1847 Closed Entry-Level Biotechnology & Life Science Job Postings
This list includes jobs asking for Associates, Bachelors or Masters degrees and is available in three formats: chronological, alphabetical and geographical. We also keep records of all the old jobs we have posted that are no longer open: Entry-level History
| Job Information | Description | Date Added | |
| 1 | Eurofins Columbia, MO Associate Scientist, Biotech MS in biological sciences or engineering Exp: 0-2 years |
Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biotech team located in Columbia, Missouri. The Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. | 10/26/2019 |
| 2 | Biotechne Newark, CA Research Associate, Probe Design BS in biological sciences Exp: 0-2 years |
We are seeking a Research Associate Scientist to join the R&D probe design team. The candidate will be responsible for ordering probes for synthesis and updating probe databases as well as other supportive functions. Prepare and send probe sequences to vendors for oligo synthesis. Communicate with internal stakeholders (Sales, Operations, etc) promptly. Prepare various files and upload to internal databases | 10/26/2019 |
| 3 | Fate Therapuetics San Diego, CA Research Associate, Cancer Immunotherapy BS in biological sciences Exp: 0-3 years in lab setting |
The candidate’s primary responsibility will be to generate lentivirus for editing and production of CAR-T cells in support of research efforts at Fate. Experience with current molecular biology techniques used for editing and engineering of hematopoietic cells is highly desired. The successful candidate will have excellent oral and written communication skills. | 10/27/2019 |
| 4 | Fluke Omaha, NE Sales Engineer BS/BA in engineering or technical field Exp: 0-3 years |
You will be working under the leadership of a Sr. Sales Engineer using your technical knowledge to support key sales efforts with our manufacturer representative agencies, distribution partners, and end-users and proactively set and meet stretch goals. Actively promote products and solutions and achieve sales quota by building rapport, providing training and support, and making end user calls with representative agencies and distribution account managers. Work under the direction of the Sr. Sales Engineer to drive the activities and performance of assigned representative agencies. | 10/27/2019 |
| 5 | Fluke Everette, WA Quality Engineer BS in engineering Exp: 1-3 years in quality improvement |
The Quality Engineer II will provide quality engineering and continuous improvement leadership to the operations, engineering, and quality organizations within Fluke at our headquarters in Everett, WA. They will be responsible for employing advanced quality engineering tools and the Fortive Business System tools in partnership with design and sustaining engineering, procurement, supplier quality, and operations to achieve continuous improvement in product safety, reliability and cost of quality. | 10/27/2019 |
| 6 | NorthStar Medical Radioisotopes Beloit, WI Process Laboratory Technician BS in chemistry or a related physical science Exp: 1+ years |
Responsible for routine (chemistry) laboratory support in one of NorthStar’s research and development laboratories. This individual will be responsible for maintaining the laboratory space to cGMP standards, creating and documenting standard laboratory solutions, and assisting in the maintenance and calibration of analytical measurement equipment. etc. | 10/21/2019 |
| 7 | Covance Dallas, TX Research Technician (On-call) BS, AS/AA or HS Diploma/GED Exp: AS/AA: 1 year clinical research experience, HS: 1-2 years |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Assist in the preparation of rooms and medical equipment. Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs. | 10/16/2019 |
| 8 | Covance Madison, WI Research Assistant I (Chemist) – Dose Analysis BS/BA in chemistry or related Exp: 1-2 years lab experience |
In this role, you will analyze biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. Organizes and conducts routine analyses in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. Sets up, operates and performs routine and non-routine maintenance on general equipment. | 10/16/2019 |
| 9 | Covance Dallas, TX Research Technician (On-call) BS, AS/AA, or HS Diploma Exp: BS: 0 years, AS/AA: 1 year, HS: 1-2 years |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Assist in the preparation of rooms and medical equipment. Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs. | 10/16/2019 |
| 10 | Dexcom San Diego, CA Mechanical Engineer 1 BS in technical degree Exp: 0-2 years |
As a member of the R&D Mechanical Engineering team this engineer will understand and articulate the current and future needs of our customers and our business, explore and evaluate new technologies and concepts for meeting those needs, and rapidly demonstrate feasibility of such technologies through rigorous modeling, analysis, prototyping, experimentation, and other risk identification and mitigation activities. Design, develop, fabricate, assemble and implement fixtures and equipment to quantify prototype device performance | 10/19/2019 |
| 11 | Dexcom Mesa, AZ Manufacturing Clerk 1 HS Diploma Exp: 0-2 years related |
Provides administrative and clerical support specifically related to manufacturing department activities. May be assigned to various administrative tasks within manufacturing support. Basic understanding of general job aspects and limited understanding of the detailed aspects of the job. Acquires job skills and learns the policies and procedures required to complete routine tasks. | 10/19/2019 |
| 12 | Editas Boulder , CO Research Associate, Medicinal Chemistry Group BS/BA in chemistry Exp: 1 year or more with synethtic organic chemistry |
This new role on the Medicinal Chemistry team in Boulder provides a unique opportunity to contribute to Editas’ efforts through the development of novel chemical compounds to improve CRISPR/Cas9 and CRISPR/Cpf1 performance. Design and synthesize compounds to improve the performance of ribonucleoproteins (CRISPR/Cas9 and CRISPR/Cpf1). Optimize synthetic methods for compounds of interest. | 10/20/2019 |
| 13 | Editas Cambridge, MA Research Associate I/II, In Vivo Pharmacology BS or MS in biological sciences Exp: 1-2 years lab experience |
The candidate will be responsible for conducting preclinical animal studies to support the development of gene-editing based therapies in multiple disease areas, including ophthalmology, oncology, and hematology. Perform basic molecular biology work such. Perform routine injections (sc, ip, iv) in mice, monitor animal health, collect tissue and blood samples, measure tumor volume, perform anesthesia and necropsies. | 10/20/2019 |
| 14 | Edwards Irvine, CA Engineer II, Automation & Process mS in Mechanical, Electronic, Mechanics, Mechatronics, Industrial Exp: 0-2 years in automation |
This is a great opportunity to lead and provide support in projects for the manufacturing area. This includes: automation projects for processes of new products, automation projects for cost reduction, quality, ergonomics and delivery improvements. In addition, validation and implementation of changes related to the projects. Develop moderately complex tests and experiments (including writing and execution of protocols) to qualify and validate manufacturing processes; follow up on protocol activities, train technicians; analyze results, make recommendations and develop reports. | 10/20/2019 |
| 15 | Edwards Irvine, CA Associate Analyst, Inventory BS/BA Exp: 1 year in finance/customer serivce/operation etc. |
Manage all consigned and customer owned inventories through a variety of processes and systems and provides insight to help improve and streamline current processes in collaboration with Commercial Contract, Finance, Sales, Supply Chain and Customer Operations. Perform basic analysis of field scan results (e.g., physical vs system of record inventory) for SOX Compliance through multiple systems, cross functional departments (e.g., Contracts, Sales, Finance, Quality, Implant Registry, Supply Chain, Customer Service, IT) and external partners to make recommendations to customer service for resolution. | 10/20/2019 |
| 16 | Edwards Irvine, CA Technician, R&D - Transcatheter Heart Valve HS Diploma Exp: 1+ years related experience |
Edwards Lifesciences is currently seeking a Research and Development Technician to perform a wide variety of tasks in support of Engineering activities for our Transcatheter Heart Valve Business Unit at our corporate headquarters in Irvine, CA. Perform set-up on textile and related machines involving mechanical components as well threading of fine textile yarns using mechanical tools . Support engineering activities such as test, check-out, modification, fabrication, and assembly under the close supervision of Engineers | 10/20/2019 |
| 17 | Edwards Irvine, CA CRA I, In House - Transcatheter Mitral and Tricuspid Therapies BS in related Exp: 1 year in documentation for clinical studies |
This is a unique opportunity to join an early-stage product development group, Transcatheter Mitral & Tricuspid Therapies (TMTT), focused on developing solutions for patients suffering from structural heart disease. The Clinical Research Associate I will ensure clinical trials are conducted and reported in accordance with all applicable regulatory requirements. Conduct reviews of documentation needed for internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations. | 10/20/2019 |
| 18 | Edwards Draper, UT Quality Engineer I, Quality BS or MS in engineering Exp: 0 years |
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Optimize Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk. | 10/20/2019 |
| 19 | Edwards Draper, UT Manufacturing Engineer II - Transcatheter Mitral and Tricuspid Therapies MS in engineering/sciences Exp: 0 years w/internships or senior projects |
Applies knowledge of technical principles and Edwards systems/procedures to optimize manufacturing processes. Improve manufacturing processes using engineering methods (e.g., LEAN methods, basic statistics) for continuous process improvement. Develop basic experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports. Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes. | 10/20/2019 |
| 20 | Edwards Draper, UT Supplier Quality Engineer I BS in engineering/sciences Exp: 1-2 years in medical devices |
Edwards Lifesciences has an exceptional opportunity for an Engineer I within the Supplier Quality group. This person will be responsible for supporting supplier quality vendor management, audits, and improvements while supporting continued Quality System improvements. In this position you will support activities sustaining quality engineering within Receiving Inspection, Manufacturing, and Product Verification as applied to supplier related issues. | 10/20/2019 |
| 21 | Myriad Salt Lake City, UT Process Technician MS in a chemical, physical, or biological science Exp: 6 months |
The Process Tech III supports the clinical diagnostic lab by troubleshooting process failures, identifying and participating in continuous improvement projects in conjunction with staff and Technical Development, and participating on cross-functional teams to implement new processes into operations. This position will work with department management and quality team members to ensure that appropriate root cause is identified, corrective actions are implemented and proactive process improvements are identified. As directed by management, this role may also support Reagent Manufacturing processes, provided they are maintaining ongoing competency to perform those duties. etc. | 10/15/2019 |
| 22 | ConMed Utica , NY Quality Engineer I BS in engineering (mechanical/biomedical) Exp: 0-3 years |
We are seeking a self-driven and continuous improvement-focused Quality Engineer I to join our Utica, NY based Quality Engineering team. In this role, you will work cross-functionally to support production lines for a variety of medical devices. You will execute projects aligned with CONMED's Quality System, ISO 13485 standards, risk management, test methods, calibration and product line support. Your efforts in problem solving, innovation and cross-functional collaboration will directly contribute to taking the site's safety, quality, delivery and cost metrics to the next level. | 10/12/2019 |
| 23 | ConMed Utica , NY Associate Assembler HS Diploma/GED Exp: 3+ months work experience |
As a Team Assembler I, you will perform basic packaging and shipping functions to include basic machine and equipment operation to fabricate parts for assembly and sub-assembly. | 10/12/2019 |
| 24 | Cook Medical Bloomington, IN Manufacturing Engineer BS/BA in related field Exp: No experience required |
Responsible for providing technical support for the day-today production activities in the manufacture of custom, plastic components used in the assemblies of various medical devices. This is a hands-on position with visibility on the manufacturing floor and requires a high level of interaction with the production, product development, and quality teams. The engineer is responsible for supporting product development activities, continuous improvement, complaint resolution, CAPA investigations and other quality initiatives. | 10/13/2019 |
| 25 | Cardinal Health Reno , NV Assoc I, Assembly - Shift (6am - 6pm) HS Diploma/GED Exp: 0-6 months |
Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. | 10/13/2019 |
| 26 | Cardinal Health Reno , NV Associate II, Warehouse Ops HS Diploma/GED Exp: 1-2 years |
Warehouse Operations is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers. | 10/13/2019 |
| 27 | Cardinal Health Mansfield, MA Engineer, R&D BS/BA Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. | 10/13/2019 |
| 28 | Cardinal Health Hazelwood, MO Product Development Engineer I BS/BA in mechanical/biomedical/plastics engineering Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. This position requires an individual to be responsible for supporting the development of new medical devices and improvements to existing products in the medical disposable area. These products are mechanical in nature, and our designs serve a global market. | 10/13/2019 |
| 29 | Millipore Sigma Burlington, MA Sales Support Specialist BS/BA in business, chemistry, biology, or related Exp: Recent graduate |
In this role as a Sales Support Specialist you will be required to interact with internal and external customers from quotation generation through the Purchase Order processing phase. You will perform research using a variety of different databases including MilliporeSigma’s customer history database, service management database, contract management database, installation database and financial database. All of which store inquiries and information that MilliporeSigma has received from a customer and/or prospective customer. etc. | 10/8/2019 |
| 30 | Millipore Sigma Burlington, MA Maintenance Contract Sales Rep. BS/BA in business, chemistry, biology, or related Exp: Recent graduate |
The role of Maintenance Contract Sales Representative will require the candidate to interact with internal and external customers from quotation generation through the Purchase Order processing phase. They will generate quotes for new and renewal of service agreements for current MilliporeSigma customers. Should be able to work independently to manage new and renewal service agreements within a defined geographical territory. etc. | 10/8/2019 |
| 31 | Millipore Sigma St. Louis, MO QC Logistics Technician AS in life or physical sciences Exp: Recent graduate |
You will assist in evaluating safety practices with regard to team activities. Work both independently and in team environment. Manage sample inventory and department stock room. Troubleshoot interruptions to the normal process flow. Manage Quality and Retain Samples. Use lean and six sigma practices to optimize efficiency and eliminate waste from process. Adhere to process requirements in a continuously changing environment. etc. | 10/8/2019 |
| 32 | Millipore Sigma St. Louis, MO Associate Production Scientist BS/BA in chemistry or other science Exp: 1+ years |
Manufacture products according to established protocols and perform operations to support a chemical manufacturing department located in St Louis, MO. Physical Attributes: Will be frequently required to wear appropriate personal protection equipment “PPE” (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes, etc.) for protection from toxic or corrosive chemicals in the forms of liquids, solids, and/or vapors. While performing the duties of this job, the employee is regularly required to sit, stand, walk, reach above the shoulder, stoop, kneel, or crouch. etc. | 10/8/2019 |
| 33 | Millipore Sigma St. Louis, MO Customer Care Associate High school diploma/AS Exp: 1+ years |
The Customer Care Associate position involves working in a dynamic, fast paced, high energy call center, and rewarding team environment focused on delivering a better customer experience. You will be responsible for ensuring each transaction is processed within customer specifications for MilliporeSigma guidelines. As a Customer Care Associate, you must be eager to learn, be respectful, honest & humble, and embrace challenges. etc. | 10/8/2019 |
| 34 | Millipore Sigma Burlington, MA Service Support Specialist High school diploma or equivalent Exp: 1+ years |
In this role you will establish and maintain service schedules with customers, prepare and process repair quotations and manage service inventory. In addition, you will support installation orders by insuring sites are prepared for service and support the service partners. You will create an efficient service schedule to maximize resources, ensure material is on site and accurate. Coordinate service-related activities as guided by service engineers and managers. etc. | 10/8/2019 |
| 35 | Bio-techne Minneapolis, MN QC Specialist 1 BS in biological sciences/chemistry Exp: 1-2 years in vitro diagnostics |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. Assist in establishing QC specifications. Performs analysis and interpretation of test results, identifies deviations, and makes appropriate recommendations | 10/3/2019 |
| 36 | Bio-techne San Jose, CA Production Chemist I AA or BS/BA in sciences/engineering Exp: 0-3 years in wet-lab manufacturing support |
The successful applicant will work with other members of the consumable production team as well as a multidisciplinary team of engineers and scientists to support routine production activities for reagent formulation/ compounding team. Principal duties and responsibilities: Help maintain and track supplies inventory. Preparation of buffers and other biochemical formulations. Conjugation of protein solutions. Record manufacturing tasks in batch records/travelers. | 10/3/2019 |
| 37 | Bio-techne San Marcos, CA Packaging Technician HS Diploma/GED Exp: 1-2 years in vitro diagnostics |
Perform kitting, liquid / powder filling and labeling functions. Assist in the setup and running of automated liquid filling, labeling and packaging equipment. Assist in the setup and running of manual liquid and powder portable filling equipment. Comply with Good Manufacturing Practices (GMP’s) and Quality Systems Regulations (QSR). Inspect all materials being issued to and returning from shop orders. Accurately count and return all materials. | 10/3/2019 |
| 38 | Bio-techne Minneapolis, MN Research Associate, Antibody Purification BS/BA in biological sciences/chemistry or related Exp: 0-2 years |
As an Antibody Purification Research Associate you will be responsible for performing antibody purifications and conducting in process testing of product. Purify monoclonal and polyclonal antibodies following appropriate SOP’s. Prepare buffers as needed for the purification process. Document the purification processes in the appropriate computer systems. Perform routine HPLC and other equipment maintenance. | 10/3/2019 |
| 39 | Bio-techne Minneapolis, MN Equipment Technician 1 HS Diploma/GED Exp: 1-2 years in equipment maintenance |
As a Equipment Technician 1 you will perform preventative maintenance and repair malfunctioning new and existing minor equipment. Respond and log supervisory alarms on TAC Monitoring System during business hours. Act as the secondary facility maintenance mechanic responsible 24/7 on call for TAC & Security System with department personnel. Assist with installing new and existing equipment, offices furniture and shelves. Perform additional duties as assigned. | 10/3/2019 |
| 40 | bluebird bio Cambridge, MA Cellular Process Development & Gene Editing Specialist BS in biological sciences Exp: 0-2 years |
The cellular process development teams are responsible for developing cellular drug product processes and introducing new technologies for stem cell and T-cell therapies. The focus of this position is to contribute to the development of next generation manufacturing processes for cell therapies. We are looking for a motivated associate scientist to drive development and characterization projects. | 10/3/2019 |
| 41 | Bausche Health Lynchburg, VA Distribution Associate I HS Diploma/GED Exp: 6 months or more |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 9/25/2019 |
| 42 | Bayer Creve Coeur, MO Software Developer-Entry BS in computer sciences Exp: Entry Level |
The primary responsibilities of this role, Software Developer, are to: Collaborate daily with a team of Software Developers, Product Manager, Product Specialists, and Agile Coach to build and support applications; Work with team and Product Manager to manage project priorities, deadlines and deliverables; Interact directly with business customers to gather and understand requirements and how they translate in application features; | 9/25/2019 |
| 43 | Bayer Woodland, CA Lab Tech II BS/BA in science-related field Exp: 1+ years in lab setting |
The primary responsibilities of this role, Lab Technician II, are to: Under the direction of Lab Operations Managers and/or Lab Coordinators complete the testing processes ensuring process control, accurate data management, timely escalation of problem solving, and error correction; Ability to learn and apply scientific methods and non-routine techniques for analysis as directed by protocols and work instructions to deliver quality results - which may include preparation of reagents, media, controls and sample preparation | 9/25/2019 |
| 44 | Bayer Indianola, PA Engineer Quality BS in engineering Exp: Entry Level |
The primary responsibilities of this role, Engineer Quality, are to: Provide focused quality engineering support to develop, support and maintain quality engineering methodologies that meets Customer, Regulatory and Bayer requirements; Lead the Material Review Board cross-functional team to investigate and address all manufacturing non-conformances; Lead and support investigations by conducting problem solving and root cause analysis to address failures identified by customer complaints, internal non-conformances and manufacturing yields. | 9/25/2019 |
| 45 | Bayer St. Louis , MO Research Associate MS in plant biology or related Exp: 0-1 year working experience |
Responsible for carrying out routine and discovery experiments in partnership with scientists. Responsible for generating highest quality research data and performing validation experiments; Responsible for organizing and recording experiment notes/best practice documents in a timely fashion to secure the company’s IP and FTO; Manage best practice documents training of new members and help onboard new team members | 9/25/2019 |
| 46 | BioAssay Systems Hayward, CA SALES ASSOCIATE HS Diploma/GED Exp: No experience required |
The Sales Associate will be responsible for processing orders, preparing shipping documents, and keeping detail records. The individual will have to communicate with our customers by phone, fax and e-mail. The position will also involve packaging products for shipment. | 9/28/2019 |
| 47 | BioAssay Systems Hayward, CA RESEARCH ASSOCIATE - MANUFACTURING BS/BA in chemistry/biology or related Exp: 1-2 years lab experience preferred |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing and packaging the finished products. This candidate may also join part time in our R&D team. | 9/28/2019 |
| 48 | BioAssay Systems Hayward, CA RESEARCH ASSOCIATE - ASSAY DEVELOPMENT BS/BA in chemistry/biology or related Exp: 1-2 years lab experience preferred |
We are currently looking for an enthusiastic research associate to join our R&D team. This position will entail developing novel assays kits and performing service projects. This candidate may also be involved in manufacturing or providing technical support to customers. | 9/28/2019 |
| 49 | Bio-Rad Dalas, TX Field Service Engineer I BS in electronics/engineering Exp: 1 year |
Provide customer site service on all LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. Act as customer advocate to ensure satisfaction and repeat business. Maintains company assets including parts inventory and leased vehicle. Administrative duties include service documentation consistent with FDA regulations. Other duties include accurate expense reporting and timekeeping.Must maintain learning plan in training database and regular product update training. Travel is required. | 9/29/2019 |
| 50 | Bio-Rad San Diego or Los Angeles, CA Proteomics Sales Specialist I BS/BA Exp: 1-3 years sales experience |
Develop and Execute a Territory Sales Plan. Promote and Sell the Bio-Rad Proteomics Portfolio to Achieve the Territory Sales Goals. Build, Manage and Grow Sales Opportunity Funnel. Utilize Various Bio-Rad Departments (Technical Support, Customer Care, Marketing and other Bio-Rad Personnel) In Order to Ensure Complete Customer Satisfaction. Proactively Communicate with Regional Manager on Activities, Market Trends, Opportunities and Forecast. | 9/29/2019 |
| 51 | Mammoth Biosciences San Francisco, CA Research Associate BS/MS in biology, chemistry, or related Exp: 1+ years |
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to support our research and product development teams. The ideal candidate will have experience with in vitro assay development, nucleic acid extraction and amplification techniques. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. etc. | 9/24/2019 |
| 52 | Merck Millsboro, DW Technician, Animal Care HS diploma/AS in relevant field Exp: 1+ years |
An Animal Care Technician is responsible for the care and husbandry of animals. Technicians will work with a variety animal species. At all times, technicians must follow Standard Operating Procedures, adhere to all safety and company policies and perform duties assigned by department supervision. etc. | 9/24/2019 |
| 53 | Merck Millsboro, DW Senior Technician, Operations BS in a biological life science Exp: None needed for BS candidate |
Objective of position: At all times technician must follow GMP and SOP and adhere to all safety and company policies while performing more advanced laboratory services in various manufacturing areas. Job Summary: Position Description: Sr. Tech is multi-skilled within own product/department and develops skills in multiple products/departments. Multi-skilled within own product/department. etc. | 9/24/2019 |
| 54 | Merieux NutriSciences Stone Mountain, GA Microbiology Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 55 | Merieux NutriSciences Gainesville, FL Chemistry Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 56 | Merieux NutriSciences Columbus, Oh Lab Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 57 | Merieux NutriSciences Crete, IL Chemist I unspecified Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food sample. The incumbent analyzes the concentration of certain components in food sample. The incumbent must accurately prepare and process the sample to obtain the needed results. etc. | 9/24/2019 |
| 58 | Merieux NutriSciences Allentown, PA Receiving Tech unspecified Exp: Entry level |
Mérieux NutriSciences is a leader in food science and testing technology. With over 6,000 employees working in 80 labs in 21 countries, our team will stop at nothing to make sure consumers around the world are protected from foodborne illness and pathogens. Each member of our team plays a critical role in our mission. We are currently seeking a Lab Assistant to provide assistance to our technicians and scientists. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 59 | Arsenal Medical Boston, MA Chemical Engineer/Materials Scientist I BS in chemical engineering/chemistry or related Exp: 0-3 years |
We have an opening for a recent graduate with experience in chemical engineering or polymer and material science to join our team. This position will be hands-on, laboratory based, and will support projects developing novel in-situ forming medical devices. Duties include: Collaborate closely with a multi-disciplinary team of scientists and engineers to develop chemical formulations. Identify, develop, and perform characterization bench test methods enabling material and formulation evaluation. Properly document experimental procedures, designs, and results in a laboratory notebook, conduct data analysis, and present experimental data in meetings | 9/22/2019 |
| 60 | Myriad Genetics Salt Lake City, UT Training Specialist BS/BA in engineering or related Exp: 0-3 years |
The Training Specialist I, Prod-Ops Support administers the training program, ensuring that employee training needs are defined and met. This position works with Training Power Users and end users to ensure that job appropriate training is available and completed. Maintain training that meets all departmental needs and follows regulatory requirements for training and competency. Develop training materials for lab processes. Create a variety of training programs including e-training, computer-based, lecture, and other training formats. | 9/22/2019 |
| 61 | Myriad Genetics South San Francisco, CA Manufacturing Associate BS in biological sciences/molecular biology Exp: 0-2 years in cGMP molecular biology |
The Manufacturing Associate is responsible for following established protocols to regularly manufacture reagents for use in the production laboratory, as well as assist in implementing upgrades to improve the quality and efficiency of manufacturing protocols and processes. They will also create, edit, and review SOPs, train junior staff, and play a key role in process scaling efforts. | 9/22/2019 |
| 62 | AstraZeneca Frederick, MD Quality Control Analyst - Operations BS/BA in sciences/biotech/pharma Exp: 0-5 years |
Performs selected quality control testing activities, dependent upon assigned area, including the following: Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. Supports preparation of validation protocols, executes experiments, and provides data for validation reports. | 9/22/2019 |
| 63 | Axsome New York, NY Clinical Trials Assistant BS in biological/physical sciences Exp: 1 year in clinical department |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. | 9/22/2019 |
| 64 | Acelity South Burlington, VT Field Servive Representative I HS diploma or equivalent Exp: 1 year |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitization and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. In addition to preparation and provision of medical equipment, employees in this function are required to learn and operate within the company defined policies and procedures to maintain compliance with the regulated requirements for medical devices. Additional responsibilities include maintenance of a safe and clean service center working environment and company vehicles. etc. | 9/17/2019 |
| 65 | Acelity Cinnaminson, NJ Field Servive Representative I HS diploma or equivalent Exp: 1 year |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitization and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. In addition to preparation and provision of medical equipment, employees in this function are required to learn and operate within the company defined policies and procedures to maintain compliance with the regulated requirements for medical devices. etc. | 9/17/2019 |
| 66 | Acelity Arlington, TX Field Servive Representative I HS diploma or equivalent Exp: 1 year |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitation and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. In addition to preparation and provision of medical equipment, employees in this function are required to learn and operate within the company defined policies and procedures to maintain compliance with the regulated requirements for medical devices. etc. | 9/17/2019 |
| 67 | AGC Biologics Bothell, WA Development Associate I-II AA/BS in life science or engineering Exp: 0-2 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. etc. | 9/17/2019 |
| 68 | AGC Biologics Bothell, WA Downstream Manufacturing Associate HS diploma to BA/BS Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. etc. | 9/17/2019 |
| 69 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/17/2019 |
| 70 | AGC Biologics Bothell, WA Manufacturing Associate III - Upstream BS in chemistry, biology, or related Exp: 1-4 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Executes bioprocess operations successfully primarily in Cell Culture/Upstream manufacturing. CIP/SIP/PT operations: cleaning, assembly, sterilization, disassembly, pressure test and operation of primary process equipment. Unit operations described in standard operating procedures and batch records (50%-100% of effort). Recommends and executes projects and changes to bioprocess operations to reduce risk and increase efficiency. etc. | 9/17/2019 |
| 71 | AGC Biologics Bothell, WA Manufacturing Support Technician HS diploma or equivalent Exp: 0-6 years |
We are seeking an experienced and highly motivated Manufacturing Support Technician to join our expanding Manufacturing team. PRINCIPAL RESPONSIBILITIES: Support product process unit operations described in standard operating procedures and batch records (100% of effort). Anticipates and minimizes deviations from support procedures. Stocking of supplies and gowning materials in GMP clean room areas. Weigh and dispensing of chemicals and processing materials. etc. | 9/17/2019 |
| 72 | Alcami St. Louis, MO Microbiology Analyst BS/BA in biology/microbiology Exp: 1-5 years |
The Microbiology Analyst is accountable for driving results in a fast-paced environment by accurately and efficiently performing sample analysis, monitoring microbial cultures and identifying microbiological contaminants and pathogens using a variety of identification methods. | 9/12/2019 |
| 73 | Alcami Charleston, SC Manufacturing Tech I HS Diploma/GED Exp: 0-1 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). | 9/12/2019 |
| 74 | Alkermes Wilmington, OH QC Analyst I BS in chemistry Exp: 0-2 years |
The position requires the individual to perform routine/non-routine physical, chemical, and in-vitro assays of clinical, commercial, process and cleaning validation samples, and process development samples to support Manufacturing. Performs physical and/or chemical analyses of product to ensure stability. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. | 9/12/2019 |
| 75 | Alkermes Wilmington, OH QA Associate I BS/BA in sciences Exp: 1-2 years in QA |
The Quality Assurance Associate will be responsible for performing functions including daily on the floor activities related to sterile manufacturing operations, on the floor batch record review, executed validation review, discrepancy identification, logbook review, AQL inspection of finished product, SAP transactions, room/utility walkthroughs, shutdown/incident form assessment/review and reconciliation, initiation of hold forms, training program support, and product shipping in a facility that manufactures sterile products in a GMP environment. | 9/12/2019 |
| 76 | Alkermes Waltham, MA Process Development Associate BS in engineering Exp: 0-3 years |
The process development engineer will provide technical support in the development, scale-up and optimization of pharmaceutical process at various phases ranging from R&D to Commercial manufacturing. Specific areas of focus include material processability characterization, 1st and 2nd principle modeling knowledge. The role is expected to have a strong lab presence with the ability to design and execute experiments, interpret the data to improve process understanding. To be successful candidate in this role the candidate needs a good understanding in material characterization and statistical modeling is required | 9/12/2019 |
| 77 | Antech Middletown, CT Laboratory Generalist BS in medical technology or related Exp: 0-1 years |
As a Laboratory Generalist I you will work with the Lead Laboratory Technician to ensure the lab is running efficiently to meet and/or exceed goals. The ideal candidate will have prior experience performing some clinical diagnostic testing. Must have experience in at least three clinical areas including Hematology, Chemistry, Processing, etc. Perform all required quality control per QA guidelines. Train on all areas to include Processing, Chemistry, Hematology, UA and Coag according to all SOP’s. | 9/15/2019 |
| 78 | Antech Fountain Valley, CA Histology Aide HS Diploma/GED Exp: 0-2 years |
Antech Diagnostics is looking for outstanding Laboratory Aides and Assistants for shift positions throughout our veterinary diagnostic reference lab locations. The ideal candidates will have experience working in either a reference or hospital laboratory, or have strong experience performing lab duties as a Vet Tech. The Laboratory Aide is responsible for setting up instruments, collection of samples, load samples into instruments and prepare samples for laboratory technicians. | 9/15/2019 |
| 79 | Antech Fountain Valley, CA QA Specialist BS in medical technology or related Exp: 1 year in clinical lab |
Our QA Specialists are responsible for ensuring consistent quality of diagnostic testing, assist with validation of methods/assays, perform QA surveys and maintain good documentation and excellent lab/business practices. You will be responsible for all quality assurance and quality control functions relating to diagnostics testing, lab safety, analytical and instrumentation. You will ensure consistent quality of diagnostics testing, assist with validation of methods/assays, perform QA surveys and maintain good documentation and excellent lab/business practices. | 9/15/2019 |
| 80 | Applied Meidcal Rancho Santa Margarita, CA Production Associate (Assembler/Machine Operator) HS Diploma/GED Exp: 1-2 years work experience |
As a Production Associate, you will be responsible for working within the framework of a team in a cleanroom or manufacturing environment, and performing the following activities: Perform all manufacturing operations in a cleanroom or non-cleanroom environment such as assembly, inspection, and machine operations. Comply with Applied Medical Quality Systems (QS) including SOPs, MIs, QIs and TMs. Perform manufacturing operations efficiently with or without tools and/or equipment | 9/15/2019 |
| 81 | Absorption Systems Exton, PA Associate Scientist - Drug Transport & Metabolism BS/BA or MS in related Exp: BS: 1-3 years, MS: 0-2 years |
Absorption Systems is seeking a candidate for either an Associate Scientist or Scientist position with drug transport and metabolism experience at the headquarter location in Exton, Pennsylvania. Conduct study projects: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conduct studies on different assays, such as drug transport, metabolism and CYP induction assays | 9/6/2019 |
| 82 | Absorption Systems San Diego, CA Research Associate – Bioanalytical BS in chemistry, biochemistry, or related Exp: 0-1 years |
The Research Associate, Bioanalytical will provide bioanalytical quantitative analysis of test compounds in biological matrices obtained from a variety of studies including preclinical safety evaluations and pharmacokinetic evaluations. Focus on small molecule analysis using LC-MS/MS. The candidate will be responsible for sample preparation from biological matrices, tissue homogenization, sample extraction techniques, and data acquisition. | 9/6/2019 |
| 83 | Absorption Systems Medford, MA Research Associate – Bioanalytical BS/BA in sciences Exp: 1+ years in industry |
TheResearch Associate will work as part of a team in a lab environment to completeclient-driven projects. Primaryresponsibilities include: Perform sample analysis following established SOPs underRUO/GLP/GMP conditions, Assist in the development and validation of new assays., General laboratory tasks including buffer preparation, samplelogging and handing, shipping samples to or for clients, equipment maintenance,lab maintenance, and ordering supplies | 9/6/2019 |
| 84 | KCI Dillon, CO Appeals Specialist I HS Diploma/GED Exp: 1 year work experience |
Provide lead with work progress reports on a daily, weekly, monthly basis or as required Investigate and analyze patient charts and wound progress reports, by reading documents and negotiating computer-based research To develop, for each Medicare Insurance claim denial, a reasonable patient product use detail and history; to develop and substantiate the product use evidence, and present the patient’s case to Medicare in the manner required or make appropriate adjustments Write a medically concise and issue focused Redetermination, Reconsideration, or Administrative Law Judge letter as required as it applies to Medicare policy | 9/6/2019 |
| 85 | KCI San Antonio, TX Quality Engineer I BS in mechanical/biomed/industrial engineering Exp: Entry Level |
The Quality Engineer I is responsible for conducting, and reporting on product, project and process activities related to medical device design and manufacturing as a team member. This position works with R&D and Manufacturing to develop and execute test protocols and reports. This position performs statistical analysis as required. The Quality Engineer I and works closely with R&D, Supplier Quality, Sustaining Engineering, and Manufacturing to ensure effective design transfer and successful on-going manufacturing. | 9/6/2019 |
| 86 | KCI Virginia Beach, VA Associate Territory Representative -- Medical Device Sales BS/BA Exp: 0-2 years |
The Associate Territory Representative (ATR) is the main point of contact on transition related sales activities. The role will focus on proactively generating sales revenue from transitions and coordinating with the Advantage Center on necessary paperwork relating to transition sales. The ATR will round floors on a daily basis to make sales and generate leads under the direction of the District Manager. The ATR will assist with account management activities including the setup of READYCARE and KCI Express and assist customers with invoicing, credit and collection issues, as well as conduct inventory management to recover lost assets. | 9/6/2019 |
| 87 | WCG Clinical Plymouth Meeting, PA Feasibility Specialist BS/BA in health care or scientific discipline Exp: 6 months of admin experience for projects |
The Feasibility Specialist is responsible for implementing site start-up activities during the Site Feasibility Questionnaire (SFQ) collection process. Coordinate project management activities, resources, equipment and information to support client and Company for project/service solutions. Liaise with clients to identify and define requirements and objectives. | 9/6/2019 |
| 88 | ADMA Biologics Boca Raton, FL QC Lab Support Associate l BS in biology, chemistry, medical technology Exp: 1-3 years in regulated lab setting |
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. Customer support functions for QC laboratories such as cleaning glassware and custodial services, monitoring temperature controlled chambers, shipping samples, sample preparation, administrative support. | 9/6/2019 |
| 89 | ADMA Biologics Boca Raton, FL QC Raw Materials Specialist BS or AS in chemistry/biochemistry/biology Exp: 0-3 years |
The Raw Material Specialist I will Perform quality control raw material processing and testing. Following general instructions on routine work and detailed instructions on new assignments. Perform quality control raw material processing, sampling and testing independently according to approved Standard Operating Procedures. Complete testing documentation and data entry as required for procedures and tests performed in-house and at contract labs. | 9/6/2019 |
| 90 | ADMA Biologics Boca Raton, FL Document Assistant - Temporary Some college Exp: 1-2 years |
The Document Assistant will Create, format, revise and proof read controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies. | 9/6/2019 |
| 91 | ADMA Biologics Boca Raton, FL Technician I, Manufacturing Purification BS/BA in life sciences/chemistry Exp: 0-2 years |
It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 9/6/2019 |
| 92 | Bio-Techne San Marcos, CA Chemist I, R&D BS/BA in chemistry, biochemistry, or biological sciences Exp: 1-5 years work in in vitro diagnostics/biotech |
Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. | 9/6/2019 |
| 93 | Bio-Techne Minneapolis, MN Production Assistant 1 HS Diploma/GED Exp: 0-2 years lab experience |
As a Production Assistant 1, you will be responsible for the processing of raw biological material for use in product manufacturing. You will also perform maintenance and cleaning of production equipment and containers to ensure safety and compliance, as well as completing required paperwork. | 9/6/2019 |
| 94 | Bio-Techne Minneapolis, MN Lab Assistant I HS Diploma/GED Exp: 0-2 years |
The responsibilities of this position are to perform lab support duties and tasks for multiple departments that include: collecting and washing used labware, preparing the labware for the autoclave, running the autoclave, and harvesting and concentration of cell culture media. Perform additional duties as assigned. This position requires a Tuesday through Saturday schedule. | 9/6/2019 |
| 95 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician AA degree Exp: 1+ years of lab/manufacturing experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain robotic and manufacturing equipment, Document production batch records/travelers, and computer data entry, Perform in-process QC and record results | 9/6/2019 |
| 96 | Bio-Techne Minneapolis, MN Product Receiving Associate HS Diploma/GED Exp: 0-2 years |
Product Receiving Associate is responsible for the receipt and delivery items from outside vendors, throughout the campus. These deliveries include materials that are of critical and temperature sensitive nature. Product Receiving Associates assist with maintaining and delivering items located in the company stores warehouse. This role works with PO data housed in our ERP system. This role will perform driving duties using company owned vehicles. Perform additional duties as assigned. | 9/6/2019 |
| 97 | Bio-Techne San Marcos, CA QC Specialist 1 BS/BA in biological sciences or chemistry Exp: 1-2 years in in vitro diagnostics/biotech |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. Coordinate, perform and maintain QC testing and scheduling for Stability program, Assist in establishing QC specifications, Assist in the validation testing of equipment and processes, etc. | 9/6/2019 |
| 98 | CAPS Phoenix, AZ Pharmacy Technician HS Diploma/GED Exp: 1 or more years in aseptic preperation |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities include: Prepares compounded sterile products using aseptic technique. Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. | 9/6/2019 |
| 99 | AGC Biologics Bothell, WA Manufacturing Associate I - Downstream BS in chemistry, biology, or related Exp: 1-8 years, depending on level |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/6/2019 |
| 100 | Agilent Wilmington, DE Analytical Instruments Technical Support BS/BA in chemistry or life sciences Exp: Entry Level |
As an Analytical Instruments Technical Support person, you will sit at our Agilent site in WIlmington, DE and join Agilent Technologies CrossLab Group's Online Technical Support Team. We support U.S. external customers. As an active team member, you will support customers requesting hardware, software and applications assistance with Analytical Products and Solutions and route those customers whom you can't help to the appropriate groups. Our group's organizational goal is that as part of a world-class technical support group, we provide insights to customers at their very first contact. In order to be successful, our response needs to be quick and well-informed. | 9/6/2019 |
| 101 | Agilent Wilmington, DE R&D Electrical Engineer BS or MS in electrical engineering or related Exp: Entry Level |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Most projects require mechanical, electrical and firmware engineers, as well as chemists and software engineers, to create a complete system. As part of those projects, you will also work with our marketing, manufacturing, purchasing and service organizations to transform your designs into shipping products. | 9/6/2019 |
| 102 | Agios Cambridge, MA Associate, Commercial Supply Chain BS in business/supply chain/management Exp: 1 year or more in GMP |
Agios Pharmaceuticals is searching for a dynamic Associate, Commercial Supply Chain to join our growing Supply Chain team. The selected individual will have full exposure across early clinical space to regular commercial production activities and exposure to new commercial product launches. With support from Commercial Supply Chain Management, oversee timelines for both internal activities and external production activities at Contract Manufacturing Organizations (CMOs) to ensure continuous supply of Commercial and Clinical materials through the supply chain. | 9/6/2019 |
| 103 | Ajinomoto San Diego, CA QC Logistics Assistant HS Diploma or BS/BA Exp: 0-2 years in QC |
In this role you will play a big part in keeping our sample testing processes running smoothing by managing sample submission, receipt, and shipping coordination of all incoming test articles into Quality Control. You may focus in a specialized area and provide routine analysis and testing according to standard operating procedures for in-process and finished formulations. | 9/7/2019 |
| 104 | Ajinomoto San Diego, CA QA Batch Release Assistant HS Diploma or BS/BA Exp: 0-2 years in QA |
The QA Batch Release Assistant ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. They have the ability to work independently, within prescribed guidelines, and as a team member. The Assistant promotes a cGMP environment and follows all Standard Operation Procedures (SOP’s). | 9/7/2019 |
| 105 | Ajinomoto San Diego, CA MQA Assistant HS Diploma or BS/BA Exp: 0-2 years in QA |
he MQA Assistant ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. This individual has the ability to work independently, within prescribed guidelines, and as a team member. This position promotes a cGMP environment and follows SOPs. | 9/7/2019 |
| 106 | Ajinomoto San Diego, CA Drug Substance Manufacturing Associate I - Upstream HS Diploma or BS/BA Exp: 0-2 years in upstream biologics manufacturing |
This position, under supervision, is responsible for executing the day to day responsibilities related to the Drug Substance Manufacturing Upstream group under the guidance of Aji Bio-Pharma's established procedures and policies. The position works under the guidance of experienced team members in support of the technical transfer and integration of processes into the Drug Substance Manufacturing Upstream department. The position will be exposed to fermentation, harvest, and TFF (UF/DF) systems employed during manufacturing campaigns. | 9/7/2019 |
| 107 | Ajinomoto San Diego, CA Drug Product Inspection Technician HS Diploma or BS/BA Exp: 0-2 years in lab/manufacturing |
In this role you will be responsible for performing a wide variety of product inspection and packaging tasks. You will complete training and pass qualification testing for visual inspection of various product forms, perform accurate visual inspection and handling of products following SOPs while working under cGMP regulations. | 9/7/2019 |
| 108 | Absorption Systems Exton, PA Associate Scientist / Scientist – Molecular Biology & Gene Expression – GMP BS/MS Exp: BS: 1-3 years, MS: under 2 years |
Absorption Systems, provides analytical support for gene and cell therapy products through every stage of development, is seeking a candidate for either an Associate Scientist or Scientist position with GMP experience in molecular biology and gene expression at the headquarter location in Exton, Pennsylvania. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. etc. | 9/10/2019 |
| 109 | WuXi AppTec Philadelphia, PA Laboratory Technician II Monday through Friday; Second Shift BS in biological science or related Exp: 1-2 years |
Performs Cell Culture and Cell-Based assays (BSL2 and BSL2+) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Completes batch records and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs daily work activities with minimal supervision. etc. | 9/3/2019 |
| 110 | WuXi AppTec Philadelphia, PA Laboratory Technician I BS in biological science or related Exp: 1-2 years |
Performs assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes test methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. etc. | 9/3/2019 |
| 111 | Zynex Medical Englewood, CO Patient Care Representative - Call Center HS diploma, Associate degree or higher preferred Exp: Entry level |
Essential Job Duties and Reporting Responsibilities Include the Ability to: Provide Top-Notch Customer Service. Ability to work in a fast-paced, professional office environment and follow all Company policies consistently. Answer every call as quickly as possible with extreme professionalism. Meet or exceed performance standards including but not limited to answer rate, handle time, and quality. Take back-to-back phone calls from patients nationwide. etc. | 9/3/2019 |
| 112 | Zynex Medical Englewood, CO Shipping & Warehouse Clerk HS diploma or equivalent Exp: 1-2 years |
Essential Job Duties and Responsibilities Include the Ability to: Cooperate with representatives from other departments in the organization to provide warehouse/shipping as requested. Help in shipping area to prepare shipments properly and place supplies into bags & envelopes. Monitor merchandise leaving the company warehouse, create shipping documents as needed, pull inventory from shelves for shipment, package correctly/accurately, print shipping labels, schedule pickup and ensure all shipments have proper postage. Trace and track shipments to ensure timely delivery with Endicia software. When requested, analyze shipping data to help maintain a high level of customer service. etc. | 9/3/2019 |
| 113 | Zynex Medical Englewood, CO Shipping & Warehouse Clerk HS diploma or equivalent Exp: Entry level |
Essential Job Duties and Responsibilities Include the Ability to: Prepare & package supplies materials into envelopes for outgoing shipments to patients. Labeling packages for shipments as necessary. Assist with other areas in the warehouse as necessary. $15 per hour; Weekly overtime possible. This is an entry level position. | 9/3/2019 |
| 114 | Zynex Medical Englewood, CO Billing Denial Analyst - Caseworker unspecified Exp: Entry level |
Essential Job Duties and Responsibilities Include the Ability to: Organize and analyze large volume of denials. Identify effective methods to appeal and fight individual denials and/or conduct bulk appeals. Perform code corrections and evaluate EOB’s when necessary. Obtain billing authorizations for the use of Durable Medical Equipment (DME) when needed. Negotiate the best pricing for Zynex for devices as well as supplies with adjustors/insurance reps as needed. Obtain information from clinics and physicians needed to provide to Insurance carriers for billing/coding support concerning devices, accessories, and supplies for recipients, insurance providers, physicians and the payer community. etc. | 9/3/2019 |
| 115 | Zynex Medical Englewood, CO Account Representative- Health Care Administration unspecified Exp: Entry level |
Zynex is seeking the best Account Representative in the state to join our team. For more than two decades, Zynex Medical has been a leading provider of opioid free, prescription-strength pain relief. Our products are fully developed, FDA-cleared, and commercially sold. We continually strive to achieve an important mission --to improve quality of life of patients suffering from debilitating pain or illness by providing effective drug-free pain alternatives and outstanding customer care. | 9/3/2019 |
| 116 | Waters New Castle, DE Building Maintenance Technician Vocational trade school Exp: 1-3 years |
Install or repairs a variety of building systems such as HVAC, compressed air systems and plumbing systems. Will install venting, plumbing and wiring required to support the production and/or development process. Performs skilled trades work, such as carpentry or painting in the construction, repair or alteration of structures such as walls, roofs or office fixtures; uses hand and power tools as directed. Makes periodic or special inspections of the premises to determine repair work necessary; performs routine repairs and maintenance to the facility. Works from blueprints, drawings or rough sketches. Produces rough sketches of projects and assists with the development of cost estimates. etc. | 8/27/2019 |
| 117 | Waters Golden, CO Chemistry Technician I BS/BA in chemistry or related Exp: 1-2 years |
ERA, A Waters Company, has an immediate opening for a full-time Chemistry Technician within it's Process Waters Consumables Product Line. PWC team produces TOC calibration and Quality Control standards, Conductivity and Turbidity standards, and other similar products. Responsibilities: Manufacturing, analytical verification, packaging, and labeling of all PWC products. Documentation of production and packaging. Creation of product labels and Certificates of Analysis. Inventory control of PWC products. etc. | 8/27/2019 |
| 118 | Waters Milford, MA Software Engineer II BS in information systems, computer science, engineering, or related Exp: 1 year |
Responsible for software development, automation, and implementation within an Agile Framework. Developnew features for established product lines using C++ along with the necessary test automation using SpecFlow. Generate Root Cause Analysis to acknowledge and assess new improvementopportunities. Set and follow priorities in collaboration with PO and the immediate Agile team. Participate in regular code reviews. Eligible for Employee Referral Program. | 8/27/2019 |
| 119 | Waters New Castle, DE Front-End Web Developer BS/BA in information sciences, graphic design, or related field Exp: 1-3 years |
TA Instruments is seeking a Digital & UI/UX Designer to join in our growing Marketing team. Typical tasks of the position include, but are not limited to: Design, implement, test, and deploy innovative new features and functionality for corporate websites and other digital media to provide an outstanding user experience. Participate in cross functional teams to conceptualize and create new digital media that drives revenue. Research emerging technologies and trends in digital and web design that fit, support, and accelerate our goals. etc. | 8/27/2019 |
| 120 | Waters Golden, CO Chemistry Technician BS/AS in chemistry or applied science Exp: 1+ years |
Waters/ERA in Golden Colorado, is currently leading a search for a Chemistry Technician to join our company. In this role, the individual will help manufacture and package products assigned to the Waters Analytical Standards & Reagents Team. This position will work daily to meet production requirements and delivery schedules of high quality products. Responsibilities - Production: Production/manufacturing of chemical solutions to specifications – may include some analytical verification. etc. | 8/27/2019 |
| 121 | WCCT Cypress, CA Research Laboratory Technician HS diploma or equivalent Exp: 1 year |
The Research Laboratory Technician assists with the biological sampling procedures required of each clinical trial and dictates tasks to Laboratory Assistants conducting the sampling activities related to each study. This position is responsible for assisting with the coordination of the preparation, collection, documentation, processing, inventory and shipment of biological specimens for clinical trials and reports to the Laboratory Supervisor. etc. | 8/27/2019 |
| 122 | WuXi AppTec Marietta, GA Associate Laboratory Technician AS/BS Exp: 1 year |
Responsibilities: Levels 1 – 4 testing with proficiency. Prep carts. Performs QA / QC checklist tasks. Perform incubator checks, contract review, assist with releases. Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required. Normally receives minimal instructions on routine work and detailed instructions on new assignments. etc. | 8/27/2019 |
| 123 | WuXi AppTec Austin, TX Clinical Project Associate HS diploma/AS Exp: 1 year |
The Clinical Project Associate I provides administrative support to clinical research projects by assisting project teams in the completion of assigned project activities. This is an in-office position with that does not require travel. Essential Job Functions: Provides operational support for Clinical Operations. Under direct supervision prepares, reviews and distributes the regulatory documentation according to Essential Regulatory Document Guidelines and Trial Master File (TMF) Plan. Under direct supervision prepares the investigator regulatory binders and other study start-up materials, following established procedures. etc. | 8/27/2019 |
| 124 | WuXi AppTec Philadelphia, PA Associate Metrology Technician AS in a technical discipline Exp: 1 year |
Calibrates instrumentation & equipment, and documents the results consistent with all applicable quality standards according to schedule. Perform preventative maintenance, troubleshooting, and repair on instrumentation and equipment when scheduled or required. Responsibilities: Ensures that all equipment is properly calibrated and qualified according to appropriate Good Manufacturing. Practices (cGMP) and/or Good Laboratory Practices (GLP) guidelines. Provides consistent cGMP & GLP documentation practices. Communicates with supervisor and other colleagues as required. Monitors contractors for calibrations, validations, and repairs as required. etc. | 8/27/2019 |
| 125 | WuXi AppTec Philadelphia, PA Laboratory Technician I BS in biological sciences or related Exp: 0-1 years |
Performs basic protein based assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes Test Methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs additional Research & Development activities as assigned by Management. etc. | 8/27/2019 |
| 126 | WuXi AppTec Philadelphia, PA Laboratory Technician II BS in biological sciences or related Exp: 1-2 years |
Performs assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes test methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. etc. | 8/27/2019 |
| 127 | WuXi AppTec Philadelphia, PA Laboratory Technician I BS in biological sciences or related Exp: 1-2 years |
Performs assays according to testing records and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under supervision, completes test methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. etc. | 8/27/2019 |
| 128 | Xbiotech Austin, TX Cell Culture Research Associate BS/MS in cell biology, biotechnology or related Exp: 1+ years |
We are seeking a highly motivated cell culture research associate to join our Cell Line Development group in the Research and Development Department. The successful candidate will be responsible for developing and culturing CHO cell lines and will work closely with other Research and Development teams to create breakthrough antibody therapies to treat infectious diseases. etc. | 8/27/2019 |
| 129 | TRC Columbia, SC Product Formulation Technician HS Diploma/GED Exp: 0-2 years in lab |
The Product Formulation Technician is responsible for operating compounding equipment and may be required to work in both the Commercial formulation area, as well as, the Development formulation area. Responsibilities also include following necessary methods and procedures to produce a functional compounding process. The Product Formulation Technician ensures that documentation and activities in the compounding area are compliant with any applicable regulations | 8/24/2019 |
| 130 | Endologix Santa Rosa, CA Manufacturing Engineer (Temporary) MS in engineering or sciences Exp: 1 year |
Maintain existing manufacturing processes and equipment to support output goals and product quality requirements through line support, dispositioning non-conforming material, and driving investigation and completion of CAPA. Evaluate, prioritize, and improve manufacturing processes to achieve cost of goods sold, product quality and cycle time targets. Collaborate with R&D, Quality Engineering and manufacturing team members to implement improvements. Help to design and develop manufacturing processes and tooling for new products from process conception through qualification. Collaborate with the R&D organization to help facilitate the successful execution of the New Product Development Process and launching products. | 8/24/2019 |
| 131 | Trucode Gene Repair South San Francisco, CA Associate Scientist, Chemistry MS in chemistry Exp: 1-2 years |
We seek a highly skilled, motivated and creative chemist ready to function in a fast-paced and collaborative environment. Candidates should have exceptional solid phase peptide synthesis and/or HPLC analysis and purifications training. Successfully prepare, purify and characterize peptide nucleic acid oligomers and conjugates via solution and solid phase methodologies. Maintain the team's peptide synthesizers, HPLCs and automated synthesis workflow. | 8/24/2019 |
| 132 | Tunnell na, PA Tech Transfer Specialist - Upstream Process MS Exp: 1+ years |
The Vaccine Process Development and Commercialization group within our client's manufacturing division focuses on late stage process development, technology transfer, and support of established vaccine products. Our client is seeking an energetic, people-oriented professional with strong scientific and technical skills to execute the tech transfer activities of multiple vaccine programs with a focus on upstream manufacturing process ( Drug Substance ). | 8/24/2019 |
| 133 | Express Scripts Byfield, MA Data Entry Pharmacy Technician HS Diploma/GED Exp: 6 months as pharma tech |
The Front End Pharmacy Tech is responsible for performing activities under close supervision that support pharmacy management operations in the administration of pharmacy benefit for lines of business. Typically a certified pharmacy technician | 8/25/2019 |
| 134 | Express Scripts North Burlington, NJ Warehouse Assistant HS Diploma/GED Exp: 0-1 years |
The Warehouse Assistant is responsible for performing tasks related to receiving product, stocking and replenishment, and inventory control. This includes safely unloading trucks and unpacking received product, comparing the purchase order to the product received for accuracy, counting quantities of product received and ensuring the quality of the product is at an acceptable level, and removing damaged or non-conforming product using data entry and retrieval devices to record receipt transaction (using scanners and computer input). In addition, this position safely transfers material from receiving area to warehouse or dispensing locations and ensures proper stock rotation—utilizing PDAs to update the inventory system. | 8/25/2019 |
| 135 | Vanda Pharmaceuticals West Palm Beach, FL Associate Neuroscience Specialty Sales Representative BS/BA in life sciences or business Exp: New graduate |
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. | 8/25/2019 |
| 136 | Vanda Pharmaceuticals Dallas East, TX Associate Neuroscience Specialty Sales Representative BS/BA in life sciences or business Exp: New graduate |
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. | 8/25/2019 |
| 137 | Vanda Pharmaceuticals Baton Rouge, LA Associate Neuroscience Specialty Sales Representative BS/BA in life sciences or business Exp: New graduate |
As an Associate Neuroscience Specialty Representative, you will be responsible for: Becoming knowledgeable of disease state, product and competitive market knowledge. Educating Healthcare providers on Vanda's product portfolio. Developing relationships with Healthcare providers in order to understand their needs. | 8/25/2019 |
| 138 | Siemens Richland, MS Manufacturing Engineer - Entry Level BS in electrical or mechnical engineering Exp: 0-2 years |
The candidate will get rotated through all the departments in the plant and once that has been completed you will be assign to the department that best fits the needs of the plant and is a fit for your background. Potential experiences include product design, customer order engineering, application engineering, quality engineering and manufacturing engineering. | 8/16/2019 |
| 139 | Siemens Richland, MS Quality Engineer - Will Consider Entry Level BS in Electrical, Mechanical, or Industrial Engineering Exp: Entry Level |
This position is in the Quality Department in Richland, MS reporting to the Quality Manager. The position is accountable for ensuring product/process integrity for high voltage circuit breakers through the development and implementation of systems that support internal processes such as the nonconformance system, final or in-process inspections, root cause analysis, 8D corrective actions, and other QC related activities. | 8/16/2019 |
| 140 | Siemens Ames, IA Software Engineer BS in Engineering, Math, Computer Science Exp: 1+ years in C++ |
Software Engineer needed to join the Teamcenter Visualization development team, with most team members located in Ames, Iowa. Design, develop, maintain and test software programming for Siemens PLM products with focus on achieving high quality and on time delivery of the software solution. Ensure the overall functional quality of the released product on all required platforms. | 8/16/2019 |
| 141 | Siemens Enid, OK Service Technician HS Diploma/GED Exp: 0.5-1 year or more as wind technician |
The Field Service Technician performs planned and unplanned maintenance including troubleshooting and replacement of parts if necessary in a safe and professional manner on Wind Turbines. Detailed records and parts used must be completed for all work performed. Technicians report to site management and communicate needs and or safety issues that arise. Perform first class work on preventive maintenances to be completed on time and right the first time. | 8/16/2019 |
| 142 | Siemens Richland, MS Engineering Management Acceleration Program BS in mechnical, aerospace, chemical, or electrical engineering Exp: New Graduate, 3.2 or higher GPA |
The Engineering Management Acceleration Program (EMAP) is a five-year development opportunity for entry-level candidates with potential for rapid advancement in the Siemens Oil & Gas business. EMAP prepares you to become a future leader of Siemens Oil & Gas by providing unique work experience, training, and mentorship. Jump start your career today! | 8/16/2019 |
| 143 | Sprint Cleveland, OH Quality Assurance Specialist BS in engineering, science or related Exp: 1-2 years in med devices |
Works with the Quality Assurance team in the processing of product complaints, including coordination of product returns. Assists with supplier approval and monitoring. Initiates and conducts CAPA (Corrective and Preventative Action) activities. Supports audits and FDA inspections. | 8/17/2019 |
| 144 | Sun Pharma Billerica, MA QC Microbiologist I BS in biology/microbiology Exp: 1+ year working in lab |
The QC Microbiologist performs GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology. Record GMP data, monitors and evaluates QC systems and equipment. Interact with internal and external auditors including government agencies and contract manufacturing representatives. | 8/19/2019 |
| 145 | Synthego Redwood City, CA Research Associate - Pre Clinical BS in biological sciences Exp: 1 or more year in bio lab |
Research Assistant - Pre-clinical will be trained to provide technical support to the senior scientist on a defined project from conception to proof-of-concept in vitro and in vivo. Process leukopacks and bone marrow to isolate primary cell culture (ie - stem cells and T cells) depending on the project. Maintain and expand primary cells. Test conditions to optimize gene editing of specific cell type | 8/19/2019 |
| 146 | Synthego Redwood City, CA Laboratory Associate, CRISPRevolution AA in chemistry/biotechnology Exp: 1-3 years in industry |
As a Lab Associate at Synthego, you will join our growing operations team and have direct responsibility for the synthesis and purification of our gRNA products. This role requires a strong attention to detail, a desire to learn and adapt to new processes, and familiarity with safe laboratory practices. This role will combine hands-on laboratory protocols with advanced automation to ensure the timely delivery of high quality products to our customers. | 8/19/2019 |
| 147 | Alexion Bogart, GA PPU Technician HS Diploma/GED Exp: 1+ years with lab animals |
The Protein Production Unit Technician (PPU Technician) will provide daily care and health monitoring of animals; follow standard operating procedures and good documentation practices; organize, clean, and maintain production rooms, supplies, and equipment for egg layers. The PPU Technician will support the production facility by working shifts, weekends, and holidays as needed. | 8/19/2019 |
| 148 | Takeda Round Lake, IL Production Associate AA/AS Exp: 0-2 years manufacturing |
The Production Associate (PA) is responsible for executing all processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, responsible for the hands-on execution of all activities in the production area | 8/19/2019 |
| 149 | Takeda Round Lake, IL Production Associate AA/AS Exp: 0-2 years manufacturing |
The Production Associate (“PA”) is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. The PA is expected to fully participate in both departmental projects and any quality working teams which may be applicable. Under the general direction of the lead technician and the overall direction of the supervisor, this position is responsible for the hands-on execution of all activities in the production area. | 8/19/2019 |
| 150 | Takeda Social Circle, GA Lab Technician BS/BA in biomedical discipline Exp: 1 or more year lab experience |
The Lab Testing Technician is responsible for performing testing in accordance with established Standard Operating Procedures (SOPs), applicable sections of the Code of Federal Regulations (CFRs), with emphasis on Good Manufacturing Practices (GMPs), the Clinical Laboratory Improvement Act of 1988 (CLIA), and applicable Takeda and BioLife policies, procedures and quality initiatives. Perform only high and moderate complexity tests for which certification has been authorized by the laboratory director or designee and deemed commensurate with their education, training, and technical abilities. | 8/19/2019 |
| 151 | Veeva Pleasanton, CA Associate Technical Writer BA in English, communications or similar Exp: 0-2 years |
Vault Clinical Data Management Systems (CDMS) is looking for an excellent technical writer who can write high-quality, usable documentation that enables our customers to use our applications successfully. If you enjoy solving puzzles and presenting complex, technical information into comprehensive, well-organized, and easy-to-understand documentation, this is the job for you! The Associate Technical Writer is expected to be located in headquarters at our Pleasanton office. This position is not available remote. | 8/19/2019 |
| 152 | Verge Genomics South San Francisco, CA In Vivo Research Associate BS in biology, neuroscience, or related Exp: 1+ years |
Do you want to be a part of a dynamic group that tests and validates novel compounds in preclinical model systems? In this position, you will support our entire in vivo team by performing efficacy, PK, and other experiments. In addition to rodent work, part of this position will require coordinating and managing samples at contract research organizations (CROs). In our newly-built South SF laboratory, you will help our in vivo team discover novel targets in neurodegenerative diseases. We are looking for detail-oriented and self-motivated individuals who are looking to make a difference in patients’ lives. etc. | 8/19/2019 |
| 153 | ViaCord (PerkinElmer) Waltham, MA Associate Scientific Services Specialist, Lab Technician AS in life sciences Exp: 1-2 years |
The candidate will conduct laboratory maintenance procedures in compliance with established protocols and in compliance with regulatory and laboratory requirements. He or she will work closely with other functional teams, providing critical lab support within the cell culture laboratory environment. Maintains suite equipment including, but not limited to: incubators, water baths, and biosafety cabinets. Monitors incubator temperature, CO2 and humidity. Responsible for the cleaning, sterilization and equipment functionality. Collaborate with Scientific Service and Asset Management teams on-site to coordinate any service-related issues. Maintains logs and accurate record keeping of worked performed. Develops and innovates continuous improvement, may collaborate with PerkinElmer technology services to implement new solutions. | 8/19/2019 |
| 154 | ViaCord (PerkinElmer) Austin, TX Associate Scientist BS/BA in relevant life sciences Exp: 1+ years |
Perform lab experiments as planned and document all observations and findings. Prepare hybridization capture NGS libraries and amplicon panel NGS libraries. Analyze and interpret data. Present experimental findings and interpretations to senior research team members. Demonstrate potential for technical proficiency and ability to collaborate with others. Participate with other R&D team members in troubleshooting and identifying new opportunities for optimization, applications, or products. | 8/19/2019 |
| 155 | ViaCord (PerkinElmer) Austin, TX Associate Scientist BS/BA in relevant life sciences Exp: 1+ years |
Perform lab experiments as planned and document all observations and findings. Prepare hybridization capture NGS libraries and amplicon panel NGS libraries. Analyze and interpret data. Present experimental findings and interpretations to senior research team members. Demonstrate potential for technical proficiency and ability to collaborate with others. Participate with other R&D team members in troubleshooting and identifying new opportunities for optimization, applications, or products. | 8/19/2019 |
| 156 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Employee Responsibilities: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. Accept or reject test results in accordance with standard operating procedures. etc. | 8/19/2019 |
| 157 | Viracor Lee's Summit, MO Laboratory Data Entry Quality Control Review I HS diploma or equivalent Exp: 1 year |
The Laboratory Data Entry QC Review associate is primarily responsible for the review and audit of order entry information and performing duties with a high degree of proficiency. Employee Responsibilities: Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other test ordering systems. Ability to prioritize and organize efficient work flow, demonstrating excellent time management skills. Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices. Make appropriate internal or external contact to resolve patient demographic issues or discrepancies. Complete correction requests as needed in a timely manner. etc. | 8/19/2019 |
| 158 | Viracor Lee's Summit, MO Laboratory Specimen Processor I HS diploma or equivalent Exp: 1 year |
This is a Full Time position. Schedule is Monday - Friday, 11:00 P.M. – 7:30 A.M., with overtime as needed. Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, stability, volume, etc.). Label samples for delivery to proper area(s). Use and maintain applicable sample storage materials (i.e. dry ice). Make appropriate internal or external contact to resolve patient demographic issues or discrepancies. Complete correction requests as needed. Adhere to all Data Management policies and protocols. etc. | 8/19/2019 |
| 159 | , Exp: |
||
| 160 | Trucode Gene Repair South San Franscisco, CA Associate Scientist MS Exp: 1-2 years |
Trucode Gene Repair Inc. is a stealth-mode therapeutics development company pioneering a novel synthetic gene editing technology to treat and cure patients with devastating rare diseases. We seek a highly skilled, motivated and creative chemist ready to function in a fast-paced and collaborative environment. Candidates should have exceptional solid phase peptide synthesis and/or HPLC analysis and purifications training. The successful candidate will be part of a dynamic and rewarding work environment where the abilities to effectively communicate and function in a team environment will be essential for success. etc. | 8/13/2019 |
| 161 | Tunnell King of Prussia, PA Analyst BS/BA in engineering Exp: 0-4 years |
The Systems Support Specialist – Operational Technology will provide basic technical support for manufacturing and manufacturing support systems in a regulated, validated environment. Provide first level technical support of manufacturing and manufacturing support systems including but not limited to; answering questions, resetting passwords Troubleshoot and maintain OT computers, peripheral equipment and software Work with vendor support contacts to resolve technical hardware and / or software problems, escort vendors on the premises, answer basic questions, oversee work being performed Enter, update and follow up supp+H10:H14ort requests in OT’s issue tracking system Provide first level systems training to end users Other duties as assigned | 8/13/2019 |
| 162 | United Animal Health Sheridan, IN Laboratory Assistant (Part-Time) HS diploma or experience Exp: None required |
The Lab Assistant will be responsible for processing samples, performing routine tests and assisting other laboratory staff. An ideal candidate will possess strong time management skills, have a high attention to detail and be able to effectively communicate with others in the lab. This is a part-time (20-24 hours/week) position with flexible hours within the operating hours of the Lab (Monday-Friday 8-5). etc. | 8/13/2019 |
| 163 | , Exp: |
||
| 164 | , Exp: |
||
| 165 | , Exp: |
||
| 166 | , Exp: |
||
| 167 | , Exp: |
||
| 168 | , Exp: |
||
| 169 | , Exp: |
||
| 170 | , Exp: |
||
| 171 | , Exp: |
||
| 172 | , Exp: |
||
| 173 | Purigen Biosystems Pleasanton, CA Research Associate I/II BS in molecular biology/biology/biochemistry, etc. Exp: 1-3 years in biotech |
The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes | 8/9/2019 |
| 174 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diplomga/GED Exp: 1-3 years work experience |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. | 8/9/2019 |
| 175 | Regeneron Tarrytown, NY R&D Associate, VelocImmune (VI) Next MS in molecular biology/biochemistry Exp: 0 years |
We are seeking a motivated, highly organized researcher to support our investigations of new antibody and cell-based therapies. Independently and as a team, conduct and support experiments. Investigating and develop new methodologies and technologies in molecular biology and biological therapeutics. Characterization of mice via NGS (next-generation sequencing) and flow cytometry-based phenotyping. Design, construct, and test DNA vectors, viral vectors, and cell-lines for in vitro and in vivo studies of candidate biologicals. | 8/9/2019 |
| 176 | Regeneron Tarrytown, NY R&D Associate (Immunology/Autoimmune Diseases) BS/MS Exp: 0-2 years |
We are seeking a motivated R&D associate to join the VI-Next group to support our effort in developing new in vivo disease models and testing the therapeutic potential of new candidate molecules. The new recruit will contribute to project advancement by performing in vivo work and in vitro assays such as cell culture, immunoassay and flow cytometry. | 8/9/2019 |
| 177 | Regeneron Tarrytown, NY R&D Associate -Analytical Chemistry BS in chemistry/biochemistry Exp: 0-5 years in protein mass spectrometry |
This role will primarily be involved in developing and executing state-of-the-art mass spectrometry and its related technologies for the analytical characterization (e.g., intact mass analysis and peptide mapping) of therapeutic proteins (e.g., monoclonal and bispecific antibodies) to support drug development activities at all stages (e.g., INDs, BLAs, comparability studies, stability studies, cell line development, process development, and formulation development), with a primary focus on supporting early stage drug candidate characterization and lead candidate selection. | 8/9/2019 |
| 178 | Regeneron Tarrytown, NY Associate Scientific Writer BS in life sciences Exp: 0-2 years supporting nonclinical/clinical development |
Provides support for the Preclinical Development department. Drafts and manages reviews for pharmacokinetics, toxicokinetics, clinical bioanalysis, clinical pharmacology, and CMC reports. In addition, drafts pharmacokinetics, toxicology, and CMC documents in support of IND and BLA submissions. Provides quality control review for regulatory documents in support of INDs and BLAs, as well as other written documents in support of development projects, as determined by management. | 8/9/2019 |
| 179 | Regeneron Tarrytown, NY Associate QC Analyst (Bioassay, 2nd Shift) BS/BA in life sciences Exp: 0-2 years lab experience |
Summary: Performs biological analyses in a GMP environment on products, in-process materials, raw materials and stability studies in support of the company’s quality program. Performs potency testing using cell based bioassays and binding ELISA assays. Maintains cell lines using aseptic technique and good cell culture practices. Maintains laboratory supplies. | 8/9/2019 |
| 180 | Regeneron Tarrytown, NY Cell Banking Associate BS/BA in life sciences or engineering Exp: 0-2 years cGMP experience |
Summary: Performs cGMP cell banking to support Manufacturing operations. Essential Duties and Responsibilities may include, but are not limited to, the following: Conducts scaled-down production procedures of newly prepared banks. Perfoms analysis of samples generated from lab scale studies and cell bank testing. Maintain cell banking inventory and perform vial transfers for shipment and prodcution. | 8/9/2019 |
| 181 | Philips Bothell, WA Manufacturing Engineer BS in engineering Exp: 1-3 years |
In this role, you have the opportunity to manage the manufacturing of Philips AED products. Within this role, you will have end-to-end responsibility for a production line, which included part delivery, manufacturing and test flows and packaging. You will implement and validate the changes required to meet maintain compliance with Internal documents and regulated industry requirements. | 8/10/2019 |
| 182 | Philips Carlsbad, CA Quality Engineer-CAPA BS in engineering Exp: 1 or more year with CAPA |
As the incumbent of this Quality & Regulatory (Q&R) role within Philips, your challenge will be to guide and support Business Groups, Markets and enabling functions to always do the right thing. This involves being a confident advisor on approval, regulatory compliance and quality management related topics, in order to achieve timely releases of innovative products that deliver high quality and outstanding reliability to the lives they will improve. | 8/10/2019 |
| 183 | Rocket Pharma New York, NY Laboratory Manager/Research Technician BS or MS in biological/health sciences Exp: 1-2 years |
Experienced and motivated lab manager and research technician to assist with daily operations of a dynamic gene therapy research lab and support development activities. The position involves managing day-to-day lab activities, including but not limited to purchase and organization of reagents and supplies, maintenance of lab equipment, and simple experimental and administrative support to a dedicated team of scientists. | 8/10/2019 |
| 184 | Semma Therapeutics Cambridge, MA Quality Control Associate (MA) MS/MA in sciences Exp: 1+ years |
This position will perform QC tests for pre-clinical and clinical material from specific manufacturing steps associated with ES-derived pancreatic Islets production, from cell bank thaw through fill/finish. QC testing will include stability tests for cell banks and final product, in-process manufacturing tests and final product lot release tests. The candidate will be expected to assume additional QC testing responsibilities associated with specific projects (e.g. cold chain custody qualification, in-use stability testing, etc). | 8/11/2019 |
| 185 | Semma Therapeutics Cambridge, MA Research Associate – Discovery Cell Biologist R&D BS in sciences Exp: 1-2 years lab experience |
he full-time role will focus on tissue culture, molecular and cellular characterization, and assay development. Under the supervision of a Senior Scientist the associate will be responsible for the day-to-day execution of specific projects in coordination with members of the Process Development team. | 8/11/2019 |
| 186 | Semma Therapeutics Cambridge, MA Research Associate – Cell Biologist R&D BS or MS in cell/molecular biology Exp: 1-2 years |
The full-time role will focus on tissue culture, molecular and cellular characterization, and assay development. Under the supervision of a Senior Scientist the associate will be responsible for the day-to-day execution of specific projects in coordination with members of the Discovery Biology team. | 8/11/2019 |
| 187 | Semma Therapeutics Cambridge, MA GMP Manufacturing Associate, Clinical Materials BS in biological/bioengineering sciences Exp: 0-1 years in development/manufacturing |
This full-time role reports to the Director of Manufacturing, and will be responsible for the technology transfer and production of cell therapy products to support Semma’s Phase I/II clinical trials. Clinical materials produced in the facility will be manufactured according to Good Manufacturing Practices (GMP) and conducted under Investigational New Drug (IND) applications with the US Food and Drug Administration (FDA). | 8/11/2019 |
| 188 | TechLab unspecified, VA Quality Assurance Officer 1 AS/BS/BA Exp: AS 1+ years, BA/BS none needed |
The Quality Assurance Officer 1 is responsible for ensuring that all TechLab® Inc. products meet the requirements of the quality system. This can include reviewing and tracking product as well as reviewing documentationto ensure it complies with regulatory standards. The Quality Assurance Officer 1 reports to the Quality Assurance Manager. etc. | 8/6/2019 |
| 189 | The Ritedose Corporation Columbia, SC Product Formulation Technician HS diploma or equivalent Exp: 0-2 years |
The Product Formulation Technician is responsible for operating compounding equipment and may be required to work in both the Commercial formulation area, as well as, the Development formulation area. Responsibilities also include following necessary methods and procedures to produce a functional compounding process. The Product Formulation Technician ensures that documentation and activities in the compounding area are compliant with any applicable regulations. etc. | 8/6/2019 |
| 190 | Paragon Genomics Hayward, CA Research Associate BS/BA in biological sciences Exp: 1+ years in NGS lab |
This is a laboratory-based position with great career potential for a junior scientist or prospective scientist who already have or wishes to gain hands-on molecular biology experience in the next-generation sequencing space. Manage orders and logistics of key account(s) to ensure smooth sales to MFG transition. Support Technical Support activities such as troubleshooting and verification studies | 8/3/2019 |
| 191 | Penumbra Alameda, CA QA Engineering Specialist BS/BA in sciences/engineering Exp: 1 or more years in quality systems |
As a Quality Assurance Engineering Specialist at Penumbra, you will support quality engineering activities designed to ensure that all processes, products and systems meet the highest standards of quality and compliance with domestic and international regulations. Verify and document accuracy of sterilization process, biological test results, and completion of Device History Records. Assemble sterile loads and complete associated documents for sterilization. Perform ongoing data entry, review, and analysis of data to support statistical process control. | 8/3/2019 |
| 192 | PerkinElmer Austin, TX Associate Scientist BS/BA in life sciences Exp: 1+ year in NGS library prep |
Perform lab experiments as planned and document all observations and findings. Prepare hybridization capture NGS libraries and amplicon panel NGS libraries. Analyze and interpret data. Present experimental findings and interpretations to senior research team members. Demonstrate potential for technical proficiency and ability to collaborate with others. | 8/4/2019 |
| 193 | PerkinElmer Waltham, MA Associate Scientific Services Specialist, Lab Technician HS Diploma/GED or AS/AA Exp: 1-2 year work experience |
The candidate will conduct laboratory maintenance procedures in compliance with established protocols and in compliance with regulatory and laboratory requirements. Maintains suite equipment including, but not limited to: incubators, water baths, and biosafety cabinets. Monitors incubator temperature, CO2 and humidity. Responsible for the cleaning, sterilization and equipment functionality. | 8/4/2019 |
| 194 | Platelet Biogenesis Cambridge, MA Research Associate, Gene Editing BS/MS in biology, immunology, molecular biology Exp: 1-3 years lab experience |
The successful Research Associate will join our Designer Platelet Team, working directly on genetic engineering of pluripotent stem cells as part of our drug delivery platform. Optimizing standard operating procedures associated with platelet loading of small-molecule and biologic drugs. Developing protocols for transgene delivery in iPSCs | 8/4/2019 |
| 195 | ProSciento San Diego , CA PT Pharmacy Technician HS Diplomga/GED Exp: 1 or more year as pharma technician |
This position is responsible for performing pharmaceutical related functions in compliance with state and federal regulations, protocol specific requirements, and the Company’s values, policies, and procedures under the direction of the Pharmaceutical Services Supervisor. Receive, label, store, organize, and return/destroy study medications for clinical trials. Prepare and update all drug inventory logs and ensure logs are current with all clinical trial drug preparation schedules. | 8/5/2019 |
| 196 | ProSciento San Diego , CA Clinical Research Coordinator BS/BA in sciences/medicine Exp: 1 or more year clinical research |
The Clinical Research Coordinator will be the main operational interface with study subjects during the conduct of a study. The CRC will participate in and manage all administrative aspects of clinical trials under the direction and supervision of the Manager, Clinical Study Management. The ideal candidate will have experience as a CRC at a clinical research site working in the fields of diabetes, metabolism, or endocrinology. Performs duties in accordance with ProSciento’s values, policies, and procedures. | 8/5/2019 |
| 197 | Biotechne Minneapolis, MN Research Associate - Protein Purification BS/BA or MS in biology or related Exp: BS: 0-2 years, MS: 1-3 years |
The responsibilities of this position are to purify proteins to restock the supply of existing products and modify existing protocols for larger scale production of proteins. This position will require assistance with basic lab operations and routine guidance on how to follow SOP’s and purification methods. | 8/5/2019 |
| 198 | Biotechne Minneapolis, MN Manufacturing Associate BS/BA or AA/AS Exp: 0-2 years |
The primary purpose of this Manufacturing Associate position is to perform manufacturing support functions. This role will require the ability to review Manufacturing DHR and perform in process quality checks throughout the day at various manufacturing lines. This includes reconciliation, kitting verification, labor collection, and coordination of scheduled activities with the Manufacturing Manager or as direction from the Manufacturing Team Leader. This position is dedicated to maintaining compliance in the manufacturing area. | 8/5/2019 |
| 199 | Biotechne San Jose, CA Manufacturing Laboratory Technician AA Exp: 1+ year lab experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain cartridge fabrication process, with good manual dexterity. Perform in-process QC and record results. Microscope inspection of chips and microfluidic devices | 8/5/2019 |
| 200 | Biotechne Minneapolis, MN QA Specialist BS/BA in sciences Exp: 0-2 or 2-5 years in QA in scientific field |
The responsibilities of this position are to support the Quality Assurance function within Bio-Techne through quality systems development, quality systems auditing, documentation review, and other QA functions. | 8/5/2019 |
| 201 | Sun Pharma Billerica, MA QC Microbiologist I BS in biology or microbiology Exp: 1+ years |
Responsibilities include: Record GMP data, monitors and evaluates QC systems and equipment. Recommend improvements to procedures, and revise SOP’s and GMP documentation as required. Interact with internal and external auditors including government agencies and contract manufacturing representatives. Perform release, stability, validation and complaint follow-up assays on raw materials, in-process and final products. Perform microbial identification related to product and environmental testing. Perform sampling of raw materials as required for QC testing. | 7/30/2019 |
| 202 | Syneos Health unspecified, PA Quality Analyst I BS/MS in biological or chemical science Exp: 0-1 years |
The QC Analyst/Microbiologist I has the responsibility to: Perform aseptic sampling Pilot Plant critical utilities and controlled environment. Perform general laboratory maintenance activities such as cleaning, inventory, and ordering of laboratory supplies. Perform sample management such as logging samples into LIMS and performing sample reconciliation. Perform basic laboratory assays such as viable and non-viable environmental monitoring, pH, and conductivity in compliance with all applicable procedures and regulations. May perform basic microbial identification testing (eg. Gram stain) with the assistance of more experienced level microbiologist. Assists with the collection of samples for qualification of critical utilities and operations environment in support of the Pilot Plant. etc. | 7/30/2019 |
| 203 | Syneos Health unspecified, NJ Lab Tech (Bulk Production) AS/BS Exp: 0-2 years laboratory experience |
A Lab Tech Ops is needed for a 6-month contract position a major biotech company in Northeast. Duties: Perform bulk production and production support duties for Operations. Performs a variety of duties relating to production operations. Follows departmental work instructions, SOP's, OSHA safety regulations and cGMPs to perform assigned tasks. Monitor and oversee lab supply inventory, generate expense purchase requisitions, if applicable, input production data and other work-output data into appropriate network (e.g. SAP / LIMS) and maintain documentation in accordance with established procedures. etc. | 7/30/2019 |
| 204 | Synexus Anderson, SC Research Assistant BS Exp: 1+ years |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Assists the Clinical Research Coordinators with updating and maintaining logs and filing in charts; Schedules subjects for study visits and conducts appointment reminders; etc. | 7/30/2019 |
| 205 | Synthego Redwood City, CA Laboratory Associate, CRISPRevolution AA in chemistry or related Exp: 1-3 years |
We are searching for motivated, enthusiastic, and hands-on individuals interested in advancing science through the manufacturing of our CRISPR products. As a Lab Associate at Synthego, you will join our growing operations team and have direct responsibility for the synthesis and purification of our gRNA products. This role requires a strong attention to detail, a desire to learn and adapt to new processes, and familiarity with safe laboratory practices. This role will combine hands-on laboratory protocols with advanced automation to ensure the timely delivery of high quality products to our customers. etc. | 7/30/2019 |
| 206 | Synthego Redwood City, CA Shipping Associate, CRISPRevolution unspecified Exp: 1+ years |
Synthego is looking for a shipping associate to execute our daily order fulfillment activities, ensuring quality and customer satisfaction are top priorities. We’re looking for a detail-oriented and highly motivated person who is comfortable working in a fast-paced, dynamic environment. etc. | 7/30/2019 |
| 207 | Synthego Redwood City, CA Research Associate - Pre Clinical BS in biological sciences Exp: 1+ years in biological lab |
Research Assistant - Pre-clinical will be trained to provide technical support to the senior scientist on a defined project from conception to proof-of-concept in vitro and in vivo. What You'll Do: Process leukopacks and bone marrow to isolate primary cell culture (ie - stem cells and T cells) depending on the project. Maintain and expand primary cells. Test conditions to optimize gene editing of specific cell type. Vector cloning and various molecular biology assays as needed. Viral production. Assist in tissue processing and analyses. etc. | 7/30/2019 |
| 208 | Takeda Lexington, MA Clinical Research Associate BS/BA Exp: 1+ years |
The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the the Clinical Project Manager(s). The CRA also provides support for existing departmental tasks and may take on developmental tasks as appropriate upon discussions with manager. The CRA performs work within established protocols under general supervision. etc. | 7/30/2019 |
| 209 | Takeda San Diego, CA Research Associate Antibody Discovery MS in molecular biology, biochemistry, or related life science Exp: Not necessary for MS candidate |
The research associate will join a fast-paced Biotherapeutic Engineering team within Global Biologics Research. The candidate will perform complex research assignments and will be responsible for the discovery and engineering of therapeutic biologics including antibodies, fusions and other platforms. The candidate will communicate results within the Biotherapeutic Engineering team and with cross functional project team members. ACCOUNTABILITIES: Under minimal supervision, execute discovery and lead optimization projects using display platform technologies with high quality and efficiency. etc. | 7/30/2019 |
| 210 | Takeda Thousand Oaks, CA Manufacturing Associate I HS diploma/BS Exp: 0-2 years |
The Manufacturing Associate I is responsible for executing all manufacturing department processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate I is expected to fully participate in both departmental projects and any quality working teams that may be applicable. This position shall be responsible for the hands on execution of activities as they relate to the manufacturing of products. Essential Duties and Responsibilities: Formulation/Filling: Participate in bulk formulation, aseptic filling, Lyophilization, and capping operations. Executes processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. etc. | 7/30/2019 |
| 211 | Takeda Thousand Oaks, CA Manufacturing Associate I HS diploma/BS Exp: 0-2 years |
The Manufacturing Associate I is responsible for executing all manufacturing department processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate I is expected to fully participate in both departmental projects and any quality working teams that may be applicable. This position shall be responsible for the hands on execution of activities as they relate to the manufacturing of products. Responsibilities: Cell Culture/Purification: Support Cell Culture/Purification operations for the production of a bulk drug substance product. Prepare media and buffer solution. Clean, Set up, operate, and teardown of equipment such as tanks, filtration systems, carton assembler, bioreactors, and production lines. etc. | 7/30/2019 |
| 212 | Takeda Round Lake, IL Production Associate AS/AA Exp: 0-2 years |
The Production Associate (PA) is responsible for executing all processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, responsible for the hands-on execution of all activities in the production area. | 7/30/2019 |
| 213 | Takeda Social Circle, GA Manufacturing Associate I AA or equivalent Exp: 1 year |
This position is expected to : clean, set up, operate, and teardown equipment such as tanks, filtration systems, chromatography columns/skids, and production lines (fill lines, inspection lines, packaging lines). In addition, the technician will operate general production equipment such as pH, UV, and conductivity meters, washers, and additional equipment associated with the production process. Monitoring and recording of critical process parameters is required. Perform basic preventive maintenance related to manufacturing equipment. Support the implementation of Kanban and 5S systems to assist the full production environment. Must be able to read and follow detailed written/electronic instructions, be comfortable with electronic documentation, and have good verbal/written communication skills. | 7/30/2019 |
| 214 | Tanvex BioPharma San Diego, CA Research Associate, Purification - #1203 BS in chemical/biochemical engineering, biochemistry, or related Exp: 0-3 years protein purification |
The Research Associate performs basic trouble-shooting of processes, instrumentation, and equipment with guidance, contributes to technology transfer from process development to clinical cGMP manufacturing (including definition of bill of materials and batch record drafting/review), and performs bench scale experiments such as sterile membrane filtration, depth filtration, tangential flow filtration, viral clearance filtration, as well as chromatography. The Research Associate will collaborate with cell culture, formulation, analytical and manufacturing for achievement of project tasks and authors internal reports at appropriate milestones with supervisory guidance. | 7/30/2019 |
| 215 | Tanvex BioPharma San Diego, CA Research Associate, Formulation - #1202 BS in chemical/biochemical engineering, biochemistry, or related Exp: 0-3 years formulation development |
The Research Associate in our Formulation group is responsible for executing experiments related to formulation development from formulation definition, to stability program design and execution to support pipeline projects. This position will effectively apply basic scientific principles in formulation screening, biochemical characterization, drug substance and drug product configuration, delivery compatibility, and technology transfer activities associated with the development of biopharmaceutical formulations. The Research Associate will execute relatively simple scientific experiments which contribute to project milestones; performs analytical test methods including but not limited to spectrophotometry, pH, liquid chromatography and capillary electrophoresis; and performs basic trouble-shooting of assays, instrumentation, and equipment with guidance. etc. | 7/30/2019 |
| 216 | Tanvex BioPharma San Diego, CA Research Associate, Analytical Sciences - #1189 BS/MS in chemistry, biochemistry, chemical/biochemical engineering or related Exp: 0-3 years |
The Research Associate will perform analytical tests using HPLC, Spectrophotometry (RP, IEX, SEC, HILIC etc.), CE, mass with high quality and efficiency; provides analytical support in R&D settings for samples from various process scales; writes experiment summaries and development reports; and assists during document review comprising of but not limited to: batch records, standard operating procedures and assay protocols. etc. | 7/30/2019 |
| 217 | Tanvex BioPharma San Diego, CA QC Associate, BioAssay - #1167 BS in molecular biology, chemistry, biochemistry, or related Exp: 0-2 years |
The QC Associate is responsible for routine and non-routine product testing using biochemical methods such. Additional responsibilities include assisting with transferring analytical methods from development into the QC laboratory and test method validation; generating test results and reporting results for the assigned GMP testing in a timely and compliant manner; sample coordination, lab equipment maintenance, QC document management and review. Knowledge of performing cell-based assay, immuno-assays, and/or QPCR assays in a GMP environment is essential. etc. | 7/30/2019 |
| 218 | Smithers Avanza Wareham, MA Entry Level Technical Report Writer BA/BS in environmental science or related Exp: 0-2 years of laboratory experience |
We are seeking a full-time Technical Report Writer to join our talented team. This position will support the needs of the Smithers Viscient organization. The candidate will be responsible for writing and editing high quality study reports for several technology groups, including ecotoxicology, environmental fate and metabolism, avian and analytical chemistry, in addition to production of other documents as needed. Prepares study reports from data presented in technical format that meets guideline requirements. Compiles and incorporates comments from several different levels of review. etc. | 7/23/2019 |
| 219 | Smithers Avanza Wareham, MA Chemistry Technician II BS in chemistry or related Exp: 6 months laboratory experience |
Position is expected to perform varied and often complex and difficult procedures somewhat independently. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Operates and may maintain, under supervision, test equipment and apparatus of moderate complexity. May provide information for initial data interpretation and test system conformance to expectations. Records, compiles and reduces laboratory data in real time in a complete and thorough manner for individual assignments. May produce reports. etc. | 7/23/2019 |
| 220 | Strata Oncology Ann Arbor, MI Laboratory Assistant AS in a relevant field Exp: 1+ years |
The ideal candidate possesses a basic working knowledge of histopathology and/or molecular biology with entry level experience in basic laboratory techniques and strong data entry skills. The Laboratory Assistant is responsible for receiving and accessioning samples into the Laboratory Information Management System as well as assisting the Histology team with basic tasks and functions required to maintain the smooth operation of the company such as clerical duties, reagent preparation, and inventory. etc. | 7/23/2019 |
| 221 | Stratos Genomics unspecified, Research Associate—Molecular Engineering MS/BS in chemistry, organic chemistry, chemical engineering, or related Exp: 1-2 years relevant laboratory experience |
We are seeking motivated Scientists and Research Associates to join our team. Candidates will be involved in synthesizing our unique building blocks for our novel DNA sequencing technology, Sequencing by Expansion, developing and optimizing synthesis protocols as well as proposing and executing innovative experiments to push our technology forward. This position requires an availability to work between the hours of 8am to 7pm with extended work hours when necessary. etc. | 7/23/2019 |
| 222 | NuVasive San Diego, CA Assoc. Development Engineer, Surgical Instruments BS in mechanical engineering or related Exp: 0-2 years |
Technical activities include projects leading to product improvement. You will also contribute on several levels including: Complete engineering models and drawings of Customized Instruments. Contribute documentation for support of Customized Instrument Design History Files. Perform quality inspection of finished devices . Interface effectively with internal and external suppliers and become educated on manufacturing methods and capabilities. | 7/19/2019 |
| 223 | NuVasive Raleigh , NC Development Engineer BS in mechanical engineering or related Exp: 1-3 years previous experience |
Technical activities include projects leading to product improvement. You will also contribute on several levels including: Contribute documentation for support of project Design History Files. Gain cadaver lab/OR experience – support Surgeon training. Interface effectively with suppliers and become educated on manufacturing methods and capabilities. Perform duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485 | 7/19/2019 |
| 224 | NuVasive San Diego, CA Clinical Research Associate BS in life sciences, biological sciences, or related Exp: 1-3 years in clinical trials |
The CRA is responsible for fulfillment of all clinical research objectives in support of product validation and ongoing verification of product safety and performance in pursuit of clinical data compliance to MEDDEV 2.7/1 rev. 4 and EU MDR. Largely site management and field-based site monitoring with additional study responsibilities as required by team. | 7/19/2019 |
| 225 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 6 months + |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Follow prioritized assignments, providing customer service support and ensure the completion of order fulfillment (picking, packing, manifesting), maintain inventory through putaway, breakdowns, replenishment, and cycle count in a timely manner, meeting or exceeding productivity and quality standards. | 7/21/2019 |
| 226 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 6 months + |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 7/21/2019 |
| 227 | Bausch Health Clearwater, FL Production Associate II HS Diploma/GED Exp: 1 or more years training lathes/milling machines |
Setup, maintain and operate production line equipment to produce intraocular lenses according to production specifications and standards. Perform inspections to verify accuracy of machining against specifications to maintain quality and performance standards using set up equipment. Conduct initial troubleshooting for defect causes and machine problems . Make minor mechanical repairs as required to maintain production specifications and standards. Report unusual conditions and problems to supervisor and practice good housekeeping. Support, encourage and participate in team related activities; report ideas or suggestions to supervisor. | 7/21/2019 |
| 228 | Pace Analytical Fort Dodge, IA Microbiology Lab Technician BS in microbiology or related Exp: 0-2 years lab experience |
This candidate will be supporting research and development of vaccines in animal care products. They will be responsible for equipment and media prep. Sterilization of equipment. Tear down and clean up of lab set-up. Preparation and sterilization of equipment and supplies. Prepare media and solutions. General microbiology tests including as needed | 7/21/2019 |
| 229 | Pace Analytical Indianapolis, IN Chemist - QA Validation BS/BA Exp: 0-5 years lab experience |
This individual's primary responsibility is to perform analytical methods and validations in order to find exceptions on the instrument and/or software side. They will be responsible for executing validation documentation on a variety of instrumentation in a pharmaceutical setting. Pharmaceutical and GMP experience is preferred, but candidates with experience with instrumentation in a regulated environment are highly encouraged to apply. | 7/21/2019 |
| 230 | Pace Analytical Maplewood, MN Physical Properties Technician BS/BA in chemistry, physics, material sciences or related Exp: 0-2 years, recent graduate |
The Physical Properties Technician will perform routine testing/characterization on a drug delivery device in a GMP laboratory setting. Perform physical properties characterization on a medical device such as appearance, adhesion, and performance. Perform wet chemistry as needed and properly dispose of samples and reagents. Operate instrumentation such as FTIR, microscopes, and other dimensional analysis tools | 7/21/2019 |
| 231 | Pace Analytical New Castle, DE Entry-Level Chemist BS/BA in chemistry or engineering Exp: 0-2 years |
Responsible for performing inspections and laboratory analysis utilizing a variety of techniques, to ensure quality of production. This includes quality checks of raw materials used in the production process to ensure they meet ISO standards; quality checks of production samples and final products prior to shipment to the customer. This includes transferring clear and accurate data from all laboratory analyses performed to the appropriate department. | 7/21/2019 |
| 232 | Pace Analytical Philadelphia, PA Entry-Level Chemist BS/BA in chemistry or engineering Exp: 0-2 years |
Responsible for performing inspections and laboratory analysis utilizing a variety of techniques, to ensure quality of production. This includes quality checks of raw materials used in the production process to ensure they meet ISO standards; quality checks of production samples and final products prior to shipment to the customer. This includes transferring clear and accurate data from all laboratory analyses performed to the appropriate department. | 7/21/2019 |
| 233 | Pace Analytical Philadelphia, PA Entry-Level Chemist BS/BA in chemistry or engineering Exp: 0-2 years |
Responsible for performing inspections and laboratory analysis utilizing a variety of techniques, to ensure quality of production. This includes quality checks of raw materials used in the production process to ensure they meet ISO standards; quality checks of production samples and final products prior to shipment to the customer. This includes transferring clear and accurate data from all laboratory analyses performed to the appropriate department. | 7/21/2019 |
| 234 | Nortech Mankato, MN Manufacturing Technician AA/AS Exp: 6 months to 1 year |
Performs machining duties and operations to include all set-ups and calculations to complete jobs independently and to meet prescribed specifications and requirements. | 7/13/2019 |
| 235 | Nortech Mankato, MN Quality Technician - Mankato AA/AS Exp: 6 months to 1 year |
coordinates the development and implementation of the quality system, researching, developing and implementing process improvements necessary to eliminate waste and reduce inventory. Responsible for development of the performance metric system used to report on continous process improvements. | 7/13/2019 |
| 236 | Nortech Mankato, MN Quality Engineer - Mankato BS/BA Exp: 1-2 years of experience/training |
As a quality engineer you will: Assure optimum quality in manufactured products in accordance with Company standards and contract requirements. | 7/13/2019 |
| 237 | Norwich Pharma Norwich , NY MDAS Research Associate MS in chemistry or related Exp: 1+ year in pharma development/QC lab |
The Method Development and Analytical Services (MDAS) Research Associate is an experienced resource in performing sample testing and validating the methods necessary to support development and commercialization of pharmaceutical products. The MDAS Research Associate is responsible for performing the bench chemistry testing of pharmaceutical products supporting development of new products, incoming transfer of existing products, and analytical support of product life cycle management. The MDAS Research Associate will assist in performing method development, transfer, validation, and/or verification for methods related to analyzing raw materials, semi-finished/finished products, and stability. Customer communication and active participation as the analytical chemistry expert on work teams may be required. | 7/13/2019 |
| 238 | Nova Biomedical Waltham, MA Chemical Filling Operator HS Diploma/GED Exp: 0-2 years as machine operator |
The Chemical Filling Operator ( Second Shift) is responsible for the proper filling, sealing and labeling of various reagents. Responsibilities: Monitoring and maintenance of the filling equipment during operation, recording necessary data into procedures, inspection of product, loading/unloading product from equipment and movement of materials. | 7/13/2019 |
| 239 | Nova Biomedical Waltham, MA Formulation Operator HS Diploma/GED Exp: 0-2 years as compounder/formulator |
The Formulation Operator will work on our First Shift and perform batch processing of various calibrators, controls, and additional reagents required to support company produced and OEM analyzers. Essential Responsibilities: formulation of various solutions including staging of tanks, weighing and mixing of chemicals per assembly procedures (AP's) and final batch adjustment and transfer of solutions. Perform incoming inspection of raw chemicals upon receipt, maintenance of formulation equipment and cleaning as needed. Ability to accurately document and complete records of batch formulations. | 7/13/2019 |
| 240 | NovoBiotic Pharmaceuticals Cambridge, MA Associate Scientist - Microbiologist BS in biology/microbiology Exp: Entry Level |
We are seeking to hire an entry-level microbiologist. The positionwill involveworking with a team of scientists to discover new antibiotics from newly cultured species from soil and marine environments. The work will include special projects as well as daily lab tasks such as reagent prep,record keeping, and equipment maintenance. | 7/14/2019 |
| 241 | Novo Nordisk Seattle, WA Assistant Animal Technician AALAS or ALAT certified Exp: 1 or more year working with rodents |
Responsible for providing a high level of animal care and husbandry, performing regularly scheduled facility maintenance tasks, and contributing technical assistance to research projects in the NNRC rodent facility. Reports to Manager, Animal Research. Internal relationships include working with Animal Technician, Attending Veterinarian, Lab Operations Specialist, Research Associates and Research Scientists locally and globally. | 7/14/2019 |
| 242 | Novo Nordisk Clayton , NC Aseptic Filling Technician I - Night Shift Job HS Diploma/GED Exp: 1+ year in manufacturing |
Filling of insulin and media preparations under aseptic conditions and operation of inspection equipment to achieve production goals. Operating, monitoring and controlling equipment, systems and processes associated with the Vial/Cartridge filling and inspection lines. Maintaining aseptic areas and performing sanitizations and environmental monitoring. Assist during equipment maintenance including restoration of lost function, predictive and preventative maintenance | 7/14/2019 |
| 243 | Novum Las Vegas, NV Phlebotomist (PT) Phlebotomy certified Exp: 1-2 years experience |
The Phlebotomist will perform highly skilled, rapid-draw venipuncture and process collected biological samples according to Standard Operating Procedures (“SOPs”), sample collection and processing instructions; verify, pack and ship samples to appropriate facility. | 7/14/2019 |
| 244 | Novum Las Vegas, NV Pharmacy Technician AS/AA Exp: 6 months to 1 year training/experience |
The Pharmacy Technician will be responsible for assisting the Pharmacy Manager with all aspects of drug handling and storage to assure drug availability and correct dosing according to the protocol. Responsible for handling the receipt, storage, and return to sponsor along with test articles used in clinical studies. Responsible for maintaining daily records of storage conditions of drugs and refrigerator temperatures. Will prepare dosage forms for clinical investigators and provide general support to the clinical operations department. | 7/14/2019 |
| 245 | Novum Fargo, ND Superviso, Phlebotomy Phlebotomy certified Exp: 1-2 years supervisory + phlebotomy training/experience |
The Phlebotomy Supervisor will be responsible for supporting study progression according to the study protocol and Standard Operating Procedures (SOPs). Also responsible for supervising the phlebotomy staff; performing rapid venipuctures, processing biological samples and providing proper documentation and verification of the same. Will label and prepare study supplies; ensure lab areas are prepared and cleaned and will review lab and tech instructions prior to study start up. Will perform document and QC documentation of all study activities as assigned. Verify, pack, coordinate and manage sample packaging and shipment/delivery to analytical labs. Will perform practical testing for phlebotomy candidates and work with manager to train and schedule staff. | 7/14/2019 |
| 246 | Smith & Nephew Memphis, TN Material Quality Tech I AS or equivalent Exp: 0-2 years |
The Materials Quality Technician I is responsible for overseeing, and maintaining the laboratory equipment and area. The Materials Quality Technician I is responsible for site-wide compliance of the activities related to Materials. The Materials Quality Technician I will be interacting on a daily basis with Quality and Manufacturing Engineers and Managers. Must be able to convey laboratory practices, policies, and procedures to regulatory bodies such as FDA and notified bodies. The Materials Quality Technician I will have the training and knowledge necessary to perform the Materials laboratory functions and the administrative functions. The Materials Quality Technician I may be assigned to special projects by the Department Management that is commensurate with their level of experience. etc. | 7/15/2019 |
| 247 | Smith & Nephew Memphis, TN Machine Maintenance Technician 2 AS in industrial maintenance technology or related Exp: 1 year |
Primarily responsible for repairs and scheduled maintenance of production machines and equipment. Also responsible for fabrication of needed parts and modifications to existing machines and equipment. Assists with training manufacturing associates to do preventive maintenance on applicable machines. Performs repairs on machinery and equipment as necessary. Performs PM’s on all manual equipment. Completes all necessary forms listing work done, parts used, parts needed, time involved, etc. Initiates requirements for machine parts and supplies. Performs installation and setup of new equipment as necessary. Installs and maintains air system. etc. | 7/15/2019 |
| 248 | Smith & Nephew Memphis, TN Quality Assurance Inspector I HS diploma or equivalent Exp: 0-2 years |
The Quality Assurance Inspector I shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. Essential Responsibilities: Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. Support the qualification/validation processes for company product. etc. | 7/15/2019 |
| 249 | Smith & Nephew Minneapolis, MN Receptionist AS/AA preferred Exp: 1-3 years |
Provide administrative support to Facility Manager and general office support to other business processes on site. Manage all aspects of office administration for smooth operation of facilities and comfortable, productive environment. Respond to all assignments and requests timely and efficiently; maintain discretion on all confidential or sensitive matters. Support corporate safety directives, policies and procedures; proactively contribute to wider HSE and housekeeping improvement goals. Uphold culture of camaraderie and employee engagement while promoting appreciation, trust and respect. etc. | 7/15/2019 |
| 250 | Smith & Nephew Memphis, TN Machinist HS diploma or equivalent Exp: 6 months |
This position requires a person to perform simple set ups and operate manual/CNC equipment to manufacture medical components from raw material in a team based environment. Must be able to comply with all governing rules including S.N.E. policies and procedures and adhere to safety and cleanliness practices in the work place. This position works under close supervision. Essential Duties And Responsibilities: Machine medical components, including but not limited to: Perform simple set ups and operate manual/CNC equipment, including turning, milling, grinding, drilling, tapping, EDM and honing. etc. | 7/15/2019 |
| 251 | Smith & Nephew Memphis, TN Machinist HS diploma or equivalent Exp: 1+ years |
This position requires a person to set up and operate CNC and manual machinery to manufacture medical components from raw material in a team based environment. Must be able to comply with all governing rules including S.N.E. policies and procedures and adhere to safety and cleanliness practices in the work place. This position works under minimal supervision. ESSENTIAL FUNCTIONS: Position Functions: Machine medical components, including but not limited to: Perform moderate set ups and operate CNC and manual metal fabricating equipment, including turning, milling, grinding, drilling, tapping, EDM and honing. | 7/15/2019 |
| 252 | Smith & Nephew Memphis, TN Graduate Engineer BS in mechanical, manufacturing, industrial or other engineering Exp: Recent graduate |
Responsible for the development of manufacturing methods to produce advanced technology products. You will work under the direction of either a Sr. Engineer or Manager in the development of new processes, introduction of new products, cost reduction projects, and capital justifications. Interface with Production Supervision, Tool Design, and Tool & Die, and Maintenance with respect to manufacturing method, tooling, and equipment. Establish routings for new products and determines manufacturing cost. Contacts and reviews projects with vendors as necessary. etc. | 7/15/2019 |
| 253 | Smithers Avanza Smithers Rapra, OH Product Testing Technician HS diploma or equivalent Exp: 1-5 years |
Performs laboratory tests to determine physical characteristics of materials and products for such purposes as quality control, process control or product development by performing essential duties and responsibilities. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform testing in accordance with relevant specification(s). Follow daily work assignments relative to test schedule. Have detailed understanding of test methods and specifications. Be able to perform basic calculations from tests. etc. | 7/15/2019 |
| 254 | Smithers Avanza Wareham, MA Program Manager BS/BA in business or science discipline Exp: 1-3 years |
Currently, we are seeking a full-time Program Manager to join our talented team. This position will support the needs of the Smithers Viscient organization in Wareham, MA and Snow Camp, NC. Job responsibilities: Manage aspects of planning, scheduling, implementation, follow-up, tracking of program tasks, and prioritization of critical program activities for our clients. Individual collects and accumulates program data from sources within the Laboratory or Organization. Responsible for writing and updating client status reports and other required client‑specific documentation. Work closely with all team members to provide services both internally and externally. etc. | 7/15/2019 |
| 255 | Smithers Avanza Wareham, MA Assistant Biologist BS in biology or related Exp: 6 months of laboratory experience |
Position is expected to perform a variety of routine tasks in support of the conduct of normal laboratory operations. Further, the individual is expected to assist in coordinating testing requirements with supporting departments (i.e. chemistry staff, Quality Assurance and reporting). Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing Standard Operating Procedures, study-specific protocol procedures and other laboratory assignments related to the testing that the individual is routinely associated with. Incumbent is able to apply a collective set of SOPs in order to assist in fully executing a study protocol. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. etc. | 7/15/2019 |
| 256 | Smithers Avanza Wareham, MA Instument Operator BS/MS in chemistry, biochemistry, or related Exp: 1-3 years (BS), 0-2 years (MS) |
The Chemistry Division at Smithers Viscient is looking for an intelligent, highly-motivated individual to operate the LC-MS instruments in support of the Ecotox, Residue, and Product Chemistry Departments. The Chemistry Division focuses on performing the necessary chemistry tests to ensure that future pharmaceuticals, agrichemicals, and industrial chemicals are safe. Our clients and the public trust our scientific judgement in this critical regulatory procedure. All Smithers Viscient team members have a hand in making sure the world is safe. The position will report to the Instrument owner and Study Director in our Residue Chemistry group. The instrument operator will be responsible for operating, troubleshooting, and performing routine maintenance for the LCMS Instruments. etc. | 7/15/2019 |
| 257 | Smithers Avanza Ravenna, OH Tire Testing Technician HS diploma or equivalent Exp: 1-3 years |
SUMMARY: Checking compliance of products to meet industry or client standards. ESSENTIAL DUTIES AND RESPONSIBILITIES: Sets up, adjusts, and operates laboratory equipment and instruments. Tests samples of manufactured products to verify conformity to specifications. Records test results on standardized forms, and writes test reports describing procedures used. Calibrates laboratory instruments, and mounts tires. Must have good attendance and attitude. Must be able to follow directions well. Must be able to learn quickly. Must follow all safety requirements and procedures. | 7/15/2019 |
| 258 | Smithers Avanza Smithers Rapra, OH F&M Technician HS diploma or equivalent Exp: 1-3 years |
SUMMARY: With the direction and lead of other Force and Moment staff, prepares and installs candidate tire/wheel assemblies for testing on MTS Flatrac® Tire Test Systems and TMSI On-Level Test Systems. Conducts tests and records results by performing the following duties: Follow safety rules and company policies. Maintains tire inventory records and coordinates all shipping and receiving. Confers with other Flatrac® Technicians or Staff to resolve operational or procedural problems relating to specifications, conditions under which tests are to be conducted, and duration of tests. Coordinates and participates in installing tire/wheel assemblies to be tested, connecting valves, pumps, hydraulic, mechanical, cabling, tubing, power source, and indicating instruments. etc. | 7/15/2019 |
| 259 | Smithers Avanza Gaithersburg, MD Sample Management Technician BS/BA/AAS in life sciences Exp: 18 months of laboratory experience |
Essential Position Responsibilities: Receive, check-in and dispose of study samples according to established guidelines and SOPs. Complete all appropriate paperwork in a timely fashion. Identify and document all discrepancies between client paperwork, Watson LIMS, and sample vials. Notify sponsor and Project Team of the discrepancies. Assures proper storage conditions for sample types. Accessions specimens using automated and manual systems. Use Watson LIMS to set-up shipments and receive shipment samples. Use Watson LIMS to edit subject ID information and assign custom IDs. Prepare sample disposition notifications. etc. | 7/15/2019 |
| 260 | Smiths Medical Southington, CT 3rd Shift Team Technician HS Diploma/AS Exp: 1-2 years |
The Team Technician is responsible for ensuring the correct operation of automatic and semi-automatic assembly production equipment in accordance with governing documentation. This person will also initiate action to prevent the occurrence of nonconformances related to the product and equipment. Additionally, this role will identify and record problems relating to the product, process and or quality system. The Team Technician will also initiate recommendations, provide solutions, and verify the affectivity of continuous operational improvements. etc. | 7/16/2019 |
| 261 | Smiths Medical Minneapolis, MN Finacial Analyst MBA Exp: 1-2 years |
The Financial Analyst will provide financial and commercial decision support. The individual holding this role will be required, with some guidance, to monitor the financial impact of his/her business function against plan and provide reliable and timely analysis to guide the business leaders in their decision-making process. Duties & Responsibilities: Provides financial support to the business function, under guidance of the Business Partner, or Regional Business Partner. Supports the annual budgeting and forecasting processes. Monitors key performance indicators and interprets financial and operational performance. etc. | 7/16/2019 |
| 262 | Smiths Medical Dublin, OH Group Leader - Airway 2nd Shift (2:30pm - 11pm) HS diploma or equivalent Exp: 1-2 years |
The Group Leader is responsible for successfully leading the department’s day-to-day activities (people/equipment/processes) with regards to safety, quality, customers, and efficiencies. Duties & Responsibilities: Demonstrate leadership and accountability in providing and sustaining a positive safety culture. Provide support for safety training, meetings, and programs. Provide recognition for safe behavior through position observations. Ensure proper instruction is provided on responsibilities and safe job performance (on the job training). Provide support for safety training, meetings, and programs. etc. | 7/16/2019 |
| 263 | Smiths Medical Dublin, OH Group Leader - Auto Assembly 3rd Shift (10:30pm-7am) HS diploma or equivalent Exp: 1-2 years |
The Group Leader is responsible for successfully leading the department’s day-to-day activities (people/equipment/processes) with regards to safety, quality, customers, and efficiencies. Duties & Responsibilities: Demonstrate leadership and accountability in providing and sustaining a positive safety culture. Provide support for safety training, meetings, and programs. Provide recognition for safe behavior through position observations. Ensure proper instruction is provided on responsibilities and safe job performance (on the job training). Provide support for safety training, meetings, and programs. etc. | 7/16/2019 |
| 264 | Smiths Medical Southington, CT Mechanical Engineer II - Medical Device Advanced degree in engineering Exp: 1-2 years |
Smiths Medical is currently hiring a Mechanical Engineer II in Southington, CT. The Mechanical Engineer II will be responsible for product and component detail design, creation of 3D models and product drawings with proper GD&T, development and delivery of Design Verification activities (test method development/fixture design/DV plans/test protocols/reports). Duties & Responsibilities: Performs engineering work requiring full competency in all conventional aspects of engineering. Plans and conducts work requiring judgment in the independent evaluation, selection and the substantial adaption of standard engineering techniques, procedures and requirements. Plans and coordinates detailed phases of engineering actions for part of a project. Conducts engineering activities of intermediate scope or degree of difficulty. This could include medium – large components/system, processes associated with a medium or large project. etc. | 7/16/2019 |
| 265 | Smiths Medical Minneapolis, MN Office Associate, Facilities HS diploma Exp: 1-3 years |
Position’s primary role is that of First Impressions Coordinator: Greeting and coordinating credentials for guests and their hosts within Smiths Medical. They also play a role in meeting site security and facility needs. They act as site concierge for all guests and employees. Supports catering activities and conference room bookings. Associate will also provide back-up for the Mail Room Associate. Position reports to Facilities Manager. Duties & Responsibilities: Welcomes visitors by greeting them, in person or on the telephone; answering or referring inquiries. Directs visitors by maintaining employee and department directories; giving instructions. Maintains security by following procedures; monitoring logbook; issuing visitor badges. etc. | 7/16/2019 |
| 266 | Smiths Medical Minneapolis, MN Product Surveillance Complaints Coordinator II BS/BA Exp: 1 year |
The Product Surveillance Coordinator II role contributes to the process of timely, high quality and consistent product complaints management, including appropriate identification and response to risks, adverse event reporting decisions, and collection and documentation of complaints. Duties & Responsibilities: Set up and manage product complaints in the global complaints database to ensure complaints are managed according to regulatory requirements and customer expectations. Communicate with customers, Affiliates and internal departments regarding product complaints and document the complaint file. Use judgment to analyze adverse event information and determine if events are reportable to regulators. etc. | 7/16/2019 |
| 267 | Solid Biosciences unspecified, Staff Accountant BA/BA in accounting, finance, or business administration Exp: 1+ years |
The Staff Accountant will support the Controller with all accounting, finance and administrative duties. Key Duties & Responsibilities: Responsible for maintaining the integrity of General Ledger accounts, structure and cost elements. Ensure monthly financial closings are in line with expectations (on time and on quality); coordinate GL resources to work according to plan (timetable, deliverables). Ensure timely and accurate financial reporting to internal/external customers (Controlling, Auditors and others). etc. | 7/16/2019 |
| 268 | Solid Biosciences unspecified, Staff Accountant/AP Specialist BA/BA in accounting, finance, or business administration Exp: 1+ years |
Solid Biosciences is looking to hire a proactive and dedicated Staff Accountant/AP Specialist to join our fast-paced Finance team. In this position, you will be responsible for the accounts payable process and assisting with the accounting close process. Key Duties & Accountabilities: Accurately process/input invoice information in G/L system and route invoices for approval to the business. Work on vendor statements. Monitor the AP inbox and respond to inquiries. etc. | 7/16/2019 |
| 269 | SomaLogic Boulder, CO Bioinformatics Analyst II/III/Sr 2019-113 MS in computer science, statistics, mathematics, biochemistry, molecular biology, genetics, or related Exp: No experience for Master's degree |
Key Job Responsibilities: Conduct routine analysis on collaborator data as it is generated by the service lab, applying standard quality assessment protocols, and providing results to collaborators. Use internally developed and off the shelf tools to process collaborator data into standard results. Apply standard quality assessment protocols to results generated and coordinate with laboratory personnel regarding assay quality and protocol deviations. Monitor and manage data flow for collaborator samples, providing regular feedback to project management. Participate in study planning calls with collaborators to discuss how their samples will be analyzed and provide recommendations based on documented best practices. etc. | 7/16/2019 |
| 270 | Sorrento Therapeutics San Diego, CA Manufacturing Associate BS in biology, biomedical science, chemical engineering, or related Exp: No experience for Bachelor's degree |
A Manufacturing Associate who will be responsible for manufacturing CAR-T cells per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. THE DAY-T0-DAY WORK INCLUDES: Weigh and measures in-process materials to ensure proper quantities are added/removed. Adheres to the production schedule ensuring on-time, internal production logistics. Records production data and information in a clear, concise, format according to proper GDPs. etc. | 7/16/2019 |
| 271 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS in life science, chemistry, or chemical engineering Exp: 1-3 years |
WHAT WE ARE LOOKING FOR: We are looking for enthusiastic and talented individuals who thrive on challenge and change, who can roll up their sleeves, put on multiple hats and have a can-do attitude without a lot of oversight or instruction. We are currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks. Including but not limited to: Tracking & control of raw material inventory. Maintenance and operation of equipment in cGMP facilities. Preparation of buffer and media. Assistance in operation of single use bioreactors for production of clinical and commercial products. | 7/16/2019 |
| 272 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS in life science, chemistry, or chemical engineering Exp: 1-3 years |
WHAT WE ARE LOOKING FOR: We are looking for enthusiastic and talented individuals who thrive on challenge and change, who can roll up their sleeves, put on multiple hats and have a can-do attitude without a lot of oversight or instruction. We are currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks. Including but not limited to: Tracking & control of raw material inventory. Maintenance and operation of equipment in cGMP facilities. Preparation of buffer and media. Assistance in operation of single use bioreactors for production of clinical and commercial products. | 7/16/2019 |
| 273 | Sorrento Therapeutics San Diego, CA Manufacturing Associate, Downstream BS in life science, chemistry, or chemical engineering Exp: 1-3 years |
We are currently seeking a Manufacturing Associate responsible for performing downstream manufacturing tasks including 1) tracking and control of raw material inventory 2) maintenance and operation of equipment in cGMP facilities, 3) buffer preparation, 4) assist in setup and operation of purification equipment for production of clinical and commercial products. etc. | 7/16/2019 |
| 274 | Sorrento Therapeutics San Diego, CA Research Associate BS/MS in chemistry, biochemistry, chemical/biochemical engineering or related Exp: 0-3 years |
The Research Associate in our Nanoformulation group is responsible for providing analytical chemistry support to research, process development, product development. This position participates in analytical method development, characterization, qualification, validation as well as method transfer. Laboratory experience in an industrial setting is desired, though applications from both recent graduates and those with more experience are welcome A sound foundation in experimental design, biochemistry, and chemistry is desired along with an ability to troubleshoot issues effectively. etc. | 7/16/2019 |
| 275 | Sorrento Therapeutics San Diego, CA QC Associate BS in microbiology Exp: 1-2 years |
This individual contributes to general operations and testing for the Quality Control and Microbiology Laboratories. This position supports in-process testing and drug substance and drug product release and stability testing programs. Works independently under general supervision. ESSENTIAL DUTIES AND RESPONSIBILITIES: Routine Environmental Monitoring in aseptic manufacturing environment” active air sampling, non-variable particulate monitoring, surface and personnel sampling. Incubation and counting of plates. Bae knowledge of microbial organisms and microbiological techniques. etc. | 7/16/2019 |
| 276 | Spark Therapeutics Philadelphia, PA Flow Cytometry Specialist BS/MS in biological sciences Exp: 1-4 years |
The Flow Cytometry Specialist will: Contribute to the advancement of gene therapy initiatives by developing, optimizing, validating and performing flow cytometry analyses on clinical, pre-clinical, and R&D samples utilizing in-depth knowledge of flow cytometric techniques. Perform complex data analyses and prepare reports and presentations to covey results and novel findings. Design antibody panels for flow cytometry analyses. Assist fellow scientists with flow cytometry experimental design, experimental setup, data acquisition, and data analysis. Train scientists in flow cytometry techniques, methods, instrumentation, etc. Maintain flow cytometry equipment. etc. | 7/16/2019 |
| 277 | Spark Therapeutics Philadelphia, PA Cell Banking Associate BA/BS in biological sciences Exp: 1-3 years |
The Scientist will: Cell banking and quality testing of prepared batches. Isolation and cryopreservation of PBMCs in the context of clinical and pre-clinical studies. Maintain cell culture facility and culture cell lines as required for experiments including but not limited to: cell expansion, cell feeding, harvesting, counting and freezing. Participate in sample management activities such as receiving, processing, storage and shipping of clinical and preclinical samples. Participate in instrument maintenance and qualification. Maintain accurate, timely and detailed records of work. With guidance and supervision from the supervisor, conduct clinical and preclinical sample analysis per SOPs and generate data with high scientific quality to meet GLP regulatory expectations. etc. | 7/16/2019 |
| 278 | Spectrum Pharmaceuticals Irvine, CA Temporary- Biostatistician BS/MS in statistics or related Exp: 0-2 years |
The position provides statistical services including analysis, analysis QC, interpretation, design, and reporting or communication of data evidence for research, development, and/or marketed drugs, devices or biologics. Activities associated with the role will require varying levels of guidance from managers and project statisticians. Primary activities include assisting senior level statisticians in reviewing data, performing analysis, QC of analysis and interpretation of the analysis. The person is expected to review all clinical trial and statistical documents such as protocol, statistical analysis plan in order to perform his/her activities. etc. | 7/16/2019 |
| 279 | Spherotech Lake Forest, IL Technical Customer Support Representative BA/BS Exp: Recent graduate |
Spherotech, Inc. seeks a college graduate for a Technical Customer Support Representative opening. Duties include, but are not limited to providing customer/technical assistance and Microparticle application support. Responsibilities also include representing the company through trade shows, technical publications, and presentations. Required laboratory skills include: Analysis of Microparticles using particle sizers, flow cytometry, fluorescence spectrophotometry, and microscopy. | 7/16/2019 |
| 280 | Spherotech Lake Forest, IL Manufacturing Associate BS in chemistry or relateed Exp: Recent graduate |
Spherotech, Inc. seeks a college graduate for a Manufacturing Associate opening. Duties include polymer synthesis, bottling, packaging, documentation, etc. This position requires a Bachelor's degree in Chemistry or related field. We offer excellent benefits including paid vacation, health insurance, dental insurance etc. Compensation commensurate with experience. | 7/16/2019 |
| 281 | Spherotech Lake Forest, IL Quality Control Associate BS in chemistry or relateed Exp: 1+ years |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This position requires a Bachelor's degree in Chemistry or related field and a minimum of 1 year of experience. We offer excellent benefits including paid vacation, health insurance, dental insurance, etc. Compensation commensurate with experience. | 7/16/2019 |
| 282 | SQZ Biotech Watertown, MA Research Associate, Analytical Development BS/MS in life science or related Exp: 1+ years |
SQZ Biotechnologies is seeking a flexible, detail oriented analytical thinker as a Research Associate to join the Analytical Development & Quality Control (AD&QC) team. The successful candidate will work within the internal AD&QC team to develop analytical methodologies for characterization of SQZ Biotechnology’s cell therapy products, support internal testing needs, and work collaboratively with Research and Development teams. The successful candidate will also work with external partners to transfer and qualify appropriate test methods. Responsibilities: Contribute to the development of: Flow cytometry methods to characterize cell therapy products, including elucidation of cell composition for blood products, in-process samples and product materials. etc. | 7/16/2019 |
| 283 | SQZ Biotech Watertown, MA Research Associate, Immunology BS/MS in biology, immunology, or related Exp: 1+ years |
SQZ Biotechnologies is looking for a highly motivated, collaborative, and dynamic Research Associate for our Immunology team within R&D. This role is an opportunity to focus on developing novel immunotherapies for the treatment of cancer. The scope of this work will encompass the design and execution of in vitro and in vivo experiments for internally- and externally-focused research programs. This position requires effective collaboration across multiple groups and the regular presentation of scientific results to multidisciplinary teams. etc. | 7/16/2019 |
| 284 | STAAR Surgical Monrovia, CA Production Operator I HS diploma or equivalent Exp: 1-2 years |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Thorough knowledge and appropriate implementation of basic production functions. Completes required production documentation accurately. Consistently meets quality and productivity targets. Appropriately follows company policies, rules, and regulations. Be able to interact well with others and work in a team environment. Maintain work area environment in a clean and orderly manner. Operate production related equipment. Other duties as assigned. | 7/16/2019 |
| 285 | STAAR Surgical Monrovia, CA Production Technician HS diploma or equivalent Exp: 1-2 years |
MAIN JOB RESPONSIBILITIES / COMPETENCIES: Thorough knowledge of all applicable SOP's: makes proper decisions in line with applicable SOPs and standards under normal conditions. Perform highly technical tasks in support of manufacturing including equipment set-up and manufacturing of product, tool changes, sterilization processes, and filtration of material and calibration activities as assigned. Troubleshoot issues on equipment and assist with preventative maintenance. Edit equipment programs (as required). Assist in revising procedures related to operation and preventative maintenance. Support qualification activities (as required). Train production operators in the processes. Other duties as assigned. etc. | 7/16/2019 |
| 286 | Scantibodies Laboratory Santee, CA Customer Service Representative II (Bilingual in Mandarin) College degree preferred Exp: 1-2 years customer service experience |
Essential Duties: Receive and respond to correspondence and phone calls from customers, including entering customer orders, researching information and tracking progress of orders. Be responsible for customer service to a variable number of directly assigned customers and be prepared to assume representation for additional customers, both as new assignments and “unassigned” customers. Be familiar with the top 10-20 products and top 30-50 customers of SLI. Be familiar with the product lines of the various production departments within SLI (i.e., who makes which products for order processing and technical support questions.) Receive, review and enter into record customer specifications, assuring proper review and approval by production, QA and other appropriate personnel. etc. | 7/8/2019 |
| 287 | Sciecure Pharma Monmouth, NJ QC Document Review BS in chemistry or related Exp: 1-2 years in GMP lab |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. Responsibilities: Review of documentation generated during method validation, method verification, stability testing, routine testing and other analyses. Review documentation, results and reports from raw material and finished product analysis for accuracy and completeness. Provide feedback from reviews to analysts and supervisor and ensure necessary action are taken to correct or prevent error. Review data using a systematic approach to ensure compliance with procedures and specifications. Review and audit projects as required. Perform other duties assigned by supervisor as needed. etc. | 7/8/2019 |
| 288 | Sciecure Pharma Monmouth, NJ ARD Intern BS/MS in chemistry, biology or related Exp: Recently graduated |
The Analytical R&D laboratory supports development and validation of methods. All activities are performed in accordance with specifications, SOPs, and regulatory requirements. This position does not require working experience; however, previous lab experiences are preferred. Full-time position at Sciecure Pharma will be considered by the end of internship. Responsibilities: Analyze data, document results, maintain laboratory notebook per cGMP and internal guidelines. Communicate results in written and oral presentations. Contribute to continuous improvement within the group. Comply with FDA, performing all work in a safe manner. Maintain proper records in accordance with all SOP's and policies. Provides support for ordering and maintaining inventory of laboratory materials and equipment. Performs other miscellaneous duties as required. etc. | 7/8/2019 |
| 289 | SDIX Windham, ME Animal Technician I HS diploma/AS Exp: Entry level |
This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. Responsibilities and Duties: Clean and disinfect cages, rooms and support areas. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. Conduct animal identification, animal breeding programs and related tasks. Conduct animal health monitoring and documentation. etc. This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. Responsibilities and Duties: Clean and disinfect cages, rooms and support areas. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. Conduct animal identification, animal breeding programs and related tasks. Conduct animal health monitoring and documentation. etc. This position participates in a team of technicians responsible for animal husbandry and antibody production activities. All job responsibilities to be conducted within standard operating procedures and regulatory compliance. Responsibilities and Duties: Clean and disinfect cages, rooms and support areas. Feed animals; maintain water systems, ventilation settings, pest control, and related tasks. Conduct animal identification, animal breeding programs and related tasks. Conduct animal health monitoring and documentation. etc. | 7/8/2019 |
| 290 | Seattle Genetics Bothell, WA GMP Support Specialist I University degree Exp: 0-2 years in a regulated environment |
This position supports Facilities GxP (GMP & GLP) compliance by acting as a liaison between Facilities, QC, GLP and QA. This position is responsible for supporting Facilities related incident investigations, CAPA, CAPA effectiveness, audits and other Quality System activities. This position supports the Master Equipment File (MEF) system by providing oversight of the document filing system. This position helps maintain departmental training compliance by providing administrative support. This position may help support validation by assisting with periodic reviews and other qualification activities. Drafts Facilities SOPs and work practices. | 7/8/2019 |
| 291 | Seattle Genetics Bothell, WA Research Associate I/II, Formulation and Drug Product Sciences BS in biochemistry, engineering, chemistry, biological sciences, or related Exp: 0-2 years |
The Formulation and Drug Product Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate to assist in the formulation development for therapeutic antibodies and antibody-drug conjugates. The ideal candidate should have a background in biochemistry or related discipline with previous laboratory experience, strong critical thinking skills, good interpersonal skills, and is self-motivated. Responsibilities: Conduct experiments and analyze results leading to development of robust formulations for antibodies and antibody drug conjugates. Generate and interpret high quality data. Perform study and instrument troubleshooting. Author technical reports. Summarize and present results in group and team meetings, contribute to discussions | 7/8/2019 |
| 292 | Seattle Genetics Bothell, WA Research Associate II, Process Chemistry MS in chemistry Exp: 0-5 years |
The successful candidate will be responsible for developing novel synthetic routes and chemical processes for anti-cancer drugs and proprietary drug linkers used for antibody conjugation. The ideal candidate should possess an in-depth knowledge of organic chemistry, reaction mechanisms, and familiarity with modern synthetic methods and analytical techniques. Candidates will have demonstrated creativity and independence in solving synthetic problems and ultimately developing robust chemical processes which he or she will work to transfer to CMO’s. Experience and expertise in peptide synthesis is desirable. Responsibilities: Conduct route scouting studies to establish novel synthetic routes for drug linkers and active pharmaceutical agents. Design and execute experiments which define parameters for robust and efficient chemical processes. etc. | 7/8/2019 |
| 293 | Seattle Genetics Bothell, WA Research Associate I/II, Target Validation BS in cell biology, biochemistry, biomedical engineering, or related Exp: 0-2 years |
The Target Validation group is seeking an energetic and highly motivated Research Associate to augment our efforts to identify and characterize molecular targets for our industry-leading ADC technology. The successful candidate will design, conduct, and interpret experiments utilizing a diverse array of techniques aimed at discovery and validation of early targets in Seattle Genetic’s drug discovery pipeline. Responsibilities: Standard target validation methodologies will include flow cytometry, in vitro cytotoxicity assays, immunohistochemistry, Western blotting, and a variety of biochemical and cell-based assays. etc. | 7/8/2019 |
| 294 | Sebela Pharma unspecified, QC Chemist BS in chemistry or related Exp: 0-2 years in a cGMP environment |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. PRINCIPAL DUTIES AND RESPONSIBILITIES: Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance. Perform training on procedures, equipment, or quality systems. Other duties as assigned. Individual contributor, but may be assigned as a project lead or trainer commensurate with experience or expertise. etc. | 7/8/2019 |
| 295 | Sedia Biosciences Portland, OR QC Technician HS diploma/AS Exp: 1 year |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. | 7/8/2019 |
| 296 | Sedia Biosciences Portland, OR Manufacturing Technician HS diploma/AS Exp: 1 year |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. | 7/8/2019 |
| 297 | Sedia Biosciences Portland, OR Scientist/Associate Scientist(R&D-Product Development) MS Exp: 1-3 years |
Sedia Biosciences Corporation of Portland Oregon is seeking a motivated, responsible, and resourceful individual to work as part of our team as a Scientist or an Associate Scientist. This position would be a full-time exempt position (40 hours per week) at our primary laboratory facility in Northeast Portland. The successful candidate will be responsible for running laboratory tests, recording data, performing some degree of data analysis, drafting protocols, and communicating with managers from R&D and other departments. They will also be asked to participate in production of prototype products, and assist in transition of those procedures (through training and/or record-keeping) to our manufacturing department. Workflow is approximately 50-70% laboratory work, with the remainder being office work. The nature of our work requires the candidate to be capable of working comfortably in a BSL 2 laboratory. | 7/8/2019 |
| 298 | Seer , CA Research Associate, Assay Development BS/MS Exp: 1-4 years |
Seer is seeking a Research Associate, Assay Development, who will implement and contribute to the design of biochemical experiments that support the development and operation of the company’s protein assays. These assays form the foundation of breakthrough products and services in proteomic data, which Seer will provide to patients and clinicians. The Research Associate, Assay Development will report to the Senior Scientist of Assay Development. The specific assays developed for Seer will leverage nanoparticles, immunoassays, as well as the use of mass spectrometry as a detection approach. The successful candidate is expected to have a background in biochemistry, biology, or pharmacology with experience in academia and/or industry, ideally within life sciences companies. Experience in industry, including the implementation of SOPs and testing in support of clinical or pre-clinical products is strongly desired. This role will be based in the South San Francisco office through late 2019. Please note, the company is moving to its permanent location in Redwood City at the end of the year. | 7/8/2019 |
| 299 | Seer , CA Research Associate, Chemisty MS Exp: 0-2 years |
Seer is seeking a Research Associate in the chemistry group, who will be empowered to support the development of the company’s core technology platform. The ideal candidate will have significant relevant experience and a track record of accomplishments in academia or in the life sciences/pharmaceutical/biotechnology industry. This role is part of a team focused on nanoparticle synthesis, characterization, and assay development. This role requires skills including particle synthesis, surface modification, and incorporates both organic and inorganic chemistry. This role will be based in the South San Francisco office through late 2019. Please note, the company is moving to its permanent location in Redwood City at the end of the year. | 7/8/2019 |
| 300 | Semma Therapeutics Cambridge, MA (Sr.) Research Associate (Scientist) – Cell Biologist R&D (MA) MS in molecular or cell biology or related Exp: 1-2 years |
Semma Therapeutics, a biotechnology company focused on developing a pluripotent stem cell-based cell therapy for Type 1 diabetes, is seeking an outstanding research associate to join its growing team. The full-time role will focus on tissue culture, molecular and cellular characterization, process and assay developments. Under the supervision of a Principal Scientist and working closely within the Cell Biology department on novel R&D programs, the associate will be responsible for the day-to-day execution of specific projects. The position will be located in Cambridge/Boston, MA. Responsibilities: Culture and differentiation of human pluripotent stem cells in various conditions, including differentiation protocol optimization. Co-design and help execute well-controlled in vitro experiments to demonstrate technological feasibility and improvements for characterization of cell product and/or achieve proof-of-concept. etc. | 7/9/2019 |
| 301 | Senseonics Germantown, MD Staff Accountant BS/BA in accounting or equivalent Exp: 1-3 years |
We are looking for a full-time Staff Accountant to support the finance team with all aspects of the day to day accounting function as needed. The ideal candidate is ready to work hard, have fun, and utilize their technical skills to further develop their accounting career. This is an excellent opportunity where you will gain valuable experience and have impact in multiple facets of operational accounting and related tasks in a publicly traded, dynamic, rapidly growing business. Qualifications: Record accounting transactions following Senseonics internal control processes. Perform account reconciliations and close procedures. Support the preparation and analysis of monthly and quarterly results. etc. | 7/9/2019 |
| 302 | SeraCare Gaithersburg, MD Research Associate II MS in biochemistry, molecular biology, or related Exp: Recent graduates |
Advance SeraCare’s purpose of understanding disease by supporting the research and development of new precision diagnostic products. Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material. RESPONSIBILITIES: Perform general molecular techniques such as nucleic acid purification, gel-electrophoresis, RNA transcription, cell culture, and bacterial culture. Perform nucleic acid analysis (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results. etc. | 7/9/2019 |
| 303 | Sigilon Therapeutics unspecified, Assistant/Associate Scientist, Biomaterials BS/MS in biochemistry, biology, engineering, or related Exp: 0-2 years |
Responsibilities: Encapsulation of cells in novel biopolymer systems. Maintenance and setting up of biopolymer device encapsulation systems. Establishing protocols and SOPs for encapsulation procedure. Work in a matrixed environment to ensure biomaterials meet the needs of the in vivo and cell biology teams. With increasing independence, plan, design and execute of a series of experiments that provide the research findings necessary for the completion of an assigned project. Demonstrate understanding and application of relevant scientific literature to the design of experimental protocols. etc. | 7/9/2019 |
| 304 | Sigvaris Group Peachtree City, GA Technician AS or equivalent certification Exp: 1-3 years |
This position is responsible for the general repair of hosiery knitting machines to ensure first quality products are produced to company specifications. Performs required/needed maintenance knitting machines to ensure machines are operating in good working order. Addresses machine stops to keep machines operating efficiently. Performs preventative maintenance as outlined in weekly PM sheets. Follows proper procedures to ensure product is knit to specifications. Sets up and sizes different styles/series on machines and ensures proper sizing to spec before released to production. etc. | 7/9/2019 |
| 305 | Smith & Nephew Memphis, TN Quality Engineer I (Medical Device-Hips) BS in mechanical, manufacturing, electrical, or industrial engineering Exp: 0-2 years |
Reporting into the Quality Department, this role has responsibility for Quality related actions in support of New Product Development (NPD, Design Quality). Works collaboratively with project team members to develop and manage project plans. Champion design control and risk management activities for assigned projects. Evaluate risk and verification implications for purposed post launch design changes. Continuously improve Design Control procedures and maintain procedural compliance. Supports new product development and implementation of new products via development of an overall quality plan, including needed inspection, test, and audit procedures; identification of needed reliability testing; identification, procurement, and maintenance of needed engineering test equipment; and support of process/product validation. Responsible for development and release of engineering design documentation. etc. | 7/9/2019 |
| 306 | Meridian Bioscience Memphis, TN Quality Systems Software Engineer BS/BA in communications, computer science or related Exp: 0-2 years |
The Quality Systems Software Engineer position at Meridian Bioscience within the Life Science Quality Assurance department supports the Quality System by developing and maintaining electronic document and data management systems. The Quality Systems Software Engineer works with cross functional teams to identify areas that can be streamlined or improved by implementing processes that meet regulatory requirements and standards associated with electronic data management. The Quality Systems Software engineer.is responsible for application systems administration within the scope of Quality Systems. This includes working with cross functional teams to identify areas that can be streamlined or improved by implementing documentation processes that meet regulatory requirements and standards for electronic documentation, developing electronic form records, document management and workflow processes, and authoring supporting documentation including but not limited to validation protocols and reports and verification test methods and procedures. | 7/4/2019 |
| 307 | Meridian Bioscience Cincinnati, OH Accounts Receivable Associate HS Diploma/GED Exp: 1 year in credit/collections |
Assist the Credit Department with wire and lock box processing, cash posting and collections. Electronic billing tasks which includes invoicing customers for shipments via email and invoice entry into customer portals. Monitoring the Accounts Receivable Email box and responding to customer requests for invoice copies and statements. Maintaining customer contact data within our collection software. Collecting and maintaining all customer sales tax documentation within Infor system. Generate and maintain rules in Cforia software system for monthly collection letters. | 7/4/2019 |
| 308 | Meridian Bioscience Cincinnati, OH Material Handler I HS Diploma/GED Exp: 1 year of warehouse experience |
The Material Handler transports all types of materials within MBI. Transports materials to the proper departments or destination by driving, carrying, pushing or hand truck. | 7/4/2019 |
| 309 | Merieux NutriSciences Minnetonka, MN Laboratory Assistant HS Diploma/GED Exp: 0 years |
We are currently seeking a Lab Assistant to provide assistance to our technicians and scientists. Responsibilities include: Carry out a number of procedures including preparing samples for analysis, sterilizing equipment, and general cleaning duties. Maintain working order of equipment and supplies necessary to perform analysis of food samples. Work closely with other team members and with the support of a department supervisor | 7/4/2019 |
| 310 | Merieux NutriSciences Madison , WI Sample Receiving Technician HS Diploma/GED Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 311 | Merieux NutriSciences Salida, CA Sample Receiving Technician HS Diploma/GED Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 312 | Merieux NutriSciences Allentown, PA Receiving Tech HS Diploma/GED Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 313 | Merieux NutriSciences Crete, IL Chemist I BS/BA or AA/AS in chemistry or related Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. This position reports to the Supervisor of Chemistry. | 7/4/2019 |
| 314 | Merieux NutriSciences Crete, IL Data Entry Specialist, Administrative HS Diploma or higher Exp: 1-2 years in data entry |
We are looking for data entry specialists with 1-2 years of experience in data entry. Fast paced work environment will require at least 60 WPM and moderate computer skills to fulfill job duties | 7/4/2019 |
| 315 | Merieux NutriSciences Madison , WI Laboratory Tech-Sample Receiving HS Diploma or higher Exp: 0 years |
Work as a member of a team to receive and log in client samples to prepare them for analysis. Review samples and documentation to assign identification numbers and enter data into our tracking system. Prepare packages for shipping and pick up by vendors. Contact clients when necessary to confirm information about test codes and sample contents. Achieve accurate, timely and consistent results to ensure samples are processed correctly | 7/4/2019 |
| 316 | MeritMedical South Jordan, UT Engineer I MS in engineering or related Exp: 0-2 years |
This Engineer I could be working in the wafer fabrication, wafer dicing, and/or electronic assembly areas. Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks. Uses limited amounts of discretionary judgment in making decisions regarding technical alternatives. Performs work of some higher technical level for training purposes, and work is screened to ensure correct application of scientific principles. Works on special projects, writes ECN's, and may create prototypes under general direction. | 7/5/2019 |
| 317 | MeritMedical Malvern, PA Quality Assurance Technician-TEMP AS/AA Exp: 1 year or more |
Performs routine quality technical assignments including data entry, storing master documents and issuing documents to authorized entities. Audits and inspects the production process to confirm that Device History Records are completed according to Device Master Record/QSR/GMP regulations. Audits and inspects finished products to ensure that it conforms with Device History Records and applicable specification and procedures. Initiates, identifies (labels) and ensures closure of NCMR's. Enters information into NCMR database. | 7/5/2019 |
| 318 | MeritMedical South Jordan, UT Material Handler I HS Diploma/GED Exp: 3 months warehouse experience |
Responsible for pulling parts from the warehouse and seeing that line production workers have the raw materials they need to perform their jobs. Obtains parts from the warehouse for use in production and verifies the part's lot number to ensure that the proper materials are used. Pulls supplies for assembly workers and ensures that supplies are stocked and readily available for assembly workers. Puts the parts in production bins for easy handling by the production workers. | 7/5/2019 |
| 319 | MeritMedical South Jordan, UT Technician II - Weekend Shift AS/AA Exp: 1 year or more |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts, and may service or repair simple instruments or equipment. Conducts a variety of tests using established and clearly defined methods. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering data from various prescribed sources and processes the data following well-defined methods, then presents the data in prescribed form. | 7/5/2019 |
| 320 | MeritMedical South Jordan, UT Packager HS Diploma/GED Exp: 6 months or more work experience |
Packages and labels products, inspects products to ensure that the number and type of product matches the label, and records the products packaged. Boxes manufactured products, checking products to ensure that they are the correct lot number and amount to be put in the box, and that the label matches the lot number and amount. Checks boxes to make sure that they are properly secured and that they are clean and neat in appearance. Obtains the correct labels for products to be boxed, matching labels with goods ordered. | 7/5/2019 |
| 321 | Merz Franksville, WI Engineer – Calibration and Reliability BS/BA in physicis, electrical engineering, electronics or related Exp: 1 year or more in calibration/reliability |
The Engineer – Calibration and Reliability is mainly responsible for the integrity of the calibration process and to ensure all documentation and procedures are up-to-date and cover all regulatory requirements. Other responsibilities include the improvement of asset reliability through predictive maintenance, analysis of data collected, risk assessments or other reliability related techniques or processes. | 7/5/2019 |
| 322 | Merz Franksville, WI Biomedical Engineer BS in biomedical engineering, engineering or life sciences Exp: 0-5 years in engineering/biotech |
The Biomedical Engineer is responsible for facilitating the transfer, scale-up, and validation of new and improved product designs and processes into manufacturing. Also responsible for assisting and providing technical product support for other functions including regulatory, quality, manufacturing, clinical, marketing and sales. | 7/5/2019 |
| 323 | Merz Mesa, AZ Engineer - NPI BS/BA in ME, IE, EE or other engineering Exp: 1-5 years in product design/development/manufacturing |
Responsibilities include: Drive efforts to design, develop, validate, and continuously improve manufacturing processes. Develop & define production control methods to monitor process output and establish critical supplier metrics. Define and coordinate the design and development of manufacturing fixturing and test equipment. Coordinate with R&D to optimize the design for manufacturing and reliability. | 7/5/2019 |
| 324 | Merz Franksville, WI Quality Control Associate I BS/BA in physical sciences or related Exp: 1-3 years in quality |
This role is responsible for executing daily activities in the QC Laboratory including support testing for the production of Merz North America product. Oversee and/or assist with tasks related to the activities associated with operation of Merz Quality System and as directed by Quality Management. Support all activities related to analytical assessment of Merz NA products and the manufacturing environment. Advise Quality Assurance, Manufacturing and MS&T departments on matters related to analytical testing and support. Provide direct support to Quality Assurance personnel regarding operation of the department and Quality System. | 7/5/2019 |
| 325 | Merz Mesa, AZ Regulatory Affrs Assoc BS/BA in sciences or healthcare Exp: 1 or more years in regulatory |
The Regulatory Affairs Associate supports the regulatory activities for development projects including new products and life cycle management. This includes assisting with regulatory strategies and timelines as well as the development and implementation of submissions under the direction of a line manager. With support from Regulatory Affairs Manager, provide ongoing support to cross functional teams to provide regulatory strategies during product development. | 7/5/2019 |
| 326 | MSD Rockville, MD Production Control Tech I BS/BA in life sciences Exp: 1 or more year in biotech lab or manufacturing |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. The position will help standardize and improve documentation, manufacturing procedures and processes to increase production efficiency and ensure best practices are followed. The position will also help implement new products, projects and processes within Manufacturing Operations. Some degree of professional latitude, creativity and self-management is expected. | 7/5/2019 |
| 327 | Metabolon Durham, NC Sofware Development Engineer BS/BA in computer sciences or related STEM Exp: 0-2 years in software development |
We are looking for exceptional self-starters who take pride in utilizing best practices to build scalable, maintainable software to provide our customers with the best user experience. We look for talented software engineers who believe in our mission, find meaning to the work that we do, and hold themselves accountable for deadlines and high-quality deliverables | 7/5/2019 |
| 328 | Mevion Medical Systems Littleton, MA Software Engineer I BS/BA in computer sciences, electrical or computer engineering Exp: 0-3 years in C/C++ programing |
Responsibilities will include various system engineering activities for the PTS-250 development, including, but not limited to: 1. Responsible for design, development, integration and testing of various tasks in support of the PTS Software development effort. 2. Work with engineers from the various project teams in order to develop the PTS-250 software. 3. Work with quality engineering to develop test plans. 4. Responsible for design documentation.Responsibilities will include various system engineering activities for the PTS-250 development, including, but not limited to: 1. Responsible for design, development, integration and testing of various tasks in support of the PTS Software development effort. 2. Work with engineers from the various project teams in order to develop the PTS-250 software. 3. Work with quality engineering to develop test plans. 4. Responsible for design documentation.Responsibilities will include various system engineering activities for the PTS-250 development, including, but not limited to: 1. Responsible for design, development, integration and testing of various tasks in support of the PTS Software development effort. 2. Work with engineers from the various project teams in order to develop the PTS-250 software. 3. Work with quality engineering to develop test plans. 4. Responsible for design documentation. | 7/5/2019 |
| 329 | Mevion Medical Systems Littleton, MA Commissioning & Support Engineer BS/BA in physics, electrical engineering, computer science or related Exp: 1 or more years |
The Commissioning & Support Engineer responsibility is two-fold: it includes both on-site, hands-on installation work and remote product support. The role of commissioning engineer involves frequent travel to customer sites to configure and commission the S250-series cyclotrons under installation. During remote weeks or between installs, this role functions more like product support, responsible for providing business critical technical support to other commissioning engineers, installers, field service engineers and customers to help ensure the highest operational status possible. | 7/5/2019 |
| 330 | Analytical Lab Group Concord, CA Laboratory Technician AS/AA in microbiology or related Exp: 0-1 years in pharma/biotech |
The technician's main duties are to ensure timeliness of testing, meeting client requirements. The technician must provide services that are compliant to the ALG-West Coast Quality Manual, client requirements and regulatory requirements as applicable such as ISO/IEC 17025:2017, USP, EU, GLP, GMP, FDA and ICH guidelines. | 7/5/2019 |
| 331 | Analytical Lab Group Concord, CA Environmental Monitoring Technician AA or BS in microbiology or related sciences Exp: 1 or more years in GMP |
Analytical Lab Group's West Coast location is looking for laboratory technicians to perform environmental monitoring at client facilities and microbiology testing in the microbiology lab. This is a full-time position. The schedule will be Monday-Friday, 7 a.m. to 3:30 p.m., but you must be able to work flexible hours, including different shifts and weekends. At this time, the starting hour is 5 a.m. and will require OT. | 7/5/2019 |
| 332 | Idex Corporation Shelby , NC Production Associate - Material Handler HS Diploma/GED Exp: 1 or more year in manufacturing |
A Production Associate is a multi-skilled employee that will perform a variety of duties to support the assembly of rescue tools and other products. Production Associates will perform a variety of activities including (but not limited to) material handling, stocking parts, quality inspections, and packaging products for shipping. Responsible for maintaining established quality standards while ensuring a safe and clean work environment. | 7/5/2019 |
| 333 | Micropoint Santa Clara, CA Quality Control Associates MS in chemistry, biology or related Exp: 0-2 years |
We are looking for highly motivated QC Associates (two openings) to join our quality team. These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. | 7/5/2019 |
| 334 | Micropoint Santa Clara, CA Manufacturing Operators HS Diploma/GED Exp: 0-2 years in food/pharma/diagnostics manufacturing |
There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging. Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection. Prepare materials used in the cartridge production process. | 7/5/2019 |
| 335 | Microvention Aliso Viejo, CA Engineer I, R&D BS/BA in related field Exp: 0-3 years |
The Engineer I, R&D supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job Duties: Develop new product concepts and products. Engineering design and process development. Generate intellectual property, write invention disclosures. etc. | 7/5/2019 |
| 336 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, chemical engineering or related Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). | 7/5/2019 |
| 337 | Merck KGaA St. Louis, MO Planning & Scheduling, Specialist BS/BA in business, mathmatics, supply chain, or related Exp: 0-1 years |
At MilliporeSigma the Planning & Scheduling Specialist reviews demand plans at a global and local level including adjusting forecast and safety stock parameters. He/she will also work with the sales group to incorporate customer demands into the planning systems and will develop operational schedules to meet customer service objectives and support sales growth plans at the lowest overall inventory costs. The specialist will also develop, test and execute models for scheduling operation and lead and/or assist process improvement initiatives. In addition, he/she will review long term plans to ensure capacity requirements are understood and met and will compile reports and metrics to ensure business has proper feedback loops on performance to objectives. | 7/5/2019 |
| 338 | Merck KGaA Rockville, MD Associate Scientist 1 BS/BA in life sciences Exp: 0-2 years |
Perform all routine and relevant laboratory techniques in compliance with BioReliance regulatory standards. Maintain and operate all laboratory equipment with some troubleshooting, as required. Perform various cell culture operations for biosafety testing. Maintains thorough records in addition to peer review of batch records. Responsible for generating deviations as required and participating in resolving investigations with support of other team members. Maintains a standard up keep of the facility through daily cleaning. Actively performs equipment and general housekeeping daily checks and notify relevant personnel of any issues. Initiates and completes projects independently, including troubleshooting during routine laboratory activities. | 7/5/2019 |
| 339 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, chemical engineering or related Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Ensure quality throughout the process. Assure you are adequately trained to perform tasks/assignments. Perform routine assays, processes and/or unit operations. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). | 7/5/2019 |
| 340 | Merck KGaA Sheboygan Falls, WI Procurement Rep 1 HS Diploma/GED Exp: 1+ year office experience |
The purpose of this position is to Initiate and expedite the transfer of inventory from and to related parties. Ensure that all materials, equipment and tools are available for production and maintenance of site processes. Solicit price and delivery information from vendors, enters into computer files and communicates to appropriate departments. Coordinate with other departments the procurement of tools, materials and equipment. | 7/5/2019 |
| 341 | Merck KGaA Bedford, TX R&D Analytical Lab Technician BS/BA or AS/AA Exp: 1+ year chemistry experience |
Must have good laboratory habits and be able to follow SOPs, procedures and protocols. Able to multi-task, handle routine as well as non-routine requests and assist other members of the group as required. Familiar with established laboratory procedures. Able to carry out experiments under close supervision. Possesses excellent record keeping skills, good written and verbal communications skills, and interacts effectively with peers and with people outside of the group. Able to work effectively with others to complete collaborative projects. | 7/5/2019 |
| 342 | Merck KGaA Carlsbad, CA Manufacturing Technician 1 BS/BA or HS Diploma Exp: HS: 6 months, BS/BA: 0 year |
The Manufacturing Technician I position will work in a cleanroom environment and adhere to cGMP batch records and SOPs to support the manufacturing of viral vector products. Employees will support projects in conjunction with other GMP Manufacturing personnel (Leads, Supervisors, Managers). Employees are expected to prepare suites for manufacturing, to document deviations, and to operate in a safe and compliant manner. | 7/5/2019 |
| 343 | Lentigen Technology Gaithersburg, MD R&D Molecular Biology Associate MS in molecular biology, immunology, or related Exp: 0-2 years |
You will use Lentigen’s expertise in lentiviral vector technology to analyze the biology of immune effector cells, stem cells and immortalized cell lines modified by lentiviral transduction. Furthermore, the unique duties of this position will allow you to master state of the art research and development techniques in molecular biology, lentiviral technology, genomics and immunology to make valuable contributions in keeping Lentigen Technologies, Inc. at the cutting edge of biomedical research. | 7/5/2019 |
| 344 | Miltenyi Biotech Sunnyvale, CA Process Development Associate BS/BA in life sciences Exp: 0-2 years |
You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. In addition to your primary responsibilities, you will document activities for reproducibility, clean and maintain laboratory equipment and support team members as needed. | 7/5/2019 |
| 345 | Miltenyi Biotech Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years GMP environment |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. | 7/5/2019 |
| 346 | Miltenyi Biotech Auburn, CA Logistics Associate HS Diploma/GED Exp: 1 or more year related experience |
As a member of the Miltenyi Biotec team, you will help ensure that the shipping and receiving process runs efficiently for our growing biotechnology organization. You will prepare and process inventory using your Enterprise Resource Planning (ERP) and shipping systems knowledge. In addition, you will record and receive incoming shipments according to established SOPs, as well as prepare and process shipments according to international regulations. There will also be occasion for employing hand-trucks and forklifts in order to move and store certain articles during routine inventory maintenance. | 7/5/2019 |
| 347 | Miltenyi Biotech Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in corporate business/accounting functions |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. | 7/5/2019 |
| 348 | Mirus Bio Madison , WI Shipping Associate HS Diploma/GED Exp: 1 or more years in shipping/logistics |
he Shipping Associate will pick orders from inventory and prepare them for shipping in an accurate and timely fashion. The Shipping Associate is also responsible for assembling finished goods for entry into inventory. This position will report directly to the Shipping Manager. Prepare and execute domestic and international shipping of Mirus products using FedEx, UPS, DHL and freight forwarders. Assemble finished goods for inventory. Follow departmental Standard Operating Procedures (SOPs) | 7/6/2019 |
| 349 | Mission Pharmacal Boerne, TX Tablet Tech-Night HS Diploma/GED Exp: 1 or more years |
Operates machines, tends the tablet press, transfers products into containers, weighs, mixes materials, records documentation, and performs basic routine maintenance. Cleans equipment and rooms per SOP’s and monitors product quality. Verifies all batches by control number, part number, and quantity per specifications prior to running the lot. Starts machine and observes operation to ensure all machinery is operating properly. Stops machine and reports any malfunction to Tableting Lead. Assist in repairs. Performs set-up of tablet press, assigned preventive maintenance procedures, parts assembly, and cleaning hardware. Ensures each product is tableted according to specifications and standard operating procedures. | 7/6/2019 |
| 350 | Moderna Norwood, MA Engineer I, Sterile Product Technology BS or MS in chemical/biomedical engineering or related Exp: BS: 0-5 years, MS: 0-2 years |
Moderna is seeking a highly skilled and motivated Engineer I/II in Sterile Product Technology, a process development team residing in Moderna’s Technical Development organization, to support mRNA lipid nanoparticle (LNP) process development that enables our clinical supply. The applicant will play a critical role helping bring medicines to patients as Moderna’s portfolio begins to shift towards late-stage development. The primary role for this position will be to support fill/finish process development and scale-up work, with eventual ownership of experimental design and execution. The applicant will collaborate closely with Technical Development, Pre-clinical and GMP Production, Quality, and Drug Product Analytical Development groups on innovative process development efforts. Applicants should have relevant pharmaceutical experience with fill/finish processes and drug product development. | 7/6/2019 |
| 351 | Moderna Cambrdige, MA (Contract) Research Associate, Process and Nucleic Acid Innovation BS or MS in molecular biology, biochemistry, biology or related Exp: 1-3 years research experience |
This role will conduct research in the Process and Nucleic Acid Innovation group to develop and test novel nucleic acid constructs for use in various interdepartmental projects. A successful candidate will be inquisitive about the science and capable of problem solving by consulting literature and colleagues and designing experiments to test hypotheses. This role will utilize various techniques associated with RNA and DNA synthesis and purification, mammalian cell culture, and in vitro molecular biology. This assignment is expected to last 12 months. | 7/6/2019 |
| 352 | Moderna Cambrdige, MA (Contract) Research Associate, Analytical Operations BS or MS in analytical chemistry, biochemistry, chemical engineering or related Exp: BS: 1-3 years, MS: 0-2 years |
The primary responsibilities of this role will be to support implementation of analytical methods and routine testing messenger RNA therapeutic drug substances and drug products, including both chemical separation and biophysical techniques. The incumbent will be expected to undertake laboratory work to support in-process sample testing of critical non-GMP large scale batches including IND enabling drug substance and drug product batches. The analyst will be responsible for generation and reporting of analytical results. | 7/6/2019 |
| 353 | Moderna Norwood, MA (Contract) Manufacturing Associate I, 2nd Shift BS/BA in biology, chemistry, chemical/biomedical engineering Exp: 0-2 years |
The individual in this role will be responsible for production of DNA for all constructs using custom automation, Hamilton liquid Handlers, and chromatography solutions. The successful candidate must demonstrate the ability to quickly master new processes and the drive to be part of a dynamic, fast paced, and highly motivated team. They must have training in chromatography (UPLC/HPLC), liquid handlers, basic molecular biology techniques, and ability to work with custom automation. The anticipated time frame for this assignment is 6 months. | 7/6/2019 |
| 354 | Moderna Norwood, MA (Contract) Manufacturing Associate I BS/BA in biology, chemistry, chemical/biomedical engineering Exp: 0-2 years |
The individual in this role will be responsible for production of DNA for all constructs using custom automation, Hamilton liquid Handlers, and chromatography solutions. The successful candidate must demonstrate the ability to quickly master new processes and the drive to be part of a dynamic, fast paced, and highly motivated team. They must have training in chromatography (UPLC/HPLC), liquid handlers, basic molecular biology techniques, and ability to work with custom automation. The anticipated time frame for this assignment is 6 months. | 7/6/2019 |
| 355 | MICR Indianapolis, IN Medical Research Study Coordinator CCRC certification + degree Exp: 1-3 years clincal research |
Individual will be responsible for implementing clinical research protocols. | 7/6/2019 |
| 356 | Molecualr MD Cambridge, MA Laboratory Assistant HS Diploma/GED Exp: 3 months or more work experience |
The Laboratory Assistant (Lab Assistant) is self-motivated and responsible for assisting the Technical Supervisor with clerical laboratory duties. They diligently strive to continually maintain a clean, professional, and safe working environment. Duties include specimen receiving and accessioning, storage of clinical specimens, assisting with lab cleaning/maintenance, equipment/temperature support, monitoring, lab supply inventory/receiving, clerical administrative responsibilities. | 7/6/2019 |
| 357 | Morphic Therapeutics Waltham, MA Research Associate, Immunology BS in biology or related Exp: 1-2 years in research |
The successful candidate will join a dynamic, multi-disciplinary team of scientists, playing a key role to evaluate new immunotherapeutic strategies and drug candidates. The candidate is expected to be multi-tasking and able to execute experiments with strong attention to detail under supervision. | 7/6/2019 |
| 358 | MP Biomedicals Santa Ana, CA Biochemicals Product Specialist MS in product management/life sciences Exp: 0-3 years |
Expand the Life Sciences business with research reagents for the fields of biochemistry, molecular biology, immunology, cell biology and neuroscience. Identify new product and market opportunities and deliver exceptional product technical support, answer questions regarding our products and present our products in the most favorable and understandable form to influence the buying decisions of our customers. Continually follow market trends and identify new sales potential through the addition of new products and application focused on select market segments. | 7/6/2019 |
| 359 | Reckitt Benckiser Parsippany, NJ Performance Marketing Associate, Comms & Content BS/BA or MBA Exp: 1-2 years |
You will be responsible for identifying and driving all digital content creation (Amazon A+/WebCollage, optimized copy, enhanced images and videos, Brand Store pages and Brand campaigns) for new and existing items across key brands. Assist sales teams for eTail such as Amazon, Walmart.com, Target.com, Costco.com to ensure content is optimized to achieve “best in class” ratings, using scorecards provided by tools such as Clavis as well as key customer dashboards. Research competitive data to understand current industry trends in order to stay competitive and develop best practices for E-Commerce content as it pertains to site merchandising and the online user experience. You are supposed to represent the end consumer and bring in their perspective and insights to add value within the broader e-commerce team. You would be the main point of contact for the various Brand teams and would work closely in understanding their brand strategy and bringing it to life within the ecommerce world. etc. | 7/2/2019 |
| 360 | Reckitt Benckiser Parsippany, NJ eCommerce Supply Fulfilment, Business Analyst unspecified Exp: Entry level or 1-2 years |
RB is driving aggressive growth in direct to consumer, E-Commerce globally. We are looking for an innovative individual to overdrive the online business with a unique combination of supply management, back office fulfilment operation maintenance and enhancements. The BA is key to the support and delivery of these overall team objectives: Responsible for developing and operating upstream end to end seamless supply chain flow for RBNA Health routes to market. Supply planning supervision is expected to ensure top level Service toward all D2C customer or consumer. Focusing on US. Manage, lead and develop robust S&OP process to allow no business disruption as well as liabilities – key stakeholder coordination is key (in market E commerce sales and marketing team, Finance, Manufacturing). Ensure Global supply processes are respected while developing new potential specific process requiring higher speed for Ecommerce. Define Logistics Strategy with key supply contact in US and CA sourcing countiresn– PNL monitoring and logistics cost optimization as key (freight mode, warehousing, potential D2C operation expansion). etc. | 7/2/2019 |
| 361 | Reckitt Benckiser Parsippany, NJ Performance Marketing Analyst BS/BA Exp: 1+ years |
Activation practitioner with experience in the media/search marketplace, who is eager to have immediate impact on RB E-Business team in its activation and optimization practice. Energized by the development of data architectures to drive performance along with executing dashboards that drive clear analysis and insights on in-market media results. Eager to create meaningful vendor partnerships & act as daily trader within self-service media platforms. ‘Hands on Keyboard’ operational activation & management of e-commerce Search/SEM strategy with stewardship of keyword, bid and pacing management Maintain relationships across Amazon AMS, AMG & Criteo Stewardship of go-to-market marketing approach across Bricks & Clicks customers, inclusive of activation of display & SEM campaigns. etc. | 7/2/2019 |
| 362 | Reckitt Benckiser Hillsborough, NJ Manufacturing Technician, Weekdays 1st shift (7:15am-3:30pm) unspecified Exp: Recent graduates |
The Manufacturing Tech is responsible for both running production lines when needed and making maintenance and technical decisions with exceptional knowledge of how the decisions will impact financial, quality and safety metrics; understanding and adhering to guidelines in the employee handbook and complying with regulatory requirements, company / plant policies, procedures, and rules in his/ her area of responsibility. The Manufacturing Tech must be able to independently perform most assignments. This is a skilled position that requires prior experience with packaging lines, equipment and processes. etc. | 7/2/2019 |
| 363 | Reckitt Benckiser Salt Lake City, UT Plant Finance Analyst (Grad Program) BS in accounting preferred Exp: 2019 graduates |
We are looking for graduating students to join our RB Finance Graduate Development Program. You may do rotations through: Supply Finance, Commercial Finance and Accounting. Responsibilities: Collect, process, verify, and report accounting related information. Perform professional analytical and management to support work assignments. Assist in preparing monthly financial reports, developing and/or utilizing spreadsheets, databases and other computer applications. Process specialized information, reports, and forms for fees, billing, project tracking, etc. Enter information reports into a financial accounting system. Other financial, accounting, and information system related tasks are to be performed as assigned. etc. | 7/2/2019 |
| 364 | Reckitt Benckiser Evansville, IN Early Innovation Scientist, Analytical Sciences BS/MS in chemistry or related Exp: Recent graduates |
Proactively support early innovation analytical and human milk assessments for front end innovation initiatives. Active participant on early innovation project teams as an Analytical Sciences and Human Milk Research representative who delivers rapid analytical technology and human milk assessments, timely responses regarding analytical and human milk research questions, project deliverables and on-going analytical research support. Supports further understanding of human milk through ability to research and synthesize published human milk research and utilize new technologies and instrumentation. Contributes to technical hypotheses regarding analytical research and human milk capabilities and carries out protocols to test those hypotheses, with possible hands-on analytical lab involvement. Builds strong internal and external collaborations and coordinates scientific research to drive innovation initiatives. Effectively communicates scientific knowledge and information to technical and non-technical audiences at multiple levels through a variety of internal and external facing formats. Represents MJPNI at scientific conferences and external meetings to communicate scientific insights and understandings. | 7/2/2019 |
| 365 | Reckitt Benckiser Evansville, IN Innovation Method Development Scientist, Analytical Sciences BS/MS in chemistry or related Exp: Recent graduates |
Proactively identifies and executes strategic analytical method development and validation initiatives to support early innovation projects, human milk research, and key quality objectives. Active participant on project teams as an Analytical Sciences representative who delivers timely responses regarding analytical questions, project deliverables, and on-going analytical support. Identifies areas of improvements for analytical methodology through utilization of new technologies and instrumentation, implementation of method validation and transfer practices, and effective networking with the internal MJN analytical community as well as external experts. Contributes to technical hypotheses regarding analytical capabilities and develops protocols to test those hypotheses. Efficiently creates and executes method validation protocols to ensure developed methods are compliant against all internal criteria. Performs instrument maintenance and repair support while building knowledge and understanding of troubleshooting methodology and instrumentation issues. Effectively communicates scientific knowledge and information to technical and non-technical audiences at multiple levels through a variety of internal and external facing formats. | 7/2/2019 |
| 366 | Regeneron Tarrytown, NY Clinical Study Specialist (Inflammatory & Immunology) MS Exp: 1-2 years |
The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs). They: Organizes and delivers analyzable reports and metrics to the clinical study lead. Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings. Collates data for assessments such as feasibility and site selection and reviews site usability database. etc. | 7/2/2019 |
| 367 | Regeneron Tarrytown, NY Associate 1, Clinical Logistics BS/BA Exp: 1+ years |
The Clinical Logistics Associate I provides support to the Clinical Logistics group and IP distribution process for one or more clinical trials. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron SOPs / WPDs. Contributes to ongoing process improvement initiatives. This role applies to internally sourced studies and/or CRO/Partnered studies. Interacts with clinical trial managers, as well as staff from quality, clinical compliance, and IOPS (CMC, external manufacturing, stability). etc. | 7/2/2019 |
| 368 | Regeneron Tarrytown, NY TEMP Clinical Study Specialist (Oncology) MS Exp: 1-2 years |
The Temp - Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The Temp - CSS may be assigned to support the execution of one or more studies across a program. The Temp - CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The Temp - CSS will support internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs). Responsibilities: Organizes and delivers analyzable reports and metrics to the clinical study lead. Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings. etc. | 7/2/2019 |
| 369 | Regeneron Rensselaer, NY Biotech Production Dispensing Technician AAS Exp: 0-2 years |
Summary: Performs all tasks necessary for the manufacturing dispensing operations. Essential Duties and Responsibilities include, but are not limited to, the following: Includes all aspects of biotech production activities related to raw material dispensing. Ensures that raw materials are dispensed as specified in Batch Sheets or Manufacturing Records to support manufacturing operations. Works with manufacturing process areas and manufacturing inventory group to schedule lots of raw materials to be dispensed. Reviews, edits, completes, and revises completed batch records (if applicable), Logbooks, and SOPs in accordance with cGMP standards and compliant with written procedure. etc. | 7/2/2019 |
| 370 | Regeneron Tarrytown, NY Process Development Associate II - Mammalian Cell Culture Medium Dev. BS/MS in chemical or related engineering Exp: 0-2 years |
The Cell Culture and Medium Development Group within Preclinical Manufacturing and Process Development is looking for a motivated person to assist in medium development for mammalian cell culture processes. He/she will perform studies at a benchtop scale to develop cell culture medium that improves cell growth, cell productivity, and/or product quality. In this role, the individual will perform innovative cell culture experiments, high-throughput model development, small-scale bioreactor development, and literature searches. The ability to design experiments, statistically interpret results, and communicate findings is required. etc. | 7/2/2019 |
| 371 | RTI Surgical Alachua, FL Donor QA Associate AA Exp: 1 year |
POSITION SUMMARY: Obtain, compile, track, review, file and disposition accurate and complete donor records (paper and electronic) to support applicable regulations, standards and departmental procedures for donor eligibility determination in a timely manner. Disposition donors in electronic system for release into production, rejection or Medical Director request for additional information. Develop and maintain effective working relationships with recovery agencies and other entities providing donor records to facilitate timely submission of accurate and complete required records. Act as departmental liaison to both internal and external customers to provide requested donor related information and/or resolve issues as requested. Comply with all applicable regulations, standards, company policies and departmental procedures. Support company and departmental quality and business objectives and initiatives. Provide information to develop and monitor quality and business metrics as requested. | 7/2/2019 |
| 372 | RTI Surgical Alachua, FL Material Tech 1 HS Diploma or equivalent Exp: Entry level |
The Materials Tech 1 position at RTI represents an entry level function. Employees will develop technical skills in their assigned areas, an understanding of the rules and regulations that RTI administers, and the basic operating approach at RTI including: reading, understanding, and following work instructions; working in a team environment; and learning to work with minimal supervision. POSITION SUMMARY: Performs tissue processing activities that produce the highest level of quality and yield outcomes in accordance with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). Responsible for accurately processing tissue products and meeting production schedules. etc. | 7/2/2019 |
| 373 | RTI Surgical Alachua, FL Tissue Processing Tech 1 HS Diploma or equivalent Exp: Entry level |
The Tissue Tech 1 position at RTI represents an entry level function. Employees will develop technical skills in their assigned areas, an understanding of the rules and regulations that RTI administers, and the basic operating approach at RTI including: reading, understanding, and following work instructions; working in a team environment; and learning to work with minimal supervision. POSITION SUMMARY: Performs tissue processing activities that produce the highest level of quality and yield outcomes in accordance with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). Responsible for accurately processing tissue products and meeting production schedules. etc. | 7/2/2019 |
| 374 | Rubryc Therapeutics San Carlos, CA Executive Assistant BA/BS Exp: 1-3 years |
The Executive Assistant reports to the CEO and will play a key support role as the Company proceeds through important developmental milestones and growth spurts in the coming years. RubrYc’s Executive Assistant will act as a crucial coordinator of meetings and contact among executives, employees, service providers, vendors, clients, investors, advisors, and other stakeholders. The Executive Assistant will manage information flow amongst and between these individuals and organizations accurately and efficiently.The Executive Assistant will have important operational roles including supporting expense reporting and reimbursement/payment, maintaining office supply inventory for the Company and laboratory materials supply inventory for R&D teams; interfacing with facilities and IT service providers; coordinating Executive Management Team calendars, arranging for travel and transportation, and managing team and Company meeting schedules. etc. | 7/2/2019 |
| 375 | Salix Pharmaceuticals Bridgewater, NJ Salix Inside Sales Associate BA/BS in business or related Exp: Recent graduates |
The Salix Inside Sales Associate program offers a unique opportunity for recent college graduates who are interested in a fast start to an exciting career in medical/medical device sales. We are seeking candidates who are highly competitive, have a strong work ethic and are motivated to accelerate their position in a company currently launching several new and innovative products into the GI marketplace. Those accepted into this exclusive program will relocate to Bridgewater, NJ for approximately 12 months. During the 12 months Sales Associates receive intensive training on: Products, Selling Skills, and Industry & Territory Management. Upon successful completion of the 12-month training program, Sales Associates ready for the field will be eligible to apply to any open Salix Territory Manager positions. Sales Associate pay, bonus and benefits are competitive. Upon placement into a field sales territory the Sales Associate is provided with a company car and necessary tools to manage a territory - including an iPad and iPhone. Some relocation assistance may be available depending on relocation distance. etc. | 7/2/2019 |
| 376 | SAMDI Tech Chicago, IL Research Assistant (Full-time) BS in biology, chemistry, or related Exp: 0-3 years |
We are seeking a highly motivated and skilled scientist to join our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include supporting the preparation of reagents and materials for running biochemical assays, assisting in executing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, integrating automated liquid handling, and supporting fundamental laboratory functions. | 7/2/2019 |
| 377 | SAMDI Tech Chicago, IL Research Associate- Biochemical Assay Specialist (Full-time) MS in biology, chemistry, or related Exp: 1-3 years |
We are seeking a highly motivated and skilled scientist to join our dynamic Research Team. The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include handling and processing of reagents and materials for running biochemical assays, designing and performing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, take a project leadership role on multiple targets/enzymes, integrating automated liquid handling, and writing and maintaining Standard Operating Protocols (SOPs). | 7/2/2019 |
| 378 | Samumed San Diego, CA DMPK, Research Associate BS in life, chemical sciences or related Exp: 0-4 years |
Samumed has an immediate opening for a Research Associate to perform bioanalytical analysis from in vivo pharmacokinetic/pharmacology studies in a variety of matrices and assist in developing novel bioanalytical methods using LC/MS/MS. Specific Responsibilities: Perform bioanalytical extractions of test article and metabolites from biological matrices. Operate, troubleshoot, and maintain LC-MS/MS and other analytical equipment. Generate high quality data in timely manner to inform project teams. Planning and executing scientific experiments as required. Analyzing and documenting experimental data in electronic notebooks in a timely and accurate manner in accordance with the company guidelines. Performing additional general duties to support the safe and efficient operation of the laboratory as required. Samumed has an immediate opening for a Research Associate to perform bioanalytical analysis from in vivo pharmacokinetic/pharmacology studies in a variety of matrices and assist in developing novel bioanalytical methods using LC/MS/MS. Specific Responsibilities: Perform bioanalytical extractions of test article and metabolites from biological matrices. Operate, troubleshoot, and maintain LC-MS/MS and other analytical equipment. Generate high quality data in timely manner to inform project teams. Planning and executing scientific experiments as required. Analyzing and documenting experimental data in electronic notebooks in a timely and accurate manner in accordance with the company guidelines. Performing additional general duties to support the safe and efficient operation of the laboratory as required. | 7/2/2019 |
| 379 | Sanofi Framingham, MA Senior Research Associate, Analytical Development I MS Exp: 0-2 years |
This position is within the Analytical Development group which develops, qualifies, and transfers analytical methods used for characterization of protein and gene therapeutics in early stage development (Phase I/II). We are seeking a highly motivated individual to participate in cGMP sample testing, as well as the development, qualification, and transfer of analytical methods, based on platforms such as enzymatic activity, gel and capillary electrophoresis, ELISA, and HPLC for the purposes of drug substance and/or drug product lot release and stability testing. Duties and Responsibilities: Perform method development and scientific procedures and experiments under minimal supervision. Plan and prioritize concurrent experimental procedures and document in an electronic lab notebook. Integrate, compile, analyze, and interpret data with minimal supervision. etc. | 7/2/2019 |
| 380 | Sanofi Westborough, MA Stability Specialist BA/BS Exp: 1-3 years |
Executes stability programs to support product expiration dating, storage and handling, shipping and patient use in compliance with industry practices and regulatory requirements. Also participates in the Periodic Product Review (PPR) process. Responsibilities: Participate in monitoring stability storage conditions, submit stability samples to analytical laboratories when required and monitor laboratory test results. Participate in developing stability study protocols and in in establishing strategies for stability studies. Perform analysis of stability data and draft stability technical reports. Escalate unusual observations, deviations or any incidence of non-compliance with established protocols or procedures. Compile stability data for inclusion in regulatory submissions. Participate in the compilation of Periodic Product Review (PPR) reports. Participate directly with external departments (e.g. Manufacturing Science & Technology, External Supply Quality Assurance, and CMOs). etc. | 7/2/2019 |
| 381 | Sanofi Allston, MA Quality Control Analyst I BS in life sciences discipline Exp: 1 year in a cGMP lab environment |
Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for CGMP operations. Various techniques are utilized in Quality Control including, HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, stability testing, assay transfers and the qualification of new instrumentation utilized in the Quality Control laboratory. Position Overview with Key Responsibilities: Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs. This position is responsible for performing routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation. etc. | 7/2/2019 |
| 382 | Sanofi Toronto, ON Packaging Technician, Day Shift Minimum 3 year college diploma in pharmaceutical technology Exp: 6+ months |
Sanofi Pasteur Limited is looking for motivated and results driven individuals to join our Filling and Packaging team as a Packaging Technician. Key responsibilities will include the following: 1. Monitor all tasks in packaging areas. 2. Maintain equipment in good condition. 3. Plan for training. 4. Ensure quality of the packaging process. 5. Provide training. etc. | 7/2/2019 |
| 383 | Sanofi Toronto, ON Packaging Technician, Day Shift Minimum 3 year college diploma in pharmaceutical technology Exp: 6+ months |
Sanofi Pasteur Limited is looking for motivated and results driven individuals to join our Filling and Packaging team as a Packaging Technician. Key responsibilities will include the following: 1. Monitor all tasks in packaging areas. 2. Maintain equipment in good condition. 3. Plan for training. 4. Ensure quality of the packaging process. 5. Provide training. etc. | 7/2/2019 |
| 384 | Sanofi Swiftwater, PA Biological Sales Associate: National Sales Network (NSN) Conference 2019 BA/BS Exp: 0-2 years |
This position is part of the Biological Sales Associate Program. This program consists of 3 developmental phases: in-house training, outbound sales responsibility based at our home office in Swiftwater, PA and a field externship period where the selected candidate would backfill one of our Vaccine Specialist positions anywhere in the US. The entire program lasts approximately 12 months with the ultimate goal of having the candidate earn a promotion to a permanent position as a Vaccine Specialist within our field sales force. This position requires that a candidate be willing to relocate to Swiftwater PA for the first half of their program and then be willing to relocate anywhere in the US upon completion. etc. | 7/2/2019 |
| 385 | Sarepta Therapeutics Burlington, MA Research Associate II, Gene Therapy Process Development - In-Process Analytics MS in pharmaceutics, chemical engineering, chemistry, or related Exp: 0-3 years |
The Research Associate will support the development of Sarepta’s Gene Therapy platform. Working as a member of Gene Therapy group within Technical Operations department, he/she will support the implementation of in-process analytical test methods for use in the development of gene therapy products. The individual will collaborate with the Analytical Development team to support the adaptation of release test methods for use in-process, will execute established test methods to better characterize product and impurities over the course of development and will collaborate with process development scientists on the design and interpretation of studies. The individual may also work with external stakeholders in supporting evaluation of processes managed outside of the organization. etc. | 7/2/2019 |
| 386 | Sarepta Therapeutics Burlington, MA Associate I, Gene Therapy Pilot Coordination BS Exp: 0-2 years |
The Associate I, Gene Therapy Pilot Coordination will help drive the development of Sarepta’s Gene Therapy platform. Working as a member of the Gene Therapy Pilot Team within Technical Operations he/she will be responsible for supporting scale-up studies and material production at a pilot scale within Sarepta’s internal laboratories. The Associate I, Gene Therapy Pilot Coordination will be responsible for documentation, product and sample inventories, as well as raw material and supply stocks. He/she will be expected to work in close collaboration with other Pilot Team members, as well as colleagues in the development and manufacturing organizations. | 7/2/2019 |
| 387 | Sarepta Therapeutics Columbus, OH Laboratory Veterinarian Technician HS Diploma, AS/BS preferred Exp: 1-2 years |
Primary responsibilities Include: Handle, transfer, and distribute mice, supplies and waste as needed to and from work area(s). Proficient in IM, IV, IP administration techniques in lab animals. Clean cages and racks. Monitor the daily health and welfare of the animals according to IACUC guidelines. Coordinate with vendors and supervisors on operational, administrative and technical responsibilities. Responsible for overseeing procurement of animals and supplies, preventive maintenance of facility equipment. Strong written and verbal English communication skills. Ability to follow written and verbal instructions. Follows standard operating procedures and maintains recordkeeping pertaining to equipment operation, animal and supply inventories in accordance with federal and state guidelines and regulations. etc. | 7/2/2019 |
| 388 | Sarepta Therapeutics Columbus, OH Research Associate I, Histology, Gene Therapy Research AS in chemical, physical, or biological science Exp: 1-3 years |
Sarepta Therapeutics is seeking a motivated individual with histology laboratory expertise/training. The qualified candidate will provide laboratory support of day-to-day GCP/GLP testing on muscle/nerve using complex histology methods in accordance with the requirements of approved protocols; maintains records of experiments; assists in analyzing data and prepares laboratory reports. This person may participate in development, GCP/GLP qualification, and validation of histology related assays to support clinical trials and clinical development decision-making. Primary responsibilities include: Performs routine and complex laboratory procedures in histology using frozen section techniques. Assist in the execution of GCP/GLP clinical study sample processing, staining and analysis using a variety of assay formats such as Histochemical special stains, Immunofluorescence and Immunohistochemistry. etc. | 7/2/2019 |
| 389 | Sarepta Therapeutics Cambridge, MA Clinical Research Associate II, Translational Development BS in biochemisty or related field Exp: 1-2 years |
Sarepta Therapeutics is seeking a motivated clinical operations specialist with experience working in clinical operations and GCP/GLP environment for a clinical operations support role. The Research Associate (RA) will assist the Clinical Research Manager in interacting with the Clinical Operations group in the planning, execution and management of clinical samples. The RA will support the transfer of clinical samples from collaborators and CROs to Sarepta and third party storage facilities. He/She will work closely with the Clinical Research Manager to facilitate the training of international biopsy surgical sites and distribution of training materials. Additionally, he/she will take on a role in tracking training documentation across studies/research protocols. The candidate must exercise discretion and judgment in handling confidential information and will follow FDA regulations, ICH guidelines and GCP in all tasks. Strong organizational skills are required, as well as the ability to balance changing priorities. The role may involve occasional travel to oversee clinical sites or vendors. etc. | 7/2/2019 |
| 390 | Lipocine Salt Lake City, UT Associate Scientist, Pharmaceutical Research and Development BS/MS in life sciences or chemical engineering Exp: 1-3 years in pharma/chem lab |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 6/27/2019 |
| 391 | Liquidia Technologies Morrisville, NC Contract Manufacturing Operator AS/AA degree Exp: 0-3 years in manufacturing |
The Manufacturing Operator will support all GMP manufacturing activities by providing daily cleaning and maintenance of manufacturing cleanrooms. This position is responsible for performing and documenting routine cleaning activities and providing support for manufacturing operations. The operator will work with the Manufacturing Operations team to ensure a 1st class manufacturing organization to drive the Company’s programs to commercial success while ensuring the highest level of quality and safety standards. | 6/27/2019 |
| 392 | Lonza Hayward, CA Manufacturing Associate I AS/BS preferred Exp: 0-2 years, Entry level |
The Manufacturing Associate Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. | 6/27/2019 |
| 393 | Lonza Portsmouth, NH Manufacturing Associate Level 1 HS diploma, AS/BS preferred Exp: 0-3 years in manufacturing |
The Manufacturing Associate Level I (Night-Shift) is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. | 6/27/2019 |
| 394 | Lonza Walkersville, MD Process Validation Scientist I BS in biology, biochemistry, chemistry, etc. Exp: 0-4 years in process validation/development |
This individual is responsible for execution of Process Validation (PV) or for PV support with intensive supervisory direction for Liquid Media, LAL and Powder Media at the Walkersville Site. The individual performs assigned duties according to specified procedures and receives detailed instructions. The individual performs a variety of routine work within established policies and procedures, and receives detailed instructions on new projects and assignments. ble to work with intensive assistance and supervision on basic PV techniques of protocol development, execution, and reporting to ensure technical content is sufficient and accurate. This individual is expected to ask questions about content. Not approved to make protocol decisions (i.e. conclusions, product impact / validation impact assessment, and corrective actions) without review of a higher level PV scientist or Manager. | 6/27/2019 |
| 395 | Lubrizol Corporation Wickliffe, OH Lab Technician BS/BA in sciences Exp: 1+ years lab experience |
The Lab Technician in the Blend Test Services Department is responsible for all facets of testing from the set-up and take-down to reporting of results. The majority of the workday is spent in a laboratory setting working with new and used oils, solvents, chemicals and equipment utilized to complete testing. This person is responsible for ensuring safety, quality, and timely delivery of test results while using good housekeeping practices during daily operations. Conduct quality tests following work instructions and ISO 9001 and ISO 17025 procedures. Ensure that all test protocols are in compliance with recognized industry or internal LZ test standards. Update work instructions and procedures as necessary. Plot reference data on control charts. Understand control charting and when to investigate potential issues. Must be able to identify, troubleshoot, and work closely with chemists and business partners to resolve issues or problems. Appropriately elevate the situation to chemist, manager and/or business partner when necessary. | 6/27/2019 |
| 396 | America Regent New Albancy, OH R&D Technical Services Chemist I MS or BS in chemical engineering Exp: BS: 1-2 years in technical services, MS: 0-1 years |
Responsible for Technology Transfer and process scale up activities associated with parenteral drug products. Supports cross-functional Production, Engineering, Quality Assurance, and Validation departments to support the trouble shooting of manufacturing issues. Conduct the experiments under the supervision of Scientists for Tech Transfer, Process R&D/Scale up/Validation, and other activities needed for introduction of a new product into cGMP manufacturing site or to support process improvements of existing products. Execute laboratory experiments as per the protocols or under supervision to study material compatibility studies and/or cleaning validation activities | 6/27/2019 |
| 397 | Lumen Bioscience Seattle , WA Lab Aid BS/BA in biology or chemistry Exp: 0-2 years, Entry level |
The position will be supporting a research biology lab actively engaged in optimizing the growth of cyanobacteria cultures. This is a full time, regular, hourly position; 40 hours per week. The work schedule is somewhat flexible, and training will be provided. Responsibilities include: Clean and maintain stocks of laboratory glassware, Maintain general laboratory solutions and other reagents, Support lab manager in maintaining stocks of consumable items, May also perform plasmid DNA purification, PCR reactions and other standard laboratory protocols | 6/27/2019 |
| 398 | Luna Roanoke, VA Electromagnetic Research/Engineering Associate MS in electrical engineering, physics, material science or related Exp: 0-5 years |
Luna Innovations is seeking a creative Electromagnetic Research/Engineering Associate to conduct research focused on the discovery and development of new electromagnetic materials technology towards commercial applications. Current areas of development in the Advanced Materials Group include electromagnetic interference (EMI) shielding composites, coatings, and sealants; radar absorbing materials; conformal antennas; and signature control coatings. It is desired that the candidate will have a background in one or more of these areas, with specific expertise in electromagnetic material properties, EMI testing and characterization, and develop skills by contributing to program management, new idea generation, and experimental design / execution. Electromagnetic modeling and simulation experience is a plus. The candidate must be a U.S. Citizen and either have a Security Clearance or be willing and able to obtain a DoD Security Clearance. | 6/27/2019 |
| 399 | Luna Ann Arbor, MI Application Engineer BS/BA in technical field Exp: Entry-Level |
This is an entry level position. The Applications Engineer will be responsible for testing and analysis of customer samples for feasibility and performance of our terahertz equipment. With increasing familiarity and experience with our product line the Applications Engineer may assist with customer training, field trials of the developed applications, and the installation and/or minor servicing of gauging solutions at the customer’s facility. The Application Engineer will provide remote hardware/software support to customers located within the United States. Remote and onsite services/support will include install, repair and troubleshooting of terahertz gauging software and equipment found within an industrial environment. | 6/27/2019 |
| 400 | United Theraputics Manchester, NH Associate Biomedical Engineer BS/BA in biomedical/chemical engineering Exp: 1+ year in 3D printing |
Support and help lead 3D organ scaffold printing, helping lead both internal and external development efforts to design and formulate fluidic devices, evaluate bio-inks, evaluate biomaterial properties required for lung scaffold printing. Provide hands-on reduction to practice for manufacturing of prototypes, including the use of fluidic devices, bio-materials, non-biologic polymers, coupling and cross-linking chemistry and coatings. Establish and maintain a deep understanding of current and emerging technology in fluidics, precision machining, and biomaterials. Follow existing test practices and develop additional experimental plans to achieve project milestones; understand and adhere to critical path activities, assemble equipment necessary to execute experimental plans for prototype development | 6/27/2019 |
| 401 | United Theraputics Research Triangle Park, NC Bioprocess Technician - Cell Biology AAS/BS/BA in biology, cmb, or biomedical sciences Exp: 1+ year lab experience |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Assist with generation and maintenance of all master and working cell banks. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays) | 6/27/2019 |
| 402 | MacroGenics Rockville, MD Manufacturing Support Technician I HS Diploma or higher Exp: 6+ months experience |
The Manufacturing Support Technician I performs tasks that support and enable the manufacturing of clinical lots for MacroGenics’ multiple clinical programs. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) and produce materials necessary the next step of the manufacturing process ensuring compliance with all required specifications and regulatory requirements. | 6/27/2019 |
| 403 | MacroGenics Rockville, MD Bioprocess Associate II – Cell Culture Sciences MS in biology, biochemistry, chemical engineering or related Exp: 0 years |
The Bioprocess Associate II is responsible for all aspects of cell culture process development, including process optimization, scale-up and characterization studies, toxicology material production, process transfer to manufacturing, and production support. This individual will also be responsible for analyzing and summarizing the data in technical reports and presentations, and troubleshooting as needed. | 6/27/2019 |
| 404 | MacroGenics Rockville, MD QC Analyst I – Analytical BS/BA in biology, biochemistry, chemical engineering or related Exp: 0 years |
This position is responsible for performing activities to support analytical testing programs at MacroGenics to ensure compliance with cGMP standards including in-process, product release and stability testing. This individual will be required to complete the testing and related documentation in a timely manner while adhering to standard operating procedures and under cGMPs. Performs basic testing such as concentration by UV absorbance, pH, conductivity, and osmolality for in-process, product release, and stability samples on a daily basis in accordance with all protocols and procedures. Enters data into Laboratory Information Management System (LIMS). Reports out of specification results from the sampling and testing to supervisor and assists with performing laboratory investigations to determine the root cause and possible resolution. | 6/27/2019 |
| 405 | MacroGenics Rockville, MD Manufacturing Associate II – Cell Culture AS/AA Exp: 1+ year in biopharma manufacturing |
The Manufacturing Associate II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. Operate expansion and production reactors, conduct harvest operations, and order and account for consumption of raw materials and components. Operate bioprocess equipment under strict adherence to cGMP, OSHA and required policies and regulations. Assist in the preparation and maintenance of reports and other documentation as applicable to the scope of operations in the manufacturing facility. | 6/27/2019 |
| 406 | MacroGenics Rockville, MD Research Associate II/ Associate Scientist I (Cell Culture) MS in biology, biochemistry, or related Exp: 0 years |
This individual will work in a cell culture laboratory and be responsible for the expression of recombinant protein molecules in mammalian cells using various vectors systems and selection methods. Responsibilities include stable and transient transfections, screening and selection of stable cell lines, evaluation of cell culture conditions, biochemical assays and data analysis. This position requires working in a collaborative environment with other team members to meet MacroGenics’ objectives in research and development of therapeutic molecules. | 6/27/2019 |
| 407 | Mallickrodt Hobart, NY Manufacturing Assoc I (tableting) - 2nd shift HS Diploma/GED Exp: 0-1 years |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. | 6/29/2019 |
| 408 | Mallickrodt Raleigh, NC Quality Tech II AS or BS in physical sciences/technical degree Exp: 1-3 years lab experience |
The Quality Tech II analyzes process samples as received and performs non-routine analysis as requested. She/he will analyze finished goods and raw materials by chemical, physical, and instrumental means to ensure quality as needed. This position will be on a rotating schedule. Performs specified analysis on all process controls samples and reports in a timely manner by telephone or computer entry using approved written procedures and proper laboratory techniques. Performs specified analysis on all finished goods using approved written procedures and proper laboratory techniques as needed. | 6/29/2019 |
| 409 | Medicomp San Francisco, CA Cardiac Monitoring Technician HS Diploma Exp: 1+ year in healthcare |
Looking for an ECG interpreter, for our San Francisco, CA office, who is excited about having the front line responsibility of triaging the patients who have our life-saving products prescribed to them. Responsibilities include: Receiving ambulatory ECG data from phone and web transmissions. Making the correct arrhythmia call, not just knowing where to place the electrodes. Using proprietary software to efficiently compose arrhythmia reports for physicians, etc | 6/29/2019 |
| 410 | Medicomp Burtonsville, MD Remote Holter Scanner HS Diploma Exp: 1+ year in healthcare |
I’m looking for a full time Remote Holter Scanner in the Burtonsville, MD area. Responsibilities include: Receiving ambulatory ECG data from web transmissions. Making the correct arrhythmia call, not just knowing where to place the electrodes. Using proprietary software to efficiently compose arrhythmia reports for physicians. Acquire and/or retain clinical certifications | 6/29/2019 |
| 411 | Medicomp Burtonsville, MD Cardiac Monitoring Technician HS Diploma Exp: 1+ year in healthcare |
Looking for an ECG interpreter, for our Burtonsville, Maryland office, who is excited about having the front line responsibility of triaging the patients who have our life-saving products prescribed to them. Responsibilities include: Receiving ambulatory ECG data from phone and web transmissions. Making the correct arrhythmia call, not just knowing where to place the electrodes. Using proprietary software to efficiently compose arrhythmia reports for physician. etc. | 6/29/2019 |
| 412 | MedImmune Gaithersburg, MD R&D Associate I/II BS or MS in chemistry or biochemistry Exp: 0-2 years |
The successful candidate will carry out analytical testing and method development using Electrophoresis, Chromatography, and Mass Spectrometry techniques in support of early and late stage development of biopharmaceutical products, such as humanized monoclonal antibodies, and recombinant proteins. The candidate will make detailed experimental observations, review and analyze data, interpret experimental results, and summarize data for presentations and reports. The candidate will author SOPs, protocols, reports and other relevant documentation. | 6/29/2019 |
| 413 | AstraZeneca Frederick, MD Technician II - Operations BS/BA Exp: 1-3 years |
As a Production Technician II in Frederick, MD, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. It offers one of the most exciting, fast paced, challenging and rewarding work environments in the world of operations, supply chain and manufacturing. Demonstrated ability to perform all process steps of upstream / downstream / central services production operations. Ability to generate SOPs, MPRs, and SPRs for equipment and procedures used in the manufacture of biological based products. | 6/29/2019 |
| 414 | AstraZeneca Gaithersburg, MD Pilot Production Technician I - BPD BS/BA or AA/AS Exp: AA/AS: 1-2 years, BS/BA: 0+ years |
The technician is responsible for the operation of equipment according to established Standard Operating Procedures and Master Production Records for the manufacture of therapeutic proteins and vaccines in accordance with Current Good Manufacturing Practices (cGMP’s). Operates production equipment such as bioreactors, centrifuges, filtration devices, chromatography equipment, washers, autoclaves, tanks. Weighs and checks raw materials, assembles and cleans process equipment, monitors processes. Performs SIP, CIP and manual cleaning and sanitization of equipment. etc. | 6/29/2019 |
| 415 | MedNet Solutions Minnetonka, MN Cloud Infrastructure Engineer I BS/BA Exp: 0-3 years with Linux Admin |
Responsible for the deployment and maintenance for critical enterprise systems within a cloud Infrastructure. Serves as a technical resource for system administration of applications, operating systems, virtual machines, containers and network infrastructure. Manages and adheres to standard configuration and deployment of applications, operating systems, and network infrastructure. Investigates and analyzes system requirements and system specifications. Provides leadership and management to deliver the highest level of service to all system users. | 6/29/2019 |
| 416 | MedPace Cincinnati, OH Entry Level Purchasing Associate AS/AA Exp: 0-1 years in business |
Responsibilities include: Create orders and purchase supplies for all Medpace entities; Maintain inventory by entering and updating item information into accounting system; Work closely with vendors to build relationships and resolve issues; Reconcile open orders on a monthly basis; Support Treasury team through new vendor setup process. | 6/29/2019 |
| 417 | MedPace Cincinnati, OH Shipping and Receiving Associate HS Diploma/GED Exp: 1+ years in similar position |
This Warehouse Worker position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your warehouse expertise and can develop and grow your career even further, then this is the opportunity for you. | 6/29/2019 |
| 418 | MedSpark San Luis Obispo, CA Product Development Engineer BS/BA in engineering Exp: 1+ years minimum |
Your primary role is driving conceptualization, development, and prototyping of new product concepts, focused on inventive uses of new and existing technologies that open up entirely new product concepts. Work hours and days are extremely flexible, based on need and your availability. Integrate Industrial Design Techniques to Create Designs with Improved Aesthetics, Ergonomics, and Usability. Select and Integrate Proper Materials, Components, Technologies, and Assembly/Manufacturing Processes. | 6/29/2019 |
| 419 | LabCorp Westborough, MA Molecular Technologist BS/BA in biology, chemistry or related Exp: 1+ year lab experience |
The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy and Fragile X syndrome to name just a few. | 6/29/2019 |
| 420 | LabCorp Phoenix, AZ Technician AS/AA in medical lab technology Exp: 1-3 years |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in a designated technical department. Interprets results, subject to verification by Technologist/Supervisor, and providing allowance by State regulations. | 6/29/2019 |
| 421 | LabCorp Chicago, IL Laboratory Support Technician / Data Entry HS Diploma/GED Exp: 1-3 years |
The Lab Support Technician will be responsible for performing clinical specimen accessioning, sample sorting, and data entry in a fast-paced, high-throughput environment according to established standard operating procedures. Please note, this position does not involve any actual hands on lab work. The role is primarily focused on accessioning, data entry, and supporting the laboratory. The schedule for this position will be Tuesday-Saturday, 9:30am-6:00pm. Saturday hours are 7:00am-3:30pm. Responsibilities: * Open incoming packages from clients, unpack and receive specimens * Perform data entry and Quality Assurance for specimen/patient information with a high degree of accuracy and in accordance with established protocols | 6/29/2019 |
| 422 | LabCorp Dublin, OH Lab Assistant/Data Entry HS Diploma Exp: 0-2 years |
We are seeking a Data Entry Lab Assistant to work in our Specimen Accessioning department. The primary function of this position is to unpack and enter all data accompanying specimens received at the laboratory to begin the testing process. Candidates must possess a passion for patient care, be goal oriented, and enjoy teamwork. | 6/29/2019 |
| 423 | LabCorp Burlington, NC Production Assembler HS Diploma/GED Exp: 0.5-1 years related work |
Perform repetitive line assembly operations to produce on-site drug test kits in accordance with Standard Operating Procedures.Make sure the proper paperwork is completed. | 6/29/2019 |
| 424 | LabCorp Burlington, NC Specimen Processing Specialist HS Diploma Exp: 1-3 years in clinical lab |
This is a multi-discipline position with 3 primary components: specimen accessioning, sample splitting/sorting and data entry. As a Specimen Processing Specialist, your responsibilities/job duties include: Preparing laboratory specimens for designated departments/locations prior to laboratory analysis and testing and routes specimens by type to various staging areas. Performing all paperwork, technical and non-technical procedures required to process and submit specimens. Operating data entry terminals and automated data systems, follows standard sequences/coding when entering data and corrects, edits, and/or verifies data entered into automated systems | 6/29/2019 |
| 425 | Medtronic Memphis, TN Sourcing Engineer II MS or higher Exp: 0 years |
This position has the authority and responsibility to be the primary integration point linking Strategic Sourcing with Research & Development and New Product Introduction (NPI) project teams. Technical Sourcing will lead the identification of Suppliers and reduction of overall supply risk and drive the adoption of capable technologies & sources in product development resulting in predictable supply & competitiveness through full product launch. Provides technical engineering expertise and leadership to the Supply Management organization and suppliers, serving as the technical liaison between Medtronic design requirements and suppliers' technical capability to assure that robust margins are achieved and maintained. | 6/29/2019 |
| 426 | Medtronic Plymouth, MN Supplier Quality Engineer MS/MA in engineering, sciences, or technical field Exp: 0 years |
Responsibilities may include the following: Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include: Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products. | 6/29/2019 |
| 427 | Medtronic North Haven, CT Quality Engineer I BS/BA in engineering, sciences, or technical field Exp: 0 years |
Responsibilities may include the following: Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications. | 6/29/2019 |
| 428 | Medtronic North Haven, CT Software Engineer BS/BA in engineering, sciences, or technical field Exp: 0 years |
You will serve as an individual contributor by providing support for the new product development and sustaining projects. The individual will assist the business in interpreting and executing against Medtronic quality system elements including software/system work products to ensure compliance. This individual will ensure that all system-level project / program work products (e.g., plans, requirements, specifications, tests, test results, traceability, risk management documents, reports) meet Medtronic’s quality, reliability, and compliance requirements. This individual will ensure Design Quality Assurance-driven initiatives meet objectives in delivering highest quality products, with supporting tools and processes. | 6/29/2019 |
| 429 | Medtronic Louisville, CO Hardware Design Assurance Engineer I BS/BA in engineering Exp: 0 years |
Medtronic is currently seeking a Hardware Design Assurance Engineer I. Daily responsibilities include: Participate in design trade-off studies. Risk assessment. Work closely with Development Engineering to assure appropriate requirement definitions are established. Work with development engineering and manufacturing engineering to translate design requirements to manufacturing requirements. Actively participate in the product development cycle to ensure quality issues are addressed and resolved prior to release. Assist in the development and implementation of methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment. Establish incoming inspection requirements and revise as necessary. | 6/29/2019 |
| 430 | Medtronic Miami Lakes, FL Supplier Quality Engineer I BS/BA in engineering, sciences, or technical field Exp: 0 years |
As an Associate Supplier Quality Engineer, you will be responsible for: Providing support to Operations and Receiving inspection teams in all areas of production quality assurance. Ensure components received in Miami lakes meet specifications, works with suppliers to investigate root cause and provide sound corrective actions in a fashion manner. May participate in supplier process development, supplier management, and maintaining supplier files. | 6/29/2019 |
| 431 | Viant Ft. Wayne, IN Manufacturing Engineer I BS/BA in technical field Exp: 0-3 years |
The primary purpose of this position is to apply engineering principles to drive process improvements in the manufacturing of medical devices to positively affect Quality, Delivery, Cost, Safety and Moral. Creates and implements lean processes in a cellular environment utilizing appropriate methods such as CNC turning and milling, Wire EDM, Laser Etch, Laser and TIG welding, Polishing, Mass Finishing, Cleaning, Assembly, and Inspection. Effectively owns and manages CAPAs pertaining to their areas of responsibility. Defines, produces and implements documents including standard work and process work instructions. | 6/29/2019 |
| 432 | Viant Ft. Wayne, IN Calibration Technician HS Diploma/GED Exp: 1+ years in calibration or related |
The primary purpose of this job is to support all calibration activities relating to the development, inspection, testing and production of product. Performs calibration, maintenance, modification, and testing on diverse types of IM&TE (Inspection, Measurement, and Test Equipment) and process control/manufacturing measuring equipment. Maintains records of all IM&TE and process control manufacturing equipment used throughout facility in compliance with FDA/ISO regulations and established procedures. Generates status reports from calibration scheduling database and works to minimize late calibrations, notifies affected areas as needed. | 6/29/2019 |
| 433 | Viant Grand Rapids, MI Customer Service Representative HS Diploma Exp: 1+ year in customer service |
The Customer Service Representative will provide customer service and support to customers, and successfully interacts with other internal departments to resolve inquiries. The CSR processes orders in an accurate and timely manner, and facilitates internal review of capacity and materials availability. The ideal candidate will have outstanding interpersonal skills, strong organization skills, be detail oriented and possess superior problem-solving skills | 6/29/2019 |
| 434 | Viant Grand Rapids, MI Production Operator HS Diploma/GED Exp: 1+ years work experience |
Under the director of the area Supervisor/Team Leader, the Production Operator is responsible for production work according to specifications and established policies, procedures, practices, and standards. Follow all standard operating procedures (SOPs), Good Manufacturing Practices (GMPs), and DOIs. Assemble components. Perform bar sealing/tray sealing duties. May operate packaging machine, etc. | 6/29/2019 |
| 435 | Quanterix Billerica, MA Receptionist HS Disploma/AS/AA Exp: 1-3 years in customer facing profession preferred |
Description of Job Responsibilities: Provide front desk telephone/reception coverage and general administrative support. Answer incoming calls, screen and forward to appropriate individuals, or take a message. Answer general inquiries. Greet Quanterix guests, direct or escort them to the appropriate individual. Upkeep of visitor sign-in/log. Schedule appointments and maintain/update calendars as needed. Update/maintain visitor signage board. Schedule and maintain customer conference rooms. Receive, sort and deliver daily mail. Assist customers in booking hotel reservations. May also assist with some travel planning. Maintain a “Visitor Guide” local hotels, restaurants, etc. etc. | 6/24/2019 |
| 436 | Quotient Sciences Boothwyn, PA Analytical Scientist II MS Exp: 0-2 years |
The position may reside in any one of the functional areas and carry out the responsibility under some supervision: Operate and troubleshoot the following instruments/equipment to test pharmaceutical samples: HPLC/UPLC, Dissolution apparatus, Karl-Fisher water content titrator, GC, FTIR, UV, Other analytical instruments as directed. Follow analytical test methods, compendial methods, experimental procedures and SOP’s. Document test results in laboratory notebook, in real-time, and communicate status of test results to supervisor. Peer review of laboratory notebooks for technical details. Maintain control of all project related samples submitted to the laboratory. etc. | 6/24/2019 |
| 437 | Quotient Sciences Garnet Valley, PA Staff Formulator MS Exp: Not required for MS candidates |
The Role: Develop stable and bioavailable pharmaceutical dosage forms. Develop and optimize manufacturing processes and manufacture clinical supplies. Responsible for developing formulations and manufacturing process for pharmaceutical dosage forms to meet customer needs. Perform pre-formulation, formulation, manufacturing process development/optimization for various batch sizes (lab to production scale), and equipment and process validation under strict cGMP guidelines. Prepare and review SOPs, batch records, protocols, development reports. Prepare and monitor stability protocols per ICH guidelines. Evaluate stability results of formulation prototypes and clinical supplies. Evaluate packaging components. etc. | 6/24/2019 |
| 438 | Radius Health Waltham, MA Quality Assurance Coordinator BS Exp: 1-3 years |
The QA Coordinator plays an essential role in the management of key GXP (Good Clinical / Manufacturing / Laboratory / Pharmacovigilance / Distribution Practices) Quality Assurance records and documents, including training curriculum management and assignment and Quality Management System records such as deviations, investigations, Audits, Audit Findings, Corrective and Preventative Actions (CAPAs), vendor qualifications and inspections. Responsibilities: Maintains training requirements matrix, tracking role-based training requirements across the company. Assigns training to new and current employees according to the training matrix. Tracks and generates compliance metrics on training completion. etc. | 6/24/2019 |
| 439 | Radius Health Wayne, PA Human Resources Coordinator BA/BS in HR, business administration, or related Exp: 1+ years in an HR position |
The HR Coordinator is a central position for the HR Function at Radius. The role will complete administrative duties to support the HR function as well as the Wayne, PA office and coordinate some activities virtually as needed for the Waltham, MA office. The role requires excellent organizational and communication skills as well as the ability to problem solve and proactively diagnose/ address issues and concerns. Responsibilities: Maintain all office needs; welcome visitors, manage office supply orders, maintain office environment, handle main phones. Primary contact on HR Connect a centralized HR service (email, phone) for all employees and external candidates. Involves timely responses, researching and diagnosing employee inquiries, running back office HR process, etc. etc. | 6/24/2019 |
| 440 | Reckitt Benckiser Parsippany, NJ Supply Graduate Development Program BS in supply chain, engineering, or business related field Exp: Entry level |
We are looking for graduating students to join our RB Supply Graduate Development Program. The program includes rotations that allow you to gain a holistic view and exposure to the entire Supply Chain function. During the rotations, you’ll be gaining valuable experience and building on functional fundamentals, as you get your feet wet with responsibilities supporting each respective function. Rotations also allow you to work in various locations throughout RB’s US offices, adding to the breadth of exposure needed to become a true success at RB! A brief description of each function is found below: Customer Service – RB’s key player in managing flow of orders and determines team ability to add value to local business. Planning (Custom Manufacturing, Demand Planning, S&OP) - Control tower of Supply Services. Serve as point of contact between RB Commercial and RB Manufacturing. Logistics (Transportation, Warehousing, Corporate Logistics) – This is where “the rubber hits the road” in terms of managing not only the key operational aspect of the Supply Services team but also the most significant costs within Supply Services. Manufacturing - Takes place in each factory; where raw and packaging materials are transformed into packaged ready products. etc. | 6/24/2019 |
| 441 | Reckitt Benckiser Parsippany, NJ IS Graduate Program BS in business or information science related field Exp: Entry level (graduating May/June 2019) |
We are looking for graduating students to join our RB IS Graduate Development Program. You will be completing IS based project work, collaborating with multiple functions such as Supply Finance, Commercial Finance, and Accounting. Responsibilities: Develop a basic understanding of each function, specifically around the organizational structure, operational processes, common issues and pain points. Perform system analysis, design, programming, testing, and documentation. Monitor and analyze existing application systems. Recommend enhancements on technical function and business utility. Constantly improve IS systems through current/best in class IS practices. etc. | 6/24/2019 |
| 442 | Reckitt Benckiser Parsippany, NJ Finance Graduate Development Program BS in accounting or finance Exp: Entry level (graduating 2019) |
We are looking for graduating students to join our RB Finance Graduate Development Program. You may do rotations through: Supply Finance, Commercial Finance and Accounting. Responsibilities: Collect, process, verify, and report accounting related information. Perform professional analytical and management to support work assignments. Assist in preparing monthly financial reports, developing and/or utilizing spreadsheets, databases and other computer applications. Process specialized information, reports, and forms for fees, billing, project tracking, etc. Enter information reports into a financial accounting system. etc. | 6/24/2019 |
| 443 | Reckitt Benckiser Parsippany, NJ Assistant Brand Manager MBA Exp: Entry level (graduating spring 2019) |
We are looking for an MBA student to join our brand management team as an Assistant Brand Manager. This position is responsible for the development of assigned brands through the achievement of specific growth objectives. The position resides within the US Marketing function and will assume support for the Brand Manager for assigned brands within the category in Equity, Activation or Innovation capacities. The Assistant Brand Manager will play a key role in supporting the development of the overall category strategy, and is expected to drive the growth of his/her assigned brands through excellent marketing execution. Responsibilities: Support in developing and delivering the vision, US in-market activation excellence and gross profit for the brand. Champion pipeline and secure incremental funding for launches. Manage the day-to-day interface and key business activities of the portfolio. etc. | 6/24/2019 |
| 444 | Reckitt Benckiser Parsippany, NJ Performance Marketing Analyst BA/BS Exp: 1+ years in media industry |
A fantastic opportunity is available for a Performance Marketing Analyst to join our Marketing team in Parsippany, NJ: Activation practitioner with experience in the media/search marketplace, who is eager to have immediate impact on RB E-Business team in its activation and optimization practice. Energized by the development of data architectures to drive performance along with executing dashboards that drive clear analysis and insights on in-market media results. Eager to create meaningful vendor partnerships & act as daily trader within self-service media platforms. ‘Hands on Keyboard’ operational activation & management of e-commerce Search/SEM strategy with stewardship of keyword, bid and pacing management Maintain relationships across Amazon AMS, AMG & Criteo Stewardship of go-to-market marketing approach across Bricks & Clicks customers, inclusive of activation of display & SEM campaigns. | 6/24/2019 |
| 445 | Reckitt Benckiser Montvale, NJ R&D Microbiology Lab Technician AS Exp: 1-2 years |
The R&D Technician will apply technical knowledge working toward multiple project goals and objectives within established timelines. Perform laboratory tasks using general microbiological laboratory techniques. Perform appropriate practices and procedures in line with standard operating procedures. Maintain laboratory records in compliance with Good Laboratory Practice standards. Prepare microbiological media, reagents, glassware, and process contaminated materials. Read and interpret microbiological test results. Maintain an adequate inventory of laboratory supplies. etc. | 6/24/2019 |
| 446 | Reckitt Benckiser Atlanta, GA Independent Pharmacy Sales Representative BA/BS Exp: 1-2 years in business sales |
The Independent Pharmacy Sales Representative (IPS) is responsible for achieving sales goals and implementing company approved programs within an assigned geographically defined territory. Sales & Merchandising responsibilities include driving front end execution for RB brands. This includes driving incremental SKU distribution, display sales as well as sustaining product distribution, shelving and promotion activities for RB branded products. Duties include successful sales of conceptual products and programs to store level decision-makers while maintaining trusting relationships. Excellent selling and negotiation skills will allow you to provide compelling reasons to purchase, or display, against the competition. etc. | 6/24/2019 |
| 447 | Regeneron Rensselaer, NY eLearning Specialist MS Exp: 1-3 years |
Analyze learning needs of internal departments, design and develop digital learning solutions for those needs, and implement them through the enterprise Learning Management System or other platforms. Essential Duties and Responsibilities include, but are not limited to, the following: Project Manage and directly Design, Develop, and Implement eLearning, learning resources (wiki, websites, manuals, job aids, etc.), and digital materials for classroom trainings; including the necessary storyboards, outlines, and project plans. Apply instructional design methodologies in creation of learning solutions and assessments. Conduct training needs analysis with internal departments to gather their training requirements. etc. | 6/25/2019 |
| 448 | Regeneron Tarrytown, NY Animal Care Technician HS Diploma Exp: 1+ years in animal care |
We are looking for a Temp Animal Care Technician. This person provides routine husbandry care and maintenance of animals, including but not limited to feeding, watering, cage changing, and health checking of animals in the vivarium as well as maintenance of the facility. The person in this role also applies technical knowledge to perform the routine care and maintenance of research animals. Responsibilities: Performs basic care of research animals for experimental purposes: daily observations to check animal health status and environment; reports changes in environment and/or animals; changes and cleans cages, equipment, water bottles and food. Unpacking and housing animals upon arrival. etc. | 6/25/2019 |
| 449 | Regeneron Tarrytown, NY Associate Editor BA/BS Exp: 1 year |
The Associate Editor will work with more senior Medical Writing Editors and Medical Writers to learn about clinical regulatory documents and the drug development process. The individual will also work with more senior Medical Writing Editors to learn how to perform a full QC check of clinical regulatory documents, to ensure that they meet company standards and Health Authority guidelines. As the individual’s QC skills, knowledge of the drug development process and knowledge of regulatory document content increase, his/her responsibilities will increase to include more editing responsibilities (eg, checks for appropriate spelling/grammar, template use, and content). The Associate Editor will focus on learning QC techniques before learning the editing processes. etc. | 6/25/2019 |
| 450 | Regeneron Tarrytown, NY Project Associate II (Temp) unspecified Exp: 1 year |
Supports non-drug project teams responsible for process design and improvement projects and change management within Global Development. Provides administrative and project support to EPIC & PMO team and EPIC & PMO project teams, others leaders/teams as assigned. Includes managing meeting invites and logistics, coordinating events, meetings and projects with administrative support for applications: Microsoft, SharePoint, Concur, as required, or other specialized support as required. Job Duties: Manage EPIC/PMO project workshops, events and meetings. Order and prepare session materials and AV equipement/support for EPIC events. Book rooms and order food from internal and external catering for events and meetings. etc.Supports non-drug project teams responsible for process design and improvement projects and change management within Global Development. Provides administrative and project support to EPIC & PMO team and EPIC & PMO project teams, others leaders/teams as assigned. Includes managing meeting invites and logistics, coordinating events, meetings and projects with administrative support for applications: Microsoft, SharePoint, Concur, as required, or other specialized support as required. Job Duties: Manage EPIC/PMO project workshops, events and meetings. Order and prepare session materials and AV equipement/support for EPIC events. Book rooms and order food from internal and external catering for events and meetings. etc. | 6/25/2019 |
| 451 | Regeneron Rensselaer, NY Engineering Technician AAS in engineering technologies Exp: 0-2 years |
Works in a medical device laboratory and/or machine shop to perform testing and development activities defined by the Combination Products Applied Research group. Essential Duties and Responsibilities include, but are not limited to, the following: Maintain, troubleshoot, and repair laboratory and/or machine shop equipment. Assist with maintenance of laboratory/machine shop supplies and testing materials. Provide subject matter expertise for operation and proper application of laboratory and/or machine shop equipment. etc. Works in a medical device laboratory and/or machine shop to perform testing and development activities defined by the Combination Products Applied Research group. Essential Duties and Responsibilities include, but are not limited to, the following: Maintain, troubleshoot, and repair laboratory and/or machine shop equipment. Assist with maintenance of laboratory/machine shop supplies and testing materials. Provide subject matter expertise for operation and proper application of laboratory and/or machine shop equipment. etc. | 6/25/2019 |
| 452 | Regeneron Rensselaer, NY Compliance Specialist Bachelor degree Exp: 0-2 years |
Essential Duties and Responsibilities include, but are not limited to, the following: Provide support, information, and assistance to individuals, groups and management with the initiation, authorship, review, submission, and followup/completion of documents such as Change Controls, EOE's, NOE's, DNF's, risk assessments, impact statements and corrective/prevention action plans. Participate/lead/author investigations and root cause analysis for department issues of non-compliance. Act as a liaison between engineering &Automation and onsite quality and regulatory groups to define and address compliance related items. etc. | 6/25/2019 |
| 453 | RegenX Biosciences Rockville, MD Regulatory Affairs Associate, CMC BS/BA in biological sciences Exp: 1-3 years in regulatory affairs |
Reporting directly to the Senior Director of Regulatory Affairs, the Associate of Regulatory Affairs, CMC is responsible for providing support for regulatory activities related to chemistry, manufacturing, and controls for each product development area from early development through BLA. The incumbent will also provide the organization with regulatory and scientific expertise to enable high quality and effective health authority and team communications to effectively support the product development process. PRIMARY RESPONSIBILITIES: Prepare CMC-related submissions and manage regulatory writing and timely delivery of high quality technical documents including, briefing books, quality modules for clinical trial and marketing applications, drug master files, and responses to regulatory authority inquiries. Interacts with colleagues in other departments, other R&D functions and RA functions to deliver high quality dossiers, documents and materials in accordance with corporate and team goals. | 6/25/2019 |
| 454 | Rejuvenate Bio San Diego, CA Research Assistant BS Exp: 1+ years |
Rejuvenate Bio is looking for a highly-motivated individual to join our energetic team and accelerate the development of our therapies. The research assistant position will directly support efforts to drive forward our future commercial offerings working with other RA's and scientists. The applicant will be performing standard molecular biology procedures as well as more advanced cell culture and virus creation. The role reports to senior or principal scientists at Rejuvenate Bio. Responsibilities will include: Following laboratory protocols and safety regulations. Performing standard cloning techniques (restriction enzyme, gateway, golden gate). Performing basic and advanced cell culture on a variety of cell lines. etc. | 6/25/2019 |
| 455 | Renaissance Pharma Lakewood, NJ Associate Scientist - Formulations BS/MS in pharmaceutical sciences, chemistry, or related Exp: 1-3 years |
The Associate Scientist supports formulation development aspects of pharmaceutical products through formulation optimization to overall candidate progression for clients’ and Renaissance’s pipeline products. Applying a working knowledge of formulation science theories, practices and concepts, the incumbent works under the direct supervision of senior R&D scientists to execute, and manage product formulations projects. Insure Standard Operating Procedures and protocols are maintained and applied. Responsibilities: Under the supervision of The R&D Manager or a Senior Scientist, perform formulation and pre-formulation activities in the development and scale-up of formulations including parenteral (solutions and suspensions), and ophthalmic (solutions, suspensions and ointments) products from bench top to pilot-scale to commercial production. This may entail technology transfer from other plants as well. Conduct routine and non-routine laboratory analyses such as finished product testing, stability testing, and manufacturing in-process test which require critical levels of accuracy. etc.The Associate Scientist supports formulation development aspects of pharmaceutical products through formulation optimization to overall candidate progression for clients’ and Renaissance’s pipeline products. Applying a working knowledge of formulation science theories, practices and concepts, the incumbent works under the direct supervision of senior R&D scientists to execute, and manage product formulations projects. Insure Standard Operating Procedures and protocols are maintained and applied. Responsibilities: Under the supervision of The R&D Manager or a Senior Scientist, perform formulation and pre-formulation activities in the development and scale-up of formulations including parenteral (solutions and suspensions), and ophthalmic (solutions, suspensions and ointments) products from bench top to pilot-scale to commercial production. This may entail technology transfer from other plants as well. Conduct routine and non-routine laboratory analyses such as finished product testing, stability testing, and manufacturing in-process test which require critical levels of accuracy. etc. | 6/25/2019 |
| 456 | ResMed Halifax, NS Inside Sales Representative BA/BS in business discipline Exp: 1-3 years |
Let’s talk about Responsibilities: Primary role is to maintain market share at current accounts by delivering exceptional service through team driven directives and assist with product training needs within the region. Develop, maintain, and grow customer relationships within assigned accounts and account managers. Develop and enhance these relationships through routine virtual customer visits, product demonstrations,educational programs, product in-services, and problem resolution. Document activities within the Customer Relationship Management (CRM) system. Work closely with the Sales Management team in evaluating business conditions and sales trends. Develop and implement a proactive plan that involves service and support with Sales Management. Let’s talk about Responsibilities: Primary role is to maintain market share at current accounts by delivering exceptional service through team driven directives and assist with product training needs within the region. Develop, maintain, and grow customer relationships within assigned accounts and account managers. Develop and enhance these relationships through routine virtual customer visits, product demonstrations,educational programs, product in-services, and problem resolution. Document activities within the Customer Relationship Management (CRM) system. Work closely with the Sales Management team in evaluating business conditions and sales trends. Develop and implement a proactive plan that involves service and support with Sales Management. | 6/25/2019 |
| 457 | ResMed Chatsworth, CA Mold Operator, LSR HS diploma or equivalent Exp: 1-2 years |
Let’s talk about the team and you: Operates and monitors equipment/process relevant to LSR moulding by following the methods and sequence of operations as defined by verbal instructions, Visual Aids, Quality Forms and/or Routers. Let’s talk about Responsibilities: Performs to individual goals established during MyDay meetings. Operate and monitor production equipment/process – relevant to LSR. Assures product meets or exceeds company and customer expectations of quality and workmanship. Accurately reports production data. Other tasks and responsibilities as assigned. Let’s talk about the team and you: Operates and monitors equipment/process relevant to LSR moulding by following the methods and sequence of operations as defined by verbal instructions, Visual Aids, Quality Forms and/or Routers. Let’s talk about Responsibilities: Performs to individual goals established during MyDay meetings. Operate and monitor production equipment/process – relevant to LSR. Assures product meets or exceeds company and customer expectations of quality and workmanship. Accurately reports production data. Other tasks and responsibilities as assigned. | 6/25/2019 |
| 458 | ResMed San Diego, CA Data Analyst BA/BS in business, information systems, data analytics, or related finance discipline Exp: 1+ years |
Let’s talk about the team and you: This position will be responsible for designing, building and maintaining financial reports, graphs and presentations globally at all levels of the commercial organization and will report to the Finance Manager. This will require becoming familiar with how financial data is generated and consumed across the business. Data analyst will also be involved in the expense allocation process including the creation and maintenance of allocation rules and inputs. Data analyst may also conduct research to determine the best means of obtaining and transforming data into management reports and dashboards. An ideal candidate must have significant technical proficiencies, is familiar with financial reporting and concepts, and has a passion for data. Proficiencies should include advanced excel knowledge including complex formulas, Power Pivot, and some VBA, SQL or other equivalent basic programming knowledge. Previous experience with financial and reporting systems such as Anaplan, TM1, Cognos, Oracle, Tableau or equivalent is a plus. etc. | 6/25/2019 |
| 459 | Respironics (Philips) Nashville, TN Sales Development Specialist BA/BS Exp: Entry level (recent graduate) |
In this role, you have the opportunity to directly impact Philips’ success by qualifying leads and uncovering opportunities adding to the sales pipeline. The Campaign Management Specialist is responsible for proactive inbound and outbound prospecting and lead management; coordinating campaign strategies focusing on development, implementation and findings. This role will act as a layer between marketing and sales for all product lines including Patient Monitoring, Ultrasound and Imaging Systems. Responsible for building relationships through marketing activity – outbound call campaign, inbound inquiries, trade shows and referrals. The goal of a Campaign Management Specialist is to take a perspective lead from a campaign, generate interest to customer, qualify the lead using the budget, authority, need, & timeframe to approach and communicate the opportunity with the appropriate Account Executive for follow up. Additionally, maintaining and updating customer information in SalesForce.com and fulfilling customer request for product information. etc. | 6/25/2019 |
| 460 | Respironics (Philips) Reedsville, PA Supplier Quality Engineer unspecified Exp: Entry level (recent graduate) |
Responsible for achieving a state of high quality performance at our Supplier partners and pursuing continuous quality improvement through the application of Quality Engineering practices on Philips products/parts/services procured from suppliers throughout the product lifecycle including sustaining change management. Responsibilities: Additions/changes/deletion to Approved Supplier List. Supplier Quality Agreement negotiation. Analysis of defects for determining if supplier caused and then notified. Supplier Quality Notifications and Supplier Corrective Action Requests (SCARs). Drive APQP Plan development, execution, monitoring and control as part of Sustaining Changes. etc. | 6/25/2019 |
| 461 | Retrovirox San Diego, CA Marketing (entry-level part-time) unspecified Exp: Entry level |
The company is seeking an entry-level marketing person available immediately. We are seeking a fast-pace individual with experience in internet-driven social network marketing strategies with focus on use of Linkedin and Twitter to generate leads. Candidates must be located in San Diego, CA. Experience in internet-based and email-based marketing strategies is needed. Experience with website design, WordPress, email marketing and design, and SEO strategies are a plus. Ideal candidate should have some scientific background to be able to understand and implement novel strategies, evaluate competition, customer’s needs, and the services provided by the Company. Compensation will be based on commissions generated from new revenue. etc. | 6/25/2019 |
| 462 | Revance Newark, CA Manufacturing Technician BS in biological sciences, chemical engineering, or related Exp: 0-3 years |
The incumbent will be a part of the manufacturing organization and provide hands-on execution of tasks related to the GMP manufacture of biopharmaceuticals working in Clinical and/or Commercial fill-finish. Essential Functions: Operate in clean room environment. Assist or perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.) in support of manufacturing intermediate, bulk or final drug product of acceptable quality to meet FDA regulatory quality requirements. Ensure compliance with established internal control procedure. etc. | 6/25/2019 |
| 463 | Roche Vacaville, CA Manufacturing Technician - BioPorcess AS/BS/BA in biological or physical sciences or engineering Exp: Entry level |
As a Manufacturing Technician, you will be responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in a current Good Manufacturing Practices (cGMP) environment. You will maintain areas in a high state of inspection preparedness and will utilize business systems for inventory and process management. You will maintain records to comply with regulatory requirements utilizing cGMP and Standard Operating Procedures (SOPs) and will participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: Upstream Manufacturing (UM), Downstream Manufacturing (DM), or Production Services (PS). etc. | 6/25/2019 |
| 464 | Rocket Pharmaceuticals unspecified, Laboratory Manager/Research Technician BS/MS in biological or health sciences Exp: 1-2 years |
Experienced and motivated lab manager and research technician to assist with daily operations of a dynamic gene therapy research lab and support development activities. The position involves managing day-to-day lab activities, including but not limited to purchase and organization of reagents and supplies, maintenance of lab equipment, and simple experimental and administrative support to a dedicated team of scientists. Responsibilities: Organize and maintain structure of the lab, managing day-to-day activities and coordinating meetings with external partners. Be responsible for shipping and receiving of materials. Participate and coordinate daily lab tasks, including maintenance of mammalian cell culture lines, and other simple lab experiments to support scientists. etc. | 6/25/2019 |
| 465 | Invitae Cambridge, MA Bioinformatics Engineer, Algorithm BS/BA or equivalient work in bioinformatics Exp: 1+ year in similar role |
As part of the pipeline engineering team, you will be responsible for maintaining, improving, and adding to our catalog of production bioinformatics pipelines across an expanding set of modern assays. You will be responsible for scaling our pipelines as we work toward our goal of providing low-cost genetic answers to billions of people. You will work and learn among an extraordinary set of peers: bioinformaticians, molecular biologists, and software engineers. Your work will directly improve the quality of our product and positively impact each tested patient. | 6/21/2019 |
| 466 | Invitae San Francisco, CA Histologist BS or MS in biological sciences, HT-ASCP or HTL_ASCP Exp: 1-4 years in clinical lab |
The Histology Laboratory Technician/Technologist will interface directly with laboratory personnel to drive the utmost quality and throughput of Invitae’s offering. Responsibilities include: Must perform clinical patient testing, assay validation testing and quality control testing along with applicable assay documentation according to all laboratory procedures under the direct supervision of a General and/or Technical Supervisor unless they too qualify for that position. Collaborate with research and development personnel in the development and optimization of new histology protocols and clinical assays. Responsible for following laboratory procedures and schedules for specimen handling and processing, test performance, analyses, and reporting and maintaining records of patient test results as well as all safety and compliance regulations | 6/21/2019 |
| 467 | Invitae San Francisco, CA Assay Tools Bioinformatics Engineer BS/BA in biological sciences or related Exp: 0-2+ years |
As part of our Assay Tools team, you will help ensure that we can grow the breadth and scale of genetic tests on our menu. You will apply your knowledge of computer science, statistics, and NGS to analyze, improve, and develop an expanding set of modern assays. You will work and learn among an extraordinary set of peers: bioinformaticians, molecular biologists, and software engineers. Your work will directly impact early development work focused on improving the quality and capability of our products. | 6/21/2019 |
| 468 | ThermoFisher Greenville, NC Formulation Technician II HS Diploma Exp: 1+ year in manufacturing |
Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Requires proficiency in; cleaning and sterilizing equipment, gowning and aseptic techniques, preparing equipment and components for operations, operating and troubleshooting mechanical equipment, following approved procedures and proper documentation. | 6/21/2019 |
| 469 | ThermoFisher Greenville, NC QC Scientist BS/BA in life sciences/chemistry Exp: 0-2 years related experience |
Job duties include: Provide routine analyses in a chemistry or microbiology environment by following standard practices. Perform analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and/or human cells. Support internal development and/or manufacturing operations. Make detailed observations and review, document, and communicate test results. Conduct routine chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. | 6/21/2019 |
| 470 | ThermoFisher Greenville, NC QC Scientist I BS/BA in life sciences/chemistry Exp: 0-2 years related experience |
Job duties include: Provide routine analyses in a chemistry or microbiology environment by following standard practices. Perform analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and/or human cells. Support internal development and/or manufacturing operations. Make detailed observations and review, document, and communicate test results. Conduct routine chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. | 6/21/2019 |
| 471 | ThermoFisher San Jose, CA Failure Analysis Engineer BS or MS in electronics or equivalent Exp: 0-2 years related experience |
The ideal candidate has a strong background in LC/MS products and a strong technical understanding of the hardware and technology. This role with play a major factor in the development of technology critical to supporting Thermo Fisher Scientific’s position as the leader in mass spectrometry in our San Jose, CA facility. Duties include; Perform detailed root-cause-analysis and work with cross-functional teams on improvements or preventative actions, along with various miscellaneous responsibilities. Perform a failure analysis of LCMS products and parts for medical device regulatory requirements.Work with R & D to ensure new products meet product design criteria for serviceability and develop hardware validation criteria. | 6/21/2019 |
| 472 | ThermoFisher Allentown, PA Project Support Associate HS Diploma Exp: 1+ year as project manager |
Duties include: Applies Good Manufacturing Principles in all areas of responsibility. Initiates the involvement of appropriate departments and maintains continuous communication with those departments. Evaluates customer clinical research packaging specifications the customer and/or Project Manager II/III or Senior Project Manager. Responsible for learning and mastering all internal systems associated with projects. (i.e JOTS (job order tracking syste, SFDC (sale force.com, etc. | 6/21/2019 |
| 473 | ThermoFisher Fremont, CA QC Engineer/Scientist I BS/BA in chemistry/biochemistry Exp: 0-2 years in QA/QC |
Major responsibilities include: Performs routine testing and analysis of components and finished kits according to established Quality Control procedures using different instrument platforms. Documents test results, complete batch records, document problems and other relevant information under cGMPs. Performs initial troubleshooting of issues which arise during routine analysis, perform out of specification (OOS investigations) and if needed, initiate non-conformance (NCAR) reports. Performs initial troubleshooting of issues which arise during routine analysis under the direction of the Supervisor and Technical Operations. | 6/21/2019 |
| 474 | ThermoFisher Greenville, NC QC Scientist I Nightshift BS/BA in related Exp: 0-2 years lab experience |
Perform Environmental Monitoring in support of production activities in classified areas. Job function includes aseptic technique including aseptic gowning working in cleanrooms to monitor the area while sterile products are filled and manufactured. Performs analyses including instrumental and automated methods utilizing prescribed procedures and techniques. Generates valid data, reports results on appropriate database compared to established specifications while adhering to GMPs. Compares laboratory results with specifications for acceptability and determines if repetition or OOS is required. | 6/21/2019 |
| 475 | iRhythm Lincolnshire, IL Sales Associate BS/BA Exp: 1-2 years in sales support |
This role will primarily focus on outbound initiatives including research and evaluation of various health care systems, identifying key medical and administrative contacts, competitive intelligence gathering, and appointment setting. A successful Sales Associate will enjoy making outbound calls to educate medical professionals about iRhythm products and services. | 6/21/2019 |
| 476 | Iridex Corporation Mountain View, CA Jr. QA Engineer BS in engineering or equivalent Exp: 1-3 years in quality/reliability engineering |
The Quality Assurance department is devoted to assuring safe, reliable and effective products that exceed patient, physician and hospital/clinic expectations. The department plays a vital role in product and process quality supporting commercial production for all Iridex products including laser consoles, delivery devices and accessories. The Quality Engineer (QE) works with a team of dedicated individuals supporting new product development and manufacturing operations to assure quality of finished product and identify quality issues related to electrical, mechanical and software subsystems. The QE evaluates product quality issues, performs root cause analysis, identifies remedial actions and follows up to ensure all actions are completed satisfactorily prior to resolution and closure. | 6/21/2019 |
| 477 | Genetech South San Francisco, CA PV Operations Associate BS/BA in life sciences Exp: 0-12 years in PV |
Key accountabilities include: Perform reconciliation related activities for Market Research Patient (MAP) support programs and responsible for tasks related to MAP Global Tracking Tool (GTT) to ensure continuous data integrity. Run operational metrics reports on a routine basis, identify follow-up’s required, and work with the appropriate PV Operations head and/or vendor lead to ensure appropriate follow-up is completed. Responsible for executing Source Data QC (SDQC) of in scope MAPs on a quarterly basis. This includes: a) Communication with MAP vendors; b) management of vendor conducting SDQC, including appropriate QC; receiving, QC and tracking data files. | 6/21/2019 |
| 478 | Genetech Vacaville, CA Manufacturing Technician - BioProcess AS/BS/BA in biological, physical sciences, or engineering Exp: 0-2 years |
Responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment; maintaining areas in high state of inspection preparedness, and utilizing business systems for inventory and process management. Maintain records to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: | 6/21/2019 |
| 479 | Jubilant Cadista Salisbury, MD Maintenance Technician HS Diploma or AS/AA in technical discipline Exp: 0-2 years |
Essential functions include: Thoroughly assess any problems with the process equipment, identifies the problems, makes necessary repairs and completes all associated GMP documentation required to appropriately record the work performed in order to minimize equipment downtime. Participates in cross functional teams to identify assignable root causes for any product or equipment related deviations or anomalies, establish and implement necessary corrective and preventive actions needed to ensure the incident or anomaly is prevented in the future. Coordinates routine and non-routine maintenance within the master production schedule, work closely with manufacturing personnel to obtain information needed to assess equipment problems in a courteous professional demeanor, as well as working with other Maintenance Technicians. | 6/21/2019 |
| 480 | Catalent Madison, WI Biomanufacturing Solution Prep, Associate 1 AS/AA or HS Diploma Exp: HS: 1+ years, AS: 0 years |
Catalent has an entry level Associate, cGMP Manufacturing position available. As an Associate, cGMP Manufacturing (Good Manufacturing Practices) you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document cGMP Biomanufacturing activities. Shift position is Wednesday to Saturday (4/10) from 7:00 a.m. to 5:00 p.m. CST. Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). | 6/21/2019 |
| 481 | Catalent St. Petersburg, FL Laboratory Technician HS Diploma Exp: 0-2 years lab experience |
The Laboratory Technician will support the needs in the laboratory for the Product Development department, including raw material sampling/ordering, maintaining inventory of supplies in the lab, preparing dissolution & HPLC media, maintaining equipment in a qualified/calibrating state, contacting vendors for equipment maintenance, working with the scientist to assist with daily lab experiments and helping to prepare samples, lead lab waste management initiatives and act as a safety officer for the lab, etc. | 6/21/2019 |
| 482 | Catalent Madison, WI Associate, Biomanufacturing Operations BS/BA in biotechnology Exp: 0 years |
As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. | 6/21/2019 |
| 483 | Catalent Madison, WI Associate I, cGMP Biomanufacturing AS/AA or HS Diploma Exp: HS: 1+ years, AS: 0 years |
The Associate I, cGMP Biomanufacturing is responsible for current Good Manufacturing Practices (cGMP) production activities, including Master/Working Cell Bank production, Upstream cell culture, Downstream protein/mRNA purification, and/or Fill/Finish. This position is a Sunday - Wednesday, 6:00 am – 4:30 pm shift. Responsibilities include: Performs aseptic techniques within in a clean room environment. Executes and properly documents cGMP Biomanufacturing activities. Operates cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. | 6/21/2019 |
| 484 | Catalent Madison, WI Associate I, Solutions Prep AS/AA or HS Diploma Exp: HS: 1+ years, AS: 0 years |
The Solutions Prep, Associate I will perform aseptic techniques within in a clean room environment. Execute and properly document cGMP Biomanufacturing activities. The Solutions Prep, Associate I will operate cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. The position is expected to follow detailed instructions and established procedures with frequent supervision. Shift position is Sunday - Wednesday (4/10) from 7:00 a.m. to 5:30 p.m. CST. The Solutions Prep, Associate I will perform aseptic techniques within in a clean room environment. Execute and properly document cGMP Biomanufacturing activities. The Solutions Prep, Associate I will operate cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. The position is expected to follow detailed instructions and established procedures with frequent supervision. Shift position is Sunday - Wednesday (4/10) from 7:00 a.m. to 5:30 p.m. CST. The Solutions Prep, Associate I will perform aseptic techniques within in a clean room environment. Execute and properly document cGMP Biomanufacturing activities. The Solutions Prep, Associate I will operate cGMP Biomanufacturing equipment, including pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and analytical equipment as applicable. The position is expected to follow detailed instructions and established procedures with frequent supervision. Shift position is Sunday - Wednesday (4/10) from 7:00 a.m. to 5:30 p.m. CST. | 6/21/2019 |
| 485 | Celgene Warren, NJ Clinical Manufacturing Associate CAR-T BS/BA in sciences or engineering Exp: 0-2 years |
Manufacture human blood derived cell therapies per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment of a multi-product clinical facility under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. | 6/21/2019 |
| 486 | Just BioTherapeutics Seattle, WA Associate Scientist, Analytical BS in chemistry/biochemistry Exp: 0-3 years |
Responsibilities inlcude: Utilize chromatography data systems and informatics platforms to analyze and distribute analytical results. The successful candidate will have some experience in chromatography, electrophoresis, and analytical chemistry. Experience with high throughput analytical testing, statistical analysis and high-performance liquid chromatography is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. | 6/21/2019 |
| 487 | Just BioTherapeutics Seattle, WA Associate Scientist, Quality Control BS in chemistry/biochemistry Exp: 0-3 years |
We are looking for a someone to join a fast-paced, collaborative, and multidisciplinary team to provide QC analysis of raw material, in-process and drug substance testing in support of our GMP operations. The successful candidate will have some experience in analytical chemistry. Experience with chromatography and ELISA techniques is a plus. The ideal candidate has a high attention to detail, is organized in their work and works well independently and in teams. Perform QC analytical testing in support of the GMP manufacturing schedule and drug substance release | 6/21/2019 |
| 488 | Katalyst Barrington, IL Chemistry Lab Technician/Client: Pepsi BS in chemistry/biochemistry Exp: 0-3 years lab experience |
Duties include: Process submitted samples into forms ready for analysis, such as grinding solid samples to a homogeneous mixture. Perform routine laboratory chemical analyses and/or instrumental test procedures using standard methods of analysis, and then calculate and report the assay results. Prepare and maintain chemicals, chemical solutions, sample dilutions, and equipment as needed for the performance of analyses. Maintain accurate records and documentation and assure the reliability of measurement systems by using appropriate GLP. | 6/22/2019 |
| 489 | KBI BioPharma Durham, NC Process Development Associate MS in biochemistry/chemical engineering Exp: 0+ years |
This is a position in the Downstream Process Development group involving the planning and execution of purification pilot/scale up and lab-scale confirmation runs for biological therapeutics using chromatography, precipitation, and filtration methods. Duties include: Use of AKTA chromatography systems with Unicorn 7 software. Use of pumps for normal and tangential flow filtration operations. Use of pH and conductivity meters. Assist in the evaluation, development and implementation of new downstream. technologies leading to process improvements and efficiency of operation. etc. | 6/22/2019 |
| 490 | KBI BioPharma Durham, NC Process Development Associate MS in biochemistry/chemical engineering Exp: 0+ years |
This is a position in the Downstream Process Development group involving the planning and execution of purification pilot/scale up and lab-scale confirmation runs for biological therapeutics using chromatography, precipitation, and filtration methods. Duties include: Use of AKTA chromatography systems with Unicorn 7 software. Use of pumps for normal and tangential flow filtration operations. Use of pH and conductivity meters. Assist in the evaluation, development and implementation of new downstream. technologies leading to process improvements and efficiency of operation. etc. | 6/22/2019 |
| 491 | KBI BioPharma Durham, NC Quality Systems Specialist I BS in pharma, biology, chemistry, or related Exp: 1-2 years in computer support/admin/pharma industry |
Responsible for quality computer system administration, providing technical/end user support for quality computer system, and maintaining close communication with management to keep stakeholders apprised of quality computer system incidents/ resolutions, project validation status, and other relevant issues. The role requires leading and/or assisting in quality computer system validation efforts and ensuring all work is carried out in compliance with cGMPs, company policies and procedures, 21 CFR Part 11, EU Annex 11, ICH guidelines, and other applicable industry regulations. | 6/22/2019 |
| 492 | KBI BioPharma Durham, NC In-Process Support Associate BS in sciences Exp: 0-2 years in QC |
We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally. Responsibilities include: Execute activities according to cGMP regulations and company SOPs. Provide STAT assay coverage including 2nd shift and weekends as required by the manufacturing schedule. Assays include A280 and RP titer. Log samples or verify sample log in outside of standard business hours. etc. | 6/22/2019 |
| 493 | KBI BioPharma Durham, NC Data Reviewer/Research Associate MS in biochemistry/chemical engineering Exp: 0+ years |
Perform data review for contract services projects, including analytical and formulations programs for monoclonal antibodies, recombinant proteins, peptides, and small molecules in a variety of dosage form such as liquids and lyophilized powders and suspensions for injection, topical gels, and other novel delivery systems. Perform timely review of cGMP data from HPLC, ELISA, CE, etc. with a high focus on data quality and integrity to ensure accuracy, completeness, and compliance. | 6/22/2019 |
| 494 | KBI BioPharma Durham, NC Microbiology Associate BS in sciences Exp: 0+ years |
Perform daily environmental monitoring and assist in collection and transfer of samples for laboratory analysis. Perform microbiological in-process and release testing in support of GMP manufacturing. Tests include, but are not limited to: bioburden, microbial purity and endotoxin. Execute environmental monitoring (EM) within all classified manufacturing areas according to approved SOP’s and cGMP’s. Provide EM support for manufacturing during specified dynamic conditions. | 6/22/2019 |
| 495 | KBI BioPharma Durham, NC Research Associate-Analytical Development BS/MS in chemistry/biochemistry or related Exp: 0+ years |
Responsible for executing and managing method transfer, method development, and/or qualification of test methods to be used for process characterization testing. Responsible for executing assays in support of process characterization studies. Responsible performing elementary data analysis and reporting of results to corresponding internal departments. Familiar with protein characterization technologies such as: HPLC, ELISA, and UV-Vis. Familiarity with automated analysis technologies such as TECAN, BioTek, or similar automated liquid handling platforms.Responsible for executing and managing method transfer, method development, and/or qualification of test methods to be used for process characterization testing. Responsible for executing assays in support of process characterization studies. Responsible performing elementary data analysis and reporting of results to corresponding internal departments. Familiar with protein characterization technologies such as: HPLC, ELISA, and UV-Vis. Familiarity with automated analysis technologies such as TECAN, BioTek, or similar automated liquid handling platforms. | 6/22/2019 |
| 496 | KCAS Shawnee, KS Analyst I, Biopharma LBA BS/BA in sciences Exp: 1+ years lab experience |
The Analyst I is responsible for preparation of reagents and solutions, as well as sample processing under required regulatory documentation. May also analyze data, interpret results or contribute to troubleshooting activities. Conducts sample inventory and carries out lab support duties as assigned, such as inventory of chemicals, washing glassware, waste disposal and/or general cleanup. | 6/22/2019 |
| 497 | Keystone Nano State College, PA Research Chemist MS in biochemistry/chemical engineering Exp: 0-2 years |
Essential job duties include: Assist in designing experiments to develop and manufacture custom specialty products. Set up and conduct chemical experiments, tests, and analyses using techniques such as spectroscopy, chromatography, physical and chemical extractions, dynamic and quasi-electric light scattering and microscopy. Compile and interpret results of tests and analyses Prepare graphs and charts to document experimental results for presentation to management. | 6/23/2019 |
| 498 | Kiniksa Lexington, MA Temporary Process Dev. Lab Specialist, Internal Dev. & Mfg. BS Exp: 0-2 years in biotech |
The individual will support buffer/media production in process development and pilot scale clinical manufacturing for products within the Kiniksa pipeline. In addition, the individual will support upstream/downstream operations in the manufacturing and process development department. This individual will also periodically support other disciplines including shipping, receiving and purchasing. It is preferred, but not required, that the candidate have experience with disposable technologies and solution preparation. The candidate must be highly motivated, eager to learn, science driven, and results oriented in a team environment. | 6/23/2019 |
| 499 | Elbit Systems of America Merrimack, NH Data Analyst BS/BA Exp: 0-2 years |
The position will support data coordination and analysis as requested and prioritized by management. Revises, analyzes and maintains data reports and conducts analysis. Prepares management and statistical summaries and reports to assist upper management in decision-making and improvement. Assists in determining means to obtain appropriate data and ensures accuracy and integrity of the data. Assists in analysis and implementation of current processes. | 6/23/2019 |
| 500 | KSQ Therapeutics Cambridge, MA Associate Scientist - Target Discovery BS or MS in biology/immunology or related Exp: 1-2 years lab experience |
The successful applicant will use their cell and molecular biology understanding to support the development of autologous T cell transfer therapies. Responsibilities include: Perform supervisor-guided cell and molecular biology experiments in the lab. Contribute to the development and characterization of genetically engineered cancer cell lines, and primary immune cells. Support process development efforts for KSQ’s autologous T cell transfer therapy programs. Document, and communicate experimental design and data | 6/23/2019 |
| 501 | KVK Tech Newtown, PA Topical Formulation Associate MS in bio/chemistry, pharma sciences, or related Exp: 1-3 years |
Responsibilities include: Assist in the development of broad range of topical product pharmaceutical formulations including gels, creams, solutions and ointments. Develop pharmaceutical formulations utilizing Quality by Design (QbD) and risk assessment concepts. Contribute and support the analytical efforts and interpretation of data generated from experimental batches. Write technical documents to support regulatory submissions and technical transfers. | 6/23/2019 |
| 502 | KVK Tech Newtown, PA QC Document Reviewer BS/BA in chemistry or related Exp: 1+ year in GMP lab |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards | 6/23/2019 |
| 503 | KVK Tech Newtown, PA Quality Control Microbiologist BS/BA in microbiology or related Exp: 0-1 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. Performs Microbiological Tests and studies by following the established procedures referenced in the official sources. Preparation of microbiological media and diluents by following laboratory procedures, etc. | 6/23/2019 |
| 504 | KVK Tech Newtown, PA Manufacturing Operator HS Diploma or higher Exp: 1-3 years in operation |
Operators are responsible for operating special purpose machines or industrial equipment to specifications on production basis in typical oral solid dose pharmaceutical manufacturing. Processes include dispensing and weighing of materials, using automatic and semi-automatic equipment for tablet manufacturing, combining materials to make blends and solutions, and packaging of finished product. | 6/23/2019 |
| 505 | KVK Tech Newtown, PA Sample Management Associate BS/BA Exp: 0 years |
Sample Management Associate provides support to Sample Coordinator and performs administrative tasks in the Sample Management Department. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Quality Control related taskslike receiving, documenting, distributing and reconciliation of all samples received in the laboratory. | 6/23/2019 |
| 506 | LabCorp Birmingham, AL Lab Assistant HS Diploma Exp: 1-2 years |
Responsibilities include: Performs all paperwork, technical, and non-technical procedures required to process and submit specimens. Assigns specific computer generated identification numbers, checks for accuracy, and records all items processed. Forwards accessioned specimens to designated laboratory location(s); and locating and correcting any discrepancies. Learns and keeps familiar with lab procedures and location of stored specimens. | 6/23/2019 |
| 507 | LabCorp Saint Paul, MN Clinical Lab Assistant HS Diploma Exp: 0-1 years |
Responsibilities as a clinical lab assistant include: Prepare laboratory specimens (blood and body fluids) for testing. Mixing of chemicals in preparation for laboratory processing. Prepare and scan documents. Maintain a clean, well-stocked, organized work area. Follow all Standard Operating Procedures including safety and quality standards | 6/23/2019 |
| 508 | LabCorp Phoenix, AZ Specimen Processor HS Diploma Exp: 0-2 years |
Job Duties/Responsibilities: Prepare laboratory specimens for analysis and testing. Unpack and route specimens to their respective staging areas. Accurately Identify and label specimens. Pack and ship specimens to proper testing facilities. Meet department activity and production goals. | 6/23/2019 |
| 509 | LabCorp Bloomington, MN Phlebotomist - Float HS Diploma Exp: 0-2 years |
Job Duties/Responsibilities: Perform blood collections by venipuncture and capillary techniques for all age groups. Collect specimens for drug screens, paternity tests, alcohol tests etc. Perform data entry of patient information in an accurate and timely manner. Process billing information and collect payments when required. Prepare all collected specimens for testing and analysis. | 6/23/2019 |
| 510 | Lantheus Medical Imaging North Billerica, MA Manufacturing Technician II AS in sciences Exp: 1-2 years in pharma/biotech |
The objective of this position is to perform operations within the Finishing Operations Team to support the manufacture of radioactive products in a timely and compliant manner based on business needs. Incumbent ensures that the integrity and quality of the products produced comply with the associated operating procedures to meet all cGMP, regulatory, and safety requirements. This position may require mandatory overtime, as needed, supporting finishing operations on holidays, weekends, and/or late and early production shifts. | 6/23/2019 |
| 511 | Lantheus Medical Imaging North Billerica, MA Cleaning Technician HS Diploma Exp: 1-3 years |
Perform cleaning and disinfection services within controlled environment manufacturing areas (i.e. clean rooms) to ensure compliance with current Good Manufacturing Practices (cGMP) and US Food and Drug Administration (US FDA). Maintain the assigned area housekeeping (per cGMP compliance) such as: cleaning walls, floors, doors, drains, windows, and other general surface areas. Follow written standard operating procedures to fulfill cGMP requirements for cleaning and disinfection of controlled clean room environments. Properly document completion of facility cleaning/disinfection in the form as required per SOP. Maintain cleaning equipment in good working condition, maintain cleaning/disinfection inventory, and keep cleaning supplies and equipment storage areas in neat and safe order. | 6/23/2019 |
| 512 | Latitude Pharma San Diego, CA Research Associate-Analytical Development BS in chemistry, pharma or biochemistry Exp: 1-5 years in lab setting |
LATITUDE is seeking a Research Associate to carry out individual drug formulation development projects for our clients. LATITUDE utilizes its extensive experience and proprietary technologies to solve issues of insolubility, instability, poor absorption and other formulation challenges over a range of dosage forms for both external clients and internal programs. A successful candidate will possess proficiency in a variety of analytical chemistry techniques including HPLC. This is a salaried, full-time position at our San Diego location. | 6/23/2019 |
| 513 | LifeMine Cambridge, MA Research Associate, Biochemistry & Biophysics MS in biology, bio/chemistry, or related Exp: 1+ years |
LifeMine is seeking a motivated Research Associate to be an integral member of the Biochemistry team responsible for discovering and developing fungal derived drugs to targets of exceptional therapeutic value. Responsibilities include: Perform enzymatic and protein-protein interaction assays for multiple targets. Execute routine screening assays. Present results at group and/or project meetings. Maintain and track an inventory of biochemical reagents. | 6/23/2019 |
| 514 | Ligand San Diego, CA Corporate Development Associate BS in finance, accounting or sciences Exp: 1-3 years in investment, management, or finance |
The Corporate Development Associate reports to the Senior Director, Corporate Development and Investor Relations and supports all aspects of Ligand’s corporate development (M&A) and general strategy functions with significant exposure to senior corporate leadership. Responsibilities include: mergers & acquisitions (Perform financial valuation and other qualitative analysis on target acquisition candidates, Assist and creation of presentation materials for senior management and Board of Directors review, Monitor market conditions, evaluate companies and/or assets and maintain potential deal list, etc.) | 6/23/2019 |
| 515 | Precision For Medicine Carlsbad, CA Biostatiscian I - Clincal Trial Services MS in Biostatistics/Statistics Exp: entry level |
What to expect day-to-day: Generating randomization schedules and providing sample size calculations. Providing input into development of case report forms (CRFs). Authoring and reviewing statistical analysis plans, including development of table and listing shells. Generating analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Providing programming support and quality control for SAS Programs and other study documents. Providing statistical analysis and reports to Data Monitoring Committees (DMCs) and preparing clinical study reports. Reviewing output across programs to ensure consistency. Participating in the development and maintenance of SOPs. Serving as the primary project team representative, delegating work as appropriate. Training and mentoring new statisticians. etc. | 6/19/2019 |
| 516 | Precision For Medicine Costa Mesa, CA Copywriter, Healthcare Advertising Agency BS/BA Exp: 1+ years in a healthcare agency environment |
As the primary “storyteller” for your assigned brands, the copywriter partners with senior writers as well as creative leaders to properly understand, articulate and develop copy. Working in a wide variety of mediums, including but not limited to print, collateral, video, digital, etc., you will ensure our content is consistent with the established strategy, brand guidelines, and industry standards. You’ll: Participating in the creation of the brand narrative, from the ground-up. Presenting creative to clients and core constituents. Engaging in productive dialogue as it pertains to brand strategy, narrative arch, and copy to ensure alignment; real-time as necessary with both internal and client teams. Participate in all concepting sessions; taking a standard creative brief to create a varied and deep set of creative entry points. etc. | 6/19/2019 |
| 517 | Precision For Medicine Chicago, IL Medical Writers - Entry & Mid-Level - Payer Marketing/Market Access Agency BS/BA in English or life sciences discipline Exp: 1-3 years |
We form teams of Medical Writers across varying levels of experience to deliver a range of medical services, including researching, developing, and writing content. You will write medical content for our clients who are developing groundbreaking medicines and treatments. Join us to make a difference in making medicines accessible and affordable. Are you an experienced writer in the medical or pharmaceutical communications industry? Do you get excited working with a respected team that ensures the highest writing quality in the work crafted for top pharma clients? If so, this is where you come in. What Your Day-To-Day Will Look Like: Writing high-quality, medically accurate print or digital documents. Acting as a subject matter authority on the supported therapeutic areas. Procuring, organizing, and handling reference materials from a various sources including peer-reviewed scientific journals, government and medical society publications, and reputable websites. etc. | 6/19/2019 |
| 518 | Precision For Medicine Gladstone, NJ Medical Writers - Entry & Mid-Level - Payer Marketing/Market Access Agency BS/BA in English or life sciences discipline Exp: 1-3 years |
We form teams of Medical Writers across varying levels of experience to deliver a range of medical services, including researching, developing, and writing content. You will write medical content for our clients who are developing groundbreaking medicines and treatments. Join us to make a difference in making medicines accessible and affordable. Are you an experienced writer in the medical or pharmaceutical communications industry? Do you get excited working with a respected team that ensures the highest writing quality in the work crafted for top pharma clients? If so, this is where you come in. What Your Day-To-Day Will Look Like: Writing high-quality, medically accurate print or digital documents. Acting as a subject matter authority on the supported therapeutic areas. Procuring, organizing, and handling reference materials from a various sources including peer-reviewed scientific journals, government and medical society publications, and reputable websites. etc. | 6/19/2019 |
| 519 | Precision For Medicine Carlsbad, CA Programmer I - Clinical Trial Services BS in statistics, mathematocs, computer science or related field Exp: entry level |
What to expect day to day: Create specifications for derived/analysis datasets. Program analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Generate SDTM domains, ADaM datasets, and Define.xml files. Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests. Perform quality control for SAS programs and other study documents (e.g., presentations and reports). Document the quality control review process. Review output across programs to ensure consistency. Review, maintain, and approve study documents per standard procedures. | 6/19/2019 |
| 520 | Precision For Medicine Oakland, CA Research Scientist MS Exp: 1 year conducting health economic research |
We are excited to invite motivated Research Scientists to consider a career with us. You will provide evidence based-research to life sciences and healthcare companies to shape strategy and inform key healthcare decisions. Successful candidates will have excellent problem solving and analytical skills; a commitment to teamwork and collaboration; an ability to communicate complex concepts to non-technical audiences; and a willingness to deliver high quality results under tight deadlines. What you can expect day-to-day: Using statistical methods and data visualizations to analyze real-world healthcare data. Creating slide decks, reports, and manuscripts that summarize the results of quantitative analyses. Helping develop simulation models for disease burden, comparative effectiveness, or cost-effectiveness studies. Collaborating across a broad portfolio of sophisticated health economic and health policy research projects. etc. | 6/19/2019 |
| 521 | Precision For Medicine Vancouver, BC Research Statistician - HEOR MS Exp: 1-3 years |
As an Associate Research Statistician you will develop and implement advanced research across a broad portfolio of evidence synthesis and decision modeling research projects. Associate Research Statisticians collaborate with project teams to execute analytical work, as well as contribute to the development of the department as a whole. Essential duties include but are not limited to: Conducting meta-analyses and network meta-analyses. Conduct statistical analyses to support projects. Draft interim and final project deliverables for clients. Clearly interpret and communicate complex quantitative results to internal and external audiences. etc. | 6/19/2019 |
| 522 | Prometrika Cambridge, MA Database Programmer BA/BS Exp: 1 year in database design and Medidata RAVE |
RESPONSIBILITIES: Build eCRFs, including dynamics and matrices in Medidata RAVE. Quality check database structures in accordance with the annotated eCRF. Write and edit check programming in Metidata RAVE. Custom function programming preferred. Perform other database related duties as assigned. | 6/20/2019 |
| 523 | Protagonist Therrapeutics unspecified, CA Clinical Trail Assistant BA/BS Exp: 1+ years as a CTA |
Core Responsibilities: Reviews, processes, and tracks study related documents (e.g. CVs, FDA 1572s, lab certifications, IRB approvals, contracts etc.) obtained directly and/or through vendors. Sets-up and maintains the Trial Master File (TMF). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site and Team Contact Lists. Prepares, ships and manages inventory of study related supplies. Gathers investigator and site information (addresses, contact numbers, fax numbers, personnel names and email addresses, etc.) Assists in preparing materials for investigator and team meetings, study manuals etc. Core Responsibilities: Reviews, processes, and tracks study related documents (e.g. CVs, FDA 1572s, lab certifications, IRB approvals, contracts etc.) obtained directly and/or through vendors. Sets-up and maintains the Trial Master File (TMF). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site and Team Contact Lists. Prepares, ships and manages inventory of study related supplies. Gathers investigator and site information (addresses, contact numbers, fax numbers, personnel names and email addresses, etc.) Assists in preparing materials for investigator and team meetings, study manuals etc. Core Responsibilities: Reviews, processes, and tracks study related documents (e.g. CVs, FDA 1572s, lab certifications, IRB approvals, contracts etc.) obtained directly and/or through vendors. Sets-up and maintains the Trial Master File (TMF). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site and Team Contact Lists. Prepares, ships and manages inventory of study related supplies. Gathers investigator and site information (addresses, contact numbers, fax numbers, personnel names and email addresses, etc.) Assists in preparing materials for investigator and team meetings, study manuals etc. | 6/20/2019 |
| 524 | ProteinSimple (Biotechne) Minneapolis, MN Research Associate BS in biotechnology or equivalent Exp: 0-2 years |
This position is for the production of a Bio-Techne product line. Duties include; Aseptic technique for the manufacture of sterile buffers. Extraction, centrifugation and dialysis of product from various materials. Sterile fill and finish in a clean room environment. Labeling and Inventory control of products. Daily and weekly maintenance of the clean room environment. Future GMP production and additional duties as assigned. Key Responsibilities: Aseptic technique, Dialysis, Buffer preparation, GMP Production. etc. | 6/20/2019 |
| 525 | ProteinSimple (Biotechne) Minneapolis, MN Kit Packer 1 HS diploma/AS Exp: HS: 0-2 years, AS: 0 years |
The responsibilities of this position are to assemble and shrink-wrap all immunoassay kits manufactured by Dept. 385 to include set-up, label printing, and computer work. Document daily Kit Packing statistics. Review and distribute weekly pack schedule. Bin product inserts in inventory system as needed. Tear down of expired kits. Participate in cycle counts as necessary. Key Responsibilities: Pack all kits per the daily schedule. Set-up for next day’s pack schedule. Print all labels for kits. Inspect components prior to packaging. Inspect and release stand-alone proteins and antibodies. etc. | 6/20/2019 |
| 526 | ProteinSimple (Biotechne) Minneapolis, MN Research Associate, Cell & Gene Therapy BS or equivalent Exp: 0-2 years |
B-MoGen Biotechnologies is currently seeking to fill the role of a Research Associate (Cellular Therapies) to expand our genome engineering team. This position would focus on completing customer projects, who are interested in transitioning to clinical therapies and or using cells for research and development. Applicants should have a solid understanding of, molecular and cellular biology and will have an emphasis on human pluripotent stem cells. Key Responsibilities: Participate in unique fee-for-service projects for the development, optimization, and manufacture of genetically modified cell lines, primary cells, mouse embryonic stem cells, and human pluripotent stem cells. Create and run flow cytometry panels. etc. | 6/20/2019 |
| 527 | ProteinSimple (Biotechne) Minneapolis, MN Facilities Maintenance Mechanic 1 HS diploma or equivalent Exp: 1-2 years |
The responsibilities of this position are to perform preventative maintenance and repair malfunctioning new and existing minor equipment. Respond and log supervisory alarms on TAC Monitoring System during business hours. Act as the secondary facility maintenance mechanic responsible 24/7 on call for TAC & Security System with department personnel. Assist with installing new and existing equipment, offices furniture and shelves. Perform additional duties as assigned. Key Responsibilities: Performs scheduled preventive maintenance on minor equipment and tasks covered under "Checks" assigned by RAM System and completes all necessary documents once work is complete. etc. | 6/20/2019 |
| 528 | ProteinSimple (Biotechne) Minneapolis, MN Advanced Research Associate, Conjugation MS in chemistry, biological science or equivalent Exp: 0-2 years |
This position is responsible for preparing conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. Key Responsibilities: Prepares conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research according to written and non written procedures. Prepares and tests other chemistry related reagents for company personnel according to written and non written procedures. etc. | 6/20/2019 |
| 529 | ProteinSimple (Biotechne) Minneapolis, MN Customer Service Representative - Temporary BA/BS in Business, Sales, Marketing or Life Sciences Exp: 1-3 years |
This is a great opportunity to get started with a quickly growing biotech company in Minneapolis! The responsibilities of this position are to answer sales and customer inquiries for availability and order status, pricing, and other order-related questions. ESSENTIAL FUNCTIONS: Enter emailed orders into ERP System. Primary point-of-contact to customer questions related to their order. Ensure customer’s needs and expectations regarding their order are met. Follow through with requests to completion or escalate to Customer Care Specialist when appropriate. etc. | 6/20/2019 |
| 530 | ProteinSimple (Biotechne) Minneapolis, MN Customer Service Representative - Specialist Team BA/BS in Business, Sales, Marketing or Life Sciences Exp: 1-3 years |
This is a great opportunity to get started with a quickly growing biotech company in Minneapolis! The responsibilities of this position are to answer sales and customer inquiries for availability and order status, pricing, and other order-related questions. ESSENTIAL FUNCTIONS: Enter emailed orders into ERP System. Primary point-of-contact to customer questions related to their order. Ensure customer’s needs and expectations regarding their order are met. Follow through with requests to completion or escalate to Customer Care Specialist when appropriate. etc. | 6/20/2019 |
| 531 | Provid Pharmaceuticals unspecified, Organic/Medicinal Chemist MS/BS Exp: unspecified |
We are seeking recent graduates and experienced candidates with strong synthetic backgrounds, excellent scientific and communication skills and who have the ability to assume a wide range of responsibilities including program leadership roles. | 6/20/2019 |
| 532 | PSC Biotech Pomona, CA Validation Engineer (Autoclave) BS Exp: 1-3 years |
We are seeking Validation Engineers with experience qualifying autoclaves. Responsibilities: Knowledgeable and experienced in performing Autoclave validations and mapping. Writing and execution of validation Protocols IQ, OQ, and PQs for Autoclave. Writing and execution of Validation Protocols for Part Washers IQ, OQ and PQs. Calibration of Thermocouples for Temperature Mapping Studies. Calculation and interpretation of data for Equipment Validation Studies. Develop, Review and modify Standard Operating Procedures (SOPs). etc. | 6/20/2019 |
| 533 | PSC Biotech Orange County, CA Entry Level CSV Engineer BS in chemical or biomedical engineering Exp: previous experience with IT or GxP industries preferreed |
We are looking for an Entry-Level Computer System Validation Engineer to support our client in Irvine, CA. This role would work alongside an amazingly talented PSC Team, and works under the leadership of one of the best in the industry! Successful candidates will have excellent verbal and written communication skills, an understanding of the IT realm, and a thirst to learn! Responsibilities: Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system. etc. | 6/20/2019 |
| 534 | PSC Biotech Pomona, CA Entry Level CSV Engineer BS in chemical or biomedical engineering Exp: previous experience with IT or GxP industries preferreed |
We are looking for an Entry-Level Computer System Validation Engineer to support our client in Irvine, CA. This role would work alongside an amazingly talented PSC Team, and works under the leadership of one of the best in the industry! Successful candidates will have excellent verbal and written communication skills, an understanding of the IT realm, and a thirst to learn! Responsibilities: Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards. Initiate/update GxP and Risk Assessments on system. etc. | 6/20/2019 |
| 535 | PSC Biotech Pomona, CA Receptionist BA/BS Exp: 1-2 years as a receptionist or administrative assistant using a multiline phone system |
PSC Biotech Corporation is seeking an Administrative Assistant / Receptionist with exceptional interpersonal skills to support the Pomona office. This is an exciting time for PSC as we continue to rapidly grow our work force. We are seeking an energetic individual to serve as PSC headquarters’ ‘first point of contact’ and a helpful “go-to” resource for our employees and clients. This is a great opportunity if you thrive in a changing and fast-paced environment. If you enjoy helping people with a smile, are great on the phone, and performing administrative functions, this is the position for you. You will be responsible for being the first point of contact for our Corporate Office. etc. | 6/20/2019 |
| 536 | Pulmatrix unspecified, Engineering Associate BS/BA or MS in chemical or biomedical engineering or related field Exp: 1-5 years in biotech/pharmaceutical R&D |
We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. Responsibilities: Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying. Support development of new technologies. Perform physicochemical property and aerosol performance characterization of solid-based inhalation dosage forms. Support batch manufacture for development, pre-clinical and clinical studies. etc. We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. Responsibilities: Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying. Support development of new technologies. Perform physicochemical property and aerosol performance characterization of solid-based inhalation dosage forms. Support batch manufacture for development, pre-clinical and clinical studies. etc. | 6/20/2019 |
| 537 | Purdue Pharma Coventry, RI Lab Technician AS/BS Exp: 1-2 years preferred |
This position will provide technical support to the product development staff as well as maintain the product development laboratory in compliant and working order. This position will primarily provide hands on support in manufacturing finished product dosage forms – tablets, capsules, liquids and semi-solids. This position will be responsible for equipment set up, product manufacturing and cleaning as per EHS, DEA and FDA regulations. In addition to assisting the product development scientists in manufacturing finished product prototypes, general support of the laboratory is required. Support activities will include managing inventories for raw materials, personal protection equipment, supplies, etc. This position will also be responsible for providing escort for equipment qualification with vendors, witnessing controlled substance receiving and dispensing, coordinating laboratory waste disposal and pickup, as well as performing and/or facilitating equipment calibrations. This role may perform other related assignments and duties as required. etc. | 6/20/2019 |
| 538 | Purdue Pharma Wilson, NC Pharmaceutical Technician, 2nd shift (Granulation/Blending) HS diploma or equivalent Exp: 1-5 years pharmaceutical industry experience or equivalent |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary Responsibilities: Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. Identify, report, and resolve quality issues. Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing and/or packaging equipment (oral solid dose manufacturing and packaging may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.). etc. | 6/20/2019 |
| 539 | Purigen Biosystems Pleasanton, CA Research Associate I/II BS in Molecular Biology, Biology, Biochemistry or similar Exp: 1-3 years |
Purigen Biosystems, Inc., a Venture-backed, life science tools start-up company in the San Francisco bay area, is seeking an experienced Research Associate to join our Operations team. The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. This is a hands-on position for the highly qualified, self-motivated candidate who wants to enable cutting-edge life sciences technologies in a fast-paced, start-up environment. Responsibilities: Set up and maintain mammalian cell line cultures and prepare cell samples by harvesting, cell-counting and lysing cells. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes. etc. | 6/21/2019 |
| 540 | Pyramid Laboratories unspecified, Manufacturing Technician No degree required. Exp: 1+ years |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. PRINCIPAL DUTIES: Familiar with related GMP procedures and requirements, as directly related to the position. Ensure that appropriate procedures and processes are utilized without unauthorized modifications. Ability to set-up, maintain and perform various manufacturing related activities as required for a GMP compliant Fill/Finish operation. | 6/21/2019 |
| 541 | QPS Newark, DE Associate Scientist I - Biotransformation BS in chemistry, biochemistry or related discipline Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of services to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. Essential Functions: Assist with quantitative and qualitative bio-analytical studies by conducting sample preparation with various analytical chemistry methodologies. Perform routine lab operations, such as sample extraction, preparing reagents, pipette, weigh, monitor, record, label tubes, order and maintain inventory of supplies, and timely disposal of study samples, in a neat/clean manner. etc. | 6/21/2019 |
| 542 | QPS Newark, DE Associate Scientist I - Protein Binding BS in chemistry, biochemistry or related discipline Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of services to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. Essential Functions: Assist with quantitative and qualitative bio-analytical studies by conducting sample preparation with various analytical chemistry methodologies. Perform routine lab operations, such as sample extraction, preparing reagents, pipette, weigh, monitor, record, label tubes, order and maintain inventory of supplies, and timely disposal of study samples, in a neat/clean manner. etc. | 6/21/2019 |
| 543 | QPS Fargo, ND Associate I, QC - Part-Time BS Exp: 0-1 year |
Through its Dermal and Transdermal Research Laboratory (DTRL), located in Fargo, ND, QPS has considerable expertise in the field of topical and transdermal pharmacokinetics, safety, and efficacy testing. We provide our clients a range of specialized research services for the pharmaceutical, cosmetic and toxicology industries. Based in Fargo, ND, this part-time staff member will be key in ensuring that all data produced by DTRL is documented in an accurate, complete, and timely manner. Essential Functions: Review all study documentation for accuracy and completeness. Monitor data and documentation on an ongoing basis, and prepare QC audit reports of findings. Inspect study documentation for evidence of non-compliance with protocols, SOPs or applicable regulations. etc. | 6/21/2019 |
| 544 | QPS Newark, DE Associate Scientist I AS/BS in analytical chemistry, biochemistry, pharmacology or related field Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of bioanalytical solutions to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our Bioanalytical department will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. If you have a Bachelor’s degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmacology, or other related disciplines and want to be part of an organization and industry that is making a difference, we would like to hear from you. | 6/21/2019 |
| 545 | QPS Newark, DE Associate I, Sample Coordination HS diploma Exp: 1+ years |
The Sample Coordination Associate is a key member of QPS’ DMPK team, ensuring that client samples and other controlled materials are received, stored, distributed, tracked and returned safely, securely, confidentially and without loss or damage. This role requires comfort with computer systems and databases, and requires independence, attention to detail, organization, and juggling multiple tasks. Essential Functions: Manage study samples according to GLPs and SOPs, including: Sample receipt - Completing inventory, documenting discrepancies, storing, and communicating with team as appropriate. Sample pulling for basic runs, boxing samples after analysis, and sample tracking as needed. etc. | 6/21/2019 |
| 546 | QPS Springfield, MO Data Management Associate HS disploma/BS Exp: 6+ months |
The Data Management Associate is an entry level position within the functions of the Data Management Department, including the maintenance of trial related source documents, as well as the timely reporting of clinical data to clients and/or regulatory authorities. The Data Management Associate must possess strong time management skills in order to effectively compile and manage source documents, perform data entry, QC source documents and transcribed data, participate in client interaction and requests, and perform short term or long term projects as required by the department manager and/or department supervisor within contractual timelines. etc. | 6/21/2019 |
| 547 | HemaCare Northridge, CA Research Associate BS in biological sciences Exp: 1+ general lab experience |
This position isresponsible for the evaluationof humanblood products for manual orautomated cell isolations, product manufacturer,andcell culture.Perform QC testing and create a certificateof analysis(COA)for products manufactured. Record isolation details on a processing worksheet usinggood documentation practices. Operate flow cytometer and basic lab equipment. | 6/14/2019 |
| 548 | HemoSonics Charlottesville, VA Associate Research Engineer BS in biomedical engineering or related Exp: 1+ years general work experience |
HemoSonics, LLC is seeking an Associate Research Engineer who will be responsible for the support of concept phase activities, including ideation, feasibility testing, and early development of new product concepts; and the support of development activities. Key responsibilities include: Design and execute feasibility tests, Test, analyze, and interpret data and development situations/events requiring evaluation of identifiable factors, Apply standard principles, theories and concepts in the field and have working knowledge of other related disciplines, etc. | 6/14/2019 |
| 549 | Heska Des Moines, IA Technician I - Immunotherapy AS in sciences or BS/BA Exp: 0-2 years |
The Immunotherapy Technician I position will work under the close supervision of the Immunotherapy supervisor to carry out the following departmental responsibilities: aseptically filling immunotherapy vials and preparing all products for final packaging and shipment. This position will require the ability to multitask as well as follow standard operating procedures at all times. Performs aseptic hand filling operations, Prepares raw materials and filling operation set-up, Inventories all of the department raw materials and products, etc. | 6/14/2019 |
| 550 | High Point Clinical Trials Center High Point, NC Lab Supervisor HS Diploma/GED Exp: 1+ years lab experience |
Applicants should have demonstrated team management skills as well as working knowledge of IATA sample shipment processes, CLIA-waivered laboratory processes, and ability to fully manage external vendors for our clinical trial testing needs. This position ensures the full reconciliation of all specimens submitted to outside client and vendors in a manner fully compliant to Good Clinical Practice under FDA guidelines. Responsibilities include: Completes all study procedures as per FDA regulations, GCP guidelines and protocol requirements, Assists with and performs laboratory procedures including sample check-in, preparation, centrifugation, storage and shipment, Assists with temperature monitoring and control of laboratory sample environments, etc. | 6/14/2019 |
| 551 | High Point Clinical Trials Center High Point, NC Research Nurse Nursing license Exp: 1+ years nursing |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Duties include: Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. Perform tasks such as EKG’s, vital signs, phlebotomy, insertion and maintenance of IV catheters. Communicates in a timely manner with physicians regarding patient safety concerns, adverse events, protocol deviations, and any study conduct issues. | 6/14/2019 |
| 552 | High Point Clinical Trials Center High Point, NC Paramedic HS Diploma/GED + Active Paramedic license Exp: 1+ years as EMS |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Duties include: Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. Perform tasks such as EKG’s, vital signs, phlebotomy, insertion and maintenance of IV catheters. Communicates in a timely manner with physicians regarding patient safety concerns, adverse events, protocol deviations, and any study conduct issues. | 6/14/2019 |
| 553 | Hikma Cherry Hill, NJ QA Inspector - QA BS in sciences Exp: 0-2 years lab experience |
The QA Inspector monitors in-process product quality for Filling and Inspection and Packaging of parenteral products. The QA Inspector is responsible for performing visual and functional testing of product against statistically based sampling plans. In addition, the QA Inspector performs routine inspection and testing of components in accordance with Standard Procedures and specifications as required by production scheduling. In performing the above duties, the individual is responsible for accurately and clearly documenting test results in accordance with cGMPs. This position participates in rotation for weekend coverage and as needed during the work week. This is a 3rd shift position | 6/14/2019 |
| 554 | Hikma Cherry Hill, NJ Fill Operator I HS Diploma/GED Exp: 1+ year operating production equipment |
Using company guidelines, the Filling Operator I is responsible for the full spectrum of duties in controlled filling and ancillary rooms. This may include but is not limited to: set-up, operation, sanitization, equipment cleaning, PM activities, airlock and ancillary room cleaning, etc. Assists with or performs preventive maintenance tasks on filling equipment, such as inspection and cleaning of machine parts, as may be required. | 6/14/2019 |
| 555 | Hikma Cherry Hill, NJ Quality Lab Associate I, Env. Monitoring BS/BA in microbiology/biology Exp: 0-2 years pharma experience |
This is a 3rd shift position. Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. Responsibilities includes: Ensure Environmental Monitoring (EM) of the facility’s controlled areas is performed as required. Document EM testing into the EM database prior to incubation, ensure samples are correctly incubated, and record sample results in the EM database following incubation. Compile trending data for EM testing to support investigations. Audit personnel aseptic technique in controlled areas including during process simulations (media fills). | 6/14/2019 |
| 556 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro BS/BA in microbiology/biology Exp: 0-2 years pharma experience |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. Other responsibilities includes: Use sophisticated laboratory instruments and computer systems to collect and record data. Perform advanced laboratory assays requiring precise analytical and aseptic technique skills. Work on special projects and protocol testing that involves new methods and instrumentation. Complete all special projects and protocol testing in a timely and appropriate manner. | 6/14/2019 |
| 557 | Hikma Cherry Hill, NJ Project Manager, Clinical Research BS/BA in sciences/technical field Exp: 1-3 years in project management |
Assist with project plan development for clinical research trials. Manage internal and external resources including subject matter experts, doctors, vendors, and drive activities to meet or exceed timelines and milestones. Identify obstacles that may negatively impact clinical trial progress and ideate viable options to maintain project advancement. Direct and manage the clinical trial project from beginning to end. Responsible and accountable for the delivery of project milestones, and maintaining timelines to successful outcomes according to the approved business case on time, expected quality and within budget. Assist with the development of full-scale clinical trial project plans and associated communications documents, and tracking tools. | 6/14/2019 |
| 558 | Hikma Cherry Hill, NJ Quality Lab Associate I, Micro BS/BA in sciences/technical field Exp: 0-2 years pharma experience |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. Other responsibilities includes: Use sophisticated laboratory instruments and computer systems to collect and record data. Perform advanced laboratory assays requiring precise analytical and aseptic technique skills. Work on special projects and protocol testing that involves new methods and instrumentation. Complete all special projects and protocol testing in a timely and appropriate manner. | 6/14/2019 |
| 559 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS Exp: 0-2 years in QSR/GMP |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. | 6/14/2019 |
| 560 | Hologic San Diego, CA Operations Test Associate BS/BA Exp: 0-3 years lab experience |
We are currently seeking an Operations Test Associate responsible for generating accurate and reliable data for biologic products or medical devices on stability. Responsibilities include: Performs routine stability testing using GMP/GLPpractices. Performs data analysis and results interpretationscomparing to stability protocol defined specifications, validity criteria, and alertlimits. Responsible for the maintenance and cleanliness ofthe laboratory, stocking shelves/drawers with testing materials. Prepares documents for storage in our documentmanagement system and manages original data files. | 6/14/2019 |
| 561 | Hologic San Diego, CA Process Development Associate 1 BS/BA Exp: 1+ years |
Responsible for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Maintains the Pilot Plant laboratory under cGMP conditions. Produces development, pilot and production materials per written instructions, Completes ERP transactions, Stocks and maintains the laboratory supplies, Keeps accurate records and documentation, Completes laboratory work and associated paperwork by assigned completion dates, etc. | 6/14/2019 |
| 562 | Hologic San Diego, CA Process Development Associate 1 BS/BA Exp: 1+ years |
Responsible for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Maintains the Pilot Plant laboratory under cGMP conditions. Produces development, pilot and production materials per written instructions, Completes ERP transactions, Stocks and maintains the laboratory supplies, Keeps accurate records and documentation, Completes laboratory work and associated paperwork by assigned completion dates, etc. | 6/14/2019 |
| 563 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS or equivalent Exp: 0-2 years |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos.Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Independently produces notebook, dev, pilot and production materials per written directions. Analyzes in-process and final oligos using state of the art analytical techniques | 6/14/2019 |
| 564 | Hologic San Diego, CA Microbiology Research Associate 2-3 BS or equivalent Exp: 1-3 years industry experience |
The Research Associate 2/3 will perform basic and advanced culture techniques, including microbiology, tissue culture and virus culture in support of assay development activities as well as product support activities. This includes sterile aerobic as well as anaerobic work technique and involves handling of infectious materials. Performs moderately complex experiments with input from supervisor. Understands experimental goal and exhibits critical thinking skillswhen evaluating data. Interprets experimental results in context of overall experimental goal, etc. | 6/14/2019 |
| 565 | Hologic San Diego, CA Research Associate 2 BS/BA or MS in molecular biology, chemistry, biochem, or related Exp: BS: 1-3 years, MS: 0 years |
Hologic is seeking a Research Associate responsible for designing and performing experiments while collaborating and communicating effectively. Responsibilities include: Understands experimental goal and exhibits critical thinking skills when evaluating data. Able to summarize related groups of experiments. Provides input to the experimental design. Performs moderately complex experiments with input from supervisor. Interprets experimental results in context of overall experimental goal. etc. | 6/14/2019 |
| 566 | Homology Medicines Inc. Bedford, MA Research Asscoiate, Analytical Development MS in biological sciences Exp: 0-4 years in QC |
Homology Medicines is seeking a Research Associate to aid in operational support for methods to characterize AAV vector products. The individual in this role will be a talented and motivated technician who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. This is a largely laboratory-based position with a focus on providing analytical support for characterizing research-grade vectors. Plans and executes AAV-specific characterization assays, including vector genome quantification by qPCR and ddPCR, viral capsid quantification by ELISA, protein analysis by SDS-Page gels, endotoxin testing and additional assays as needed | 6/14/2019 |
| 567 | Homology Medicines Inc. Bedford, MA Research Associate, Downstream Process Development BS in chemical engineering, biochem, or bioengineering Exp: 0 years |
The successful candidate will be an integral part of a fast paced and rapidly growing group of scientists and engineers developing purification processes for the manufacture of Homology’s novel and proprietary adeno-associated virus (AAV) viral vectors. Responsibilities will include helping to develop scalable unit operations supporting viral vector purification such as chromatography, filtration and ultrafiltration. Critical to this role is the ability to concisely interpret and summarize data and to be able to effectively communicate results through high quality technical reports and oral presentations. | 6/14/2019 |
| 568 | Hovione Hovione, NJ QC Analyst- Drug Product BS/BA in chemistry or related Exp: 0 years |
The Quality Control Analyst ensures all Quality Control (QC) activities at Hovione LLC are carried out in compliance with Corporate Operating Procedures (COP), Standard Operating Procedures (SOP), Internal Operating Procedures (IOP), and Federal Food and Drug Administration (FDA), International Conference on Harmonization (ICH), Occupational Safety and Health Administration (OSHA), and Environmental Protection Agency (EPA) requirements. Responsibilities include: Perform analytical testing (i.e. raw materials, intermediates, API, stability, cleaning, method validation and cleaning) in a timely manner to meet deadlines; Execute qualification tests contained in protocols for equipment qualification; Perform instrument calibrations on Balances, High Pressure Liquid Chromatography (HPLC) and Gas Chromatography (GC); Carries out routine tasks, routine housekeeping related to the laboratory, and maintenance of analytical equipment. | 6/14/2019 |
| 569 | Hovione Hovione, NJ Process Technician - Drug Product Continuous Manufacturing BS in engineering (chemical engineering preferred) Exp: 1-2 years in process operations |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. Main responsibilities include: Work in a GMP environment area, executing chemical and physical operations following approved written instructions and in accordance with cGMPs and EHS regulations. Clean/verify proper cleaning of equipment and production areas according with cGMPs. Adhere to the necessary gowning requirements and in alignment with the various room classifications. Ensure that performed activities are recorded in applicable documentation. | 6/14/2019 |
| 570 | Hovione Hovione, NJ Process Engineer BS in chemical engineering, chemistry or related Exp: 1-3 years industrial experience |
The Process Engineer will ensure that the use of the best process engineering knowledge will be applied in scaling up chemical and spray drying projects to maximize customer satisfaction and Hovione’s interests and in compliance with all Federal, State, Local and internal policies. Main responsibilities include; Plan and design manufacturing processes based on chemical procedures to run safely and effectively in a pilot plant/kilo lab in accordance with the best known practices ensuring cGMP compliance. Contributes to the Process Hazard Analysis (PHA) of all processes under his/her responsibility and assures that all identified hazards are addressed prior to performing any activities within operations. Prepares Mass balance sheet, instructions for unit operations, production batch records, Bill of Materials and other GMP related documentation for all processes run in operations. etc. | 6/14/2019 |
| 571 | Hovione Hovione, NJ Associate Quality Assurance Specialist BS in chemistry or chemical engineering Exp: 1-2 years in cGMP industrial environemnt |
The Quality Assurance Associate Specialist promotes high quality standards and a continuous improvement culture within the Quality area of the New Jersey site in order to ensure that these are aligned with applicable quality regulations and the company's high quality standards. This role provides support in achieving the department objectives and supports the cGMP programs (i.e. validation, qualification, stability, and environmental control). Main responsibilities include: Reviews completed batch records and associated deviations for final product release; Reviews executed protocols and other GMP related documentation; Responsible for evaluation/approval of equipment cleaning; Prepares SOPs, quality related reports, and change control documents when appropriate; etc. | 6/14/2019 |
| 572 | HTG Tucson, AZ Operations Laboratory Technician I AS or BS/BA in sciences Exp: AS: 1-2 years, BS: 0-1 years |
The successful candidate will have responsibilities for reviewing and updating lab quality control processes, reviewing and analyzing results of tests to improve product quality level and maintaining product inventory. Tasks will include preparing product for internal and external customers and operation, maintenance and calibration of laboratory equipment. They will utilize standard procedures to formulate, test, fill and assemble product. Operates and maintains automated laboratory equipment, such as pipettors, scales, incubators, PCR/qPCR instruments and nucleic acid sequencers. Assembles reagents, kit orders, and other products for shipment to customers in accordance with standard protocols. Formulate reagents and solutions utilizing Standard Operating Procedures (SOP’s) and approved Work Instructions (WI’s). etc. | 6/14/2019 |
| 573 | ICON Farmingdale, NY Sample Mgmnt Coordinator HS Diploma Exp: 1-2 years |
Responsible for coordinating the shipment of diagnostic samples as per client specific requirements. Maintaining sample integrity at all times, ensuring correct procedures are followed and correct documentation accompanies the shipment of samples. Quality checking of shipments to ensure correct samples are included and documentation accompanies shipments. Shipment of samples to other ICL locations or referral laboratories per protocol specific requirements. Coordinate courier collections with Logistics to ensure shipments are sent as per protocol specific requirements | 6/15/2019 |
| 574 | ICUMED Salt Lake City, UT Equipment Operator I HS Diploma/GED Exp: 0-1 years |
A Equipment Operator I is responsible for the safe and efficient operation of simple automated assembly machines. This individual will ensure the continued operation of assembly machines through interpretation of and appropriate response to machine faults and through infrequent alignment of stations and fixtures. This individual will perform simple, repetitive tasks associated with machine operation and will operate machines that require a low level of attentiveness. The operator is also responsible for ensuring that medical devices are assembled with the highest quality possible. | 6/15/2019 |
| 575 | ICUMED Salt Lake City, UT Quality Inspector I HS Diploma/GED Exp: 0-1 years |
Independently performs inspections on parts, materials, and supplies received from vendors, perform in-process production inspections, and ensure products comply with quality standards prior to shipment. Issues acceptance or rejection tags based on outcome of inspections, checking with supervisor on more difficult determinations. Familiar with manufacturing environment, inspecting, testing, sampling, and sorting of products / goods being manufactured. | 6/15/2019 |
| 576 | Imbed Biosciences Fitchburg, WI Production Technician, Medical Device Manufacturing BS/BA in sciences/technical field Exp: 1-4 years |
Technician will assist Manufacturing team in production of medical devices. Successful candidate will work within a high-energy, small, focused team environment and maintain a strong sense of shared responsibility and shared reward to make work fun and interesting. Work with Medical Device Production team in a moderate-volume commercial laboratory to fabricate polymeric films, perform and assist in daily laboratory tasks and work flow, maintain and edit standard operating procedures and work instructions, record data, write reports and communicate results. Ensure quality control of materials and end products of the company in a consistent manner. | 6/15/2019 |
| 577 | Immucor Inc Norcross, GA Medical Laboratory Technologist I AS or BS/BA in sciences Exp: 0-1 years |
As a Medical Technologist I, you will perform all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. blood borne pathogens and chemical hazards). You will assist the department supervisor and/or manager with investigations, root cause analyses, and reports of out-of-specification results and deviations. You will also be responsible for maintaining and compiling Device History Records. | 6/15/2019 |
| 578 | Immucor Inc Mountain View, Ca Research Associate BS/BA Exp: 1-3 years research experience |
As a Research Associate, you will be responsible for performing a variety of standard molecular biology techniques such as the extraction, isolation, and identification of biological molecules that are relevant to the generation of important clinical information using molecular methodologies such as polymerase chain reactions, real-time PCR, sequencing technologies, and standard or novel methodologies for protein detection. | 6/15/2019 |
| 579 | Immucor Inc Norcross, GA Laboratory Technician AS in biomedical engineering, or biomedical technology Exp: 1 year experience |
As a Laboratory Technician, you will be responsible for performing routine and preventative maintenance on all Automated Instrumentation in the R&D labs. You will also maintain and order department supplies and raw materials for R&D labs including stocking supplies and performing cycle counts. Repairing and replacing parts as necessary on all automated instrumentation in R&D labs. Assuring all personnel are in compliance with all departmental laboratory procedures, OSHA safety regulations and other safety related procedures. | 6/15/2019 |
| 580 | Immucor Inc Norcross, GA Solid Phase Technician AS/AA in life sciences, engineering, or automation Exp: 0-1 years |
As a Solid Phase Technician, you are responsible for performing manufacturing operations according to department procedures, specifications or work instructions and completing tasks within procedure/work-instruction-defined time frames. Specific duties include: Preparing reagents as bulk and for use in Manufacturing processes, Following appropriate control measures to prevent mixing of dissimilar solid phase components or products, Following applicable laboratory OSHA safety regulations with respect to chemical hazards, blood-borne pathogens, etc. | 6/15/2019 |
| 581 | Immunomedics Morris Plains, NJ Validation Engineer BS/BA in engineering or sciences Exp: 1-2 years hands-on validation |
The Validation Engineer will be responsible for the completion of assigned validation projects encompassing equipment, instruments, computers, cleaning, and process areas for the entire validation lifecycle. Satisfactorily completes assigned validation projects. Performs IQ/OQ/PQ of facility, including building management system and appropriate manufacturing and QC equipment; executes process/cleaning and specified system validations. Investigates and writes Notice of Events/Deviations when applicable. | 6/15/2019 |
| 582 | InCube Labs San Jose, CA Scientist BS in biochemistry or related Exp: 0-3 years research experience |
Research Associate plays a pivotal role in our R & D teamwork on novel projects involving drug-device combinations for treating chronic diseases with the potential to dramatically impact patient outcomes. Responsibilities include: Independently carry out technical aspects of research projects including formulation work, sample preparation, conducting experiments, recording and managing data, and communicating results to supervisors and research team. Conduct bioanalytical assays and analyze data for the quantification of analytes. Record and manage data from complex experiments including preliminary statistical analysis | 6/15/2019 |
| 583 | Indivior Indianapolis, IN Specialty Pharmaceutical Sales Rep/Clinical Specialist BS/BA Exp: 1+ years in pharma/medical/health sciences |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Responsibilities include: Invest the time and the effort to achieve the established goals for the territory such as sales, market share, doctor calls, appropriate program planning, etc. Plan and organize daily sales call activities to optimize the use of time and maximize the achievement of sales objectives. | 6/15/2019 |
| 584 | Indivior Jacksonville, FL Specialty Pharmaceutical Sales Rep/Clinical Specialist BS/BA Exp: 1+ years in pharma/medical/health sciences |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Responsibilities include: Invest the time and the effort to achieve the established goals for the territory such as sales, market share, doctor calls, appropriate program planning, etc. Plan and organize daily sales call activities to optimize the use of time and maximize the achievement of sales objectives. | 6/15/2019 |
| 585 | Indivior Portland, ME Specialty Pharmaceutical Sales Rep/Clinical Specialist BS/BA Exp: 1+ years in pharma/medical/health sciences |
The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Responsibilities include: Invest the time and the effort to achieve the established goals for the territory such as sales, market share, doctor calls, appropriate program planning, etc. Plan and organize daily sales call activities to optimize the use of time and maximize the achievement of sales objectives. | 6/15/2019 |
| 586 | Inova Piagnostics San Diego, CA Chemist I - IFA Controls BS/BA in biological or chemical sciences Exp: 0-2 years lab experience |
Assists with preparation of autoimmune diagnostic Immunofluorescence Assay (IFA) slide, control and conjugate products in accordance with established procedures. Major duties include preparation activities for IFA controls and conjugates and the growth of cloned antigens in insect cells. Maintains detailed Device History Records, laboratory notebooks and/or any associated documentation for all manufacturing and evaluation activities in accordance with current Quality Systems Regulations (QSRs). Tests IFA slide products for acceptable titer and pattern reactivity according to written Manufacturing Documents. Assists with the maintenance and growth of insect cells and the harvesting of various cloned antigens from these cells according to established procedures. | 6/15/2019 |
| 587 | Inova Piagnostics San Diego, CA QC Analyst I BS/BA in biological or chemical sciences Exp: 1+ years lab experience |
This is an entry level position responsible for performing the QC functions for release of intermediate and finished products, including conducting stability studies, according to standard operating procedures. This position will assist in maintaining the work environment in state of compliance for GMP, OSHA and other applicable regulatory requirements. Performs QC testing/inspection of intermediate and finished products according to established house specifications accurately and on time. Inspects labels and finished components and kits to ensure compliance to all requirements before distribution. Assists with the maintenance and proper organization of the QC patient samples to ensure availability of the samples at all times and ease of retrieval. | 6/15/2019 |
| 588 | Inova Piagnostics San Diego, CA Technical Services Support Specialist I BS/BA in medical technology, biological science, or related Exp: 1-2 years with diagnostics/instruments |
As a member of the Technical Support Team, provides product and technical support to customers via phone and email on all Inova products. Responsible for assessing customers’ needs and delivering exceptional customer service to provide remote support, basic troubleshooting, and issue resolution for Inova customers. Responds to customer product inquires on a broad range of technical questions regarding instrument and assay performance, instrument capabilities, quality control, and other product concerns. Interpersonal skills and technical product knowledge, judgement and decision making expertise are critical to responding to daily customer-centric activities. | 6/15/2019 |
| 589 | Omnipod Salt Lake City, UT Inside Sales - Omnipod Associate BS/BA Exp: 0-1 years in medical device sales |
This role works closely and collaborates with the field sales and internal team members to provide the best patient experience possible. This role is responsible for communicating insurance benefit guidelines and cost share information with patients and assists them with their decisions regarding insulin pump therapy. Promote and sell Insulet’s products to prospective customers. Responsible for making outbound calls to patients who have expressed interest in the OmniPod System. Responsible for handling inbound calls from patients generated through physicians’ offices or marketing programs. | 6/15/2019 |
| 590 | Integer Plymouth , MN Manufacturing Engineer I BS/BA in manufacturing, mechanical, or industrial engineering Exp: 0-3 years |
The primary purpose of this position is to perform work which involves conventional engineering practice. Ensures Integer's internal and external customer expectations are met or exceeded. Accountabilities & Responsibilities: Adheres to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. | 6/15/2019 |
| 591 | Integer Plymouth , MN Process Engineer BS/BA Exp: 0-3 years |
Participate in cross-functional project teams to implement creative solutions. Monitors performance of equipment, machines and tools and correct equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with Quality and R&D to integrate new products or processes. Responsible for identifying and correcting manufacturing process nonconformance's identified during prototype builds. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. | 6/15/2019 |
| 592 | Integer Chaska, MN Manufacturing Team Member I HS Diploma Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. Assembles component parts as per print. Utilizes both manual and automatic machine operation. | 6/15/2019 |
| 593 | Integer Chaska, MN Manufacturing Team Member I HS Diploma Exp: 0-2 years |
The primary purpose of this position is to develop competency in and performance basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Sets up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Understands own tasks and how they relate to others on their team. Works under close Supervision where duties are clearly defined. Will follow Standard Work where applicable. Assembles component parts as per print. Utilizes both manual and automatic machine operation. | 6/15/2019 |
| 594 | Integer Alden, MN Manufacturing Team Member: 1st Shift (Mon - Fri) HS Diploma Exp: 0-2 years |
Primary Purpose: To develop competency in and perform basic assembly and/or inspection operations at Integer. The incumbent is expected to follow written procedures to meet production and quality requirements. Responsibilities include: Set up equipment needed for assembly/inspection as per Manufacturing Process Instructions (MPI's) and Quality Work Instructions (QWI's). Assembles component parts as per print. Utilizes both manual and automatic machine operation. Visually and/or dimensionally inspects parts and/or completed assemblies for conformance to specifications. Identifies and escalates quality non-conformances. | 6/15/2019 |
| 595 | Integer Trenton, GA SPI Operator I - Weekend Night Shift HS Diploma Exp: 1+ years in manufacturing |
Position summary: Perform most of the tasks and procedures required to ensure the timely and efficient processing of jobs through the manufacturing area. Maintain and update production and material control systems as needed to ensure proper job and material tracking is maintained. Maintain work area and equipment in a clean, neat, and organized fashion. Complete off-schedule notifications. | 6/15/2019 |
| 596 | Integra LifeSciences Plainsboro, NJ Materials Handler HS Diploma Exp: 0-1 years Quality Inspection |
The individual will be responsible for all material handling on 1st and 2nd shifts as well as aspects of receiving, shipping, inventory control and inventory movement. Other responsibilities include processing returned materials. Transact receipts, shipments, movements and work orders in a MRP system. Use department databases to track and manage Finished Goods and Raw Material Inventories. Effectively follow SOPs, policies and ISO/QSR requirements. etc. | 6/15/2019 |
| 597 | Integra LifeSciences Plainsboro, NJ Associate Sales Representative, Wound Reconstruction BS/BA Exp: 0-2 years outside sales experience |
The Associate Sales Representative will be a responsible Integra’s Integra Skin and Primatrix 6X6 > product line and solely responsible for supporting these products within for sales of these products for a defined territory within the Hospital OR/Surgery setting. Your primary responsibility will be to support and grow business in order to achieve or exceed sales revenue targets. You will provide case coverage, transport trays, and develop select accounts by building relationships, demonstrating extensive product knowledge and providing exceptional customer service. Your primary call points will be plastic surgeons, podiatric surgeons, orthopedic surgeons, and general surgeons. 50% of your time will be spent in the Operating Room. You will work side by side with an experienced Account Manager for approximately 18 months. | 6/15/2019 |
| 598 | Integral Medicine Philadelphia, PA Research Associate I BS/BA in biology, bioengineering or related Exp: 1-2 years lab experience |
We seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. Conduct laboratory research and support general R&D efforts for customer-based biomedical research. Projects may involve cell culture, virology, DNA preparation, and liquid-handling automation. Perform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry) | 6/15/2019 |
| 599 | Integral Medicine Philadelphia, PA Biotechnology Sales Associate BS/BA in biology, bioengineering or related Exp: 1+ years lab experience |
We are seeking a Technology Sales Associate to join our Philadelphia-based sales, marketing and business development team. Responsibilities include: Lead generation and data entry into customer relationship management (CRM) system. Conduct marketing and sales efforts targeting large and small antibody biotech customers. Prepare sales reports on product performance. | 6/15/2019 |
| 600 | Integrated DNA Technologies San Diego, CA Production Scientist I BS/BA in sciences Exp: 0-2 years |
The Production Scientist I synthesizes, purifies, formulates and ensures the quality of custom oligonucleotides according to the customer’s order and internal specifications. This generally includes, synthesis, cleavage, deprotection, purification, desalting, QC sampling, QC analysis and final packaging and formulation of the oligos and chemical reagents being made. | 6/15/2019 |
| 601 | Integrity Bio Camarillo, CA Quality Control Associate II BS/BA in sciences Exp: 1+ years in QC |
We are currently seeking a QC associate to work in both laboratory and cleanroom environments under strict SOP’s for performing environmental monitoring and other lab testing. Responsibilities include; sampling using EM equipment, sample handling, testing, reporting results with accurate documentation, investigation of OOS’s, and determination of root cause as appropriate | 6/15/2019 |
| 602 | Integrity Bio Camarillo, CA Research Associate BS/BA in biochemistry, chemistry, biological sciences or related Exp: 1-5 years in biotech/pharma |
Job duties as a research associate include: Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Set up and perform HPLC, as well as other assays, to characterize protein and peptide molecules. Analyzes, records, and reports the results and conclusions for laboratory experiments. Summarizes and interprets data. The candidate should also be open to learn new laboratory techniques and work under the guidance of experienced researchers. | 6/15/2019 |
| 603 | Integrity Bio Camarillo, CA Manufacturing Associate BS in sciences Exp: 1+ year in biotech/pharma |
Manufacturing Associate will be responsible for the manufacture of pre-clinical/clinical products. Responsibilities include: Operates the production processes according to the determined daily production planning. Performs defined production processes according to GMP and SOP procedures (e.g., set-up, machine handling, close down, reconciliation,line cleaning, line clearance, waste disposal, storage, etc.). | 6/15/2019 |
| 604 | Intuitive Multiple Locations, US Field Service Engineer AA in electronics or mechanical engineering Exp: 1-3 years field service experience |
Primary Function of Position: Install and support the Intuitive Surgical products and ensure service agreements and warranty obligations are fulfilled. Exceed customer expectations and maintain customer satisfaction to the highest possible level. Responsibilities includes: Pre site verifications to prepare site for system installation. Assist in coordination of system delivery (e.g. confirming site readiness) Troubleshoot and repair Intuitive Surgical products and associated equipment failures as required. etc. | 6/15/2019 |
| 605 | Intuitive Albany, NY da Vinci Clinical Territory Associate BS/BA, sales preferred Exp: 1+ year in leadership or sales |
The Clinical Territory Associate (CTA) will work closely with the Clinical Sales Manager to gain knowledge in all aspects of our business to include technical, clinical, and sales. He or She will train to be a da Vinci® Surgery technical and sales expert across all primary surgical specialties to develop surgical robotics programs in the assigned territory. During the first year of the job, the CTA will focus on the technical and clinical aspect of the job, and during the second year of the job, the CTA will progress and begin to focus on the sales aspect of the job. The CTA will have the opportunity to support a specific region by maximizing the utilization of installed da Vinci® Surgical Systems by leading product demonstrations/in-services and sales activities. | 6/15/2019 |
| 606 | Invicro Boston, MA Associate Scientist, in vivo BS/BA in biology, animal sciences, or related Exp: Entry Level |
The open associate scientist position is one that will support all in vivo, small animal medical imaging studies. These studies include nuclear medicine (PET/SPECT), computed tomography (CT), and magnetic resonance imaging (MRI). The Associate Scientist will maintain the animal and imaging facility, provide study support in mouse and rat disease models ranging from basic injections to surgical procedures, and assist in image acquisition procedures. This position will be an immersive cross-functional opportunity where an ideal candidate will identify areas in which to excel and focus a career in research. A qualified applicant is enthusiastic about biomedical research, able and willing to rapidly learn new skills and begin applying them immediately. | 6/15/2019 |
| 607 | PRA Health Sciences Phoenix, AZ Client Delivery Analyst, Custom Analytics BS Exp: 1-3 years work experience in a data analytics environment |
The Client Delivery Analyst leads independent data analysis, preparing comprehensive reports and presentations of data analysis findings for internal and external clients per established service level agreements. Job functions include understanding of data inputs to dimension, executing programs, assessing data accuracy, drawing research conclusions, and formatting and presenting output. This person is an expert in recommending procedural changes or participating in new project implementation from start to finish. Furthermore, they will support new client implementations and ad-hocs to support revenue needs. etc. | 6/14/2019 |
| 608 | Precision BioSciences Durham, NC Research Assistant - Molecular Biology BS Exp: 1+ year experience with relevant laboratory bench work |
Precision BioSciences is seeking a detail oriented molecular biologist with recent laboratory experience for a Research Assistant position. The position will be responsible for routine cloning, DNA preparation and manipulation of bacterial and mammalian cells. The candidate must be a fast learner, meticulous and have a track record of successful bench work. The position is working closely with a large, friendly team in a fast-paced, collaborative environment. As a member of the Core Technology team, the Research Assistant will be responsible for: cloning a variety of constructs into plasmid DNA, plasmid DNA purification, genomic DNA purification, PCR, generation of electrocompotent bacteria. etc. | 6/14/2019 |
| 609 | Precision BioSciences Durham, NC Research Assistant - In Vivo AS, BS or MS Exp: 0-3 years |
Under specific direction, the Research Assistant, In Vivo Models will assist and perform a variety of routine technical procedures related to the execution of animal studies including: animal identification, colony management, injection of cells and new constructs, imaging, monitoring animal behavior, collecting specimens and euthanasia. May perform tasks related to the research project independently, but within specific guidelines. Strong communication skills and comfort in interdisciplinary lab required. Some evening and weekend work required. etc. | 6/14/2019 |
| 610 | Precision for Medicine Oakland, CA Associate Research Economist MS or equivalent in economics or related discipline Exp: 0-1 years |
The Associate Research Economist is responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. The Associate Research Economist will have a familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and the ability to utilize specific discipline knowledge gained through academic and/or work experience (e.g. economics, etc.). This position will perform a wide range of activities including: literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. etc. | 6/14/2019 |
| 611 | Precision for Medicine Los Angeles, CA Associate Research Scientist - Health Policy MS Exp: 1 year conducting health economic research |
What you can expect day-to-day: collaborating across a broad portfolio of sophisticated health economic and health policy research projects, performing a wide range of activities including: literature reviews; regression analysis; preparing content for reports and manuscripts, slide decks and meeting notes; quality assurance/review; and other activities. | 6/14/2019 |
| 612 | Precision for Medicine Oakland, CA Associate Research Scientist - HEOR MS Exp: 1+ years in a research role |
As an Associate Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. etc. | 6/14/2019 |
| 613 | Precision for Medicine Boston, MA Associate Research Scientist - HEOR MS Exp: 1+ years in a research role |
As an Associate Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. etc. | 6/14/2019 |
| 614 | Precision for Medicine Vancouver, BC Associate Research Statistician - HEOR MS Exp: 1-3 years |
As an Associate Research Statistician you will develop and implement advanced research across a broad portfolio of evidence synthesis and decision modeling research projects. Associate Research Statisticians collaborate with project teams to execute analytical work, as well as contribute to the development of the department as a whole. Essential duties include but are not limited to: conducting meta-analyses and network meta-analyses, conduct statistical analyses to support projects, draft interim and final project deliverables for clients. etc. | 6/14/2019 |
| 615 | Precision for Medicine Indianapolis, IN Business Intelligence Analyst - Pharmaceutical Analytics BS Exp: 1-3 years using Microsoft SQL Server |
Ready to take your technical and data analysis skills and use them to tackle problems facing clients in the pharma & biotech space? Are you proficient in SQL development? Do you have a positive, can-do attitude, are self-motivated and take excellent pride in your work product? If yes, then your dream job is waiting and we'd love to talk to you. We are excited to bring a bright, motivated Business Intelligence Analyst onto our growing team. Read on to learn more about the day to day responsibilities. etc. | 6/14/2019 |
| 616 | Precision for Medicine Costa Mesa, CA Copywriter, Healthcase Advertising Agency BS/BA Exp: 1+ years in a healthcare agency environment |
As the primary “storyteller” for your assigned brands, the copywriter partners with senior writers as well as creative leaders to properly understand, articulate and develop copy. Working in a wide variety of mediums, including but not limited to print, collateral, video, digital, etc., you will ensure our content is consistent with the established strategy, brand guidelines, and industry standards. You’ll: participate in the creation of the brand narrative, from the ground-up, present creative to clients and core constituents, engage in productive dialogue as it pertains to brand strategy, narrative arch, and copy to ensure alignment. etc. | 6/14/2019 |
| 617 | Progenity Irving, TX Medical Billing Trainee BS/BA Exp: 1+ years in a billing office or recent graduate degree |
The Medical Billing Trainee works within the Billing and Reimbursement department to understand the revenue cycle and provide strategic insight. This person is dedicated to career growth and is looking to learn more about the functions of a business and how each department works together. Responsibilities: receives training and performs duties focused on improving the revenue cycle, learns various staff functions, including operations, management viewpoints, and company policies and practices affecting each phase of business, meets performance goals and objectives set by upper management and determined upon accepting position. etc. | 6/14/2019 |
| 618 | Progyny unspecified, NY Cash Application & Payroll Specialist BS/BA in accounting or finance Exp: 1-2 years cash application expericence |
What you'll do... Cash applications: timely and accurate application of daily payments received against outstanding invoices in the General Ledger, accurately report Member AR aging report and Member cash received by Month, perform other duties and special projects as assigned. Payroll: process semi-monthly payroll for all employees (hourly and salaried), provide routine monthly reports requested from payroll. etc. | 6/14/2019 |
| 619 | Progyny unspecified, NY Business Analyst BS/BA Exp: 0-2 years |
What you'll do... Build automated reports to support internal and external data requests. Build interactive dashboards in Cognos or PowerBI to increase both operational effectiveness and senior management decisions across functions supported by BI: patient care services, provider relations, claims management, network contracting, pharmacy, sales, account management, legal and marketing. You will need to understand the business’ goals, know how to find the data measuring the effort put into meeting those goals, and analyze the information to find trends. etc. | 6/14/2019 |
| 620 | Promega Madison, WI Environmental, Health & Safety Technician AA/BS in life sciences, chemistry, environmental, or related field Exp: 0-2 year experience working with hazardous materials |
Assist and support the Environmental, Health and Safety (EH&S) department by performing tasks that ensure a safe workplace and sustain Promega’s compliance with Local, State, and Federal environmental, health, and safety regulations. ESSENTIAL DUTIES: 1. Collect chemical, biological, and radiological waste from satellite accumulation areas in all facilities. 2. Properly identify, segregate, process, label and store chemical, biological, and radiological waste according to standard operating procedures and applicable regulations. 3. Schedule, organize and oversee the packaging, labeling, shipment and disposal of chemical, biological, and radiological waste at all facilities. Complete, track and file hazardous and non-hazardous waste manifests and other shipping papers for chemical, biological, and radioactive waste shipments from all facilities. etc. | 6/14/2019 |
| 621 | Promega Madison, WI Production Scientist 1 AD or BS in a scientific discipline Exp: 0-3 years |
ESSENTIAL DUTIES: 1. Manufacture a variety of Genetic Identity products so as to meet product specifications. Follow production schedules to assure on-time delivery of product. Understand basic laboratory concepts and perform basic lab techniques. 2. Perform assays to assure that products meet existing requirements for purity, activity and functionality. 3. Follow the quality requirements that relate to area. Demonstrates good documentation practices and consistently produces quality products and documentation. Follow existing policies for data recording and record keeping. 4. Understands and complies with ethical, legal and regulatory requirements applicable to our business. etc. | 6/14/2019 |
| 622 | PharPoint Research unspecified, NC Clinical Data Manager AS required, BS preferred in science or computer related disciplines Exp: 1 year experience in clinical data management |
Perform the execution of Clinical Data Management functions with delegated authority. Interactively participate in the day to day development of the client deliverables while providing supervision and mentorship to Data Management Interns. | 6/12/2019 |
| 623 | Physical Sciences Inc. Wilmington, MA Battery Scientist BS Exp: 0-2 years |
Physical Sciences Inc., with offices located in Andover and Wilmington, is looking for an entry level Scientist to support advanced Lithium ion battery research and development programs at its Wilmington facility. The individual will be involved in day-to-day hands-on laboratory experimentation, data collection, and analysis. The responsibilities for this position include: battery scientist, assist in the development of advanced anode, cathode, separator and electrolyte components for next generation Li-ion batteries, perform routine lab operations including preparing electrode slurries and building cells for electrochemical evaluation, collect, analyze and present data and findings in informal and formal reports, follow safety procedures and prepare standard operating procedures for new processes developed. | 6/12/2019 |
| 624 | Physical Sciences Inc. Andover, MA Energetic Formulations Chemist BS/MS in chemistry Exp: MS unspecified; BS work experience in RDT&E in related disciplines |
Physical Sciences Inc., located just north of Boston in Andover, is looking for a chemical scientist to conduct research, development, test and evaluation (RDT&E) of innovative energetic materials for propulsion and munitions systems. Emphasis is placed on laboratory scale and pilot scale processing of ingredients and formulations for fuels, oxidizers, propellants, and explosive compositions. We are seeking an individual with a strong background in wet chemistry and analytical instrumentation to join a multi-disciplinary team of engineers and scientists. This individual will play a key role in growing a diverse portfolio of technologies funded by the DoD and NASA. etc. | 6/12/2019 |
| 625 | Platelet BioGenesis Cambridge, MA Research Associate, Gene Editing BS/MS in biology, molecular biology, cell biology or immunology Exp: 1-3 years lab experience, in vivo is a plus |
We make platelets. We have developed and patented a microfluidic bioreactor and shown that functional platelets can be generated from human induced pluripotent stem cell cultures. We are now scaling platelet production for human clinical trials and leveraging our platelet platform for cell-based drug delivery. The successful Research Associate will join our Designer Platelet Team, working directly on optimizing and characterizing our drug delivery platform, and providing support for ongoing and emerging research projects. The ideal candidate has experience with platelets, pluripotent stem cells, genetic engineering and enjoys working with a team of scientists in a fast-paced and highly matrix environment. etc. | 6/12/2019 |
| 626 | Plexxikon Berkeley, CA Research Associate 1, Medicinal Chemistry BS in chemistry Exp: up to 2 years hands-on, relevant experience in organic synthesis |
The Research Associate 1, Medicinal Chemistry will be a critical member of the research team reporting directly to one of our Scientists. This is an exceptional opportunity to gain experience in a successful biopharmaceutical company and bring drugs from ideas to the clinic. Responsibilities include, but are not limited to: Multi-step synthesis, purification and characterization of small molecules for evaluation as potential drug candidates, maintain various lab equipment, maintain current knowledge of synthetic methodology through literature readings, present progress at chemistry group and project team meetings. etc. | 6/12/2019 |
| 627 | PMI BioPharma Solutions Nashville, TN Chemist I, Analytical Development BS in chemistry, biology, or related science Exp: 1-2 years of pharmaceutical experience |
PMI Biopharma Solutions is looking for an Analytical Development team member that is passionate and driven regarding his/her work. PMI Biopharma Solutions desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. The Chemist I position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. etc. | 6/12/2019 |
| 628 | PMI BioPharma Solutions Nashville, TN Facilities Technician I, MSAT unspecified Exp: 1-2 years maintenance experience in regulated manufacturing environment (pharmaceutical/biotech preferred) |
PMI Biopharma Solutions is looking for a Facilities Technician team member that is passionate and driven regarding his/her work. PMI Biopharma Solutions is in need of a motivated individual to provide their expertise in the delivery of results for the company and its clients. Reporting to the Supervisor of Engineering, the Facilities Technician will be responsible for PMI’s maintenance and equipment support activities. The Facilities Technician performs with minimal supervision preventive maintenance, demand maintenance and calibration tasks on critical equipment, utilities, and facilities. etc. | 6/12/2019 |
| 629 | PMI BioPharma Solutions Nashville, TN Microbiologist I, Analytical Development BS in biology or related field Exp: 0-1 years pharmaceutical experience |
PMI Biopharma Solutions is looking for an Analytical Development team member that is passionate and driven regarding his/her work. PMI Biopharma Solutions desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. Reporting to the Microbiology Supervisor, the Microbiologist I will be responsible for performing environmental monitoring sampling of ISO class environments and assisting with preparation, characterization, and identification of environmental isolates. He/she will perform raw material and drug product method development and cGMP testing. etc. | 6/12/2019 |
| 630 | Portola Pharmaceuticals San Francisco, CA Clinical Data Manager (temporary) BS/MS in relevant field Exp: 1-3 years experience handling clinical research data |
The Temporary Clinical Data Manager will support the Data Management group from study start-up through database lock and clinical study report. The successful candidate will deliver high quality data, on time and on budget. In this role, the candidate will be expected to lead and provide oversight for the execution of data management activities for more than one compound in a therapeutic area. This role will report to the Associate Director, Clinical Data Management. Works collaboratively with Clinical Programmers, Statistical Programmers, Biostatisticians, Clinical Research, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for moderately complex clinical data acquisition, quality checking and reporting. etc. | 6/12/2019 |
| 631 | Poseida Therapeutics San Diego, CA Process Development Associate MS Exp: 1+ years experience with immunology, molecular biology, or related field |
Poseida Therapeutics, Inc. is seeking an outstanding candidate to join our Cell Therapy Development group at our La Jolla, San Diego, CA location. The Development Associate will be a key member of a dynamic team that develops and implements characterization strategies to support and enable process and clinical development of gene-engineered cell products. This is a lab-based position that will involve hands-on development of clinical manufacturing processes for selecting, gene-modifying and growing T cell subsets. This position will interface with our Research and Development team as well as with outside Contract Manufacturing Organizations. etc. | 6/12/2019 |
| 632 | PPD Richmond, VA Lab Support Tech Technical AS Exp: 1 year coursework in laboratory science |
Second shift position to perform routine maintenance tasks on laboratory robots, in support of daily lab operations under the direction of a senior staff member. Must be able to maintain a schedule and perform regulated tasks and documentation. The laboratory technician will work with various teams (automation, lab, etc.) to assist in maintenance of laboratory systems and resources and assist with preparation of laboratory reagents, solutions and chores. etc. | 6/12/2019 |
| 633 | PPD King of Prussia, PA Associate Scientist- ELISA, qPCR BS or equivalent Exp: 1+ years |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. In this position you will perform a variety of validated or experimental analytical procedures such as ELISA. You love science and have keen observation skills. You are a self-directed learner with excellent attention to detail. You have an inherent scientific curiosity and enjoy working with instrumentation. etc. | 6/12/2019 |
| 634 | PPD Highland Heights, KY Assoc Sample Coordinator - Global Central Labs HS Diploma or equivalent Exp: 0-1 years |
Part-Time Position. Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory. Provides support to Sample Coordinator and performs administrative tasks in the Sample Management department. Follows SOPs, applicable client procedures, and fulfills laboratory requests with modest direct supervision. Performs a variety of simple inventory tracking procedures (receipt, check-in, login, labeling, inventory, transport, check-out, etc.) and administrative tasks in support of laboratory operations. Communicates status of tasks to supervisor and/or appropriate laboratory staff. etc. | 6/12/2019 |
| 635 | PPD Palmer Square, NJ Associate Scientist - Lab Operations Support Tech (Pathology) BS in biology or related field or equivalent Exp: 0-1+ years |
We are seeking a passionate, highly organized, sharp individual seeking to begin a career in Operations in a lab setting. As an Associate Scientist/Lab Ops Tech you will perform a variety of tasks such as arranging supplies and supporting the Immunohistochemistry, Pathology and Histology in the Translational Medicine group. Your role will strictly be laboratory operations, and not include any bench work. You, as the Associate Scientist will assist scientists through tasks such as shipping and receiving, reagent and supply ordering, inventorying and stocking, lab cleanliness, safety, setting up equipment service & maintenance and record keeping for the labs. etc. | 6/12/2019 |
| 636 | PPD Richmond, VA Associate Scientist - Immunochemistry BS or equivalent Exp: 1+ years |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Grow your career within the scientific ladder, pursue project management, or develop into a leader. These are just a few career pathways available once you become a part of the PPD team. etc. | 6/12/2019 |
| 637 | Edwards Irvine, CA Quality Engineer II MS in engineering or sciences Exp: 1-2 years w/medical devices |
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc.Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc.Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc.Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Responsibilities include: Key Responsibilities: Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports. etc. | 5/31/2019 |
| 638 | Edwards Irvine, CA Technician, R&D/QA Engineering - Transcatheter Heart Valve AS or equivalent Exp: 1+ years required |
The R&D Technician will support a wide range of engineering activities such as test, check-out, modification, fabrication and assembly under minimal supervision of Engineers and may propose technical solutions. Responsibilities include: Build complex prototypes, sub-assemblies, test samples, and prepare feasibility test units, samples, and/or chemical solutions. Perform complex work using drawings, diagrams, written and verbal instructions, layouts or defined plans to perform testing, checkout, and trouble-shooting functions. | 5/31/2019 |
| 639 | Edwards Draper, UT Manufacturing Engineer I BS/BA in engineering or sciences Exp: 0-2 years |
Applies knowledge of technical principles and Edwards systems/procedures to tptimize manufacturing processes. Responsibilities include: Improve manufacturing processes using engineering methods for concinous process improvement. Develop basic experiements and tests to qualify and validate manfactruing process, etc. | 5/31/2019 |
| 640 | Eisai Woodcliff Lake, NJ Clinical Trial Assistant BS in life sciences or related Exp: 1-3 years in clinical operations or related |
Supports all phases of clinical study activities including: TMF review, assist with filing and archiving project documentation in theTMF within a 20 day timeframe. Assist with creating, updating and maintaining project trackers in EPIC. Provides support for document preparation. Attend internal study team meetings, and prepare and distribute study team agendas and minutes. etc. | 5/31/2019 |
| 641 | Eisai Woodcliff Lake, NJ Clinical Trial Assistant BS in life sciences or related Exp: 1-3 years in clinical operations or related |
Supports all phases of clinical study activities including: TMF review, assist with filing and archiving project documentation in theTMF within a 20 day timeframe. Assist with creating, updating and maintaining project trackers in EPIC. Provides support for document preparation. Attend internal study team meetings, and prepare and distribute study team agendas and minutes. etc. | 5/31/2019 |
| 642 | Elanco na, IN Associate - Corporate IT Auditor - Fixed Duration Employee BS/BA in computer sciences/engineeirng Exp: 1+ years in audit or IT operations |
The auditor works with 2-5 person audit teams on domestic and global audits designed to test compliance with good internal control practices, external regulations, and corporate policies and procedures, in alignment with Institute of Internal Audit standards. Responsibilities include identifying and assessing risks, scoping engagements, testing policy compliance, automating test procedures, influencing action plans, partnering with affiliate management and audit team members to complete and improve audit processes, sharing of best practices and key learning across the organization. | 5/31/2019 |
| 643 | Elanco Clinton, IN Mfg Engineering Associate BS/MS engineering Exp: Entry Level (graduating by August 2019) |
Multiple positions. Position titles include but are not limited to Plant Engineer, Process Engineer, Project Engineer, Development Engineer, Automation and/or Control Engineer, and are available in manufacturing and development areas supporting: Bulk processing (Animal health products), facilities/utilities engineering, process development. | 5/31/2019 |
| 644 | ELITechGroup Bothell, WA Shipping and Receiving Associate HS Diploma Exp: 0-1 years |
Verifies and keeps records on outgoing shipments and prepares items for shipment. Receives product and inspects items to ensure conformance to specifications. Duties include: Confirming shipped/received products/packages. | 5/31/2019 |
| 645 | Elstar Cambridge, MA Research Associate / Senior Research Associate - Immunology BA or MS in biology or related Exp: 0-3 years |
The successful candidate will be responsible for developing and performing cell-based assays within the Immunology team achieving common team goals. Responsibilities include: Perform ex-vivo and in-vitro cellular assays with an emphasis on flow cytometry and immuno-assays including ELISA and MSD. Analyze and interpret data and generate high-quality summary reports in a timely manner, and present findings in the inter and intra departmental group meetings. Document experimental data and results and maintain a current and accurate electronic notebook (ELN) | 5/31/2019 |
| 646 | MilliporeSigma Rockville, MD Flexible Resource Associate Scientist BS/BA or MS in biology/chemistry/related Exp: BS: 1+ year, MS: 0-1 years |
The Flexible Resource Associate Scientist conducts pre-designed assays, makes scientific observations, maintains detailed workbooks and ensures all documentation fulfills generally accepted GLP or GMP industry standards. Functional area and period of deployment to a specific laboratory will be controlled via Sales and Operations Planning process. An individual able to follow the SOPs, protocols and relevant compliance regulations regarding safety procedures, documentation and scientific responsibility. You can maintain an understanding of technological principles and applications of the organization’s services; independently analyze data, interpret results and advise the supervisor and study director of any factors that may affect quality and usefulness of data. | 5/31/2019 |
| 647 | MilliporeSigma Rockville, MD Associate Scientist BS/BA in sciences (biology, microbiology, chemistry, etc.) Exp: 0-2 years |
The Associate I (ASI) will perform safety testing required to manufacture clinical and commercial products. The ASI is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of BioReliance services, technical principles and applications. | 5/31/2019 |
| 648 | EMD Serono Billerica, MA Associate Scientist - In Vitro Pharmacology BS/BA in biology, immunology, or related Exp: 1+ year with cell culture |
We have an opening for a talented Associate Scientist to join the ImmunoOncology platform at EMD Serono, Billerica, MA. The successful candidate will support the discovery of novel cancer immunotherapies. In his/her role, the candidate is expected to develop and conduct cellular immune assays to characterize small molecules or biologics that modulate the tumor immune environment and enhance the anti-tumor immune response. | 5/31/2019 |
| 649 | MilliporeSigma Sheboygan Falls, WI Quality Assurance Associate BS/BA in life sciences or chemistry Exp: 0-3 years |
Provide Food Safety and Quality systems support for the Flavors and Fragrances product line while ensuring adherence to GMPs and working to improve the Supplier Quality Management program. The Flavors and Fragrances facility is FSSC 22000 certified as well as ISO900. Responsibilities include: ensuring compliance with FSSC 2200 and ISO9001, support customer complaint management, etc. | 5/31/2019 |
| 650 | MilliporeSigma Miamisburg, OH Scientist, Production Associate (QC) BS/BA in chemistry or life sciences or engineering Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Essential functions include: ensure quality through process, perform routine assays/processes and/or unit operations, complete work volume, stay in compliance with change control procedures, improve processes, etc. | 5/31/2019 |
| 651 | MilliporeSigma Billerica, MA Associate Scientist, Immuno-Oncology BS/BA in biology, immunology, or related Exp: 1+ years in research |
We have an opening for an Associate Scientist to join the Immuno-Oncology platform at EMD Serono, Billerica, MA. The successful candidate will support the discovery of novel cancer immunotherapies. In this role, the candidate is expected to develop and conduct cellular immune assays to characterize small molecules or biologics that modulate the tumor immune environment and enhance the anti-tumor immune response. The Associate Scientist will also develop, evaluate and implement well-controlled in vitro experiments to interrogate target biology, and generate proof of concept data supporting target Go/No Go decisions. | 5/31/2019 |
| 652 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma Exp: 0-1 years in cGMP |
Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. Maintain state of facility environmental control including: preparation of defined concentrations of cleaning solutions, daily, monthly, quarterly and annual cleaning of manufacturing surfaces and equipment per Standard Operating Procedures. etc. | 5/31/2019 |
| 653 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma Exp: 0-1 years in cGMP |
Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. Maintain state of facility environmental control including: preparation of defined concentrations of cleaning solutions, daily, monthly, quarterly and annual cleaning of manufacturing surfaces and equipment per Standard Operating Procedures. etc. | 5/31/2019 |
| 654 | Emergent BioSolutions Gaithersburg, MD Associate Engineer, Process Development BS in engineering Exp: EIT certificate and/or 1-2 years related experience |
Under the direction of Process Development management, the Associate Engineer will perform experiments (hands-on) to develop, scale-up, and improve the performance of unit operations. The Assoc. Eng. will apply technical training to assess risks, solve problems, and analyze data sets coming from experiments and present results. This includes: preparation of solutions/media, cell culturing and related processes, tubing assembly and sterilization, development studies, etc. | 5/31/2019 |
| 655 | Emergent BioSolutions Baltimore, MD Analyst I, Validation BS in science or engineering Exp: 0-2 years |
The Analyst I position will design and prepare all protocols and reports related to novel and diverse validation activities. The candidate will focus on Equipment, Utilities, and Software Validation. Responsibilities include: Write and execute validation and re-validation protocols and reports, (IQ / OQ / PQ), for the validation of new and existing processes, equipment, systems, etc. Write summary reports, following good documentation practices. Use Kaye Validator, DataTrace dataloggers, and/or Veriteq dataloggers to perform mapping studies. Analyze statistical data to verify acceptable criteria. etc. | 5/31/2019 |
| 656 | Emergent BioSolutions Lansing, MI Analyst II, Microbiology - 3rd Shift MS in pharmaceutical or biochemistry Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. | 5/31/2019 |
| 657 | Endiotix Boston, MA Executive Assistant/Office Manager HS Diploma Exp: 1-5 years, entry level will be considered |
The right candidate must be organized and calm under pressure. Excellent communication skills are essential for this role for external interactions. This position requires a professional demeanor and a high level of discretion in regards to handling of confidential company information. Must enjoy a “start-up” atmosphere and be flexible, show initiative, good judgment and be willing to take on additional tasks and responsibilities as needed to achieve goals and deliverables. Must have strong knowledge of Microsoft Office (Outlook, Excel, Word, PowerPoint) | 5/31/2019 |
| 658 | Endo Pharmaceuticals Horsham, PA QC Analyst I - Microbiology BS in biological sciences Exp: 0-3 years in pharma/biotech |
The QC Analyst I – Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, and inventory forms. Additionally, this role is responsible for assisting with the writing of standard operating procedures (SOPs) and revision of existing documentation. | 5/31/2019 |
| 659 | Endo Pharmaceuticals Horsham, PA Manufacturing Associate I USP BS in biological sciences Exp: 0-3 years in pharma/biotech |
The Manufacturing Associate I – Fermentation works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture Collagenase Clostridium Histolyticum (CCH) bulk drug substance (BDS). This role is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. | 5/31/2019 |
| 660 | Endologix Irvine, CA Supplier Quality Engineer BS in engineering or related Exp: 0-4 years in medical devices |
Responsible for supporting the Supplier Quality program and supporting cross-functional departments to acquire highest quality materials from suppliers that meet the requirements while improving the cost of quality of parts, processes and products. Provides support in the development and maintenance of company’s Quality Systems. Day to day activities include; supplier auditing, SCAR management, Supplier NCMR investigations, Supplier file maintenance, Supplier metrics, ASL and ACL | 5/31/2019 |
| 661 | Stryker Portage, MI Associate Quality Assurance Technician HS Diploma Exp: 1-2 years of assembly |
Under general supervision performs repetitive inspection tasks on assembled products using Standard Work Instructions and Device History Records (DHRs) while maintaining training certifications. Will work from written and/or verbal instructions while maintaining pace with production requirements. Will interact with internal customers to help resolve, inspection and/or components issues. etc. | 5/31/2019 |
| 662 | Stryker Kalamazoo, MI Design Engineer BS in software/electrical engineering, or computer sciences Exp: 0-2 years, experience is a plus |
As part of this team, you will interface with cross functional team members both on a local and global scale. Be responsible for creation to manufacturing of your design, this will include modeling, prototyping, and proving your design through testing. Specifically, this team member will join the team working to enhance the surgical environment for healthcare providers. Design, develop, test, work on compliance, traceability, documentation and refinement of embedded and application level software for medical device electro-mechanical systems | 5/31/2019 |
| 663 | Stryker Chicago, IL Associate OnSite Repair Specialist AS/AA Exp: 1-2 years in reprocessing or surgical instrumentation |
The Surgical Instrument Repair Excellence (SIRE) Apprenticeship Program is a two to three-year process that is monitored by the Department of Labor (DOL). The first 4 – 6 months of initial training will be based out of the Houston Training Center (HTC). After completion of the training at HTC you will be required to spend the remainder of the introductory 6 months with established field personnel at their home sites. Learn and become proficient in all aspects of handheld stainless steel instrument sharpening, repair and maintenance (Maintain an average score of 80% on all written and technical assessments). | 5/31/2019 |
| 664 | Stryker Sacramento, CA ENT Sales Associate BS/BA Exp: 1-2 years of sales support |
This position is a sales support role responsible for assisting and achieving regional goals. Responsibilities included building strong customer relationships, utilizing product knowledge, and case coverage support. You will proctor physicians during their initial procedures to provide guidance, gather procedure data and provide customer feedback on the Company’s product to appropriate individuals. Travel is extensive with temporary relocation dependent on the company needs. | 5/31/2019 |
| 665 | Stryker Portage, MI Quality Engineer - Electrical/Software BS/BA in eletrical/software engineering, computer sciences, or related Exp: 0-2 yeras |
As an Advanced Quality Engineer, you will support the development of one or more products from concept generation through production, having the unique opportunity to realize the entire product lifecycle. Specifically, you will: Partner with marketing and design to understand user needs and translate those into engineering specifications that constitute the basis of the design. Lead the development of a safety risk management strategy including implementation of risk controls. etc. | 5/31/2019 |
| 666 | Stryker San Jose, CA Packaging Test Engineer BS in packaging engineering/sciences Exp: 1-3 years in packaging/test engineering |
Test Engineers work closely with R&D to experiment with early prototypes and vet out product designs throughout the design process. Manages, improves, and maintains sterile and non-sterile packaging validations and associated procedures within Total Endoscopy. Maintains internal packaging validation work instructions are compliant and comprehensive per industry accepted procedures. etc. | 5/31/2019 |
| 667 | Envigo Indianapolis, IN Maintenance Technician HS Diploma Exp: 1-2 years experience/training |
Maintenance Technicians are responsible for general repairs and maintenance on buildings, structures and equipment. Maintenance Technicians are generally tasked with day-to-day upkeep of facility equipment that provides vital resources for animal breeding. Performs electrical, electronic, mechanical, hydraulic, and pneumatic maintenance and repair of machinery, equipment, and HVAC system. Performs diagnosing malfunctions in machinery and equipment. Performs dismantling, assembling, and installing industrial machinery. etc. | 6/3/2019 |
| 668 | Envigo Princeton, NJ Analyst, Immunoassay BS/BA or AS/AA Exp: 0-1 yeras |
Responsible for all aspects of validation, sample analysis and data preparation in support of pre-clinical and clinical studies. Ensure all work is conducted in accordance to GLP/GCP regulations. Conduct validation and sample analysis as per study method, in life study plan and or analytical/validation plans and SOPs in accordance to GLP/GCP. Promptly prepare and submit results after analysis. Work as a team and as directed by Study Managers and Lab Managers. Provide status reports on projects and accountable for meeting agreed timelines and performance quality. etc. | 6/3/2019 |
| 669 | Enzo Farmingdale, NY Medical Technologist - Immunology BS in clinical lab sciences. License by NYSED as Clinica Lab Technolgist required Exp: 1+ year |
The technologist will perform qualitiative and quantitative tests and examinations using various analyzers and/or manual methods. Assist in peforming established quality assurance procedures (quality control testing, instrument function checks and calibrations). Mainatains appropriate documentation and reports irregularities. | 6/3/2019 |
| 670 | Enzo Farmingdale, NY Medical Technologist- Generalist (Chemistry, Hematology, Coagulation, Urinalysis) BS in clinical lab sciences. License by NYSED as Clinica Lab Technolgist required Exp: 1+ year |
Several shifts avalible. The Medical Technologist will perform qualitative and quantitative tests and examinations using various analyzers and/or manual methods on specimen sources such as blood, urine, and other body fluids using established procedures. They will also be responsible for performing established quality assurance procedures (quality control testing, instrument function checks and calibrations). Maintains appropriate documentation and reports irregularities. | 6/3/2019 |
| 671 | Epic Laurelton, NY Analytical R&D Scientist MS in chemistry or biochemistry Exp: 1+ years |
Conduct analytical runs for R&D purposes using a set of analytical techniques such as HPLC, UPLC, GC, including writing related protocols and reports. Develop, evaluate, validate analytical methods for raw materials and finished products. Support the transfer of developed and qualified assays to relevant clients. Provide support, as related to analytical, plant trouble shooting/investigations and product regulatory submission. Provide full analytical development support in accordance with cGMP/GLP practices to product development programs within strict timelines to successfully meet internal and client program milestones. Support the AR&D related activities for filing of new ANDA. Support the generation of pharmaceutical development reports and related documentation. | 6/3/2019 |
| 672 | Abcam Burlingame, CA Research Associate BS/BA in biological sciences Exp: 1+ year working in lab setting |
The position is primarily responsible for the screening and characterization of monoclonal antibodies. The successful candidate will play a hands-on role in the company’s use of a wide variety of analytical assays such as ELISA, flow cytometry, Octet, and HTRF. He or she will partner closely with other team members within the group, assisting with every step of antibody development. The candidate will make observations, analyze data, and interpret results with full supervision. | 6/3/2019 |
| 673 | ERT Philadelphia, PA Project Coordinator BS/BA or equivalent Exp: 0-2 years, experience is a plus |
Duties include: deliver customer service by providing support using ERT's products. Work and collaborate with project teams in development and delivery of ERT products. Etc. | 6/3/2019 |
| 674 | Eurofins Fremont, CA Biochemist- Biacore/Protein Binding MS Exp: 1-2 years protein characterization |
Duties include: performing routine biopharmaceutical characterization studies including UV/Vis, size exclusion, cation exchange chromatography. Support other methods such as mass spec, or immuno-based assays. Conduct experiments and record/interpretate data. | 6/3/2019 |
| 675 | Eurofins St. Charles, MO Associate Scientist AS/AA or BS/BA Exp: 0-1 years |
Duties as an associate scientist include: performs lab work including preparing buffers/reagents/media. Maintain cell cultures in BSL2 lab. Conducts production assays in ADMET, ion channel, immunosignaling, OncoPanel, etc. | 6/3/2019 |
| 676 | Eurofins Columbia, MO Assistant Scientist I, Method Dev BS/BA in chemistry or life sciences or engineering Exp: 1+ years related experience |
The Associate Scientist I position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. | 6/3/2019 |
| 677 | Eurofins Easton, MD Assistant Scientist I, Aquatics BS/BA in chemistry or life sciences or engineering Exp: 1+ years related experience |
Carries out routine experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs). Assist/run toxicology studies, including preparing test solutions and daily maintenance of test systems. Feed, water, and examine animals for signs of illness, disease, or injury sustained in the laboratory. Performs analysis, first level, and peer review of data for accuracy and completeness. | 6/3/2019 |
| 678 | Eurofins West Point, PA Analytical Scientist BS in biology, chemistry, or related Exp: 1+ year in cGMP lab |
Responsibilities include: Execute experiements utilizing analytical methods to support preclinical pharamceutical product development. Use techniques/instrumentations such as HPLC and spectroscopy. Prepare test solutions, compounds, and reagents. Maintain lab instruments. etc. | 6/3/2019 |
| 679 | Eurofins San Diego, CA Analytical Chemist BS/BA in analytical chemistry, biochemistry, or pharmaceutical sciences Exp: 1-2 years in lab/research |
Responsibilities include: Develop, qualify and validate analytical test methods for drug products, intermediates and excipients. Design and execute analytical development studies. Write protocols and repors. Maintain and write SOPs. etc. | 6/3/2019 |
| 680 | Eurofins Lancaster, PA 2nd shift - Pharmaceutical Stability Project Management Specialist BS/BA in sciences, business or related Exp: 0-2 years, experience is a plus |
2nd shift. Responsibilities include: manage all aspects of stability studies assigned by clients. Take responsibilities for quality and TAT of assigned studies. etc. | 6/3/2019 |
| 681 | Exactech Gainesville, FL Clinical Research Associate AS/AA or BS/BA preferred Exp: 1+ years in clinical research |
Responsibilities include: Monitor the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), GCP, and all applicable regulatory requirements. Conduct visits to assess the qualification of potential investigative sites, initiate sites, instruct site personnel on the proper conduct of studies and use of Electronic Data Capture (EDC) system, review and ensure accuracy of data collected, and terminate studies | 6/3/2019 |
| 682 | Exelixis Alameda, CA Risk Analyst BA in business admin, finance, risk management or related Exp: 1-2 years in insurance, project management or consulting |
The Risk Analyst will provide appropriate business risk assessments, identify areas of risk of loss, quantify the impact, develop and evaluate policies and provide guidance to the Company’s decision makers. The Risk Analyst is important role within the organization to minimize the impact of operational and financial risk to the enterprise. | 6/3/2019 |
| 683 | Exsurco Wakeman, OH Assembly Technician HS Diploma Exp: 0-1 years factory work |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). | 6/3/2019 |
| 684 | First Light Diagnostics Chelmsford, MA Research Associate - Microbiology BS in bioengineering, biochemistry, microbiology or related Exp: 0-2 years, experience is a plus |
Candidates should love laboratory science and should enjoy technology innovation. You will work with a group of creative inventive scientists on developing novel state-of-the-art methods that are the basis for important new products to improve medical outcomes for patients with serious infections. Responsibilities include: developing experimental designs, preforming microbiological/molecular biological experiments, and other lab-related work. | 6/3/2019 |
| 685 | Fluidigm Markham, CA Reagent Manufacturing Associate I BS/BA in biology, biochemistry, or related Exp: 1-2 years in lab/research |
The Reagent Manufacturing Associate is a member of our Proteomics Reagent Operations team. The scientist will be accountable for QC testing of raw materials, in-process materials and finished goods for release. This individual will also be a subject matter expert in the development and testing of new QC procedures. | 6/3/2019 |
| 686 | Fluidigm South San Francisco, CA Research Associate - Microfluidics BS/BA or MS in chemistry, biomedical engineering or related0-3 years Exp: |
Responsibilities as a research associate include: serving as a key member for testing, analyzing, and developing microfluidic devices. Integrate biochemical reactions in microfluidics. etc. | 6/3/2019 |
| 687 | Fluidigm Markham, CA Product Development Scientist MS in immunology, molecular biology, biochemistry, or related Exp: 1+ years in research |
The Product Development Scientist will play an active role in developing high-quality Fluidigm reagents. Responsibilities include: write application, product or system validation test plans. Work with product managers and product applications group. Ensure all valudation tests are in concordance with customer and product requirements. etc. | 6/3/2019 |
| 688 | Fluke Everett, WA Test Engineer BS in electrical engineering or related Exp: 0-2 years |
Responsibilities as a test engineer at Fluke iclude: plan/implement test systes for new product introductions. Support/maintain/improve test systems throughout factory. Advise design engineering of existing production capabilities. etc. | 6/3/2019 |
| 689 | Fluke Houston, TX Medical Physics Assistant MS Exp: 0-4 years |
Basic Duties and Responsibilities: Assisting in clinical medical physics coverage, as well as supporting the commissioning team's project | 6/3/2019 |
| 690 | Foxx Life Sciences Salem, NH Wuality Engineer BS in engineering or related Exp: 1+ years in quality engineering |
Duties include: develop and implement all quality-related processes and documentation. Direct manufacturing process development to meet quality metrics. Monitor faility performance and associated metrics. Etc. | 6/3/2019 |
| 691 | Fresenius Kabi Melrose Park, IL Validation Engineer BS/BA in science or engineering Exp: 1-3 years in cGMP |
Responsible for providing technical support to operations in terms of equipment/system/process initial validation and equipment/system/process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. Individual must also perform HEPA filter integrity/velocity testing and critical area (class 100) airflow pattern testing. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 6/3/2019 |
| 692 | Fresenius Kabi Grand Island, NY Associate Scientist - Chemistry Technical Services BS or higher Exp: 1+ years |
Reports to manager, QC chemistry technical services. Responsibilities include: Method transfers/method verification/Co-Validations of compendial and non-compendial analytical methods utilized across Fresenius Kabi according to written procedures. Testing of routine and non-routine samples where specialized training is essential. etc. | 6/3/2019 |
| 693 | Freudenberg Jeffersonville , IN Medical Device Assembly/ Manufacturing Associate - 1st Shift HS Diploma Exp: 0-1 years |
Responsibilities include: hand assembly manufactured components, complete required documentation for work performance, quality inspect work performed. etc. | 6/3/2019 |
| 694 | Freudenberg Gloucester, MA Program & Quoting Engineer BS/BA in mechanical engineering or related Exp: 1+ years (coops and internships) |
Ensures that opportunities introduced are a strategic fit to the Lead Center. Coordinates costing activities with the Project Management Team. Ensures that all cost assumptions and cost drivers are optimized and technically feasible. Understands cost assumptions and challenges cost drivers where appropriate. Develops pricing and submits final quotes to the sales team. Establishes acceptable pricing for new business opportunities by optimizing minimum margin requirements and target pricing from the Business Development team. Leads quote meetings within the lead center and acts as the single point of contact at the Lead Center for the Commercial Team specific to the support of new business opportunities. Ensures that all quotations consider Lead Center resources, capabilities, profitability, strategic plan, and product liability and insurance concerns. Utilizes Salesforce.com as the single CRM (customer relationship management) tool for inputs and outputs to the quoting process. Measured by accuracy, clarity, and timeliness of quotation. | 6/3/2019 |
| 695 | Fujifilm College Station, TX EHS Specialist I BS/BA in safety science, environmental science/engineering or related Exp: 1+ years |
Responsibilities include: Assist with all aspects of EHS, including applicable OSHA regulations, environmental record keeping, safety audits, and accident investigations. Ensure the Emergency Response Plan remains current with regulatory requirements and site needs, assist with the readiness of FDBT personnel and facilities to respond to emergencies. Conduct environmental and safety audits and inspections; assist EHS Management with reporting to Senior Leadership. | 6/3/2019 |
| 696 | Fujifilm College Station, TX Downstream Manufacturing Technician I AS/AA in biological sciences or engineering Exp: 0-1 years |
The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation. | 6/3/2019 |
| 697 | Codexis Redwood City, CA Research Assistant, Molecular Biology BS in molecular biology or related Exp: 0-2 years |
Responsibilities include: Construction of gene libraries and expression vectors. Characterization of gene variants. Primer design. DNA isolation. DNA sequencing. Cloning of genes and genetic pathways. Work with project teams to provide support and assistance to all phases of directed evolution projects, contribute to team presentations and written reports. | 5/25/2019 |
| 698 | Codexis Redwood City, CA Research Assistant (Biochemistry) BS in molecular biology or related Exp: 0-2 years |
We are looking for an entry level Research Assistant interested in analytical method development and protein biochemistry. Successful candidates will be part of an interdisciplinary, dynamic and enthusiastic protein engineering team responsible for implementing Codexis’ core technologies and delivering commercially-relevant and highly-evolved proteins. Responsibilities include; Assist in developing relevant enzyme assays in HTP format. Grow cultures, express proteins, and test enzyme activity in high throughput and in larger scales. Analyze HTP samples in HPLC, UV-Vis Spectrophotometry, GC, LC-MS, or GC-MS to identify and quantify small-molecule products. | 5/25/2019 |
| 699 | Codiak Cambridge, MA Associate Scientist II Protein Sciences MS in biology, chemistry or related Exp: 1+ years research experience |
Codiak is seeking a qualified associate scientist to join our growing Research organization and contribute to the development of the company’s innovative exosome engineering platform. Responsibilities include: Produce, purify, and characterize engineered exosomes from conditioned cell culture medium; Execute biochemical and cell-based assays to validate target and pathway engagement of therapeutic candidates; Express and purify recombinant proteins, including antibodies, enzymes, and fusion proteins, at the milligram scale to support assay development for ongoing projects;etc. | 5/25/2019 |
| 700 | Cogent Terre Haute, IN Laboratory Technician HS Diploma Exp: 1+ years pharma lab experience |
The Laboratory Technician ensures the quality of products by developing, validating and documenting analytical methods and performing physical and chemical analyses of raw materials, in-process and finished products in support of the manufacturing process. Perform test sample extractions or dilutions and execute instrumental analysis using high performance liquid chromatography (HPLC). Perform other laboratory testing as required, including but not limited to, GC, LOD, Ash, and particle size analysis (sieve method). etc. | 5/25/2019 |
| 701 | Cogmedix Westborough, MA Electrical Engineer I BS in electrical engineering Exp: 0-5 years |
As a member of the engineering services team, the Electrical Engineer I will solve complex problems and participate in the specification, design, prototyping and testing of a diverse range of tooling, fixtures, design for manufacturability projects, and other customer product design needs. Under the direction of the Electrical Engineering Manager, the engineer in this role will be performing design tasks of a complex technical nature requiring investigation of new technologies, and applying engineering design principles and practices. | 5/25/2019 |
| 702 | Coloplast Mankato, MN QA Chemist BS in chemistry or related Exp: 0-5 years |
As a QA Chemist, you will be is responsible for performing inspections and tests on raw materials, in-process products, bulk products, finished goods and stability samples to ensure conformance to established specifications. Perform in-process inspections and determine any adjustments required. Perform bulk and finished product inspections, testing and analyses. Confirm samples meet established standards and specifications and release items as appropriate. Develop and validate analytical methods based on USP requirements and local needs and available instrumentation. Record test data and results using standard laboratory data calculations. Verify notebook entries and calculations for lab staff. Assure equipment is calibrated prior to use and complete preventative maintenance. etc. | 5/25/2019 |
| 703 | Complete Genomics Montreal , Ca Lab Technician BS in molecular biology or related Exp: 1-2 years |
The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. Execute on and assist in the development of process instructions that ensure accuracy, throughput, and quality. Operate and monitor laboratory automation and instrumentation. Communicate issues and failures as necessary to the appropriate parties. General lab duties, such as restocking supplies and maintaining inventory. | 5/25/2019 |
| 704 | Complete Genomics San Jose, CA Lab Technician BS in molecular biology or related Exp: 1-2 years |
The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. Execute on and assist in the development of process instructions that ensure accuracy, throughput, and quality. Operate and monitor laboratory automation and instrumentation. Communicate issues and failures as necessary to the appropriate parties. General lab duties, such as restocking supplies and maintaining inventory. | 5/25/2019 |
| 705 | Conformis Billerica, MA Design Engineer I BS in mechanical or biomedical engineering Exp: 1-2 years |
The Design Engineer I will be responsible for design and development of new orthopedic implants and related instrumentation systems and the creation of documentation in support of quality systems and concept to medical device which achieve quality, cost and time to market requirements. Understand the objectives, responsibilities, and mission of the Engineering department and works towards those goals. Develop protocols for design verification and validation (V&V), including outside test and research labs. Complete corresponding test reports. Communicate with customers, sales, marketing and independent entities to gain knowledge of product design requirements. | 5/25/2019 |
| 706 | Conformis Billerica, MA Hip Cell Programming, 1st Shift HS Diploma Exp: 1-3 years |
This position is responsible for operation of Pre/Post machining from start to finish for hip stem and hip acetabular Cups. Responsibilities include: Printing DHR’s for production release of hip stem and acetabular cup . Programming of acetabular cup and hip stem . CNC operation of acetabular cup and hip stem . Comply with all company policies and procedures including safety regulations, personal protective equipment requirements, Standard Operating Procedures, Work Instructions and Good Manufacturing Procedures | 5/25/2019 |
| 707 | ConMed Utica, NY Pricing Analyst I BS in business or finance Exp: 1-3 years |
Supports management, sales, marketing, contracts, and other administrative areas by providing timely and accurate financial projections, price quotations, contracts, and profit analyses. Performs financial analyses, including forecasts, projections, and historical assessments. Produces quotes for capital and/or disposables not covered by existing contracts. Facilitates communication among management, sales, and contracts staffs regarding contract and price. | 5/25/2019 |
| 708 | ConMed Largo, FL Machining Associate HS Diploma Exp: 1+ years |
Purpose: Produce parts that meet requirements using a variety of manual and/or automated equipment through established procedures. Accurately perform basic metrology tasks utilizing basic measurement devices such as calipers, micrometers, etc. Set-up and operate various manual and automated production machines where set-up is well defined and operate simple CNC type machines that are already set-up for production. Must be willing and able to continually rotate through a variety of manufacturing processes and duties, performing all types of tasks in a cell/team environment. | 5/25/2019 |
| 709 | ConMed Largo, FL Quality Engineer I - New Product Development BS in related field Exp: 0-3 years medical device experience |
The Quality Engineer New Product Development (NPD) is responsible for supporting all quality engineering activities to support the new product life cycle, from concept through commercialization and sustaining changes, as part of a cross-functional development team. Serves as the key resource for ensuring compliance to ISO, MDD and QSR requirements for Medical Devices. Takes the lead with quality initiatives with inter-organizational impact following QSR, ConMed Policies and standards. Works under direction from Quality Management. | 5/25/2019 |
| 710 | ConMed Utica, NY R&D Engineer I BS in electrical or biomedical engineering Exp: 0-2 years |
e are seeking a R&D Engineer I to join the Cardiology and Critical Care R&D team, based in Utica, NY, to work on new product development and sustaining engineering activities for this product portfolio. This engineer will have immediate opportunities to contribute in a fast paced and hands on environment. Support the development of new and existing product specifications and requirements based on design input requirements, in collaboration with the project engineer. Write technical reports, risk management documents, VOC summaries, test protocols and design input and output documents. Perform sustaining engineering activities including problem troubleshooting, root cause analysis, investigations, and resolving part obsolescence issues | 5/25/2019 |
| 711 | ConMed Denver , CO Mechanical Engineer I BS in electrical, mechanical, or biomedical engineering Exp: 0-3 years engineering experience |
The Mechanical Engineer will work with a cross-functional teams on new product development and sustaining engineering activities. Support the development of new and existing product specifications and requirements based on design input requirements, in collaboration with the project engineer. Supports the writing of technical reports, risk management documents, VOC summaries, test protocols and design input and output documents. Create detailed 3D CAD models and drawings of mechanical and electrical parts and assemblies | 5/25/2019 |
| 712 | Cook Bloomington, IN Quality Engineer BS in sciences/engineering Exp: 0-2 years |
The Quality Engineer at Cook Medical is responsible for executing and/or monitoring key processes in support of the Quality Management System: auditing; complaint investigation; corrective and preventive action (CAPA); control of non-conformances; document, data, and change control; process control; risk management and supplier quality management. The Quality Engineer fulfills the role of Independent Reviewer of many key process outputs | 5/25/2019 |
| 713 | Cook Pittsburgh, PA Quality Control Microbiology Assistant AS degree in life sceicenes Exp: 1-3 years in lab/GMP environment |
The Quality Control Microbiology Assistant at Cook MyoSite will assist GMP testing and perform environmental monitoring activities to support lot release and in-process testing. Preparation of equipment and instrumentation for further use in analytical assay and/or microbiological testing. Perform environmental monitoring activities such as collecting viable air, surface EM samples, non-viable particulate samples, and reading of EM plates. Support to maintain cleanroom environment below alert limits by participating in and following established cleaning practices and cleanroom behavior | 5/25/2019 |
| 714 | Cook Spencer, IN Regulatory Engineer BS/BA in engineering or sciences Exp: 0-4 years |
The Regulatory Engineer provides technical support to Regulatory Affairs for the development of regulatory documentation for compliance with FDA and international regulatory requirements. Develop new, and refine existing, systems that provide the necessary information for successful submission to global regulatory bodies . Assist various Regulatory Affairs staff with technical assessment and writing of regulatory submissions and responses to regulatory agencies. Prepare regulatory submissions for new products, product changes, and re-registrations, as required. etc | 5/25/2019 |
| 715 | Cook Bloomington, IN Research and Development Packaging Engineer MS in packaging sciences Exp: 0-3 years |
The Packaging Engineer II procures and develops packaging for new and existing products. A Packaging Engineer II leads packaging activities with a cross-functional team including SBU Product Management, Regulatory Affairs, Operations, Quality Assurance, Clinical Affairs, and other Engineering personnel. | 5/25/2019 |
| 716 | Cook Winston-Salem, NC Regulatory Affairs Specialist I BS/BA in related field Exp: 0-2 years |
The Regulatory Affairs Specialist I is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified Class I, II, III and IV medical devices in specific markets. In addition to submissions, the Regulatory Affairs Specialist will serve as a communication liaison between the Cook manufacturer and the Cook Local Office / Cook Distributor. | 5/25/2019 |
| 717 | Cook Winston-Salem, NC Quality Engineer - Post Market BS/BA in related field Exp: 0-2 years |
The primary purpose of the Quality Engineer (Post Market) position at Cook Winston-Salem is complete and review post market quality engineering activities, including complaint investigations, risk assessment, post market feedback, and product quality issues. Responsibilities include: Perform complaint investigations, including technical assessment of returned products. Complete risk assessments using post market data. Assist with the investigation, risk assessment and resolution of product quality and quality system issues. Implement, support and maintain post-production quality activities. | 5/25/2019 |
| 718 | CryoLife Austin, TX Component Processing Technician - Final Assembly HS Diploma Exp: 1-4 years in manufacturing |
Position Overview: Perform work station assembly operations including sewing and packaging of heart valves in a clean room. Inspect incomplete and finished components for conformance to written specification with the aid of a microscope, and follow standard work methods and practice safe work habits to ensure production is as efficient and safe as possible. | 5/25/2019 |
| 719 | CSL Kankakee, IL QAO Specialist I BS/BA in sciences/technical field Exp: 0-2 years in cGMP environment |
Provide an overview of the responsibilities of the position by providing a summary of the most important aspects and duties of the position. This is an entry level position into Quality Assurance Operations. Developing responsibilities include assisting with investigating deviations, relevant to area of responsibility. Responsible for driving continuous improvement on production floor to ensure compliance to cGMPs. Real time review of batch records, including critical processing steps with production floor presence. | 5/25/2019 |
| 720 | CSL Holly Springs, CN Associate I/II/III, Manufacturing (Upstream) Night Shift HS Diploma or BS/BA Exp: HS: 1+ years, BS: 0 years |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (be trained in) the technical skill-sets necessary to manufacture high quality biologicals or sterile injectables safely in a compliant, efficient, and cost effective manner. Responsibilities include; Becomes trained on basic processes and equipment and serves as a hands-on resource in Production. Cleaning, preparing, and sterilizing production equipment. Assembly, set-up, and disassembly of production equipment. Handling biologically and chemically hazardous goods | 5/25/2019 |
| 721 | CTI Covington, KY Clinical Research Associate BS in health fields Exp: 1+ years in clinical research monitoring |
The Clinical Research Associate completes project activities associated with monitoring functions of phase I through phase IV clinical research studies while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP) and applicable local regulations; provides clinical and technical support for CRAs and administrative staff; and performs management of study site activities to ensure integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs). | 5/26/2019 |
| 722 | LivaNova Houston, TX Entry-Level Electrical Engineers BS/BA in electrical engineering Exp: recent graduates |
We are looking for only the most driven Electrical Engineers with solid engineering fundamentals. Responsibilities include: Circuit simulation/modeling, Bench data collection, Scripting & overall test automation, Chipset evaluations (e.g Bluetooth, MCUs, accelerometers…), PCB design & layout, etc. | 5/26/2019 |
| 723 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS Exp: 0-2 years |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos. Responsibilities include: Independently produces notebook, dev, pilot and production materials per written directions, Analyzes in-process and final oligos using state of the art analytical techniques, Troubleshoots simple manufacturing process problems, etc. | 5/26/2019 |
| 724 | Hologic San Diego, CA Process Development Associate 1 BS/BA Exp: 1+ years |
Responsible for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes. Responsibilties include: Maintains the Pilot Plant laboratory under cGMP conditions. Produces development, pilot and production materials per written instructions. Stocks and maintains the laboratory supplies. Completes laboratory work and associated paperwork by assigned completion dates | 5/26/2019 |
| 725 | Hologic Methuen, MA Shipper 1 HS Diploma Exp: 1+ years in shipping/warehouse |
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Responsible for picking, packaging, and preparing product for shipment. Assists in loading trucks and running end-of -day reports for carriers. Works with other members of the Distribution Team to ensure all orders are prepared and shipped daily. Runs packing lists and prepares finished goods for shipment. etc.The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Responsible for picking, packaging, and preparing product for shipment. Assists in loading trucks and running end-of -day reports for carriers. Works with other members of the Distribution Team to ensure all orders are prepared and shipped daily. Runs packing lists and prepares finished goods for shipment. etc.The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Responsible for picking, packaging, and preparing product for shipment. Assists in loading trucks and running end-of -day reports for carriers. Works with other members of the Distribution Team to ensure all orders are prepared and shipped daily. Runs packing lists and prepares finished goods for shipment. etc. | 5/26/2019 |
| 726 | Hologic San Diego, CA Oligo Process Development Chemist 1 BS/BA or equivalent Exp: 0-2 years |
Responsible for the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Responsible for research, development and production manufacturing activities associated with oligos. Independently produces notebook, dev, pilot and production materials per written directions. | 5/26/2019 |
| 727 | Hologic San Diego, CA Operations Test Associate BS/BA or equivalent Exp: 0-3 years lab experience |
We are currently seeking an Operations Test Associate responsible for generating accurate and reliable data for biologic products or medical devices on stability. Responsibilities include: Performs data analysis and results interpretations comparing to stability protocol defined specifications, validity criteria, and alert limits. Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials. Responsible for the maintenance and cleanliness of equipment, calibrating or submitting items for calibration as needed. etc. | 5/26/2019 |
| 728 | Hologic Malborough, MA Electrical Engineer I BS/BA in electrical engineering Exp: 1+ years |
The ideal candidate is one who understands complex electro-mechanical systems, and how they interact with software, manufacturing, service, and external vendors, to fulfill product requirements. This position would report to the Director of Research and Development. Designs and directs engineering personnel in fabrication of test control apparatus and equipment, and determines methods, procedures, and conditions for testing the engineered products and associated apparatus. Applied electrical engineering knowledge concerning the research, design and development of new products having state-of-the-art sophistication for X-ray generators, data acquisition, signal processing, power supplies, etc. | 5/26/2019 |
| 729 | Evotec Watertown, MA Associate Scientist BS/BA in biology, chemistry, or related Exp: 1+ years in lab |
Cyprotex US, an Evotec Group, is looking for an Associate Scientist (Cell Biologist) based in Watertown, MA to assume responsibility for the routine screening of compounds in various in vitro ADME assays and reporting to the Associate Director or Senior Scientist. Responsibilities include: Design molecular or cellular laboratory experiments, oversee their execution, and interpret results. Conduct research on cell function, including mechanisms of gene expression, cell signaling, or cell differentiation. Compile and analyze molecular or cellular experimental data and adjust experimental designs as necessary. | 5/26/2019 |
| 730 | Cytovance Biologics Okalahoma City, OK Manufacturing Sciences Technician BS in life sciences or related Exp: 1-3 years in GMP production |
The main responsibility of the Manufacturing Sciences technician is to support the manufacturing team as a technical advisor and operator. Manufacturing Sciences technicians adapt processes demonstrated at the R&D scale to final manufacturing scale. Secondary roles include driving/contributing to continual improvement initiatives and providing input to production scheduling | 5/26/2019 |
| 731 | Decibel Theraputics Boston, MA Research Associate, Histology BS or MS in biological sciences Exp: 1+ year in lab |
The Research Associate will work closely with colleagues in platform development, biology, and pharmacology. In addition, the Research Associate will be responsible for restocking lab supplies and maintaining lab equipment. Core responsibilities include: Conduct whole body perfusion and collect tissue for histological analysis. Micro dissect and process inner ear tissues. Perform immunohistochemistry staining protocols. etc. | 5/26/2019 |
| 732 | Deciphera Lawrence, KS Scientist - Biological Sciences BS or MS in biotechemistry Exp: 0-5 years |
This position will report to the Principal Investigator – Biological Sciences in the Lawrence, KS research facility. Key responsibilities include: Perform primary screening of small molecules utilizing cell-based assays. Primary responsibility will be in the area of screening small molecule kinase inhibitors. Perform routine mammalian cell culture. Together with supervisor, responsible for validating new biochemical or molecular biology-based assays and trouble-shooting when needed to establish reliable screening platforms. | 5/26/2019 |
| 733 | Deciphera Lawrence, KS Scientist - Benzymology BS or MS in biotechemistry Exp: 0-5 years |
This position will report to the Senior Scientist – Enzymology in the Lawrence, KS research facility. Key responsibilities include: Perform routine drug screening assays for kinase inhibitors. Quality control of high throughput screening equipment. Together with supervisor, responsible for validating new biochemical assays and troubleshooting when needed to establish reliable screening platforms. Track and record data into corporate database and notebooks. Generate reports and create presentations as required by the organization. | 5/26/2019 |
| 734 | Deciphera Waltham, MA Associate/Sr. Associate, Regulatory Affairs BS/BA or higher Exp: 1-3 years in clinical research or FDA regulation |
This position will report to the Sr. Manager, Regulatory Affairs and be located in the Waltham, MA office. Responsibilities include: Under supervision, the Regulatory Affairs Associate will work with cross functional colleagues in providing support for clinical and CMC regulatory filings, creation of internal regulatory documents, and assist with ensuring internal compliance with GXP regulations and policies. Define contributions for submissions, communicate to functional contributors and track delivery according to agreed timelines. Identify and compile all materials required in U.S., EU, and other ex-US regulatory submissions, this includes annual reports, DSURs for INDs, CTAs, IND/NDA/MAA applications, etc. as necessary | 5/26/2019 |
| 735 | Dendreon Richmond, VA Immunotherapy Sales Specialist - Richmond, VA BS/BA in sciences/technical field Exp: 1+ year in biotech/medical device sales |
Dendreon’s Immunotherapy Sales Specialist is responsible for achieving sales objectives in an assigned territory through the development, maintenance, and enhancement of the business. Customers include oncologists, urologists, nurses, pharmacists, pharmacy and therapeutics groups, tumor boards, teaching institutions, hospitals and formulary committees. The role is responsible for ensuring customer’s clinical conviction in the product as well as guiding the customer through the logistics process and seeing the sale through to its conclusion. The territory alignment for this role is the state of Virginia. | 5/26/2019 |
| 736 | Dexcom San Diego, CA Mechanical Engineer 1 BS/BA in technical discipline Exp: 0-2 years |
Under the direction of the Operations Mechanical Engineering Manager, the Mechanical Engineer provides technical support for the projects, functions, and strategic objectives of the Operations Mechanical Engineering department, focusing on: engineering support for new product development; development of fixtures and equipment as standalone and in support of automated systems; failure mode analysis and corrective action of process equipment and instruments; sustaining engineering for the legacy and newly deployed manufacturing systems; engineering and quality documentation development. | 5/26/2019 |
| 737 | Dexcom San Diego, CA Quality Assurance Analyst 1 BS/BA in technical discipline Exp: 0-2 years |
Supports the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality assurance processes and standards for manufacturing and production. Performs evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Identifies risk and evaluates deficiencies while working with internal departments/business units to appropriately remedy them. Facilitates internal training on quality assurance requirements, processes, and procedures. May perform audits and risk assessments. | 5/26/2019 |
| 738 | Dexcom San Diego, CA Engineering Technician 1 HS Diploma or AA/AS Exp: 1-2 years in production equipment operations |
Responsible for preventative and reparative maintenance of the equipment, process and/or electronics located in the Production and R&D Departments. Prepares and maintains appropriate documents in RAM, Agile and Track-It. Helps with Process and Equipment Validations, IQ's and OQ's and process protocals. Equipment project work and validations assigned as needed. Follows Good Manufacturing Protocals. | 5/26/2019 |
| 739 | Dexcom San Diego, CA Clinical Data Associate MS in technical dicipline Exp: 0-2 years |
Collaborates with various departments on the design, documentation, testing and implementation of clinical data studies. Develops systems for organizing data to analyze, identify and report trends. Analyzes the interrelationships of data and defines logical aspects of data sets. Prepares reports of clinical trial studies for internal validation and cross validation studies. May evaluate and resolve issues regarding contents of reports. | 5/26/2019 |
| 740 | Dexcom San Diego, CA Research Associate 1 BS/BA in technical discipline Exp: 0-2 years |
Performs research and/or development in collaboration with others to complete science-based projects. Makes detailed observations, analyzes data and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Maintains high level of professional expertise through familiarity with scientific literature. May participate in scientific conferences and contribute to scientific journals. May be responsible for identifying patentable inventions. May act as principal investigator in conducting own experiments. | 5/26/2019 |
| 741 | Dexcom San Diego, CA Mechanical Engineer 1 BS/BA in technical discipline Exp: 0-2 years |
Under the direction of the Operations Mechanical Engineering Manager, the Mechanical Engineer provides technical support for the projects, functions, and strategic objectives of the Operations Mechanical Engineering department, focusing on: engineering support for new product development; development of fixtures and equipment as standalone and in support of automated systems; failure mode analysis and corrective action of process equipment and instruments; sustaining engineering for the legacy and newly deployed manufacturing systems; engineering and quality documentation development. | 5/26/2019 |
| 742 | Dexcom San Diego, CA Quality - Quality Assurance Analyst 1 BS/BA in technical discipline Exp: 0-2 years |
Supports the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality assurance processes and standards for manufacturing and production. Performs evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Identifies risk and evaluates deficiencies while working with internal departments/business units to appropriately remedy them. Facilitates internal training on quality assurance requirements, processes, and procedures. May perform audits and risk assessments. | 5/26/2019 |
| 743 | DiCE Molecules Redwood City, CA Research Associate - Assay Science (Biology) BS or MS in biochemistry, molecular biology, or related Exp: 0-4 years in biotech |
Responsibilities to include: Performing key assays to support drug discovery using biochemistry, cell biology and/or biophysics. Generating high-quality, reproducible data by leveraging liquid handling, laboratory robotics and advanced data analysis tools. Identifying and developing new assays as the project requires. Communicating experimental results to project teams. | 5/26/2019 |
| 744 | Dicerna Pharmaceuticals Cambridge, MA Research Associate/Associate Scientist, RNAi Pharmacology BS or MS in biochemistry, molecular biology, or related Exp: 1+ years |
Key responsibilities include: Rodent dosing, sampling and necropsy; planning and performing of all technical aspects of in vivo experiments; contributing to experimental design and strategy. Cross-functional collaboration to help enable efficient operation of our on-site animal care facility (ACF). Performing laboratory assays according to SOPs, troubleshooting as needed; assay development. Generating data using both standard and novel molecular technologies. Contributing to a team tasked with evaluating novel experimental medicines in preclinical models of disease, and advancing our technology to enable development of the next generation of innovative RNA-based therapeutics. | 5/26/2019 |
| 745 | Dicerna Pharmaceuticals Cambridge, MA Research Associate/Associate Scientist, RNAi Discovery BS or MS in relevant field Exp: 0-5 years |
Dicerna Pharmaceuticals is looking for a BS/MS scientist to help in its drug discovery efforts. This is a hands-on research position that requires strong expertise in molecular and cellular methodologies. Key responsibilities include: siRNA drug candidate screening, hit identification, and lead optimization. In vivo drug candidate testing (e.g. mouse dosing; sample analysis) | 5/26/2019 |
| 746 | DMS Health Technologies Wausau, WI Medical Assistant (Technologist Assistant) HS Diploma Exp: 0-1 year |
The technologist assistant assists the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. The technologist assistant demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. The individual demonstrates knowledge of the principles of growth and development over the life span. He/she is able to identify and categorize each patient’s age-specific grouping of needs, such as those for infant, pediatric, adolescent, adult or geriatric patients. | 5/26/2019 |
| 747 | DMS Health Technologies Santa Maria, CA Medical Assistant PRN HS Diploma Exp: 0-1 year |
The technologist assistant assists the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. The technologist assistant demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. The individual demonstrates knowledge of the principles of growth and development over the life span. He/she is able to identify and categorize each patient’s age-specific grouping of needs, such as those for infant, pediatric, adolescent, adult or geriatric patients. | 5/26/2019 |
| 748 | DMS Health Technologies Minneapolis, MN Medical Assistant HS Diploma Exp: 0-1 year |
The technologist assistant assists the technologist with patient care by transporting patients between the facility and scanner; sanitizing and cleaning patient care and staff areas; changing table linens; entering exam and patient information electronically or on paper; and answering the telephone. The technologist assistant demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served. The individual demonstrates knowledge of the principles of growth and development over the life span. He/she is able to identify and categorize each patient’s age-specific grouping of needs, such as those for infant, pediatric, adolescent, adult or geriatric patients. | 5/26/2019 |
| 749 | DMS Health Technologies Glen Burnie, MD Cardiac Stress Tech AS or BS/BA Exp: 1+ years in emergency care setting |
Under the direct supervision of the site physician, performs various professional and administrative duties related to nuclear medicine stress testing including but not limited to: patient preparation-including IV start and EKG lead placement interpretation, administration of exercise and pharmacological stress tests, and application of ACLS measures to patients when directed. Activities not performed at the physician site are supervised by the Area Supervisors and Business Directors. | 5/26/2019 |
| 750 | DJO Vista, CA Maintenance Technician 1 HS Diploma Exp: 1+ years |
Performs basic and routine functions associated with the maintenance or repair of the manufacturing process including machines and equipment. Utilizes fundamental knowledge of a select number of machines, equipment and manufacturing processes to perform duties that may include but are not limited to: performing electronic, electrical or mechanical troubleshooting to determine problems in non-functioning equipment or machinery used in the manufacturing process; dismantling, adjusting, repairing and assembling equipment and machinery according to layout plans, blueprints, operating or repair manuals, rough sketches or drawings; using test and diagnostic equipment to perform checkouts; rebuilding or modifying manufacturing equipment as required. May troubleshoot software as it pertains to test equipment or machinery as needed. | 5/26/2019 |
| 751 | DJO Vista, CA Product Assembler HS Diploma Exp: 1+ years |
Utilizes a developing to full understanding of operational processes and procedures to perform an assortment of assembly activities of moderate scope on a mixture of products, components, assemblies or sub assemblies. Follows methods, and sequence of operations according to specifications, blue prints and bills of materials. Ensures quality and product conformance. Sets up assembly for production. Performs various tasks which may include but is not limited to: wiring, component installation, hand soldering, cable harnessing, welding, painting, milling, filling, sewing, templating and fitting on assembly units. Performs maintenance responsibilities as needed and keeps surrounding area clean, safe and organized. Develops and recommends new methods to improve processes. Follows and complies with Company policies, standards and practices. | 5/26/2019 |
| 752 | Dragonfly Therapeutics Waltham, MA Laboratory Operations Coordinator BS/BA in natural sciences Exp: 1+ years |
Dragonfly Therapeutics seeks an experienced and motivated Laboratory Operations Coordinator to help supportnovel cancer immunotherapy programs. The candidate must be independent, goal-oriented, flexible, and able to work efficiently in a laboratory environment as well as an office setting. Responsibilities include: Monitor day to day lab operations and support equipment maintenance, stock lab consumables, and collect asset and maintenance data. Provide office operational support to colleagues, partners, and ongoing research collaborators by helping with procurement, researching supply issues, and providing supply options. Create, manage, and participate laboratory and office protocols such as safety procedures, lab emergency response, and communicating general lab rules and company policies. | 5/26/2019 |
| 753 | Dynosense San Jose, CA QA Engineer BS in computer science, eletrical engineering or related Exp: 0-2 years |
Job duties include: Estimate, plan, and coordinate testing activities. Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications. Perform ad hoc, functional, integration, and regression testing. Identify software defects and submit problem reports via bug-tracking system. Perform regression testing on fixed issues. | 5/26/2019 |
| 754 | Editas Cambridge, MA Research Associate, Cellular Process Development BS/BA in life sciences Exp: 1+ years |
This individual will also assist in the development and execution of isolation and cryopreservation procedures for various cell types (PBMCs, T cells, CD34+, etc.). Candidate must be experienced with aseptic technique and be versatile to assist in the development and execution of processes for normal donor cellular products derived from different lineages of cells. Candidate must be experienced with aseptic technique and be versatile to assist in the development of processes for autologous or normal donor cellular products derived from different lineages of cells (T cells, HSCs, etc.). | 5/26/2019 |
| 755 | Editas Cambridge, MA Research Associate I/II, Screening BS or MS in cell biology or related Exp: 1-3 years lab experience |
Editas is seeking a highly motivated Research Associate I/II to join our Screening Team. In this role, you will contribute to the pre-clinal development of gene-edited cell products. An ideal candidate should have a strong background in cell and molecular biology. Demonstrated culture experience with both IPSC or primary cell lines and a strong interest in genome editing. Experience and interest with lab automation and liquid handling robots, Biomek Fx / I7 or similar, is a plus. | 5/26/2019 |
| 756 | Editas Cambridge, MA Research Associate I/II, Immunotherapy BS or MS in, immunology, biology or related Exp: 1-3 years lab experience |
An ideal candidate should have a background in immunology, cancer biology, and a strong interest in genome editing. Responsibilities include: Develop and optimize protocols for gene editing, including: delivery methods, culture conditions, scale up, and multiplexing. Culture primary cells and cell lines. Perform basic molecular biology work such as DNA and RNA extraction and PCR. Develop and perform immune cell activation, cytotoxicity, and other cellular and ELISA-based assays to evaluate gene editing approaches in cell therapeutics in vitro and in vivo. etc | 5/26/2019 |
| 757 | BioPharmGuy Anytown, US Contract Data Confirmation Some college Exp: 0 years |
Looking for a contract worker to confirm contacts we have on file. Job mostly involves searching on LinkedIn and company websites. Must be able to accept payment via PayPal. Must be eligible to work for any U.S. Employer. Send a message through our contact form. | 05/20/19 |
| 758 | C4 Therapeutics Watertown, MA Research Associate - Target Biology BS in biology or related Exp: 1-5 years lab experience |
The candidate will play a significant role in the implementation of in vitro studies to characterize and differentiate the biological consequences of our small molecule therapeutics to advance early drug discovery programs. Responsibilities include: Perform cell-based studies to support identification/validation/differentiation of small molecule mechanism of action. Routine implementation of a wide variety of laboratory techniques: mammalian cell culture, cell-based genetic engineering (lentiviral, CRISPR), flow cytometry, etc. Maintain written records of laboratory experiments, data, conclusions and communicate results in a clear/concise manner. | 5/15/2019 |
| 759 | CSL Holly Springs, NC Specialist I QA (Quality Engineering) BS in science or engineering Exp: 0-3 years |
The incumbent will be a member of the QA-Engineering team at the Holly Springs Influenza Vaccine manufacturing facility, supporting QC/Bulk and/or Fill-Finish Operations. The QA-Engineering Specialist applies Seqirus quality principles related to equipment qualification, method validation, process validation, Cleaning validation, shipping validation and technology transfers. Utilizes integrated commissioning and qualification principles to ensure compliance of equipment and system qualification. Supports the development and maintenance of quality procedures and systems related to Quality Assurance oversight. Provides technical support for the US FCC site in all cGMP compliance related matters, including assurance that all aspects comply with cGMPs, legal, and regulatory requirements. | 5/15/2019 |
| 760 | CSL King of Prussia, PA Business Systems Analyst I - Identity and Access Management BS in information technology/management or computer sciences Exp: 0-2 years in IT |
Key responsibilities include: Participates in gathering requirements (user requirements, business process requirements) from business users using appropriate mechanisms and following CSL standards. Responsible for identifying the design of approved changes and updating/creating the required system design documentation (design details, diagrams and charts, functional and configuration specifications) to ensure the visualization of the technical implementation. Contributes to the compilation of validation testing. Responsible for the ongoing operation and maintenance of applications for the assigned IT functional areas. This includes providing 2nd or 3rd level incident support, change management, and maintaining the upkeep of technical records and documentation. | 5/15/2019 |
| 761 | CSL Holly Springs, NC Associate I, Manufacturing (Support) Day Shift HS Diploma/GED or BS/BA Exp: HS: 1+ years, BS: 0 years |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (or be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. Responsibilities include: Ability to learn basic processes and equipment and serves as a hands-on resource in Production. Cleaning, preparing, and sterilizing production equipment. Assembly, set-up, and disassembly of production equipment. Interfacing with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, LiveLink) | 5/15/2019 |
| 762 | CSL Holly Springs, NC Associate I, Manufacturing (Upstream) Night Shift HS Diploma/GED or BS/BA Exp: HS: 1+ years, BS: 0 years |
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (or be trained in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost effective manner. Responsibilities include: Ability to learn basic processes and equipment and serves as a hands-on resource in Production. Cleaning, preparing, and sterilizing production equipment. Assembly, set-up, and disassembly of production equipment. Interfacing with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, LiveLink) | 5/15/2019 |
| 763 | Cambrex Charles City, IA Quality Engineer BS in chemical engineering or chemistr Exp: 1-3 years in manufacturing |
The Quality Engineer will be responsible for oversight and management of open items in the TrackWise system and help facilitate closure of items to achieve site quality goals. This role will help manage all open items to ensure items assigned to others are being completed in the required timeframe and/or assist with updating scope or completion timeframe. This role will also provide hands on work such as completing training, revising documents, completing investigations/CAPA, and executing action plans as it pertains to Project Records (PR) within the TrackWise system. | 5/15/2019 |
| 764 | Cambrex Whippany, NJ Microbiologist I BS/BA in biology or microbiology Exp: 1-2 years |
The Microbiologist will maintain product quality by conducting microbiology associated tests and monitoring on the manufacturing and packaging environments and systems while adhering to cGMP guidelines. Responsibilities include: Perform Environmental Monitoring by sampling: Total Particulates, Viable Air, Surfaces. Support aseptic processing in a clean room environment including the ability to aseptically gown in to an area and monitor the environment. Sample the water systems and perform the microbiology testing on water samples: Bioburden and Bacterial Endotoxin testing. | 5/15/2019 |
| 765 | Cambrex Longmont , CO QC Scientist BS/BA Exp: 1-2 years in chromatography or wet analytical chemistry |
As an Analytical Scientist in our Quality Control unit, you will perform release and stability testing of materials for manufacturing of drug substances and drug products including raw materials, starting materials, intermediates, excipients and cleaning samples. You will operate HPLC, Dissolution, GC, KF, FTIR, and other laboratory equipment in a cGMP environment. Additionally, you may write standard operating procedures (SOPs), stability protocols and reports. | 5/15/2019 |
| 766 | Cambrex Longmont , CO Formulation Scientist BS/BA Exp: 1-2 years in industry |
The Scientist will be responsible for developing oral solid dosage formulations for drug product process development and analytical method development to primarily support early stages of the CDMO projects. In addition to extensively interacting with cross functional teams, individuals are responsible for carrying out and overseeing formulation development and stability testing of lyophilized and liquid formulations. Uses fit for purpose analytical methods to support formulation development, and research stability testing. Authors and reviews formulation development sections of regulatory and technical documents, study reports and technology transfer documents. | 5/15/2019 |
| 767 | Cambrex Agawam, MA Quality Assurance Specialist II MS degree Exp: 1+ years |
QA Specialist II will be required to: Support the quality team to achieve quality goals. Assist the quality team daily to accomplish efficient and effective review and approval of records as assigned including, but not limited to: calibration and maintenance work, procedures, validation protocols, validation reports, deviations and change controls. Communicate effectively with internal personnel, as well as external customers (if applicable). | 5/15/2019 |
| 768 | Cardiovascular Systems, Inc Houston, TX Assembly Technician HS Diploma/GED Exp: 1+ years |
The Assembly Technician I will be expected to perform basic functions to complete day-to-day production activity. The position requires a highly motivated, positive individual that can work both independently and in a “team” environment. Assembly Technician I level employees will be expected to perform all job duties in the areas they are assigned under basic supervision. They will stay on task and complete quality work with accurate documentation. He/she will be a valuable and trustworthy asset to their work area through quality work of trained processes. This individual must be dedicated to the success of CSI and its quest to continually improve its operations, as well as perform duties to manufacture CSI products, meeting FDA, OSHA, GMP/MDD and ISO compliance requirements. | 5/15/2019 |
| 769 | Caris Life Sciences Denver, CO JIT Network Associate BS/BA preferred Exp: 1-3 years at clinical sites |
This role has the responsibility to assist in developing and maintaining site research relationships, ensure sites are appropriately trained on JIT research technologies and clinical trial portfolios, and ultimately create an outstanding site research experience. The individual will work closely with the Senior Director, JIT Trials and JIT Network Manager to develop and execute network management and development programs. Arrange and organize sales oriented presentations or trainings for new research sites interested in joining the JIT Network and/or current sites in the JIT Network. | 5/15/2019 |
| 770 | Caris Life Sciences Phoenix, AZ Laboratory Operations Specialist HS Diploma/GED Exp: 1-3 years in lab |
The Laboratory Operations Specialist is responsible for supporting all CMI laboratory departments with all clerical and ancillary duties in keeping all equipment ready to run for patient output. While maintaining job functions, the Laboratory Operations Specialist is to progress in their learning of the regulations (CLIA, CAP and NYS) which the laboratory functions by. Laboratory Operations Specialists support Specimen Processing Clerks, Histology Technicians, Histology Technologists, Pathology Assistants, Pathologists and Molecular Technicians. This position works under the direction of the Supervisor and follows standard laboratory procedures and policies. | 5/15/2019 |
| 771 | Zeiss Orlando, FL Field Support Engineer I BS in electronics, engineering, or computer technology Exp: 0-3 years in field service |
The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 5/15/2019 |
| 772 | Zeiss Kansas City, MO Field Support Engineer I BS in electronics, engineering, or computer technology Exp: 0-3 years in field service |
The Field Support Engineer I, under close supervision and direction, installs, repairs, upgrades and performs preventative maintenance on specified Carl Zeiss Meditec instrumentation in a designated field service territory. Represents Carl Zeiss Meditec at customer locations and works to achieve a high level of customer satisfaction. Maintains all company property (inventory, tools, diagnostic equipment, vehicle, etc.) in accordance with company policies. Maintains a high level of professional communication with team, customers, management, Sales and Technical Support. | 5/15/2019 |
| 773 | Zeiss Boston, MA Field Applications Scientist MS in biological sciences or bio-engineering Exp: 0-3 years |
The job involves training and working with scientists and microscopy users across the territory on a regular basis. The Field Applications Scientist will represent ZEISS as an expert in topics including, but not limited to Widefield, Confocal, Airyscan, Superresolution, Lightsheet and Automated microscopy, Image Processing and Image Analysis. Exceptional documentation and organizational skills are essential to succeed in this position. In addition to effectively communicating complex microscopy concepts to our customers, effective coordination between members of the sales and service team is an integral part of the daily routine. | 5/15/2019 |
| 774 | Zeiss Marlborough, MA Applications Engineer - Metrology Services BS/BA in engineering, math or physics Exp: 0-5 years |
Job Duties include: Consistent delivery of acceptable customer results. Ability to setup and run all lab measurement equipment. Ability to select and use the best software for the job (Calypso, VG StudioMax, etc.). Deliver inspection reports per the job request. Monitor each system’s performance for accuracy/repeatability issues. Peer review job results with colleagues. Assist Site Manager with quoting as necessary. Results review with customer (within 2 days of job completion – if possible). | 5/15/2019 |
| 775 | Casebia Therapeutics Cambridge, MA Process Development Engineering Associate MS in biologica/chemical sciences Exp: 1+ years |
The position will be responsible for downstream purification of recombinant viruses and will be a key member of the team developing expression and purification strategies for novel gene editing/gene therapy vectors. Responsibilities include: Contribute to a smart, integrated development approach for definition of scalable viral vector processes and suitable control strategies. Plan and perform experiments to develop purification process steps including chromatography (affinity, IEX, HIC, SEC, etc.) and filtration (depth filtration, UFDF, and sterile filtration). Perform experiments to develop robust downstream unit operations, using DoE, multivariate analysis, and other statistical tools. | 5/15/2019 |
| 776 | Casebia Therapeutics San Francisco, CA Research Associate, in vivo BS or MS in biology or realted Exp: 0-2 years |
The successful candidates will be integral in discovering and developing the next generation of therapies for hematological diseases. The successful candidates will have experience executing and analyzing in vivo experiments in hematology, specifically the hematopoietic and immune system. Basic cell and molecular biology skills are desirable. | 5/15/2019 |
| 777 | Casma Therapeutics Cambridge, MA Research Associate - Cell Lines, Biology MS in biology or related Exp: 1-3 years |
The individual should possess strong core competencies in cell biology, molecular biology, assay development. Responsibilities include; Cell culture and cell line development using retro- and lenti-virus, CRISPR and downstream analysis of autophagy and signaling. Perform western blotting, FACS and imaging analysis to analyze autophagy and specific target activity in primary cells and cell lines. Aid in conducting genome-wide CRISPR screens for novel target ID. Use mouse tissue to both aid in the development of novel biomarkers and analyze key targets by protein and gene expression. | 5/15/2019 |
| 778 | Catalent Madison, WI Biomanufacturing Upstream, Associate Two BS/BA in biotechnology or reated Exp: 0-2 years |
As a Biomanufacturing Upstream, Associate Two you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) Biomanufacturing activities. Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Perform basic cell culture work, including but not limited to working inside of a biosafety cabinet, cell counting (automated and manual), performing manipulations of required cell cultures in an ISO 5 environment, and analysis of cell culture samples using applicable analyzers. | 5/15/2019 |
| 779 | Catalent Madison, WI Associate, Biomanufacturing BS/BA in biotechnology or reated Exp: 0-2 years |
As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position. Work hours are Sunday to Wednesday (4/10). Responsibilities include: Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations and change control/protocol execution, by established due dates. | 5/15/2019 |
| 780 | Catalent Madison, WI Associate Quality Assurance Systems, Document Control BS/BA in biotechnology, engineering, or life sciences Exp: 0-2 years |
The Associate Quality Assurance Systems, Document Control is responsible for managing the flow of document review, making documents effective and distribution according to standard operating procedure (SOP). The Associate Quality Assurance Systems, Document Control will correspond with customers to obtain document approval. Responsible for the process of document control, including managing drafts, editing, approval, change control, distribution and archiving, of all controlled documents (e.g. Standard Operating Procedures (SOPs), Batch Production Records, Stability Protocols, Qualification Protocols, Specifications, Equipment Records, etc). Edits Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and reports independently and accurately. | 5/15/2019 |
| 781 | Catalent Madison, WI Laboratory Associate Buffer Prep, Manufacturing AS/AA in biotechnology or reated Exp: 0-1 years |
Catalent has an opening for a Laboratory Associate Buffer Preparation, Manufacturing position. Responsibilities will include performing aseptic techniques within a clean room environment. As the Laboratory Associate Buffer Preparation, Manufacturing you will learn to execute and properly document biomanufacturing activities. Work schedule is Wednesday to Saturday, 7:00 a.m. to 5:00 p.m. CST. Operates cGMP Biomanufacturing equipment, including pH/conductivity, meters, mix tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). | 5/15/2019 |
| 782 | Catalent Morrisville, NC Laboratory Associate BS/BA in chemistry or realted Exp: 0 years |
Performs tasks from detailed instructions and established procedures. After conducting basic analysis, interpretation and evaluation of results, work is reviewed for soundness of judgement and adherence to procedure. Execute laboratory work plan / schedule developed by supervisor or senior team member. Edits technical documents, such as test methods, with direct guidance from a supervisor or senior level scientist. | 5/15/2019 |
| 783 | Catalent Woodstock, IL Formulation Technician HS Diploma/GED Exp: 1+ years in manufacturing |
The Formulation Tech reports to the Production Manager. The position is entry level and responsible for learning the basic BFS technology, personal protective equipment, equipment use, and comprehension of formulation processes and methods such as: tank sterilization process, temperature recorder function, reading set-up drawings, tank compounding, and batch record documentation. This position is responsible for aseptic gowning certification as prerequisite to entering the Aseptic Suites. New hire is not intended to stay in this position long term. Once training and qualification is completed at this level, employee advances to Formulation Technician Level 1. | 5/15/2019 |
| 784 | Cato Research Durham, NC Biostatistician I BS or MS in sciences Exp: 1-2 years |
Responsibilities include: Write and review statistical analysis plan. Write and review the statistical and related sections of clinical protocols. Provide statistical guidance and input to authors of clinical study reports, development plans, and other regulatory documents to ensure accuracy and quality. Interacts with sponsors, investigators, and other consultants to determine the best clinical trial design. Performs the design, development, modification, and evaluation of technical infrastructure to expedite conduct and evaluation of clinical trials and basic research | 5/15/2019 |
| 785 | Celerion Montreal, QC Clinical Data Programmer I BS in statistics, math, computer sciences or related Exp: 1+ years |
Responsibilities as a clinical data programer include: Provide data programming support to project teams for reporting and analysis of clinical data in early clinical studies. Develop, maintain and process SAS programs for standard studies that create case report forms (CRFs), edit checks (clinical), data listings, analysis data sets and electronic data transfers. | 5/15/2019 |
| 786 | Celerion Lincoln, NE Clinical Data Programmer I BS in statistics, math, computer sciences or related Exp: 1+ years |
Responsibilities as a clinical data programer include: Provide data programming support to project teams for reporting and analysis of clinical data in early clinical studies. Develop, maintain and process SAS programs for standard studies that create case report forms (CRFs), edit checks (clinical), data listings, analysis data sets and electronic data transfers. | 5/15/2019 |
| 787 | Celerion Lincoln, NE Associate Quality Control Analyst AS/AA or BS/BA in chemistry, biology, or related Exp: 0-1 years |
Responsibilities include: Verify Excel spreadsheets and calculations. Assist in paperwork routing, document assembly, and verification of information packet completeness. Verify raw data against information in Methods or Standard Operating Procedures: Ensure Compliance with general SOP requirements, Verify Solution composition or concentration, including calculations used to determine the concentrations are correct, Verify volumes used and any processing step documented are as explained in the sample processing procedures | 5/15/2019 |
| 788 | Celgene Summit, NJ Manufacturing Associate, CAR-T BS/BA Exp: 0-2 years |
Manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. This position is for the Weekday Shift Start and end times are subject to change based on business demands. | 5/15/2019 |
| 789 | Cell Signaling Technology Danvers, MA Research Associate - Monoclonal Development BS/BA in biological sciences Exp: 1+ years lab experience |
The Research Associate is a member of the Monoclonal Development team which is a core function for antibody development at CST. This individual will be responsible for preparing rabbit and mouse monoclonal antibodies as one of the key first steps in our product development process. This will be a focused role that will provide exposure to the broader monoclonal antibody development process. Coat and block plates for ELISA preparation, Process and document resulting ELISA data in accordance with CST hard copy and electronic laboratory documentation requirements (e.g. notebooks, electronic LIMS, Jira, PDP, PLM, etc.) Make culture media | 5/15/2019 |
| 790 | Cell Signaling Technology Danvers, MA Lab Assistant II HS Diploma/GED, BS/BA preferred Exp: 1+ years |
We are seeking a Lab Assistant who will work as part of the Development Materials Management Core (DMMC), which serves as a centralized resource for the Product Development organization. The DMMC manages the inventory of antibody materials integral to antibody validation pipeline and enables reduced product development cycle times through the efficient, effective, and timely delivery of materials between the Antibody Discovery teams, other groups in Product Development, and Production teams. Responsibilities include: Accurately track and properly store antibody samples and other materials used to validate antibodies. Receive and log new materials, both made in-house (e.g. those produced by the Validation Systems Core (VSC)) and ordered commercially, into inventory management system on a timely basis. etc | 5/15/2019 |
| 791 | Cell Signaling Technology Danvers, MA Research Associate BS/BA in biological sciences Exp: 1+ years lab experience |
We are seeking a Research Associate to join our Validation Systems Core (VSC) team within our Product Development organization. The VSC serves as a centralized resource for innovation in the culture, treatment, lysis, and storage of cell lines. The Research Associate is responsible for providing well-characterized, high quality cells and lysates to the organization to support Product Development efforts focused primarily on affinity research reagents such as primary antibodies, in addition to other product types such as assay kits, conjugates, and ELISA pairs. | 5/15/2019 |
| 792 | ImmunoSpot Cleveland, OH Laboratory Assistant BS Exp: 1+ years in GLP/GCP lab |
We are seeking a Laboratory Assistant for our Contract Research Laboratory who will perform immunology testing of client specimens collected from both pre-clinical and clinical studies using the following test methods: ELISPOT, ELISA, flow cytometry, etc. You will help support our quality improvement projects in conjunction with QA, support our quality system by data quality control, communicate with fellow laboratory personnel, maintain laboratory equipment, write reports, etc. All work is performed according to general laboratory safety standards, internal standard operating procedures (SOPs), client protocols, and applicable international, federal and state regulations. | 5/17/2019 |
| 793 | Cepheid Sunnyvale, CA Manufacturing Associate II HS Diploma/GED Exp: 1-2 years |
Responsibilities as a manufacturing associate include: Follow documentation procedure (filling out Data History Records (DHRs), reading and understanding instructions from Work Release (WR), Planned Deviation Report (PDR) or Non-Conformance Report (NCR). Read and follow Standard Operating Procedures (SOPs) and Manufacturing Work Instructions. Maintain dry room and cleanroom standards, practices, and housekeeping according to standard operating procedures. Set up and operate manufacturing equipment. Monitor machines and inform Supervisor and/or Lead of problems. Clean and maintain equipment and work area as needed. | 5/17/2019 |
| 794 | Cepheid Sunnyvale, CA Reagent Manufacturing Technician HS Diploma/GED Exp: 1-2 years |
The position will be working in a chemical lab that manufactures liquid reagents in bulk quantities. Responsible for the overall operation of the bulk lab throughout the shift and ensure that all activities are compliant with the company’s Quality, Safety and departmental policies and standards. Essential functions include: Formulate bulk liquid reagents following standard operating procedures. Work safely with hazardous chemicals and follow all Safety policies to ensure zero incidents in the lab. Recommend or suggest improvement ideas in the lab that will positively affect production efficiency, Quality and Safety compliance | 5/17/2019 |
| 795 | Cepheid Sunnyvale, CA Software Engineer BS/BA Exp: 0-2 years |
Cepheid is looking for a Software Engineer to join our product software team developing molecular diagnostics applications using Java and Angular predominantly. You will be a member of the software team responsible for designing, developing, testing, and implementation of Cepheid next generation software products. Repsonbilities include: Design, develop, troubleshoot and debug software products using Java and Angular. Maintain robust software applications by participating in software debugging and testing. Adhere to software development and source control processes. | 5/17/2019 |
| 796 | Synchorgenix Philadelphia, PA Regulatory Submission Specialist BS/BA Exp: 0-3 years |
The Regulatory Submissions Specialist will serve as a team member for electronic submission publishing (primarily eCTD format) and SPL conversion projects. He/she will collaborate with the Synchrogenix team and interact with clients on routine project related correspondences. The Regulatory Submissions Specialist will be responsible for completing publishing tasks that are assigned in order to meet submission deadlines. Prepare, compile, scan, render, and maintain regulatory submissions to Regulatory Health Authorities and other government agencies worldwide. Publish documents by creating bookmarks and hyperlinks into submission files according to Synchrogenix and client policies. | 5/17/2019 |
| 797 | Ceva Lenexa, KS Live TCO/CEO Lab Technician I AS/AA or BS/bA in life sciences Exp: AS: 1-2 years, BS: 0 years |
The Manufacturing Lab Technician I will work directly with Viral seed culture and Virus propagation techniques, prepare buffer/media solutions and equipment preparations, and inactivation methods following aseptic technique and cGMP procedures. Operators will be in a full gowned environment and will be need to use strict aseptic techniques. | 5/17/2019 |
| 798 | Champions Oncology Rockville, MD Veterinary Technician I, Veterinary Services BS in biology, pharmacology, or related Exp: 1+ years |
Support in vivo oncology studies in mice as a member of the Veterinary Services Team. Conduct daily and weekly assessments and treatments of animals identified with abnormalities. Administer the health surveillance program as described, including animal and sample submission and tracking of results. Proficiently perform survival animal surgeries and provide perioperative care. Collect blood and tissue samples as dictated by study protocol or veterinary need | 5/17/2019 |
| 799 | Champions Oncology Rockville, MD Research Technician I, Necropsy BS in biology, pharmacology, or related Exp: 1+ years |
Support in vivo oncology studies in mice as a member of Necropsy Services. Allocate animals to study. Assist with gross necropsies (dissection, tissue trimming/collection/preservation, sample collection). Perform preparation activities, including container and tube labeling and room set-up. Collect, process and maintain blood and tissue samples. Assist with the tracking and shipment of samples to sponsors and diagnostic laboratories. | 5/17/2019 |
| 800 | Champions Oncology Rockville, MD Research Associate, Preclinical Flow Cytometry BS in biological sciences Exp: 1-3 years in cell biology |
The position will work in the flow cytometry laboratory handling samples and preparing for flow cytometry evaluation. Perform standard cell biology techniques to process blood and tissue samples from multiple species. The laboratory process samples in a high-throughput, plate-based manner, requiring ability to use multichannel pipetting. Solid tissue and tumor samples will be dispersed into single cell suspensions. Samples may require cell counting and viability determination using cellometer, hemocytometer, flow cytometer, or other techniques. Sample handling may include cell washing, red blood cell depletion, stimulation, intracellular staining, fixation. Staining of samples with multicolor antibody cocktails. Some PBMC isolation and freezing down cells to create cell banks. Some tissue culture work may be required. He/she will follow SOPs and methods, and carefully record and document processes performed within the laboratory. | 5/17/2019 |
| 801 | Champions Oncology Rockville, MD Formulation Technician I BS in chemistry, pharmacology, or related Exp: 1+ years |
Provide chemistry and formulation support for vivo oncology studies. Collect and document pertinent data, including lot information, COA, and MSDS, for the receipt, distribution, preparation and disposition of test compounds, reagents, and carriers/vehicles in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines. Prepare and dispose of test materials, vehicles, and reagents according to study protocols and SOPs. Monitor test materials and help maintain facilities for cleanliness, safety, and regulatory compliance. This includes glassware and waste processing. | 5/17/2019 |
| 802 | Champions Oncology Rockville, MD Cell Culture Assistant BS in biology, pharmacology, or related Exp: 1+ years |
Support in vivo oncology studies in mice as a member of Cell Culture Team. Prepares passaged and primary cells for use by in vivo and in vitro technicians as directed. Produces, maintains and characterizes cultured cells, as directed. Performs related general duties such as inventorying supplies and reagents, general lab housekeeping, and maintaining safety records. Maintain accurate and detailed records using laboratory information management systems and Microsoft Office suite programs | 5/17/2019 |
| 803 | Charles River Wilmington, MA Lab Technician I BS in biological sciences Exp: 0-2 years |
Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Perform within the Bacteriology laboratory process internal and external rodent samples by for microbiological identification. Reconcile customer paperwork with submission documentation to ensure accuracy. Make detailed observations and maintain documentation of all laboratory work. Comply with all Standard Operating rocedures (SOPs) and operating equipment and hazardous and non-hazardous chemicals and biological material according to laboratory safety policy | 5/19/2019 |
| 804 | Charles River Reno, NV Necropsy Technician I HS Diploma/GED Exp: 1+ years in pathology lab |
Perform basic necropsy laboratory procedures. Participate in the documentation of all activities as required. Receive and ship samples. Assist with and perform basic necropsy procedures (basic dissection, tissue collection/preservation, fresh tissue trimming, sample collection, etc.). Learn/know correct anatomic terms. Receive samples, complete tracking documentation, and prepare pathology materials and data for shipment and archiving | 5/19/2019 |
| 805 | Charles River Mattawan, MI Quality Assurance Auditor 1 BS/BA in life scienes Exp: 1-2 years in QA GLP role |
The following are responsibilities related to the Quality Assurance Auditor 1: A Quality Assurance (QA) Auditor I is responsible for performing audits of basic records and reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. | 5/19/2019 |
| 806 | Charles River Ashland, OH Research Technician I, Inhalation HS Diploma/GED Exp: 0.5-1 years in animal lab |
We are seeking a Research Technician I for our Safety Assessment Group site located in Ashland, Ohio. Collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. | 5/19/2019 |
| 807 | Charles River Kingston, NY Technician I HS Diploma/GED Exp: 0.5-1 years in animal lab |
The Technician I will perform routine animal husbandry and other production duties, and maintain supplies and environment of environmentally-controlled work area(s). Other essential duties and responsibilities include: Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals. Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s). Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (cGMPs) and/or Standard Operating Procedures (SOPs). Maintain recordkeeping pertaining to equipment operation, animal or supply area inventories. | 5/19/2019 |
| 808 | Charles River Shrewsbury, MA Lab Operations Technician I BS/BA in sciences Exp: 1-3 years lab experience |
In this position, the Laboratory Operations Technician I will be responsible for performing a variety of tasks involved in sample receiving and processing, and inventory management of critical components, laboratory supplies, specialty reagents, and client-supplied reagents and controls. Perform activities related to sample log in, processing, storage, shipping of materials client support, laboratory and facilities order placement, and order tracking, receiving, and processing. | 5/19/2019 |
| 809 | Charles River Reno, NV Research Assistant I (Formulations) BS/BA in sciences Exp: 0-2 years in biology/chem/pharma labs |
This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 5/19/2019 |
| 810 | EyeCRO Ann Arbor, MI Research Assistant - Chemistry BS/BA in chemistry or chemical engineering or related Exp: 1+ years as research technician |
This person will be responsible for participating in a wide variety of lab-based activities inlcuding: Routine wet chemistry. Operation of various analytical instruments (HPLC, LC/MS, and liquid handlers). Animal handling/husbandry. Animal procedures. Record keeping. etc. | 5/19/2019 |
| 811 | ChemBio Medford, NY Regulatory Affairs Associate BS or MS in life sciences Exp: 0-3 years in FDA regulated industry |
Primarily to assist in the regulatory filings of new products as 510(k), PMA and / or BLA submissions for in-vitro diagnostic devices as well as post approval related regulatory filings for the lawful marketing of Chembio products. Review change control process as it pertains to reportable changes to FDA CBER and CDRH. Assist in 180-day supplements and clinical filings to regulatory agencies etc. | 5/19/2019 |
| 812 | CHeminPharma Branford, CT Associate Scientist, Medicinal/Synthetic chemistry BS or MS in synthetic chemistry Exp: 0-5 years in lab setting |
The successful candidate will be an experienced chemist with state of the art knowledge of synthetic organic chemistry and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members and external customers. Major responsibilities will involve design, synthesis, purification, and characterization of novel chemical entities and the management of general chemistry lab operations under the direction of senior scientific staff. The qualified individual is expected to contribute to process development and scale-up of key intermediates. | 5/19/2019 |
| 813 | ChemPacific Baltimore , MD Chemist MS in chemistry or organic chemistry Exp: 1+ years |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 5/19/2019 |
| 814 | CliniLabs na, TX Clinical Research Associate (CRA) – Texas BS in life sciences or nursing degree Exp: 1+ year as clinical mentor |
The Clinical Research Associate (CRA) monitors activities at clinical trials sites to assure adherence to Good Clinical Practices (GCP), standard operating procedures, and study protocols. The CRA reviews regulatory documents as necessary, and prepares site visit reports. The person in this position is involved in the selection of potential clinical investigators and determines if facilities are adequate based on protocol requirements. | 5/19/2019 |
| 815 | Clovis Oncology San Francisco, CA Clinical Research Associate BS/BA in sciences or health Exp: 1-2 years clincal research experience |
Assist in managing all aspects of clinical trials to ensure that studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines. Assist with the management of key study parameters (e.g. start-up activities, enrollment, site management, data collection, data reviews, site feasibility, database lock, etc.) and proactively identify solutions within the clinical team when issues arise. Develop and review informed consent forms, case report forms, study manuals, and other clinical trial materials. Assist in the evaluation and management of CROs and other vendors and systems. Negotiate and manage contracts/budgets with CROs and other vendors. | 5/19/2019 |
| 816 | Clovis Oncology San Francisco, CA Clinical Trial Assistant BS/BA in sciences or health Exp: 1-2 years clincal research experience |
The Clinical Trial Assistant provides support to the clinical operations department to assist with execution and maintenance of clinical studies. Acts as a central support for the clinical team for designated project communications, correspondence, and associated documentation. Maintains, updates, and may establish various databases for clinical activity tracking. Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites. | 5/19/2019 |
| 817 | Cochlear Centennial, CO Insurance Verification Specialist HS Diploma/GED Exp: 1-2 years customer service |
In order to support cochlear implant clinics and recipients, we are recruiting for an Insurance Verification Specialist. To be successful in this role, you will facilitate all pre-claim activity for reimbursement orders while providing exceptional service to internal and external customers. You will act with a sense of urgency to address inquiries while demonstrating a high degree of knowledge, integrity, and empathy in all aspects of team performance and operations. | 5/19/2019 |
| 818 | Bioclinica The Villages, FL Psychometric Rater BS/BA in mental health-related field Exp: 1+ year in psychometry or related |
The Psychometric Rater I is responsible for administering and interpreting quantitative tests for the measurement of psychological variables related to diseases and disorders, examples of which include, but are not limited to, Alzheimer’s disease, Mild Cognitive Impairment, Multiple Sclerosis, Depression, Anxiety, and Parkinson’s Disease. This position is responsible for managing the psychometric ratings aspect of clinical trial performance at the site level in order to ensure that the data collection is in congruence with the philosophy and mission of the company, as well as with the specific scale administration guidelines. The Psychometric Rater I follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff, sponsoring agencies, and others to effectively perform required testing and related research activities. | 5/10/2019 |
| 819 | Bioclinica The Villages, FL Clinical Research Coordinator BS/BA in health field Exp: 1+ year in clinical research |
The Clinical Research Coordinator I (CRC I) is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the philosophy and mission of the company. The CRC I plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned research projects. The CRC I follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff, sponsoring agencies, and others to effectively perform clinical research and to coordinate research activities. All duties carried out by the CRC I are done so in accordance with company policies and SOPs, as well as all applicable local, state, and federal regulations. Professionals in this role actively participate in outstanding customer service and accept responsibility for developing and maintaining mutually respectful relationships. | 5/10/2019 |
| 820 | Bioclinica Nashville, TN Imaging Analysis Technician BS/BA in sciences or health Exp: 0-1 years |
Responsibilities include: Communicates with Clinical Project Managers, Clinical Operations Associates and/or Specialists regarding image quality, deliverables, and data discrepancies. Communicates with Image Analysis Lead, Clinical Operations Manager, and/or Scientific Director regarding troubleshooting of reading systems, image quality concerns, and deliverables. Maintains study-specific reading tracking tools. Performs quality control of site qualification- scans using phantom or patient, and on-going patient data within study-specific turnaround times to Clinical Project Manager, Clinical Operations Associate, and/or Specialist responsible for the study. Completes validation of relevant central analysis types by meeting pre-defined validation requirements. | 5/10/2019 |
| 821 | Bioclinica Durham, NC Associate, Validation Services BS/BA in computer science, engineering, etc Exp: 1+ year in software validation |
Ensures software applications are accurate, complete and conform to all user, company and regulatory requirements by: Tracking all software versions, features, bugs and validation efforts for all software created and/or modified by the Development teams. Creating and executing manual test scrips which includes testing software applications for quality and functionality using defined validation protocol and testing techniques. Working with application developers in resolving issues and retesting applications. Partnering with technical and business teams to achieve understanding of current and future functionality. | 5/10/2019 |
| 822 | Bioclinica Ocala, FL Medical Assistant HS Diploma Exp: 1+ year as medical assistant |
Medical Assistant works in a clinic setting and handles basic clinical task and performs administrative/office duties. Interacts with patients and assist physician to ensure operations run smoothly and efficiently. Responsibilities include: Answer incoming calls, take messages and/or respond to all calls within 24 hours. Schedule patient appointments. Perform clinical task including but not limited to vital signs and height/weight; document medical history in patient charts. Call and/or fax RX request to pharmacy and obtain preauthorization, if necessary once approved by physician | 5/10/2019 |
| 823 | Bioclinica Orlando, FL Laboratory Assistant HS Diploma Exp: 1+ year clinical/lab experience |
The Laboratory Assistant must demonstrate knowledge of specimen collection and processing and handling requirements as relevant to Bioclinica Research and must have a thorough knowledge of lab procedures and practices. Responsibilities include: Perform blood draws, specimen collection, take vital signs, perform EKG testing and able to record accordingly. Timely specimen preparation for processing and shipping. Effectively and professionally interact with patients, visitors, peers and other healthcare professionals | 5/10/2019 |
| 824 | Bioclinica Orlando, FL Laboratory Technician BS/BA in chemistry, biochemistry, or biology Exp: 1+ year lab experience |
The Lab Technician is responsible for the overall specimen processing and handling according to specific protocol requirements and Bioclinica Research SOP. Responsibilities include: Specimen handling, Perform lab tests, Prepare and process blood, urine and other samples for in house test, reference lab or central lab according to specific study protocol and/or SOP, Perform blood draws, specimen collection, take vital signs, perform EKG testing and able to record accordingly | 5/10/2019 |
| 825 | Biodesix Boulder, CO Laboratory Technician BS/BA in chemistry, physical, biological sciences Exp: |
Biodesix is accepting resumes for a Laboratory Technician to process molecular and proteomic Laboratory Developed Tests (LDT’s) from blood based specimens. Laboratory Technicians must have the technical training and experience required to perform regulated clinical laboratory testing, including sample accessioning and processing using standard in-vitro laboratory techniques which include DNA and RNA extraction from whole blood, ddPCR (digital droplet PCR), Mass Spectrometry for proteomic testing and to operate a proprietary LIMS. | 5/10/2019 |
| 826 | BioDuro San Diego, CA Quality Assurance Associate – Analytical & Manufacturing Support BS/BA in sciences Exp: 6 months + |
This function includes: Analytical Support – Support functions include, but are not limited to: review and approval of in-process testing, release testing of products, stability testing, other data summaries, method validation data, laboratory equipment validation protocols, product certificates of analysis, generation of environmental chamber monitoring reports. Other duties as deemed appropriate by Head of Quality. Manufacturing Support, Document Control, Internal Audits and Client / Regulatory Audits, Equipment and Facilities Calibration, Maintenance, Validation, Preventive Maintenance | 5/10/2019 |
| 827 | BioLegend San Diego, CA Manufacturing Associate - Tissue Culture AS/AA in biology, biochemistry, or related Exp: 6 months + |
The primary functions of this position include culturing, setting up, feeding, maintaining, and harvesting of bioreactors with hybridoma cells, finding, testing, and developing new procedures to increase the quality and efficiency of our product and processes, and maintenance of regularly used equipment. This position offers a varied work load and will enable you to gain solid experience that will allow you to grow and increase your skill set within a fast-growing and stable biotech company. This position will also allow you to gain experience in all areas of tissue culture and cross training on a variety of other supporting tasks such as downstream processing, ELISA assays, qPCR, mycoplasma detection, and NOVA BioProfile 400 use and maintenance. | 5/10/2019 |
| 828 | BioLegend San Diego, CA Product Development Research Associate - Recombinant Protein Group BS/BA in biological sciences Exp: 1 year |
The Product Development Research Associate will be responsible for developing cutting edge recombinant protein research products for the Molecular Cellular Immunology group. This position will be involved with developing a new line of recombinant protein products by supporting other team members. The typical duties include preparing buffer solutions and cell culture media, performing bacterial and mammalian cells cultures, purifying recombinant proteins with affinity tag, and performing PCR and DNA purification according to standard operating procedures. | 5/10/2019 |
| 829 | BioLegend San Diego, CA Manufacturing Associate - Conjugation (1st Shift) AS/AA in biochemistry, chemistry or related Exp: 1+ year |
The Manufacturing Associate will be an integral member of a team that ensures the highest quality of our finalized antibody products. This position offers the opportunity to gain experience with different types of conjugation chemistries and different chromatography methods to purify antibodies and offers the opportunity to work in small scale to large scale product projects and to learn to utilize the (Enterprise Resource Planning) ERP database to track production schedules and deadlines and to enter production results. This position will also perform scale ups and perform troubleshooting of problematic products, including continuous improvement methodologies for efficiency. | 5/10/2019 |
| 830 | BioLegend San Diego, CA Quality Control Associate - Custom Solutions Team BS/BA Exp: 1+ year in flow cytometry |
BioLegend is currently seeking a talented, detail-oriented Quality Control Associate to join our growing Custom Solutions Team. This position will be responsible for assisting with flow cytometry based QC testing, analysis, documentation, and will help maintain relevant databases. | 5/10/2019 |
| 831 | BioLegend San Diego, CA Research Associate - ELISA BS/BA in immunology or biological sciences Exp: 1+ year in industry/lab |
BioLegend has an immediate opening for an ELISA Research Associate who will become an active member of our team who develop high quality ELISA products including proteins, antibodies and assay kits. The Research Associate will participate in all stages of the produce development process from product design, material sourcing, optimization, validation and product launch. | 5/10/2019 |
| 832 | BioLegend San Diego, CA Quality Control Associate BS/BA in sciences Exp: 1 year in lab |
BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. This position will also perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. | 5/10/2019 |
| 833 | BioLegend San Diego, CA Research Associate-Recombinant Protein BS or MS in biological sciences or related Exp: 1+ year in biotech or research |
This position is responsible for developing recombinant protein research products in the Molecular Cellular Immunology group by using cutting-edge synthetic biological technology. The duties include preparing buffer solutions and cell culture media, performing bacterial, insect, and mammalian cell expression, purifying recombinant proteins with chromatography, and performing molecular cloning, PCR, and DNA purification according to standard operating procedures. This position offers a significant opportunity for learning protein production techniques and career growth in biotechnology industry. | 5/10/2019 |
| 834 | BioMarin Novato, CA Research Associate 1, Manufacturing Science and Technology MS in biological sciences, engineering, or chemistry Exp: 0-2 years |
This laboratory based position requires technical expertise in protein characterization and purification systems in support of ongoing manufacturing operations. He or she participates in monitoring and troubleshooting existing processes to build a detailed process understanding and developing process improvements consistent with cGMP. This position involves collaboration with process development, manufacturing, quality control, and quality assurance groups. Travel is limited to attending relevant professional conferences and workshops. | 5/10/2019 |
| 835 | BioMarin Novato, CA Research Associate II, AAV Production (TEMPORARY) BS in biochemistry/molecular biology Exp: 1-4 years lab experience |
We are looking for highly motivated and hardworking Research Associate I/II for molecular biology and AAV production to coordinate and perform activities required to generate early stage material for the therapeutic programs at discovery stage. Responsibilities include: Operations of bench-scale bioreactor, Cell culture for insect and mammalian cell lines, Molecular cloning and PCR based quantitation | 5/10/2019 |
| 836 | BioMarin San Frafael, CA Research Associate, BioAnalytical Testing I (TEMPORARY) BS/BA in biological sciences Exp: 0-2 years lab experience |
Responsible for efficient and effective laboratory operations, the Research Associate I has a significant impact on the company's ability to reach project goals in a timely manner with respect to delivery of data to support pre-clinical and clinical studies critical to advancing programs through the development process. The Research Associate I will perform bioanalysis, using validated PK or immunoassay methods, on non-clinical and clinical samples in a GLP compliant environment. Responsibilities can include sample preparation, sample analysis, GLP documentation, report generation, assay validation and troubleshooting, and interaction with BioMarin’s GLP quality assurance unit. | 5/10/2019 |
| 837 | BioMarin Novato, CA Research Associate, Cell Culture Process Development MS in biological sciences Exp: 1+ years lab experience |
The Research Associate will be part of a stablished team of scientists and RAs working to develop and optimize AAV vectors production processes and assists team members in molecular biology and cell culturetasks including:Nucleic acid/plasmid purification. Cell propagation and plasmid transfection.Clone screening and selection. DNA analysis by agarose electrophoresis. PCR. DNA quantification by qPCR or ddPCR. etc | 5/10/2019 |
| 838 | BioMarin Novato, CA Analyst, QC I (TEMPORARY) BS/BA in sciences Exp: 0-1 years lab experience |
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. Duties as an Analyst include: Perform, under direct supervision, chemical analyses of incoming raw materials under cGMP to meet specified timelines. Evaluate results and trend data. Maintain raw materials log and control of laboratory inventories. Maintain the laboratory in an inspection ready state. | 5/10/2019 |
| 839 | Biomerieux Salt Lake City, UT Engineering Tech I AS/AA in engineering or related Exp: 0-4 years |
This technician works within a project team under the leadership of a more experienced individual such as a team lead, project lead, or project manager. The technician is expected to perform various types of technical activities including design, development, testing, verification, and documentation. This technician is expected to work and communicate well with other members and leadership of the team in order to meet the goals of the project. | 5/10/2019 |
| 840 | Bio-Rad Hercules, CA Chemist I BS/BA in biological sciences Exp: 1-3 years |
The Chemist I will support the manufacturing of various reagents in Bio-Rad’s PCR product line. The Chemist will be expected to plan, prepare, and perform the manufacturing of reagents and consumable products. This position will interact with the planning, purchasing, and warehouse groups. | 5/10/2019 |
| 841 | Bio-Rad Santa Rosa, CA Manufacturing Associate I HS Diploma Exp: 0-2 years |
Processes a variety of work orders associated with the manufacture of assays and other consumable reagent materials. The work orders consist of execution of a combination of tasks that include receipt and verification of issued materials, calibration of equipment, operation of equipment, coding of labels, sealing bags and pouches, dispensing of solutions, capping and torqueing of bottles, label application, assembly of components and kits, executing calculations and filling out required documentation such as work orders, procedures and logs. | 5/10/2019 |
| 842 | Bio-Rad Hercules, CA Chemist I BS/BA in life sciences Exp: 0-2 years lab experience |
Bio-Rad Laboratories is seeking a chemist to support routine testing and logistical activities in the PCR Quality Control group. The incumbent will execute core laboratory testing involving qPCR, Real-Time PCR and droplet digital PCR, SDS-PAGE and other lab techniques. Other duties would include assisting with laboratory and general maintenance to support compliance to ISO13485 regulation standards. The incumbent will ensure adherence to documentation requirements and interact with peers and collaborating departments as needed. | 5/10/2019 |
| 843 | Bio-Rad Hercules, CA Data Analyst I BS/BA in computer sciences or related Exp: 0-3 years |
This job may become a full time Data Analyst position with the Sales and Marketing team or the Customer Support team. We extract data from our Salesforce and SAP systems, transform that data into meaningful information, and load that data into our data lake to help drive sales. The Data Analyst is responsible for using a broad range of technologies, analytical techniques and methodologies in order to retrieve and analyze a broad range of data from various sources to provide predictive insights and support business decision making. | 5/10/2019 |
| 844 | LGC Petaluma, CA R&D Research Associate BS/BA in chemistry or biology Exp: 1-2 years |
This position requires an individual with strong problem solving skills, good laboratory technique, and the ability to execute complex experiments. The successful candidate will have a desire to learn and the strong attention to detail. This position will entail running of automated oligonucleotide synthesizers as well as synthetic chemistry and/or molecular biology laboratory work to support new product development. | 5/10/2019 |
| 845 | LGC Petaluma, CA Therapeutic Production Chemist BS/BA Exp: 1+ years |
The Therapeutic Production Chemist is responsible for performing manufacturing activities in compliance with company procedures and external regulatory requirements as directed by the departmental supervisor, manager or director. The Therapeutic Production Chemist will work closely with experienced group members and may interact with other LGC facilities to support GMP activities, such as produce and release GMP batches. | 5/10/2019 |
| 846 | Brooks Chelmsford, MA Mechanical Engineer MS Exp: 0-1 years |
Responsible for design/development, modification, and evaluation of primarily mechanical systems, equipment and packages. May contribute to total systems engineering, including other eng. disciplines. Conducts feasibility studies and tests new and modified designs. Is involved in all phases of development from initial concept to manufacturing. Directs support personnel in the preparation of detailed design, design testing and prototype fabrication. Provides design information to drafting for packaging documentation. Depending on level may function as a project engineer/leader with the resident responsibilities of proposals/project plan, schedules, work assignments, prime contact, technical presentations, cross functional issue resolution, etc. | 5/10/2019 |
| 847 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations BS/BA in biological sciences Exp: 0-2 years lab experience |
The responsibilities of this position are production, bottling, and packaging of methylcellulose-containing and other cell culture media. Perform QC testing of methylcellulose-containing cell culture media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Skills used include cell culture, high attention to detail, strong communication and organizational skills. Perform additional duties as assigned. This will be a Sun through Thurs work schedule. | 5/11/2019 |
| 848 | Bio-Techne Minneapolis, MN Research Associate, Cell Culture and Stem Cell Media Operations BS/BA in biological sciences Exp: 0-2 years lab experience |
The responsibilities of this position are production, bottling, and packaging of methylcellulose-containing and other cell culture media. Perform QC testing of methylcellulose-containing cell culture media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Skills used include cell culture, high attention to detail, strong communication and organizational skills. Perform additional duties as assigned. This will be a Sun through Thurs work schedule. | 5/11/2019 |
| 849 | Bio-Techne Minneapolis, MN Research Associate, Q Kit Assay Development BS or MS in biological sciences or related Exp: 0-2 years lab experience |
The responsibilities of this position are to primarily develop immunoassay kits including reagent evaluation, feasibility, assay optimization, stability studies and product transfer. Develop new immunoassay products. Under general supervision, independently schedule, plan, perform and report experiments for the feasibility, optimization, transfer and validation of immunoassay kits. Communicate effectively in writing and in verbal communications, including formal presentations. Write official product documentation. | 5/11/2019 |
| 850 | Bio-Techne Minneapolis, MN Research Associate/Advanced Research Associate Antibody Development BS/BA of biochemistry, cell biology, chemistry Exp: 0-5 years |
The responsibilities of this position are to characterize monoclonal and polyclonal antibodies on natural samples using Western blot and Simple Western. Screen multiple sera or hybridoma culture supernates to select potential products. Validate purified antibodies using natural samples. The person will develop problem solving and decision-making skills, while maintaining appropriate contact and communication with the supervisor. Maintain and treat cell lines for needed lysates. Refer to pertinent literature, databases and competitor product information on specific antibody targets. Maintain clear notebook, enter data in PDPT and perform calculations. | 5/11/2019 |
| 851 | Bio-Techne Minneapolis, MN Kit Packer I HS Diploma Exp: 0-2 years |
The responsibilities of this position are to package and release all kits manufactured by bio-techne (including set-up, component inspection, label printing) as defined in the packaging procedures. Inspect and release proteins and antibodies to Finished Goods Receiving. Cap and label proteins and antibodies as necessary. Break down expired kits and properly dispose of all components. Participate in annual cycle counts and/or as needed. | 5/11/2019 |
| 852 | Bio-Techne San Marcos, CA Manufacturing Chemist I BS in chemistry/biochemistry, or biological sciences Exp: 0-2 years |
The Manufacturing Chemist I is responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 5/11/2019 |
| 853 | Bio-Techne Minneapolis, MN Research Associate - New Technologies/Luminex MS in chemistry, biology, or related Exp: 0-2 years |
The responsibilities of this position are to assist with validation, feasibility, product development, and technical support of immunoassays. Optimize components and performance, develop manufacturing procedures, transfer product/process to production, and perform necessary troubleshooting. Work on problems of moderate scope where analysis of situation or data requires a review of identifiable factors. Perform additional duties as assigned. | 5/11/2019 |
| 854 | Bio-Technical Resources Manitowoc, WI Assistant Research Scientist, Microbiology/Molecular Biology BS/BA or MS in biological sciences/microbiology Exp: 1-3 years |
Bio-Technical Resources is seeking an Assistant Research Scientist to work with supervision as a microbiologist and molecular biologistas part of a team developing new strains for the production of antibiotics, enzymes, metabolites, and proteins. The position involves generating and improving strains using strain engineering molecular biology techniques or classical mutagenesis,screening and selection.Routine microbiology tasks | 5/11/2019 |
| 855 | Bio-Technical Resources Manitowoc, WI Assistant Research Scientist, Analytical Support BS/BA or MS in chemistry, biochem, or chemical engineering Exp: 1-3 years |
Bio-Technical Resources is seeking an Assistant Research Scientist to work with supervision as an analytical research assistant supporting teamsdeveloping fermentation and biotransformation processes for the production of antibiotics, enzymes, proteins, chemicals, and metabolites. The position involvesimplementation of HPLC, chromatography, enzyme assays, and gel-basedanalytical methods.Common tasks include analytical separations and quantitative analyses | 5/11/2019 |
| 856 | Biotronik Lake Oswego, OR Clinical Trials Assistant AS or BS/BA in health or sciences Exp: 1+ years |
This position will provide support for clinical research functions of project teams by supporting all aspects of project initiation through project closure. This will include performing administrative functions, maintaining general and study site files, data entry and interfacing with site coordinators, field clinical staff and other company representatives, as well as other project-specific duties. | 5/11/2019 |
| 857 | bluebird bio Cambridge, MA Associate Scientist, Molecular Biology BS or MS in biological sciences or related Exp: 1-3 years |
This new Research Associate will join our group to develop and evaluate novel gene therapies for oncology and severe genetic disease. Responsibilities include: Independently perform routine protocols for qPCR and RNA-seq. RNA sample preparation, including (but not limited to): RNA isolation, library preparation for NGS and qPCR, quantification and QC. Prepare and sequence cDNA libraries using Illumina sequencing instruments (NextSeq). Analyze and communicate findings to cross-functional group members through presentations, face-to-face meetings and email. | 5/11/2019 |
| 858 | Boehringer Ingelheim Fremont, CA Manufacturing Associate Upstream-Nights AS or BS/BA in biotechnology or biological sciences Exp: 1+ years lab experience |
(Associate Level) Executes routine unit operations in Upstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures. Executes, with oversight of qualified staff, complex unit operations including but not limited to batching and inoculation of bioreactors, operation of bioreactors, process monitoring, and harvest operations. Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies. | 5/11/2019 |
| 859 | Boston Analytical Salem, NH Analytical Chemist *All-Levels* BS/BA in chemistry or related Exp: 0-5 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. Responsibilitiesi include: Prepares and analyzes products to determine chemical and physical properties. Follows all safety rules and regulations and conducts periodic safety audits. Under close supervision confers with chemists and other client personnel regarding research, procedures performed, related results and prepares reports. Performs routine data generation and problem solving with a minimal rework. | 5/11/2019 |
| 860 | Boston Analytical Salem, NH Sample Management Technician HS Diploma Exp: 0-2 years |
Non-Lab position. The Sample Management Technician is responsible for ensuring that all samples are entered into the Laboratory Information Management System (LIMS) and made available to the lab staff in a timely manner. This position reports to the manager of Stability and Sample Management. The Technician’s responsibilities include, but are not limited to, the following: Performs any combination of sample management tasks, including labeling, preparing for shipping, transporting to labs, inventorying and disposing. Reviews and verifies sample paperwork against samples to ensure accuracy and communicate discrepancies. Distributes sample information and paperwork. | 5/11/2019 |
| 861 | Boston Scientific Tampa, FL Rhythmia Mapping Specialist BS in biomedical engineering or related Exp: 0-2 years |
The Rhythmia Specialist will provide expert clinical product and technical assistance and training to physicians, EP Lab Staff, and sales representatives on the effective and safe use of the Rhythmia System during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals. Serves as primary resource for clinical support in the areas of case coverage, basic troubleshooting, system/software development for Rhythmia System and catheters. Educates customers and internal BSC employees on the merits and proper clinical usage of Rhythmia by giving presentations and demonstrations using a wide variety of formats and platforms (e.g., slides, transparencies, manuals) to keep all abreast of the latest product and technology developments for Rhythmia system. | 5/13/2019 |
| 862 | Boston Scientific Coventry, RI Process Engineer I BS/BA in mechanical or chemical engineering Exp: 0-2 years |
The Process Engineer I is responsible for developing and maintaining capable processes and ensuring efficient and effective sterilization operation. This person will apply problem solving skills to enable sterilization innovation while using technical and collaboration skills alongside his/her passion for innovation and continuous improvement to drive growth through efficient and effective process improvements. Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on multiple and moderately complex processes. Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation. | 5/13/2019 |
| 863 | Boston Scientific Valencia , CA Research Scientist II MS in biomedical engineering, neuroscience, or related Exp: 1+ years in neural engineering |
The Research Scientist II will support execution of neuromodulation research projects (computational, preclinical, and exploratory clinical studies). The successful candidate will primarily focus in the area of deep brain stimulation, supporting future technologies and participating in the definition and execution of multiple projects that address strategic, scientific, and technological needs for the organization. | 5/13/2019 |
| 864 | Brammer Bio Alachua, FL Scientist - Downstream PD BS/BA or higher Exp: 1+ years |
The Scientist will provide biologics process development support to ensure that the Brammer Bio Downstream Process Development (DSPD) unit operates to provide clients with new purification methods and investigational materials for pre-clinical and clinical use. The incumbent will assist in the design and execution of experiments under the supervision of the technical project lead. This will involve researching and sourcing reagents, equipment, and materials; preparing columns; purifying viral vectors utilizing working knowledge in filtration technologies, column chromatography (SEC, affinity, HIC, AEX), ultracentrifugation and scale up principles. This position will also be expected to technically review data, prepare experiments/data for presentation, participate in laboratory investigations, interpret this data and work with the project lead to trouble-shoot technical problems. The incumbent will participate in the optimization of purification methods and the writing and troubleshooting of protocols. The incumbent is expected to prepare and modify documents (SOPs, Batch Records, Raw Material Specifications, etc), maintain a GLP culture, and assist in maintaining the process development laboratory. | 5/13/2019 |
| 865 | Brammer Bio Cambridge, MA Manufacturing Investigator I BS/BA Exp: 1-5 years |
The Manufacturing Investigator I in this role will be part of a cohesive team responsible for Deviations and CAPAs for all phases of manufacturing. The Manufacturing Investigator I uses expert knowledge of cGMP regulations and project management to ensure manufacturing readiness. The incumbent will also support investigations and improvement initiatives within the manufacturing operations. Works independently with minimal supervision and direction. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion. | 5/13/2019 |
| 866 | Brammer Bio Cambridge, MA Associate, Manufacturing Science & Technology BS in biochemical or chemical engineering, or realted Exp: 0-2 years |
The primary responsibility is to support the technology transfer teams for the late stage, PPQ and commercial manufacturing of viral vectors. This position requires close interaction with the MS&T colleagues, Manufacturing, Process Development, and other departments. This role will focus on aspects of ensuring a robust, scalable and efficient manufacturing processes to produce late-phase human clinical trial and commercial gene transfer vector products. Supports cross functional technology transfer teams for cGMP DS manufacturing of viral vectors. Collaborate with another site or clients to ensure success of scale up/ process transfer. Includes authoring of upstream or downstream plan documentation and associated detail process descriptions (DPDs). | 5/13/2019 |
| 867 | Brammer Bio Cambridge, MA Associate I, Quality Control (Microbiology) BS/BA in biology, chemistry, or related Exp: 0-2 years |
(Overnight Position) The QC Associate I will work in the QC cGMP compliant Laboratories to develop, qualify, and conduct microbiological assays that support quality control of biopharmaceutical products being developed and manufactured at Brammer Bio under contract. Normal working hours will be 7:00 pm - 7:00 am on a shift rotation. Occasional off-shift work/holiday work will be required to support business needs. Duties include performing routine microbiological assays and testing including but not limited to environmental monitoring, bioburden and endotoxin testing. The QC Associate I will also troubleshoot and optimize assays under the supervision of QC Microbiology management . Functions also involve raw data review and document management, maintenance (routine and preventive operation) of equipment, and supporting routine laboratory operations (cleaning the laboroatory, inventory control, etc) | 5/13/2019 |
| 868 | Bristol-Myers Squibb Devens, MA Associate Scientist/Engineer MS in pharma, biological, or chemical sciences/engineering Exp: 0-2 years |
Responsibilities include: Conduct experiments to support cryogenics manufacturing processes of commercial and late-stage biologics drug substance. The candidate will support bulk container selection and freezing, storage, and thawing operations for biologics drug substance. Support validation of the freezing and thawing processes of commercial and late-stage biologics drug substance across BMS global network and contract storage/manufacturing sites. Follow appropriate GLP/GMP procedures. Study design, execution and analysis of results, data verification, preparation of study protocols and final reports, and the presentation of findings at internal and external forums | 5/13/2019 |
| 869 | Bristol-Myers Squibb New Brunswick, NJ Process Engineer BS or MS in chemical engineering/chemistry/engineering Exp: 1-3 years |
As API Process Engineer, you will work as part of a cross-functional matrix team to ensure successful manufacture of active pharmaceutical ingredients, chemical intermediates and specialty materials to support development of R&D pipeline products. Provide process engineering expertise within process planning workflows and document reviews for internal and external manufacturing implementation including: tech transfer documentation, data/process knowledge collection, equipment setup, process modeling, process flow diagrams, compatibility assessments, risk management, etc. Perform engineering analysis of process execution, recommends opportunities for improvement with plant efficiency and risk mitigation as goals, and captures analysis in campaign summary documents | 5/13/2019 |
| 870 | Bristol-Myers Squibb Hopewell, NJ Associate Research Scientist MS in analytical chemistry, biochemistry, or related Exp: 0-2 years |
This associated scientist position within the analytical methods team has the opportunity to drive the development and validation of robust separation methods (e.g., CE-SDS, iCIEF, SEC, RP, IEX, HIC) for biotherapeutic drug candidates in the portfolio spanning early and late stage clinical programs. Bristol-Myers Squibb's biologics pipeline includes approved biologics products such as OPDIVO®, YERVOY®, EMPLICITI®, ORENCIA®, and NULOJIX®, and a number of exciting clinical stage compounds as well as antibody combination products. Development of methods utilizes state-of-the-art analytics as well as modern concepts of quality attribute monitoring of biotechnology products. Science-based research and molecular-level understanding of protein properties are critical for successfully performing method development. Innovation is central to establishing robust analytical control and define our overall biologics development strategy. The successful candidate will also support regulatory filing activities including IND and BLA, as necessary. This position reports to manager in Methods and Analytical Development function of the Biologics Development organization. | 5/13/2019 |
| 871 | Bristol-Myers Squibb Devens, MA Engineer/Scientist Rotational Program BS in chemical engineering/life sciences Exp: 0-2 years |
Support the operation of GMP / Non GMP manufacturing systems (Systems include Process Automation Systems, Manufacturing Execution Systems, Process Development, Technology Transfer, Laboratory, Manufacturing Operations) in the associated facilities. Provide Troubleshooting support and guidance of systems in support of manufacturing, process development, and/or Lab operations within a collaborative team. Collaborate in investigations of proprietary automation software/hardware, manufacturing operations, process development, along with vendors when necessary. Documentation of data and results, data verification, interpretation of small scale and at scale data supporting the manufacturing processes and preparation of final reports to summarize the findings. | 5/13/2019 |
| 872 | Bristol-Myers Squibb Devens, MA Assistant Engineer/Scientist Rotational Program BS in chemical engineering/life sciences Exp: 0-2 years |
Support the operation of GMP / Non GMP manufacturing systems (Systems include Process Automation Systems, Manufacturing Execution Systems, Process Development, Technology Transfer, Laboratory, Manufacturing Operations) in the associated facilities. Provide Troubleshooting support and guidance of systems in support of manufacturing, process development, and/or Lab operations within a collaborative team. Collaborate in investigations of proprietary automation software/hardware, manufacturing operations, process development, along with vendors when necessary. Documentation of data and results, data verification, interpretation of small scale and at scale data supporting the manufacturing processes and preparation of final reports to summarize the findings. | 5/13/2019 |
| 873 | Brooks Chelmsford, MA Mechanical Engineer MS Exp: 0-1 years |
Responsible for design/development, modification, and evaluation of primarily mechanical systems, equipment and packages. May contribute to total systems engineering, including other eng. disciplines. Conducts feasibility studies and tests new and modified designs. Is involved in all phases of development from initial concept to manufacturing. Directs support personnel in the preparation of detailed design, design testing and prototype fabrication. Provides design information to drafting for packaging documentation. Depending on level may function as a project engineer/leader with the resident responsibilities of proposals/project plan, schedules, work assignments, prime contact, technical presentations, cross functional issue resolution, etc. | 5/13/2019 |
| 874 | Bruker Kennewick, WA Manufacturing Engineer & Quality BS in mechanical, electrical or industrial engineering Exp: 1-5 years |
As a Manufacturing Quality Engineer, you will be the primary quality interface for new and existing products. You will design, develop, and execute quality assurance and control systems. Use your expertise and judgment in implementing a wide variety of quality concepts, practices, and procedures. You will contribute to product and manufacturing process design, as well as the methods for verification and validation of product to ensure adherence to company and customer requirements. You will work toward the prevention and/or resolution of product and manufacturing process non-conformance. You are well versed in working with Contract Manufacturers (CM) and Component Suppliers. You will lead teams to ensure products are designed and built to Bruker’s high standards of quality and performance. You will evaluate the product designs and create the processes, tools and procedures behind Bruker’s world leading Handheld X-Ray Fluorescence (XRF) products. You will collaborate with Commodity Managers and Design Engineers to determine Bruker’s manufacturing and product specifications | 5/13/2019 |
| 875 | BD Tempe, AZ R&D Engineer II MS in engineering Exp: 0-3 years |
This position designs, develops and implements new products, processes, test methods and equipment. This position is responsible for conducting engineering studies for process improvements and validations. Initiates new or revised documentation and tracks through appropriate approval cycles and implementation. Maintains a professional working relationship with internal and external customers and support staff. Develops physical and functional test requirements to ensure specifications and regulations are met. Writes and approves protocols, reports and data. | 5/13/2019 |
| 876 | BD Woburn, MA Associate Manufacturing Engineer BS in chemical engineering Exp: 0-1 years |
Responsible for coordinating and providing engineering support throughout the manufacturing facility in areas such as process improvements, technological advancements, cost improvements, facility maintenance, safety, and environmental regulation. Coordinate and participate in plant CIP and process improvement programs as required.Support, or lead as required, activities such as failure investigation, design of experiments, process capability studies, qualifications, and validations of processes and equipment. Coordinate tactical plans geared towards timely completion of line extensions and major equipment installations, modifications, or enhancements. | 5/13/2019 |
| 877 | BD Covington, GA Quality Engineer I BS in engineering/sciences Exp: 1-3 years in regulated industry |
This position is responsible for working in the Bard Complaint Laboratory to perform product testing as well as planning, organizing, and tracking work activities. Quality results are expected to ensure the integrity of Bard complaint investigations. Additionally, the Quality Engineer functions as a subject-matter resource for Engineering, Operations, Sterilization and outside suppliers. Responsible for all products testing in the Complaint Laboratory. Creates investigation files in the BARD Global complaint system (Trackwise). | 5/13/2019 |
| 878 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I BS/BA in engineering or STEM field Exp: |
As a Quality Engineer I, you will learn and develop skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Responsibilities include: Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. Design engineering test protocols and use a data-driven approach to collect, analyze and summarize data into engineering reports. Perform root cause investigations for design and manufacturing | 5/2/2019 |
| 879 | Applied Medical Rancho Santa Margarita, CA Associate Customer Relations Representative BS/BA Exp: 1-2 years customer service |
As an Associate Customer Relations Representative, you will be responsible for working within the framework of a team and performing the following activities: Enter customer orders and understand the Customer Relations department’s processes. Comprehend and comply with safety rules and company policies. Work directly with external customers as well as Applied Medical internal departments such as Credit, Field Operations, Shipping, etc. Assist with other tasks and projects as needed | 5/2/2019 |
| 880 | Applied Medical Rancho Santa Margarita, CA Corporate Communications Associate BS/BA in communications, english, or related Exp: 1+ years in corporate communications |
As a Corporate Communications Associate, you will work on a wide variety of projects that help to communicate the company’s brand, purpose and programs to both internal and external audiences. You will be responsible for working within the framework of a team and performing the following activities: Edit and proofread a variety of communication materials, primarily for in-house teams and other internal programs. Build relationships within various internal departments to best understand each team and help identify communication needs and opportunities. Create posts and provide content support to community managers for the company’s social media platforms including Facebook, Twitter, YouTube and LinkedIn | 5/2/2019 |
| 881 | Applied Medical Technologies Brecksville, OH Mold Process Engineer AS/AA in plastics/plastic technologies Exp: 1-4 years |
This list is not comprehensive but meant to represent the most common or important duties of the position. Develop, document and implement standard molding processes and methodologies. Use scientific molding method to validate new molding processes and re-validate existing/legacy molds. Research, design and develop manufacturing processes and new technologies. Participate in Tool Design Reviews and recommend improvements to optimize molding, setup, and overall manufacturing. Work with design, manufacturing, production, engineers and tooling during the entire development cycle. Emphasis on new mold sampling prior to transfer to production. Research, develop and implement manufacturing process controls, machinery modifications and improvements. | 5/2/2019 |
| 882 | Applied Stem Cell Milpitas, CA Document Control Specialist BS/BA in literature/english Exp: 1 years in document control |
Duties include: Write, revise and review SOPs. Track and control document flow. Achieve manufacturing and quality records. Ensure auditing and manufacturing documentation is kept up to date. Maintenance of Quality Assurance documentation. Train Production staff training on quality procedures, protocols, and documentation | 5/2/2019 |
| 883 | Applied Stem Cell Milpitas, CA Research Associate, Cell Biology (iPSCs) BS or MS in biological sciences Exp: 1-2 years lab experience |
This is a hands-on lab-based role in Induced Pluripotent Stem Cells (iPSCs) group with a focus on iPSC genome engineering and differentiation using ASC’s gene editing technologies. Responsibilities include: Work closely with a multi-function team to deliver engineered iPSCs cell lines and a variety of other cell types. Work on gene editing projects in iPSCs/stem cells, preparing reagents, performing cell culture and cell-based assays. Work on iPSCs generation, differentiation and characterization. Apply scientific knowledge, critical thinking, and problem-solving abilities to troubleshoot and refine methods and assays. Interpret genotyping data from Sanger sequencing and Nextgen sequencing | 5/2/2019 |
| 884 | Aptar Pharma Congers, NY Microbiology Technician BS in microbiology or biological sciences Exp: 1-3 years in cGMP lab |
The Microbiology Technician supports Injectable manufacturing at Congers. The Technician performs duties as needed related to environmental monitoring in the pump manufacturing facility and assists in the technical and quality efforts in the lab. Responsibilities include: Perform microbiology & particulate testing of product and processes (clean room, WFI loop) by accurately following all testing as specified by the appropriate quality documentation. Perform environmental monitoring in manufacturing areas, including tracking & trending test results and performing bioburden sampling in controlled areas. Assist in investigations related to Lab OOS (Out of Specification) and support Production OOS investigations. | 5/2/2019 |
| 885 | Aptar Pharma Congers, NY Plastics Process Technician HS Diploma Exp: 1-3 years working in manufacturing |
The primary mission of our Technicians is to operate injection molding equipment to successfully meet production demands and quality standards. Duties include but are not limited to: Utilize your mechanical skills to install, remove and adjust Injection Molding machinery and equipment. Troubleshoot Injection Molding machines, follow process to resolve failures, other problems. Coordinates and sets up machines, robots and other equipment performing necessary tests to ensure company compliance. Trains employees in the correct procedures for operation as needed. Assist in preventative maintenance and repair of molding machines, molds and peripherals (robots). | 5/2/2019 |
| 886 | Evotec Brandford, On Lab Technician BS in sciences Exp: 1-2 years |
The purpose of this position is to perform laboratory processing of client orders; the majority of which will involve manual weighing and liquid handling of compounds. The position requires a highly motivated individual, able to work independently and as part of a team to ensure successful project support. This role will be expected to have increased understanding of Compound Management workflows, set forth SOPs, etc. Tasks will include, but are not limited to, performing the day to day laboratory work and direct communication with local and remote lab colleagues in a cross-functional environment. | 5/2/2019 |
| 887 | Arbor Cambridge, MA Research Associate (Bioengineer) BS or MS in biological sciences Exp: 0-5 years |
At Arbor, Research Associate Bioengineers use a combination of molecular biology, high-throughput techniques, and next-generation sequencing to systematically search through nature’s gene diversity to discover and engineer new protein technologies. In this interdisciplinary position, you will be expected to perform high-throughput functional screening to further Arbor’s mission of biodiscovery, and accelerate the company’s platform technologies through protocol development and testing. | 5/2/2019 |
| 888 | Arbor Cambridge, MA Software Engineer - Infrastructure BS or MS in software engineering Exp: 1-2 years |
On the Software Engineering Infrastructure team, you will apply your expertise in Python and large scale distributed systems, building data processing pipelines and interactive tools. | 5/2/2019 |
| 889 | Arbor Cambridge, MA Research Associate (Assay Development) BS or MS in biochemistry, molecular biology or related Exp: 1-3 years lab experience |
The ideal candidate will have significant research or industrial experience in protein purification, assay development and optimization. They will also possess a strong background in molecular biology, excellent organizational skills and attention to detail, as well as a strong desire to learn and the ability to work independently. Responsibilities include: Routinely perform the established assays. Optimization of assays to increase throughput and performance . Document, compile, and analyze experimental data. etc | 5/2/2019 |
| 890 | ArcherDX Boulder, CO cGMP Manufacturing Associate II BS in physical/biological sciences Exp: 1-2 years |
Associate level position for manufacturing medical devices in accordance with controlled procedures (SOPs) in compliance with Good Manufacturing Practice (GMP) regulations and current GMP (cGMP) guidelines. Manufactures solutions, labels and fills containers, labels and assembles kits. Compiles auditable electronic or paper records of manufacturing, maintains equipment logs and monitors supplies. Manufacture product as specified in controlled manufacturing procedures, and in compliance with cGMP regulations and guidelines. Accurately complete documentation in cGMP manufacturing batch records, using Good Documentation Practices | 5/2/2019 |
| 891 | Arcus Biosciences Hayward, CA QB2-Research Associate BS or MS in biology/biochemistry Exp: 0-3 years |
The job requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. Responsibilities include, but are not limited to: Performing routine assays to support chemistry efforts. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro assays. Contribute during lab meetings and assist in the analysis and reporting of experimental data to project teams. | 5/2/2019 |
| 892 | Arcus Biosciences Hayward, CA QB1-Research Associate BS or MS in biological sciences Exp: 0-3 years |
The job requires the application of creative problem-solving approaches to the execution of new biochemical and cell-based assays. The successful candidate will have excellent practical laboratory skills, coupled with aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities include, but are not limited to: Transient and stable mammalian cell protein expression. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro assays. | 5/2/2019 |
| 893 | Arcus Biosciences Hayward, CA Research Associate II MS Exp: 0 years drug discovery |
The Biology group is seeking a self-motivated, collaborative and highly skilled individual who wishes to play a key role in advancing novel immunotherapy drug candidates from the discovery phase into the clinic. The data generated by the in-vivo team is central to advancing our understanding of the mechanism of action of our drug candidates and potential combination partners. Specific responsibilities will include collaborating with the project team to conduct tumor efficacy studies in both syngeneic and xenograft models. In addition to taking point on in-vivo efficacy studies the successful candidate will be involved in the ex-vivo analysis of tumor samples. Additional duties could also include in-vitro responsibilities such as the maintenance and preparation of cell lines for tumor studies. | 5/2/2019 |
| 894 | Arcus Biosciences Hayward, CA Research Associate: Quantitative Biology BS or MS in molecular biology/biochemistry Exp: 0-3 years |
The successful candidate will have strong organizational skills and attention to detail, coupled with excellent practical laboratory skills, and aptitude and enthusiasm for automated laboratory assay techniques. Responsibilities include, but are not limited to: Mammalian cell culture. Biological sample banking. Biology and tissue culture lab management, safety program support. Execution of new biochemical and cell-based assays. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. Utilizing liquid handling systems and laboratory robotics to implement in vitro assays. | 5/2/2019 |
| 895 | Ardelyx Fremont, CA QA Specialist I BS in sciences/engineering Exp: 1-7 years in quality |
This role will be responsible for QA oversight of all GxP Computer Systems. The incumbent, working with the functional teams must ensure that all GxP regulated systems are purchased, audited, installed and maintained based on industry best practices (e.g. GAMP5) and regulatory requirements (e.g. 21CFR Part 11 and relevant FDA Guidance). The position plans and organizes all QA activities for computer system validation projects. Duties include, but are not limited to, oversight and approval of validation - related documents, leading risk assessments and working with project team to determine which elements should be validated, conducting and/or coordinating impact assessments of proposed changes to computerized systems and leading inspection (external/internal) readiness activities related to computer system validation. The candidate will ensure that all GxP computer systems are maintained in a validated state in addition to designing work processes for users and administrators of the aforementioned systems. | 5/2/2019 |
| 896 | Arkray Minneapolis, MN Laboratory Assistant 1 HS Diploma Exp: 1+ years in clinical lab |
ARKRAY is currently seeking a Laboratory Assistant to perform laboratory testing, data entry, support evaluation studies for quality testing, complaint investigations, and support ARKRAY products. Responsibilities include: Performs laboratory testing and assists in clinical studies to meet QS specifications and to support Operations and D&S activities. Prepares samples for product evaluation including blood, urine, and saliva. Maintains documentation in compliance with applicable regulatory programs. Perform computer entry of data. | 5/2/2019 |
| 897 | Array Biopharma Boulder, CO Cell Culture Biologist BS or MS in life sciences Exp: 1+ years maintaining cell culture |
We are seeking a highly motivated Cell Culture Biologist with excellent organizational, problem solving, and communication skills to join our Structural Biology group located in Boulder, Colorado. This scientist will be responsible for maintaining and scaling up (≥5L) insect cell and E. coli cultures in suspension for recombinant protein expressions. The individual will also be involved in molecular cloning and construct design. A track record of excellent aseptic techniques and experience in molecular biology and protein expression are essential for this role. | 5/2/2019 |
| 898 | Array Biopharma Boulder, CO esearch Associate / Associate Scientist - Medicinal Chemistry MS in organic chemistry Exp: 0-2 years |
The ideal candidate will have ability to work closely with others in a collaborative manner. Responsibilities include: Demonstrates technical competency in reaction set-up, product isolation, purification and analysis, from milligram to multigram scale. Work efficiently with minimal supervision in the lab. Adhere to all safety requirements. Develop an understanding of SAR, contribute to analog design. Collaborate closely with colleagues to discuss data and generate new ideas. Demonstrate curiosity and interest in furthering knowledge of drug discovery. | 5/2/2019 |
| 899 | Arrowhead Pharmaceuticals Madison, WI Associate Chemist, CMC BS or MS in chemistry/biochemistry Exp: 0-3 years lab experience |
This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. The successful candidate will be expected to: Perform solid-phase synthesis and purification of oligonucleotide drug candidates. Analyze small-molecule and macromolecular targets using standard methods, such as HPLC, UV-Vis spectrophotometry, mass spectrometry, NMR, etc. Track progress against project timelines, generate regular status updates, and communicate progress and issues to management, including presentation of findings at team meetings | 5/2/2019 |
| 900 | Arthrex Ave Maria, FL Quality Control Inspector I HS Diploma Exp: 1+ years in QC |
The QC Inspector will perform a variety of quality control test and inspection functions on materials, components and finished goods at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products. Responsibilities include: Performs and documents dimensional inspections on inventory parts using engineering prints, Inspection procedures or work instructions. Selects products at specified stages in the production process, if applicable, and inspects products for variety of qualities, such as dimensions and functionality. Detects non-conformances during production operations effectively. | 5/2/2019 |
| 901 | Arthrex Ave Maria, FL Automation Engineer I BS in mechanical/electrical engineering Exp: 1-2 years |
We are actively seeking an Automation Engineer I to provide automation and equipment development and support expertise to the Final Device Assembly and Packaging engineering group. This engineer will be a resource for all activities required to build, program, install, debug, and implement automated equipment. The successful candidate will have strong communication and analytical skills, knowledge of manufacturing process and a Bachelor’s degree in Engineering or Engineering Technology. | 5/2/2019 |
| 902 | Myriad Genetics Austin , TX RBM Software Engineer I BS/BA in computer sciences Exp: 0-2 years computer programing |
We are looking for a Software Engineer I candidate to work within the broader Informatics team who will use their computer programming skills to develop solutions for the company’s lab operations and other business needs. You will be expected to collaborate with other departments throughout the development lifecycle from planning thru acceptance testing. Ressponsibilities include: Responsible for developing and testing of computer programs, databases and spreadsheets. Collaborate with team members to determine requirements and participate in design discussions. Display ownership and responsibility for the projects you work on. | 5/3/2019 |
| 903 | Myriad Genetics Austin , TX RBM Laboratory Technician - Testing BS/BA in sciences/biomedical engineering Exp: 0-3 years |
The goal of the Lab Technician I is to ensure that process’s required for a production run as it pertains to samples and reagents are done in an organized and expedient manner. The Technician is accountable for following company procedures and working to the best of their ability to ensure quality in all aspects of the job. Responsibilities include: Processing of biological samples required for production runs, including locating and verifying sample identification, thawing, mixing, and centrifugation. Transferring samples to the production sample plate in a manner that maintains the integrity of the sample identity, and accurately pipetting the amount of sample required for the run, etc. | 5/3/2019 |
| 904 | Myriad Genetics Salt Lake City, UT Clinical Research Associate I BS/BA in sciences Exp: 1+ years in clinical research |
Under the direction of the Program Manager and Clinical Trial Manager, the Clinical Research Associate I contributes to the tactical implementation and conduct of clinical research studies. The CRA I ensures the quality of each research study through on-site and centralized monitoring of protocol and regulatory compliance. The CRA I represents Myriad at the research site level and maintains collaborative relationships with investigator sites and the internal clinical development team. This position can be based in Salt Lake city, Utah or Mason, Ohio. | 5/3/2019 |
| 905 | Astellas Seattle, WA Research Associate 2, Cell Editing MS Exp: 0-2 years lab experience |
The Cell Editing RA 2 will work as part of a team evaluating, planning, and executing all aspects of gene-editing and engineering of pluripotent stem cells. Will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. Will assist with complex laboratory operations and take on more responsibility to provide content for various documents and reports. Will be able to execute protocols with minimal guidance, and the ability to summarize results independently. | 5/3/2019 |
| 906 | Astellas Seattle, WA Research Associate 2, Process Developmen MS Exp: 0-2 years lab experience |
The Process Development Research Associate 2 will work as part of a team evaluating processes, and planning/executing experiments to improve all aspects of culturing, gene-editing, and engineering of pluripotent stem cells. The Research Associate 2 will acquire further versatility in routine procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. Will assist with complex laboratory operations and take on more responsibility to provide content for various documents and reports. Will be able to execute protocols with minimal guidance and will have the ability to summarize results independently. | 5/3/2019 |
| 907 | Atex Carlsbad, CA Biomechanical Testing Engineer BS or MS in mechanical/biomedical engineering Exp: 1-2 years in med devices |
Responsibilities as a testing engineer include; Performs mechanical tests according to recognized standards and internal policies and procedures. Compiles, critically analyzes and interprets test data. Prepares clear, complete and accurate technical engineering documentation. Assists with the calibration, safety, maintenance, and efficient utilization of testing equipment. Designs and oversees fabrication of test fixtures as needed. Provides technical support to other department (e.g., R&D, Regulatory, Marketing, Sales). Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. | 5/3/2019 |
| 908 | Atreca South San Francisco, CA Research Associate, Target Biology BS in molecular biology/biochemistry Exp: 1-6 years |
In this position, the successful candidate will apply their skills and expertise in protein biochemistry to identify targets bound by patient derived antibodies using protein biochemistry and molecular biology techniques. These include protein and carbohydrate arrays, immunoprecipitation, and other protein biochemistry techniques. Responsibilities include: Perform immunoprecipitation and array screening of antibodies selected for testing in in-vivo tumor models. Generate lysates and subcellular fractions from tissue culture cells (including radiolabeled cells) and mouse tumors. Perform pilot immunoprecipitation screens on lysates from tumors and radiolabeled cells. | 5/3/2019 |
| 909 | Atreca Redwood City, CA Research Associate - FACS (Temporary to FTE) BS/BA in biology or related Exp: 1+ years research in cell biology |
In this position, a successful candidate will apply her/his skills in biology and flow cytometry to Atreca’s Immune Repertoire Capture™ technology. The RA will isolate peripheral blood mononuclear cells (PBMCs), isolate various B and T cells and sort them into microplates in a biosafety level 2 (BSL2) environment. The RA will work in a collaborative environment in the team. Responsibilities include: Isolate peripheral blood mononuclear cells from human blood. Freeze/thaw and stain PBMCs or primary tissues. Sort cells into microplates through Fluorescent-Activated Cell Sorting (FACS). Follow laboratory safety guidelines and practices. | 5/3/2019 |
| 910 | Atricure Cincinnati, OH Associate Process Engineer BS/BA Exp: 0-7 years |
The Associate Process Engineer is responsible for on-going production, validations, and continuous improvement of new and existing manufacturing processes. He/she contributes in a creative and collaborative ways to achieve the company’s goals of producing market leading products through positive patient outcomes. Responsibilities include: Team member of projects involving design, manufacturing, and quality resources, both internal and external. Knowledge of general manufacturing technologies (plastic injection molding, stamping, milling, turning, assembly methods, various fastening techniques) including low to medium volume manufacturing processes. Able to define, communicate, and develop fixture concepts using internal and external resources. Able to incorporate the capabilities of typical production association into these concepts | 5/3/2019 |
| 911 | Atricure Cincinnati, OH Associate Manufacturing Engineer BS/BA Exp: 0-7 years |
The Associate Manufacturing Engineer is responsible for the development, qualification, verification and validation of manufacturing processes. The Associate Manufacturing Engineer will contribute in creative and collaborative ways to achieve the company’s goals of producing market leading products through positive patient outcomes. Responsibilities include: Review of component designs and identification of Design for Manufacturing opportunities. Work with outside suppliers to define, document, analyze and qualify their manufacturing processes. Able to define, communicate, and develop fixture concepts using internal and external resources.Able to incorporate the capabilities of typical production association into these concepts | 5/3/2019 |
| 912 | ATUM Newark, CA Production Associate - Synthetic Biology Manufacturing BS/BA in biology or related Exp: Entry Level |
This entry-level position is within our production group. The work includes following standard operating procedures for using automated liquid handling stations, interfacing with our in-house database, providing support in various lab functions including PCR, making agarose gels, growing culture from stock, organizing/purging storage plates, and interacting with our bioinformatics department. | 5/3/2019 |
| 913 | Avedro Burlington, MA Associate Research Formulation Scientist MS or BS in biochemistry, analytical chemistry, etc Exp: 0-2 years |
Avedro is seeking a highly motivated and versatile individual to join our R+D team as an Associate Formulation Scientist. In this role you will be responsible for assisting with the formulation development and testing efforts within our ocular drug development program. Located primarily at our labs in Burlington, MA and interfacing with other group members in our Waltham, MA offices, you will join a growing dynamic team of interdisciplinary scientists at a world leading company on the forefront of corneal crosslinking science. | 5/3/2019 |
| 914 | Avion Pharmaceuticals Austin , TX Pharmaceutical Sales Representative BS/BA Exp: 1 year of business/pharma sales |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. | 5/3/2019 |
| 915 | Avion Pharmaceuticals Worcester, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year of business/pharma sales |
We are currently hiring a field-based Specialty Pharmaceutical Sales Representative who will be able to drive branded prescription sales in their assigned territory. The Specialty Pharmaceutical Sales Representative will promote our growing portfolio of innovative, branded prescription pharmaceutical and dietary supplement products in Women’s Health, Hematology, Dermatology, and related specialties. The primary call point will be OB-GYN’s offices in their territory, calling on assigned healthcare providers, informing those providers on the features and benefits of our products to effectively grow our market share. | 5/3/2019 |
| 916 | Avomeen Analytical Services Ann Arbor, MI SAMPLE COORDINATOR BS/BA in chemistry Exp: Entry Level |
This is an entry level position in a chemistry-based contract research organization. A background in the sciences, particularly chemistry, is preferred. Responsibilities include; Reporting to the Manager of Quality, responsible for logging in samples and chemicals for use in the laboratory. Keep chemical inventory program up to date. Keep chemical storage areas free of expired chemicals and uncluttered. Ensure chemicals in the laboratory are in the correct locations. Ensure glassware is in properly labeled locations | 5/3/2019 |
| 917 | Axsome New York, NY Clinical Trials Assistant BS in biological/physical sciences Exp: 1 years in clinical environment |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. | 5/3/2019 |
| 918 | Bausch Health O'Fallon, MO Manufacturing Associate I HS Diploma Exp: 0-1 years |
Perform tasks within full-scale production manufacturing operations, including routine assembly; or quality assurance and reliability testing following established methods and procedures. Operators are to be cross-trained and expected to perform any/all essential tasks within the production/manufacturing operations within the standard run time associated with each assembly. Use of basic hand tools. | 5/3/2019 |
| 919 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 0-1 years |
The Distribution Associate I is responsible for performing the following: As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader. | 5/3/2019 |
| 920 | Bausch Health Lynchburg, VA Distribution Associate I HS Diploma Exp: 0-1 years |
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and/or group leader. This position is third shift, Sunday-Thursday | 5/3/2019 |
| 921 | Baxter Aibonito, PR Engineer I BA/BS in mechanical/industrial/chemical engineering Exp: 0-2 years |
Must be bilingual (English and Spanish). Responsibilites include: Provide technical support to Manufacturing, Engineering and Quality areas. Improve manufacturing processes. Participate on the evaluation of customer complaints and provide suggestions for process/product improvements. Generate validation protocols and reports for the qualification of process equipments or process changes. Develop and update standard operating procedures for new and existing processes and equipment. | 5/3/2019 |
| 922 | Baxter Marion, NC Quality Lab Assoc I Chemistry (8th Shift- 7PM-7AM) BS/BA in micro biology/biological sciences Exp: 0-2 years |
Duties and responsibilities include: Conduct critical chemical and physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision. Use sophisticated laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles. Complete all testing, including special project / protocol testing in a timely and appropriate manner. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. | 5/3/2019 |
| 923 | Baxter Marion, NC Quality Laboratory Associate I – Microbial ID BS/BA in microbiology/biological sciences Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. Essential Duties and Responsibilities include: Operate lab equipment such as laminar flow hoods, autoclave, incubators, and other equipment. Read plates and enter test results and other data into LIMS. Initiate paperwork for microbial out of limit investigations and provide needed information to Investigators. Perform monthly safety audits | 5/3/2019 |
| 924 | Baxter Cleveland, MS Engineer I BS in engineering Exp: 0-2 years engineering/manfacturing |
This position is a key role in Maintenance in our Manufacturing Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support working within the Operations Group and Engineering. Cross-functional project management will be involved in this role as well. Duties include: Design/modify precision assembly and/or manufacturing equipment. Manage multiple projects with minimal supervision. Prepare estimates for various tasks and projects. Manage capital projects both directly and through coordinating engineers. | 5/3/2019 |
| 925 | Baxter Medina, NY Quality Engineer-Investigations BS in engineering Exp: 1-3 years of medical device experiences |
This position has primary responsibility for investigation, review, and completion of all Quality Engineering complaint issue analysis tasks utilizing various quality system inputs. Responsibilities include: Review individual complaints and associated service data to determine risk level and complete investigation into the “as “determined” problem code and cause codes for each complaints. Analyze data from various quality inputs (including but not limited to : Field Corrective Action (FCA), Complaints, FDA Medical Device Reports (MDR), etc.) to determining trends and systemic issues. Prepare and issue reports based on information analysis. Review existing investigation reports and identify gaps for GMP compliance. Develop strategies and plans to close the gaps in an efficient and technical manner. | 5/3/2019 |
| 926 | Baxter Round Lake, IL Associate Regulatory Affairs-R&D BS/BA in sciences/pharmacy Exp: 0-2 years |
Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical and scientific data and reports required for submission in support of Baxter’s products. Responsibilities include: Track of status and progress of regulatory documentation. Review, edit and proofread regulatory documentation. Assist in preparation and review of labeling, SOP’s, and other departmental documents. Compile under supervision regulatory documents for submission | 5/3/2019 |
| 927 | Baxter Round Lake, IL Engineer II BS in engineering Exp: 1-3 years |
Responsibilities as Engineer II include: With supervision, perform standard engineering assignments which are typically a significant portion of a larger project. Lead small project teams through the planning, execution, and completion of smaller projects or defined pieces of larger projects. With supervision, lead projects within Baxter’s change control management process, from initiation through closure. Change Owners assign and prepare impact assessments, develop change plans, write and execute engineering studies, while working closely with manufacturing plants, quality, regulatory, purchasing, and various scientific/technical groups. | 5/3/2019 |
| 928 | Bayer West Sacramento, CA Data Engineering Graduate Scholar MS in computer science, chemistry, statistics, or related Exp: 1+ years |
The primary responsibilities of this role, Data Engineering Graduate Scholar, are to: Design and develop pipelines to connect external data sources to a data lake in a collaborative effort with Bayer R&D IT and Bayer Biologics; Design and develop workflows to link datasets in the data lake based on shared ontologies; Design and develop REST APIs and web-based UIs to provide access to linked datasets in the data store; Gain expertise in frameworks for schema discovery from schema free sources and use expertise gained to extract knowledge from existing schema-free sources; Design and develop workflows to link datasets in the data lake based on shared ontologies; | 5/3/2019 |
| 929 | Bayer Multiple Locations, US Graduate Scholar, Medical Affairs MS in computer science, chemistry, statistics, or related Exp: 1+ years |
The position will allow someone who has completed advanced studies in a science or engineering field or a physician to work closely with the radiologists, engineers and physicists at Bayer and take on a project that supports the use of contrast enhanced imaging and associated informatics software. They will be able to understand what the scientists and physicians do in Radiology at Bayer through an in-depth project. A specific project that fits their background and training will be assigned. Projects typically involve the investigation of improvements to imaging in radiology. They involve programming, data analysis and innovative thinking. They may also help develop scientific materials for presentations and help answer scientific questions internally and externally with collaborators or customers. | 5/3/2019 |
| 930 | Beam Therapeutics Cambridge, MA Research Associate, RNA editing & Novel CRISPR nucleases BS or MS in biological sciences Exp: 1+ years of research |
he ideal candidate will support efforts in developing next-generation RNA base editing technologies as well as exploration of novel CRISPR nucleases for enhancing our base editing tool-box. Experience with molecular biology techniques and mammalian cell culture is required. Responsibilities include: Molecular biology support: Vector and primer design, cloning, PCR, DNA/RNA isolation, Sanger sequencing analysis, plasmid preparation, etc. NGS sample preparation. Mammalian cell culture and non-viral transfection. Yeast cell culture. Data analysis and visualization to determine gene editing outcomes. | 5/3/2019 |
| 931 | BD Woburn, MA Manufacturing Engineer I BS in engineering (chemical engineering preferred Exp: 1-3 years in manufacturing |
This position is responsible for coordinating and providing engineering support throughout the manufacturing facility in areas such as process improvements, technological advancements, cost improvements, facility maintenance, safety, and environmental regulation. Essential job functions include: Coordinate and participate in plant CIP and process improvement programs as required. Support, or lead as required, activities such as failure investigation, design of experiments, process capability studies, qualifications, and validations of processes and equipment. Coordinate tactical plans geared towards timely completion of line extensions and major equipment installations, modifications, or enhancements. | 5/3/2019 |
| 932 | BioAgilytix Durham, NC Sample Management Technician HS Diploma Exp: 1+ years in cGMP environment |
The Sample Management Technician is responsible for GxP-compliant processing of incoming and outgoing samples and reference materials. Responsible for GxP-compliant accessioning of incoming samples and reference material, as well as the outgoing shipment of samples, reagents and reference materials. Reviews study sample demographic data to confirm consistency between the tube labels, study paperwork and electronic sample management systems (eSMS). Resolves discrepancies, with responsibility for investigating and correcting sample anomalies identified in the eSMS system. | 5/5/2019 |
| 933 | BioAssay Hayward, CA RESEARCH ASSOCIATE - ASSAY DEVELOPMENT BS/BA in biochemistry, chemistry, or biology Exp: 1-2 years lab experience |
We are currently looking for an enthusiastic research associate to join our R&D team. This position will entail developing novel assays kits and performing service projects. This candidate may also be involved in manufacturing or providing technical support to customers. | 5/5/2019 |
| 934 | BioAssay Hayward, CA RESEARCH ASSOCIATE - MANUFACTURING BS/BA in biochemistry, chemistry, or biology Exp: 1-2 years lab experience |
We are currently looking for an enthusiastic research associate to join our manufacturing team. This position will entail preparing reagents for our assay kits, QCing and packaging the finished products. This candidate may also join part time in our R&D team. | 5/5/2019 |
| 935 | BioAssay Hayward, CA SALES ASSOCIATE HS Diploma Exp: 0-1 years |
The Sales Associate will be responsible for processing orders, preparing shipping documents, and keeping detail records. The individual will have to communicate with our customers by phone, fax and e-mail. The position will also involve packaging products for shipment. | 5/5/2019 |
| 936 | Bioclinica Ocala, FL Medical Assistant HS Diploma Exp: 1+ years medical assistant |
Medical Assistant works in a clinic setting and handles basic clinical task and performs administrative/office duties. Interacts with patients and assist physician to ensure operations run smoothly and efficiently. Answer incoming calls, take messages and/or respond to all calls within 24 hours. Schedule patient appointments. Perform clinical task including but not limited to vital signs and height/weight; document medical history in patient charts. Prepare patient for examination. Ensure examination room is clean, well-equipped, and ready at all times | 5/5/2019 |
| 937 | Bioclinica Orlando, FL Laboratory Assistant HS Diploma Exp: 1+ year lab experience |
The Laboratory Assistant must demonstrate knowledge of specimen collection and processing and handling requirements as relevant to Bioclinica Research and must have a thorough knowledge of lab procedures and practices. Maintain continuity of office operation. Perform blood draws, specimen collection, take vital signs, perform EKG testing and able to record accordingly. Effectively and professionally interact with patients, visitors, peers and other healthcare professionals. Timely specimen preparation for processing and shipping. Maintain laboratory inventory and ordering supplies. | 5/5/2019 |
| 938 | Akoya Menlo Park, CA Associate Scientist, Reagent Development MS Exp: 0-2 years in histology/microscopy |
You will beresponsible for developing applications and products for Opal Multiplex Fluorescent IHC Reagents which are designed specifically for Akoya’s cutting-edge Mantra and Vectra Polaris multispectral imaging systems.The desired skillset for laboratory work includes the ability to perform immunohistochemistry (IHC) procedures to support theproductdevelopment. Your work will involve manual laboratory work and the use of automated stainersystems for monoplex and multiplex fluorescence tissue staining. | 4/26/2019 |
| 939 | Akrevia Therapeutics Cambridge, MA Sr. Research Associate, Immuno-Oncology(FACS) MS Exp: 1+ years in biotech/pharma |
We are seeking a Senior Research Associate to join our Immunology group. This person will be responsible for developing, qualifying, and performing assays to assess immune function in support of Immuno-Oncology programs. Responsibilities include: Support the characterization of the immune state of ex vivo and in vivo tumor models through a variety of means including FACS analysis. Develop assays to assess immune function including T-cell, NK cell, macrophage function in a variety of formats. Integrate technologies that improve or expand the ability to assay molecules by working with teammates, collaborators, vendors, and staying abreast of the literature | 4/26/2019 |
| 940 | Alan Laboratories San Diego, CA Chemistry Lab Technician BS in chemistry or chemical engineering Exp: 0-2 years |
To conduct formulation preparation or analytical test in direct support of the drug development team, including writing documents and reports. Responsible for the maintenance of lab instrumentation and general lab duties. Prepare drug formulations according to established procedures. Analyze test data, recognize results that are abnormal or deviate from those expected. Recognize equipment malfunction and factors affecting measurements and testing. Evaluate and solve problems related to sample preparation, variation and processing | 4/26/2019 |
| 941 | Alcami Germantown, WI Process Chemist (Night shift) BS in chemistry or sciences Exp: 0-4 years |
The Process Chemist I is accountable for driving results in a fast-paced environment by understanding reaction mechanisms and applying them to practical execution of given synthesis. Optimization of conditions to proposed and designed synthetic routes including but not limited to purity, loadings, equivalents, cycle times, work up procedures, and yields. The Process Chemist I must understand and able to perform routine analytical procedures to monitor reaction progress (i.e. TLC, GC, NMR, HPLC, KF) and be able to isolate and purify products and intermediates by using standard laboratory techniques . The Process Chemist I must document using GMP Good Documentation Practices and prepare final reports for completed projects, including final procedures and compiling all analytical data. | 4/26/2019 |
| 942 | Alcami Germantown, WI Chemical R&D Associate Scientist II MS in chemistry or related Exp: 0-2 years |
The Associate Scientist II, under the direction of a senior scientist, executes chemical reactions on a gram to multi-kilogram scale and performs routine analytical procedures to monitor reaction progress. This role requires the incumbent to efficiently organize routine work with supervision and properly evaluate and interpret generated data. Exercises judgment within defined procedures and practices to determine appropriate action. The Associate Scientist II will exercise judgment within defined procedures and practices to determine appropriate action | 4/26/2019 |
| 943 | Alcami Wilmington, NC Associate Scienstist, Biotech MS in pharma sciences, chemistry, or related Exp: 0 years |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this position HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company) | 4/26/2019 |
| 944 | Alcami Durham, NC Associate Scientist MS in pharma sciences, chemistry, or related Exp: 0 years |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this position HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 4/26/2019 |
| 945 | Alcami Wilmington, NC Associate Scientist MS in pharma sciences, chemistry, or related Exp: 0 years |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this psotion HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). | 4/26/2019 |
| 946 | Alcami Germantown, WI Analytical Chemist I BS in chemistry or related Exp: 0-2 years in API GMP manufacturing |
The Analytical Chemist I is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by Alcami). | 4/26/2019 |
| 947 | Aldevron Fargo, ND Quality Control Analyst I - Research Grade Manufacturing BS in sciences Exp: 1+ years in lab |
Our Quality Control Analysts are responsible for performing testing and sampling of our products in a laboratory environment. Responsibilities include; Perform all established assays as well as routine and non-routine laboratory testing. Act as primary analyst for production projects and complete appropriate documentation. Perform testing and sampling to support manufacturing, validation, and process development | 4/26/2019 |
| 948 | Abbott San Diego, CA Production Chemist I BS/BA in chemistry or biological sciences Exp: 0-2 years |
Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. Responsibilities include: Carry out production tasks in support of manufacturing goals and objectives. Operate laboratory equipment safely, as trained and directed, in accordance with established practices. Maintain records and notebooks as directed in a neat, thorough and accurate manner. Perform required data entry on company planning and materials management system. Report results to supervisor. Perform complex formulations, component and material evaluations, equipment calibrations and maintenance | 4/26/2019 |
| 949 | Abbott San Diego, CA Process Engineer I BS in engineering Exp: 0-2 years |
In this role, you will provide technical expertise and tactical coordination for successful implementation of components, processes and equipment for product development and/or production. Responsibilities include: Design and implementation of manufacturing processes from the laboratory and concept stage through pilot plant and manufacturing scale-up. Responsible for identifying and implementing improvements to both day to day operations and high-level systematic changes associated with ensuring all processes and functions come together to achieve throughput and quality goals. Interfaces with various departments to ensure processes and designs are compatible for new product technology transfer and to establish future process and equipment automation technology. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Acts as advisor and/or supervises subordinates in solving technical problems. Frequently interacts with departments, peers management and scientists. | 4/26/2019 |
| 950 | Abbott Scarborough, ME Production Specialist I Nights HS Diploma/GED Exp: 0-2 years |
The position of Production Specialist I is within our Infectious Disease Developed Markets business unit located at Scarborough, Maine. In this role you will perform work required for the assembly of components, devices, and/or the final product depending on the trade assigned. Duties include: Performs work required for the assembly of components, devices and/or the final product with supervision. Ensures quality of product using standard operating procedures, templates, training and supervision, and good judgment. | 4/26/2019 |
| 951 | Alexza Mountain View, CA Quality Control Analyst I BS in sciences or related Exp: 0-2 years in cGMP QC environment |
Responsibilities include: Provide timely analyses to support manufacturing and stability. This includes routine analysis of raw materials, in process and release of commercial product or clinical supplies. Under general guidance, perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications . | 4/26/2019 |
| 952 | Alexza Mountain View, CA Research Associate I BS or MS in chemistry or chemical/bio engineering Exp: 0-2 years research experience |
Responsibilities include: Conduct research on various drug/device interactions as part of the drug delivery and device development process. Analyze and interpret data from various product development experiments. Exercise technical discretion in the design, execution and interpretation of experiments that contribute to project objectives. Contribute to stability studies. Ensure reproducible and reliable results for protocols related to development of drug delivery systems. | 4/26/2019 |
| 953 | Align San Jose, CA Regulatory Affairs Specialist BS in engineering or sciences Exp: 0-2 years |
The primary responsibilities of this position will be premarket regulatory activities to support U.S. and international filings. Responsibilities include creating regulatory strategy for new products, supporting submission related activities, and interfacing with outside regulatory agencies. This position reports to the Director of Quality Assurance and Regulatory Affairs. Support assigned U.S. and international product/software registration activities; including assisting with the development of the regulatory strategy, 510k and international filing determinations, Technical Files, and international product registrations. Compile information from multiple sources for submissions, providing support to the project teams in creating documentation for submissions and assuring compliance with Design Control and Software Life Cycle SOPs. | 4/26/2019 |
| 954 | Alkahest Inc San Carlos, CA Research Assistant/ Research Associate (in vivo) - Wednesdays thru Sundays BS/BA in life/biomedical sciences Exp: 1+ years |
The role will use in vivostudies to primarily assess CNS mechanisms through rodent behavioral, histological and biochemical techniques. The role is critical in assisting the scientific team in advancing our therapeutic understandings. This person will be involved in establishing, validating, and implementing methodologies in Alkahest’s laboratories and is thus pivotal to the company’s mission. The studies performed will involve cutting edge science and require innovative concepts and strategies. The role requires dedication to drive science, flexibility, excellent communication and organization, and will interact with a team of scientists and research associates to drive multiple projects in parallel. | 4/26/2019 |
| 955 | Alkermes Waltham, MA Engineering Coordinator AS or BS/BA in relevant field Exp: 0-2 years |
The Alkermes Site Operations department has an opportunity for a full-time Engineering Coordinator. This position will coordinate service and project-related activities for the Site Operations department while providing technical and administrative assistance to other Site Operations team members as directed. Responsibilities include: Serve as the administrative contact / liaison with internal departments and external parties in order to develop engineering requirements and manage resource availability. Develop written documentation and correspondence for the department; screen and evaluate incoming and outgoing responses as appropriate. Gather, enter, and/or update data to maintain departmental and equipment records / databases, as appropriate. Establishes and maintains files and records for the department. Responsibilities include administration of the Maximo (CMMS/EAM) system including managing work schedules / work orders as well as keeping the system up-to-date. Ensure high Good Manufacturing Practices (GMP) and Environmental Health and Safety (EHS) standards are maintained, while adhering to schedules to meet the business requirements. Assist as needed in regulatory agency inspections. | 4/26/2019 |
| 956 | Allergan Branchburg, NJ Associate Regulatory Compliance Analyst BS/BA Exp: 0-2 years |
Under the supervision of Regulatory Compliance management, the Regulatory Compliance Auditor/Analyst will support all aspects of the Regulatory Compliance processes which include but not limited to the activities listed below. Complies with FDA, ISO, AATB, and all other applicable international and state regulatory requirements, best industry practices and internal processes. Compile Quality metrics for QSMR, Tier board etc. and identify and bring issues to management when a compliance gap or quality issue is identified. Supports LifeCell’s internal audit program and performs assigned internal audits under the guidance of lead auditor in accordance with internal procedures and relevant standards/regulations. | 4/26/2019 |
| 957 | Allergan Branchburg, NJ Associate Supplier Quality Engineer I BS/BA Exp: 0-2 years |
Under the supervision of supplier quality management, the Supplier Quality Engineer I will support all aspects of the Supplier Quality processes which include but not limited to the items listed below. Complies with FDA, ISO, AATB, and all other applicable international and state regulatory requirements, best industry practices and internal processes. Identify and bring issues to management when a compliance gap is identified. | 4/26/2019 |
| 958 | Allergan Irvine, CA Laboratory Ops Associate AS or BS/BA in life sciences or chemistry Exp: 0-2 years lab experience |
The Lab Ops Associate is based in Irvine, CA and will support Allergan R&D by ensuring optimal operation efficiency of the laboratories. Primary area supported is Research and External Scientific Innovation, and includes multi-disciplinary interaction with EH&S, Managed Lab Services, Facilities & Corporate Engineering, and Pharmaceutical Development with emphasis on planning, coordinating and executing logistical lab operations. Responsibilities include: Scheduling technician visits and escorting the technicians into restricted lab spaces. Tracking research lab equipment including inactive, new, movement, and repair or calibration schedules. | 4/26/2019 |
| 959 | Alliance Spine San Antonio , TX Full-Time Inventor Expeditor HS Diploma/GED Exp: 1+ years warehouse/inventory operation |
The inventory expeditor will work with other members of the inventory team to increase company profitability and customer satisfaction by delivering complete, accurate and on-time deliveries to the company’s customers. Responsibilities include: Deliver orders/inventory via the most effective route to ensure devices/products are delivered according to established time frames. Maintain communication with the Inventory Manager during deliveries to ensure any updated instructions are received. Operates a motor vehicle according to applicable state laws as needed. | 4/26/2019 |
| 960 | Alnylam Cambridge, MA Associate Scientist: RNA Synthesis BS or MS in chemistry, biochem, or related Exp: 0-4 years |
The successful candidate will help to synthesize and purify oligonucleotides for research studies. Additionally, they will evaluate new chemical modifications for their use in the RNAi pathway via synthesis, purification, and characterization of synthetic oligonucleotides. Other responsibilities include: Utilize analytical instrumentation such as UV-Vis spectroscopy, HPLC, and/or LC-MS for the analysis of both crude and purified synthetic products. Effectively troubleshoot synthetic/process issues and independently find solutions. Improve upon and/or develop new methods and automation for the downstream processing of synthetic oligonucleotides and their subsequent analysis/purification and annealing into siRNA duplexes. | 4/26/2019 |
| 961 | Ambry Genetics Aliso Viejo, CA Research Associate I BS or MS in life sciences Exp: 0-2 years lab experience |
Research Associate I is responsible for assisting senior R&D staffs to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. Duties include: Aid in the design and development of clinical diagnostic assays for use in a CLIA/CAP regulated setting. Participate in drafting Standard Operating Procedures for new assays. Perform research experiments, such as primer design and preparation, PCR, electrophoresis, gel imaging and analysis, Sanger Sequencing, Next-Gen sequencing library preparation, aCGH microarray labeling, and sequencing analysis. | 4/29/2019 |
| 962 | Ambry Genetics Aliso Viejo, CA Research Associate I - ATG Lab BS or MS in life sciences Exp: 0-2 years lab experience |
The Research Associate I is responsible for assisting senior ATG Lab staff to design and perform research diagnostic assays spanning a wide range of PCR and Next-Generation sequencing technologies. Perform research experiments, such as primer design and preparation, PCR, electrophoresis, gel imaging and analysis, Sanger Sequencing, Next-Gen sequencing library preparation, and sequencing analysis. Aid in the design and development of diagnostic assays for use in a CLIA/CAP regulated setting. Participate in drafting Standard Operating Procedures for new assays. | 4/29/2019 |
| 963 | Ambry Genetics Aliso Viejo, CA Lab Assistant, Quality Control HS Diploma/GED Exp: 0-1 years (entry level) |
As a Lab Assistant under our Quality Control (QC) team, you will be overseeing Clinical Lab Quality Control, including equipment maintenance and reagent QC support. Responsibilities include: Oversee equipment preventative maintenance/routine maintenance and systems, as well as driving routine multi-system testing. Manage general temperature & humidity monitoring. Supervising general reagent quality control and systems. Regularly communicate with vendors/suppliers and coordinate on-site maintenance or repairs. Maintain current knowledge of reagent stability and storage, proper handling of reagents, and associated safety protocols. Maintain laboratory safety by ensuring work area is safe and clean, noting any problems that may require prompt and proper repair. | 4/29/2019 |
| 964 | Ambry Genetics Aliso Viejo, CA Quality Assurance Engineer BS/BA in computer sciences Exp: 0-2 years in software QA |
You will be working in a team that is handling one or two applications. You will be getting requirements from a QA manager and will be with the QA development team. You are responsible for the documentation, development and execution of basic manual test cases. You will also be working with the application development team for creating data sets for testing, debugging issues, and improving products. Your end users are mostly internal and need to be able to support them when necessary. | 4/29/2019 |
| 965 | Ambry Genetics Aliso Viejo, CA Clinical Assistant I BS/BA Exp: 0-2 years |
The clinical assistant I will provide support and help organize work flow for the genetic counselors, laboratory directors, and medical directors in the clinical diagnostics department. He or she will also share some general responsibilities of the Client Services department, such as providing testing information to clients about our products and services, patient test status, and routing calls throughout the organization as needed. Providing detailed information (technical and clinical) about genetic tests offered by Ambry Genetics, communication of relevant results, and basic results interpretation, if necessary. Work collaboratively with the Clinical Diagnostics team, laboratory personnel, accessioning department and sales & marketing department to make sure the needs of our clients are met. | 4/29/2019 |
| 966 | Ambu Noblesville, IN CAD CAM Engineer AS or BS/BA in engineering Exp: 0-2 years |
Responsibilities include: Draw and design parts, fixtures, tooling and test equipment. Write programs for CNC machines and support the tool room in the manufacture of designs. Update all modifications to part prints and 3D data. Measure and determine proper machine function for finial sizing of components. Create new designs for products, production machinery, injection molds, and mold shop tooling and fixturing. etc | 4/29/2019 |
| 967 | Ambu Noblesville, IN Quality Assurance Inspector - 2nd and 3rd Shift HS Diploma/GED Exp: 1-3 months |
Monitor compliance to in-house standard operating procedures (SOP's) and Current Good Manufacturing Practices (CGMP's), pertaining to the manufacturing, packaging, storage, and distribution of finished product. Inspect and test components, labeling, sub-assemblies and finished product for conformance to all written specifications. Ensure complete, accurate, and proper performance of all QA functions, including documentation. Monitor all processing steps to ensure conformance to Manufacturing specifications (work order) and processing methods. Assist in verifying the complete, accurate and proper performance of all Quality Assurance functions, including documentation to ensure compliance with CGMP's, and ISO 9001, MDD, EN46001, production and corporate standards. | 4/29/2019 |
| 968 | Amgen Thousand Oaks, CA Bioprocess Development Sr. Associate MS Exp: 0-2 years |
The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advancement of Amgen programs. The successful candidate will design and execute experiments at the bench scale, spanning the end-to-end drug substance process, including both cell culture and purification operations. The candidate will apply established platform approaches and utilize problem-solving skills to rapidly solve day-to-day experimental challenges. Additionally, the candidate will utilize out-of-the-box thinking to contribute to technology development. | 4/29/2019 |
| 969 | Amgen Thousand Oaks, CA Associate Manufacturing BS/BA Exp: 0-4 years |
This Cell Culture Manufacturing Associate position will support the on going commercial operations for drug substance intermediate and the start-up of new clinical and commercial drug substance manufacturing operation in Thousand Oaks, CA. The Associate will execute production operations on the manufacturing floor including execution and coordination of commissioning and qualification of process equipment. This role will interface between the GMP manufacturing teams in the plant and our partner organizations. | 4/29/2019 |
| 970 | Amgen Rhode Island, RI Associate Manufacturing BS/BA Exp: Graduation by June 2019 |
Under general supervision, Associate Manufacturing will perform operations in the Manufacturing area, specifically Purification processes. Operations will be performed according to Standard Operating Procedures (SOPs). Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams and represent the Purification group. Associate may also have the responsibility of owning NC/CAPA’s and Change Control records. In addition, Associate may identify, recommend, and implement improvements related to routine functions. | 4/29/2019 |
| 971 | Amgen Thousand Oaks, CA Associate Scientist MS in life sciences or engineering Exp: 0-2 years |
The Associate Scientist’s responsibilities include, but are not limited to, the following: Design and execute experiments for analytical support of biotherapeutic proteins using HPLC, LCMS, and capillary electrophoresis. Develop and optimize analytical methods. Troubleshoot and maintain analytical equipment in good working order. Analyze and clearly document experiments in Electronic Lab Notebook (ELN). | 4/29/2019 |
| 972 | Amicus Greater Philadelphia, PA Research Associate, Discovery Biology AS/BS in sciences Exp: 0-2 years lab experience |
The Research Associate position will be responsible for supporting lab operations in the purification of target proteins and bio-reagents. Responsibilities include: Performing experiments for the bench scale purification of protein therapeutics and reagents. Performing necessary assays in support of both upstream and downstream activities. Supporting therapeutic protein drug substance process development and scale up. Evaluating technologies to improve downstream processes. Serving on departmental, interdepartmental, and project teams. | 4/29/2019 |
| 973 | Amicus Cranbury, NJ Clinical Trial Associate BS/BA Exp: 1+ year in clinical trial operation |
The Clinical Trial Associate is responsible for assisting the Clinical Operations team(s) to provide efficient execution of assigned studies, including appropriate filing of all documentation. Responsibilities include: Assist with documents during study start-up including CDAs and CTAs. Assist with compilation of regulatory documents. Coordinate investigator payments for studies where the Sponsor is responsible for this activity. Verify investigator payment details submitted for payment by CROs for studies where CROs are responsible for this activity. etc. | 4/29/2019 |
| 974 | Amicus Greater Philadelphia, PA Associate Scientist, Protein Expression Analysis - Gene Therapy MS in sciences Exp: 0-2 years lab experience |
This position will be responsible for the transfection or transduction of gene therapy-related constructs for the characterization of protein expression efficiency and protein product characteristics across a wide range of therapeutic targets. Duties include: Maintenance of the appropriate cell systems for evaluation of protein expression. Transfection or transduction of transgene constructs into an appropriate cell system to evaluate protein expression and characteristics. Measurement of protein expression level and quality. Tracking progress of multiple protein expression projects and prioritization of parallel projects to ensure timely delivery. | 4/29/2019 |
| 975 | Amicus Greater Philadelphia, PA Associate Scientist, Bio-reagent Development MS in sciences Exp: 0-2 years lab experience |
This position will be responsible for the expression and purification of enzymes and antibodies required as bio-reagents for the evaluation of gene therapy-based protein products. Duties include: Collaboration with Therapeutic Target Leads to identify required Bio-reagents. Collaboration with Molecular Biology Core and Protein Expression Analysis teams for required DNA constructs. Expression and purification of bio-reagents. Screening of commercial antibodies against targets of interest. etc./ | 4/29/2019 |
| 976 | Amneal Piscataway, NJ Safety Engineer BS/BA in environmental health/safety Exp: 1+ year in health/safety |
The Safety Engineer works with the Supervisor to plan, direct and implement Amneal's environmental health and safety programs to ensure a positive, safe, healthy and incident-free work environment and is responsible for the compliance by Amneal with all environmental and safety regulatory agencies. Responsibilities include: Walk each plant periodically to observe operations and identify safety issues, assess and correct any problems. Ensure fire extinguishers are in working order, not blocked, conduct annual inspections with outside contractor, and verify that they are properly placed and hung. For NJ position: Weekly inspections of Laboratory and hazardous waste area required. Obtains OEL, SDS and SFS for all products with a focus on NPL and R&D projects. Ensures that proper information is communicated to user department and training is provided, as required. | 4/29/2019 |
| 977 | Amneal Brookhaven, NY QA Inspector I HS Diploma/GED Exp: 1+ years in QA |
To monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run. Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability. | 4/29/2019 |
| 978 | Amneal Brookhaven, NY QA Inspector I HS Diploma/GED Exp: 1+ years in QA |
To monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run. Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability. | 4/29/2019 |
| 979 | Amneal Bridgewater, NJ IT Support Associate HS Diploma/GED Exp: 1+ years |
The IT Support Associate will support team members by providing prompt response to members' problems and requests while managing and maintaining the closing of tickets within Servicedesk Plus ticketing system. As a team member, he/she will function as the primary interface for the Corporate IT Team providing a positive experience for Amneal's team members through tailored IT solutions. He/she will be responsible for team members' computer and account management provisioning and de-provisioning as well as inventory management of equipment. Installation, configuration, and support of network resources including printers, VOIP phone system and other peripheral devices among many other tasks will be a part of daily duties. IT Support Associate will work on all aspects of problem resolution for team members; this includes but is not limited to driving the resolution from IT Support teams, cross-functional organizations, and external vendors. Using your expertise, you will identify opportunities for continuous process improvements and if needed, partner with other Amneal technology teams to design, plan and implement a resolution. | 4/29/2019 |
| 980 | AMPAC Rancho Cordova, CA Quality Assurance Analyst BS/BA in sciences Exp: 1-5 years |
Duties may include: Review and/or conduct investigations for process variances, product non-conformances OOS results. Ensure compliance of current processes and planned process improvements to cGMP. Be responsible for the timely review of records, to include confirming the completeness of the record and the accuracy of relevant entries. Manage the release of intermediates and final products in accordance with the approved systems, procedures and specifications.. | 4/29/2019 |
| 981 | Amphastar Pharmaceuticals Inc El Monte, CA Validation Technician BS/BA Exp: 0-2 years |
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties maybe assigned. Coordinates and performs validations on equipment and process such as autoclaves, ovens,aseptic processes, product assembly lines, filling machines, sterilization processes, and cleaning process. Performs basic validation techniques and activities to report on product,equipment, and process performance to assure Company's standards are met. Works with Operations to assure work is completed without manufacturing interruption | 4/29/2019 |
| 982 | Amphastar Pharmaceuticals Inc Inland Empire, CA Microbiologist BS/BA in biological sciences Exp: 1-2 years |
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Performs test preparation and setup, and runs required tests for pharmaceutical raw material and finished products, such as bioburden, sterility and endotoxin tests. Performs a variety of tests which directly or indirectly affect product release, and test for the sterile quality of products manufactured by performing the following duties. Analyzes test data collected from experiments using laboratory equipment and chemicals to determine the sterile quality of products produced. Interpret EM plates and RCS strips. Identify isolates recovered from EM plates/strips and bioburden tests. Writes test results and submits reports including required calculations and statistical verifications. | 4/29/2019 |
| 983 | International Medication Systems South El Monte, CA Operations Assistant - Engineer BS/BA in chemistry, biochemistry, or engineering Exp: 0-2 years |
Plans and coordinates activities of pharmaceutical production processes, process improvement and development, equipment renovation, quality assurance/quality control, training, and other duties by performing the following tasks personally. Coordinates and conducts daily operational activities and provides support to all departments. Plans, coordinates, and directs programs for pharmaceutical, medical product order fulfillment, product development, improvement of manufacturing processes; or for analysis and testing of substances to support quality control efforts. Generates and revises standard operation procedures. Reviews protocols from Validation and Quality Control Laboratory and engineering reports. | 4/29/2019 |
| 984 | AMRI Grafton, WI QUALITY ASSURANCE ASSOCIATE BS in chemistry or related Exp: 1-3 years |
The Quality Assurance Associate is an integral part of the AMRI team, contributing to our success by assuring that all documentation, procedures and protocols comply with GMP and FDA guidelines. In this role you will: Conduct batch record and test data reviews, and approve batches for release. Assist in maintaining compliance of Environmental Monitoring, Equipment Calibration, and the Equipment Maintenance Program. Issue Deviation, CAPA, and OOS investigations. Track investigations and outcome. Review and recommend approval of indicated actions to senior associates or quality management. | 4/29/2019 |
| 985 | AMRI Alburquerque, NM Microbiologist I BS in life sciences Exp: 0-2 years lab experience |
Prepare, collect, and test plant purified water, manufacturing raw materials, product in-process, and finished product, and perform environmental monitoring. With limited supervision, learn and perform critical laboratory techniques and complete original work. Author problem reports and participate in investigations. This description is inclusive of EM and testing duties: actual percentages of time spent on each duty may vary based on business needs. | 4/29/2019 |
| 986 | AMRI Burlington, MA Microbiologist BS/BA in sciences, microbiology preferred Exp: 1+ years in GMP/GLP environment |
The Quality Control Microbiologist performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. This includes: Perform microbiological testing (endotoxin, bioburden) for water. Perform microbiological testing (endotoxin, sterility and bioburden) for raw materials, in-process materials, intermediates and final product. Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results. Maintain historical files on organisms found in classified areas; microbial identification and trending. etc. | 4/29/2019 |
| 987 | Analogic Peabody, MA Associate Mechanical Engineer BS in mechanical engineering or related Exp: 0-3 years |
Performs mechanical design tasks on subunits of larger projects. Requires knowledge of engineering principles and concepts, an ability to understand the integration of designs and subunits within the overall project, and consistent application of acquired knowledge. Designs, modifies and evaluates mechanical and electro-mechanical apparatus components and processes. Applies original and creative approaches to design tasks. Plans and conducts engineering research, design, development or manufacturing engineering assignments. Estimates engineering personnel requirements. Schedules work to meet completion dates and technical specifications. Makes changes in methods, design or equipment where necessary. Generally operates with appreciable latitude for unreviewed action or decision. | 4/29/2019 |
| 988 | ARL BioPharma Oklahoma City, OK Laboratory Technician - Microbiology Lab AS or BS/BA in microbiology or related Exp: 0-2 years |
Under the supervision of the laboratory supervisor the Microbiology Lab Technician provides support tasks in a fast-paced laboratory setting. Funtions include: Media preparation, Glassware cleaning, Inventory / ordering, Lab cleaning and sanitization, Autoclaving various reagents and supplies, Assist laboratory personnel in daily activities to maintain high scientific quality and compliance with SOPs, protocols, and safety standards | 4/29/2019 |
| 989 | ANI Pharmaceuticals Baudette , MN Operator I - Manufacturing and Packaging (1st and 2nd Shift) HS Diploma/GED Exp: 1-2 years |
Position Responsibilities: Assists in material handling, equipment set-up and breakdowns, documents process according to Master Production Records, and works with trained operators at assigned work centers to learn all aspects of the position, including batch record documentation, equipment set-up, operation and clean up. | 4/29/2019 |
| 990 | ANI Pharmaceuticals Baudette , MN Contracts Support Associate AS Exp: 1-2 years |
This position is responsible for daily data entry as it relates to Contract Support related activities. This includes order processing, shipping paperwork, invoicing, advanced ship notices, product returns and other duties as assigned. Position Responsibilities: This includes: 1. Order Entry – Receipt/entry (EDI, Fax, e-mail). 2. Shipping/Invoicing – Prepare all docs pre and post shipment, maintain files, send invoices and advanced ship 3. CSII Orders – Process, verify, track orders, and maintain electronic 222 log. 4. Receive and update returns log for all return requests received by customers. 5. Evaluate each return to determine the appropriate return policy. 6. Create Disposition Authorization. 7. Coordinate with return company and/or customer on return or destruction authorization. 8. Create credit request for approval once material returned or destruction notice received. 9. Enter approved credits/debits into customer accounts. 10. Provide customer with credit and any supporting documentation. 11. Performs other duties as assigned or requested. | 4/29/2019 |
| 991 | Antech Diagnostics Columbia, OH Laboratory Generalist AS/BS in sciences or veterinary technician Exp: 1+ years lab experience |
You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: Hematology, Urinalysis, and Chemistry/endocrinology. | 4/29/2019 |
| 992 | Antech Diagnostics Mississaugua, CA Specimen Processor HS Diploma/GED Exp: 1+ years lab experience |
The Specimen Processor receives and prepares samples for laboratory analyses and tests. Prepares samples on slides or other testing format, records required information and sends to appropriate specialty lab area. Receives and prepares samples for laboratory analyses and tests to diagnose various pet and other animal illnesses, injuries and diseases in support of veterinarian animal treatment. Records information about specimens. Labels and numbers slides, specimens and submittals. Enters specimen data into tracking system. Make copies of submittals. Matches test slips with incoming specimens. Prepares work lists for each testing department. Verifies accuracy of information. | 4/29/2019 |
| 993 | Antech Diagnostics Fountain Valley, CA Laboratory Aid HS Diploma/GED Exp: 1+ years lab experience |
Antech Diagnostics is looking for outstanding Laboratory Aides and Assistants for Overnight Shift positions throughout our veterinary diagnostic reference lab locations. The ideal candidates will have experience working in either a reference or hospital laboratory, or have strong experience performing lab duties as a Vet Tech. The Laboratory Aide is responsible for setting up instruments, collection of samples, load samples into instruments and prepare samples for laboratory technicians. | 4/29/2019 |
| 994 | Antech Diagnostics Irving, TX Laboratory Aid HS Diploma/GED Exp: 1+ years lab experience |
Antech Diagnostics is looking for outstanding Laboratory Aides and Assistants for Overnight Shift positions throughout our veterinary diagnostic reference lab locations. The ideal candidates will have experience working in either a reference or hospital laboratory, or have strong experience performing lab duties as a Vet Tech. The Laboratory Aide is responsible for setting up instruments, collection of samples, load samples into instruments and prepare samples for laboratory technicians. | 4/29/2019 |
| 995 | Applied Medical Rancho Santa Margarita, CA Product Quality Engineer BS/BA in mechanical, biomedical, or electrical engineering Exp: 1+ years in med device industry |
As a Product Quality Engineer, you will be responsible for working within the framework of a team and performing the following activities: Evaluate the performance of products returned by the customer. Perform device analysis in accordance with model-specific procedures and protocols. Perform root cause analysis to investigate alleged product deficiencies. Propose corrective/preventive actions as required. Compose detailed reports describing results from investigations. | 4/29/2019 |
| 996 | Applied Medical Rancho Santa Margarita, CA Process Engineer I BS in mechanical, biomedical, industrial, or manufacturing engineering Exp: 0-2 years in engineering |
As a Process Engineer I, you will learn and develop skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. Responsibilities include: Sustain manufacturing processes. Debug manufacturing processes and equipment via root cause analysis. Develop and update engineering documents such as process maps, process FMEA, manufacturing/quality Instructions, test methods, drawings, and test reports. Collaborate with the Engineering team for fixturing design and development, tolerancing and design for manufacturing | 4/29/2019 |
| 997 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I BS in engineering or STEM Exp: 0-2 years in engineering |
As a Quality Engineer I, you will learn and develop skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. Responsibilities include: Conduct experiments to prove hypotheses. Create and validate test methods for design verification and manufacturing inspection testing by using measurement system analysis, gauge R&R and other relevant techniques. Implement statistical techniques to determine sample sizes and levels of confidence. Design engineering test protocols and use a data-driven approach to collect, analyze and summarize data into engineering reports | 4/29/2019 |
| 998 | BioPharmGuy Anytown, US Contract Pipeline Research Assistant Some college Exp: 0 years |
We are looking for someone to confirm/correct our drug pipeline data on a contract basis. You should have some knowledge of drug indications and clinical phases of drug development. If interested, send us a message via our contact form. Must be able to accept payment via PayPal | 4/15/2019 |
| 999 | zPredicta San Jose, CA Research Associate, Cell Biology MS in life sciences Exp: 1+ years |
You will be responsible for executing projects for our pharmaceutical clients ranging from screening of investigational compounds to exploring the mechanism of action of drug candidates. Key responsibilities includes: Run customer projects under the guidelines and in collaboration with our pharma partners. Analyze data from multiple readout platforms including, but not limited to, flow cytometry, microscopy, viability and proliferation assays. Assist in adoption of zPREDICTA’s platform for high throughput use. | 4/19/2019 |
| 1000 | Zymergen San Francisco, CA Research Associate, Automation BS or MS in biology or life sciences Exp: 0-2 years lab experience |
The RA in this role will conduct experiments to test and validate new automation processes for high throughput engineering of microbial genomes. They will help to invent new techniques, create cutting edge protocols, and extend existing Zymergen protocols to provide newer and better workflows to our microbe engineering Factory. They will work together with other scientists, RAs, automation engineers, and software engineers to deploy these new technologies into production. The RA will contribute to the overall mission of Zymergen by helping to bring new technologies into our workflows. | 4/19/2019 |
| 1001 | Zymergen San Francisco, CA Research Associate I/II, Strain Banking BS/BA in biology, chemistry, engineering, or realted Exp: 0-2 years |
The Research associate will assist in supporting a number of cell banking activities, working with diverse microbes, following standard operating procedures (SOPs). The Biorepository team plays a key role in managing large collection of engineered microbes and DNA constructs which is key to enabling our engineering pipeline and the protection of Zymergen’s intellectual property. Key Responsibilities include: Executing day to day cell banking workflows for different projects, varying by type of host strains. Responsible for ownership of each project workflow, troubleshooting, as well as maintaining operational integrity . Adapting to complex multi-day experimental schedules and evolving standard operating procedures. | 4/19/2019 |
| 1002 | Zymergen San Francisco, CA Manufacturing Engineer, High Throughput Screening MS in life sciences Exp: 0-2 years |
Zymergen is hiring Engineers into the Manufacturing Engineering group to focus on the continual improvement of manufacturing workflows across our factory. These Engineers are required to be able to identify and implement improvements in existing processes and establish protocols for new programs. Typical responsibilities will include: Operation of multiple types of robotic systems, including but not limited to, liquid handlers, colony pickers, barcoders, and automated plate readers for implementation of new or improved processes. Process modeling using a bpmn based MES and workflow optimization in collaboration with software and automation teams. Development and implementation of data tools (JSL, Python, R, etc.) to support existing workflows. | 4/19/2019 |
| 1003 | Zymergen San Francisco, CA Research Associate I-III, DNA/Plasmid/Strain Production BS/BA in biology or related Exp: 1+ years in lab or manufacturing |
This Research Associates position will be responsible for either the DNA, Plasmid or Strain manufacturing processes within Production. The Research Associate will run a diversity automated workflows in a high-throughput environment. Key responsibilities include: Entering and processing data using custom software. Working with diverse integrated automation platforms to perform high-throughput cell and molecular biology workflows. Recognizing opportunities to improve workflows and communicating appropriately to manager and/or adjacent teams. | 4/19/2019 |
| 1004 | Zymergen San Francisco, CA Research Associate II/III, Genome Sequencing MS in biology, computer sciences, or related Exp: 1+ years professional experience |
This role is for an RA that will be an integral part of carrying out the sequencing core’s most essential function - sequencing. In particular this role is for an Reserach Associate that will be skilled at PacBio library preparation and instrument usage. Responsibilities will include preparing PacBio Sequencing libraries, writing SOPs for library preparation and instrument usage, work with Bioinformaticians and Software Engineers and IT staff to integrate PacBio sequencer into existing or new infrastructure and prepare sequencing libraries for other instruments. | 4/19/2019 |
| 1005 | Zymo Research Irvine, CA Research Associate MS in biology or rleated Exp: 0-2 years |
The incumbent will have demonstrated clear leadership potential with ability to efficiently multi-task and manage a scientific research project, starting from the initial idea through to completion and publication in a peer-reviewed journal. The successful candidate will also be a quick learner, have strong interest in science, and be passionate about a career in research. Responsibilities include: Assist in experimental design. Conduct complex, high-level scientific research activities. Optimize experimental procedures. Read scientific literature pertaining to project and apply relevant findings to research project. | 4/19/2019 |
| 1006 | 10xGenomics Pleasanton, CA Microfluidics Engineer BS or MS in engineering Exp: 0-2 years |
The candidate must be able to learn complex procedures, efficiently execute microfluidic characterization experiments, perform data analysis, and communicate results and observations effectively. Key responsibilities include: Perform experiments and analyze data to help us develop robust microfluidic consumables. Use your understanding of microscale transport phenomena and troubleshooting skills to engineer new products. Communicate results clearly and contribute data for making critical design decisions | 4/19/2019 |
| 1007 | 23andMe Mountain View, CA Software Engineer-Research Services BS/BA Exp: 1+ years |
Responsibilities include :Build web applications and APIs aimed at scientific researchers. Improve access to data and metadata throughout the company. Develop data visualizations. Secure customer data and protect customer privacy. Set up reliable, automated infrastructure in AWS. Deliver quality Python and Typescript code. | 4/19/2019 |
| 1008 | 23andMe Mountain View, CA Software Engineer - Machine Learning MS Exp: 1+ years |
Responsibilities include: Build applications, libraries, and services to make machine learning more available within the company. Expand the variety and complexity of machine learning modes we can use. Develop checks and tests to ensure we're delivering reliable, quality results. Optimize machine learning, computational, and data processing pipelines. | 4/19/2019 |
| 1009 | 3M Menomonie, WI UR – Corporate Engineering – Resident Project Engineer BS in engineering Exp: 0 years |
The successful candidate will have the opportunity to be involved with numerous 3M manufacturing processes, equipment and techniques, in numerous locations throughout the United States and the world. Responsibilities include: Manage project timelines and budgets for assigned projects. Successfully interact with multiple discipline teams including 3M plant personnel, consultants and suppliers. Specify equipment performance and design criteria. Estimate capital equipment and installation costs. Oversee plant equipment layout and design. | 4/19/2019 |
| 1010 | 3M Maplewood, MN UR - Cloud Analyst BS in engineering Exp: 0 years |
he person hired for the position of Cloud Analyst will work with the global process teams to build and deploy standardized global cloud solutions as part of the Polaris project. Responsibilities include: Design, develop and test data pipelines established to deliver data into data storage based on a function design specification. Analyze, design, code/develop and implement changes to resolve break/fix issues to resolve and close tickets during both testing cycle of project and in production. Understand the functionality of relevant process area and data that will be required to Build, Test and implementation. | 4/19/2019 |
| 1011 | 3T Biosciences Menlo Park, CA Computational Biologist BS/BA or MS in bioinformatics Exp: 1-2 years in bioinformatics or related |
We’re looking for enthusiastic and self-motivated individuals to bring their talents to a fast-paced environment. Responsibilities include: Processing next-generation sequencing data, such as RNA sequencing. Developing and applying algorithms such as clustering, principal component analysis and others to biological data such as gene expression information and immune repertoire data. Working with Amazon Web Services to process data. Working with a team of consultants, data scientists, and computational biologists | 4/19/2019 |
| 1012 | Abbott Abbott Park, IL Associate R&D Scientist, Diagnostics BS/MS in life sciences Exp: 0-2 years |
Main Responsibilities include: Experimental procedures: Conducts experiments, accomplishes established milestones and summarizes data. Recommends options for other experiments. Presents data within team. Expertise and Problem Solving: Troubleshoots instrumentation or experiments; recognizes and assists with technical problems. Project Planning: Participates in planning project tasks; providing input to accomplish assigned tasks. Lab Safety: Participates in routine maintenance and lab safety. Documentation: Appropriately documents experimental procedures and results according to established guidelines. Quality: Responsible for implementing and maintaining the effectiveness of the quality system. | 4/19/2019 |
| 1013 | Abbott Westford, MA Quality Engineer MS in related field Exp: 0-2 years |
Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. Core responsibilities include: Identifies and controls Manufacturing process defects (scrap, nonconforming material, custom complaints)by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria.; Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and FMEAs.; | 4/19/2019 |
| 1014 | Abbott Temecula, CA Quality Engineer MS in related field Exp: 0-2 years |
Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. Core responsibilities include: Identifies and controls Manufacturing process defects (scrap, nonconforming material, custom complaints)by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria.; Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and FMEAs.; | 4/19/2019 |
| 1015 | Abbott Santa Clara, CA R&D Engineer MS in related field Exp: 0-2 years |
Responsibilities as an R&D Engineer include: providing engineering support in the creation and development of new medical device products. Main responsibilities include: research, develop, and designs mechanica/electromechanical materials, components, assemblies, and processes. Conducts feasibility studies to verify capability and functionality. Developes new concepts from initial designs, etc. | 4/19/2019 |
| 1016 | Abbott Santa Clara, CA Associate R&D Engineer BS in related field Exp: 0-2 years |
Responsibilities as an R&D Engineer include: providing engineering support in the creation and development of new medical device products. Main responsibilities include: research, develop, and designs mechanica/electromechanical materials, components, assemblies, and processes. Conducts feasibility studies to verify capability and functionality. Developes new concepts from initial designs, etc. | 4/19/2019 |
| 1017 | Abbott Scottsdale, AZ Quality Engineer I BS in electrical engineering or technical field Exp: 0-2 years |
This position is responsible for supporting and improving quality engineering methodologies and providing quality engineering support within manufacturing, or system/services support. Responsibilities include: Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. Assist in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues. Design and conduct experiments for process optimization and/or improvement. etc. | 4/19/2019 |
| 1018 | Abbott North Chicago, IL Quality Technician BS in sciences Exp: 0-2 years |
Candidate will undertake the role of technician quality with some supervision. Daily responsibilities include: CAPA -Provides inputs to facilitate CAPA investigations as required. Investigates standard complaints. Identifies and prioritizes medical and reportable complaints. Monitor performance of manufacturing processes and implement required improvement activities. Manage Product and Process Improvements - Participate in Project and Process improvement activities. Quality/Compliance -Support manufacturing and testing operations as required; adhering to Good Manufacturing Practices and Good Laboratory Practices. etc. | 4/19/2019 |
| 1019 | AbbVie Lake County, IL Associate Scientist I/II, Biotransformation DMPK BS or MS in chemistry Exp: BS: 1-4 years lab, MS: 0 years |
The candidate for this Associate Scientist I/II position will be working in the Biotransformation group of AbbVie’s Bioanalysis and Biotransformation department. This position will be focused on preparing biological samples and performing LCMS assays to characterize biotransformation of large molecules, including antibodies, antibody-drug conjugates, and proteins. The individual will be expected to have solid experience working with analytical instruments, especially HPLC and MS, and preferred to have experience working with protein samples and protein chemistry techniques. | 4/19/2019 |
| 1020 | AbbVie Lake County, IL Associate Scientist I, DMPK MS in life sciences Exp: 0 years |
The ideal candidate will have a strong background quantitative laboratory methods and mammalian cell culture. The position will require ability to generate precise, reliable and reproducible data in a timely manner. Demonstrate strong data interpretation skills, ability to troubleshoot experiments and instrumentation, ability to learn and understand new experimental techniques and be able to place data in proper scientific context by consulting and citing relevant literature. | 4/19/2019 |
| 1021 | AbbVie Worcester, MA Associate Scientist I/II, Modality Analytics BS or MS in chemistry Exp: BS: 1-4 years lab, MS: 0 years |
The candidate will be part of the New Modality Analytics Group within Protein Analytics that is mainly focused on method development and implementation of various HPLC, UPLC, and CE based analytical methods of AbbVie’s Biologics. The successful candidate will contribute to the development and testing of analytical assays and will contribute to the continuous improvement and innovation within the group and the PA department. | 4/19/2019 |
| 1022 | Abcam Burlingame, CA Research Associate, IVD BS in biochemistry, pathology, or life sciences Exp: 1+ years lab experience |
This position will contribute to the development and validation of qualified reagents and generate data to support IVD products. Protocols and associated data may include immunohistochemistry (IHC), western blots, ELISA or other immunoassays, immunofluorescence or others as required. In addition, this position will be expected to complete scientific and technical tasks on aggressive timelines and to work as part of a team on varied tasks with changing priorities. | 4/21/2019 |
| 1023 | Abcam Burlingame, CA Project Coordinator (Custom Antibody Development) BS in biology or other life sciences Exp: 1+ years |
The project coordinator will join a dynamic team within a rapidly growing organization and will be responsible for supporting custom antibody development projects, driving them toward major milestones and successful completion. This position will be an important addition to the US Custom Services team within our Burlingame office. The role will support project management functions including the sourcing of reagents, scheduling immunizations, supporting customer interactions, populating work reports and product datasheets. In addition, the appointed person will assist with the receipt and shipment of critical reagents and data entry. | 4/21/2019 |
| 1024 | Abpro Woburn, MA Research Associate, Antibody Engineering BS or MS in biology or life sciences Exp: 0-3 years |
We are seeking a motivated individual for a research associate/senior research associate position that will specialize in antibody/protein engineering, gene sequencing, mammalian cell culture, and antibody expression/purification. This person will have good opportunity to experience many different areas in therapeutic antibody discovery, molecular biology and cell biology as an integral part of our Antibody Discovery and Engineering team. Responsibilities include: Sequence antibody variable (VH/VL) regions. Construct and validate gene and plasmid constructs. Express antibody/protein genes in mammalian cell systems. Purification of antibodies/proteins | 4/21/2019 |
| 1025 | Absci Vancouver , WA Research Associate I BS in biology, biochemistry, or related Exp: 1-2 years lab experience |
The Research Associate I, under direction of the Molecular Sciences team, will support innovative experimental research that advances AbSci’s proprietary E. coli expression platform. Primary responsibilities include providing core support to ongoing DNA construction, strain engineering, and small-scale protein expression activities. Daily activities will include management of the Molecular Sciences laboratory consumables and sample libraries, preparation of common research reagents, and providing assistance to ongoing experiments. The ideal candidate will demonstrate rapid mastery of assigned tasks and the capacity to take on additional technical responsibilities within an expanding team. | 4/21/2019 |
| 1026 | Accuray Madison, WI Product Development Technician AS or BS in electrical technology or related Exp: 1+ years |
The Product Development Technician is responsible for assisting in various Product Development projects. Duties include: maintaining, modifying and repairing H-Series and Radixact Radiation Delivery Systems; maintaining and repairing test and lab equipment; performing tests, measurements, and analysis; assisting Engineers with various Product Development tasks; selecting and purchasing supplies, components, and assemblies for maintaining and testing. Duties include: Maintain, test, troubleshoot and repair radiation delivery systems and associated bunker support instrumentation, in accordance with quality system requirements and associated manufacturing and service procedures. Manage inventory of spare and alternate parts necessary to maintain and reconfigure radiation delivery systems; procure replacement/new parts through supply chain, manufacturing, and/or service as-needed. Obtain required data sets; assist in analyzing and presenting findings. | 4/21/2019 |
| 1027 | ACell Columbia, MD Materials Associate HS Diploma Exp: 0-3 years in manufacturing |
The Materials Associate I is primarily responsible for completing general warehouse functions. This includes, but is not limited to labeling and boxing product, verifying incoming product counts, conducting inventory counts, and reviewing documentation in order to maintain up-to-date inventory records. The Materials Associate I is also responsible for the packaging and shipping of finished devices to customers and sales representatives. | 4/21/2019 |
| 1028 | ACell Columbia, MD Biotechnician HS Diploma Exp: 0-3 years |
Employee will carry out manufacturing practices in a cGMP biotechnical facility. The job involves the manual processing of porcine urinary bladders, which includes all aspects from collection of raw materials to packaging of the final product. Following training, work will be expected to be performed independently to a high degree of standard in biomaterial handling. | 4/21/2019 |
| 1029 | Acutus Medical Carlsbad, CA Engineer I - Field Service BS in sciences/engineering Exp: 1+ years |
The Engineer 1 - Field Service is the responsible for providing highly visible onsite and remote technical support to customers of Acutus Medical. This includes but is not limited to installation, general servicing, repairing, problem solving and supporting customers and medical centers using the Acutus’ electromedical equipment. This Engineer works closely with Acutus’ internal teams to ensure customer feedback, experiences and input is communicated to the appropriate internal team members. | 4/21/2019 |
| 1030 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma Exp: 0-1 years in cGMP environment |
Responsibilities as an assistant manufacturing associate include: Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. | 4/21/2019 |
| 1031 | Emergent BioSolutions Baltimore, MD Associate Specialist Metrology Tech Sys BS in engineering or related Exp: 1-2 years |
The Associate Metrology Technical Systems Specialist is responsible the execution of the metrology functions required to support the facility and process equipment at the Baltimore fill/finish facility. Perform calibrations and schedule vendor calibrations of instrumentation and equipment. Repair and troubleshoot electronics and instrumentation as well as other equipment as able. Duties include: Designs, develops, implements and maintains calibration processes and procedures for new and existing equipment and instrumentation and train key personnel on proper use. Coordinates and performs calibration of instrumentation necessary for maintaining production equipment, laboratory equipment and other auxiliary measurement systems. Maintains detailed calibration record. | 4/21/2019 |
| 1032 | Emergent BioSolutions Baltimore, MD Analyst II, QC Microbiology MS in microbiology/biology Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. | 4/21/2019 |
| 1033 | Emergent BioSolutions Baltimore, MD Analyst I, QC Microbiology BS in microbiology/biology Exp: 0-2 years |
Analyst I of QC microbiology has responsibilities that include: Responsible for conducting qualitative and quantitative microbial analyses in support of environmental monitoring, cGMP manufacturing and stability of drug products and incoming raw materials. Perform various microbiological testing procedures as per manufacturing/Quality Control batch records, stability protocols, raw material requests for testing, etc. Perform environmental monitoring and utility testing of the facility. Performs environmental monitoring during fill operations. | 4/21/2019 |
| 1034 | Adaptive Biotechnologies Seattle, WA Research Associate I SB/BA in biology, chemistry, or related Exp: 1+ years lab experience |
The position will design and coordinate experiments which leverage Adaptive’s unique platform to realize the company’s strategic objectives in hematology, immunology and oncology. Responsibilities include: Develop new assays for immune system profiling by next generation sequencing in collaboration with a team of other researchers. Develop new methods and technologies for project advancement including novel molecular biology methods, streamlined protocols, and automating tasks. Transfer developed methods and/or assays into SOPs for the development laboratory and/or production laboratory . Responsible for analyzing data and reporting findings to their supervisor | 4/21/2019 |
| 1035 | Adaptive Biotechnologies Seattle, WA Quality Systems Associate I (GMP) BS or MA in sciences Exp: 1+ years in QA |
The Quality Systems Associate is responsible for supporting day-to-day operation and may have individual responsibility for working with new, or transferred, products to provide quality oversight to ensure regulatory compliance. The position is accountable for the applications of industry standard quality practices and tools as applied by Adaptive Biotechnologies. The position requires the ability to manage priorities from multiple projects and tasks utilizing effective written and oral communication skills. This position will apply quality systems knowledge, problem solving, and judgment skills to ensure the appropriate balance of quality, compliance, and business needs. | 4/21/2019 |
| 1036 | Adaptive Biotechnologies Seattle, WA Quality Systems Associate I BS in relevant sciences Exp: 1+ years in QC/manufacturing etc. |
This position is responsible for supporting the Quality Management System (QMS) by working with production staff to ensure compliance with regulatory and internal process requirements. The position is accountable for the applications of industry quality requirements, standards, and tools to continually improve the quality systems established at Adaptive Biotechnologies. The position requires the ability to manage priorities from multiple projects and tasks while utilizing effective written and oral communication skills. This position will develop quality systems knowledge, and apply that knowledge through reasoning and judgment, to ensure an appropriate balance of quality, compliance, and business needs. | 4/21/2019 |
| 1037 | Adimap Lebanon, NH Research Associate - Antibody Discovery BS or MS in biology, chemical engineering, biochemistry, or related Exp: 1+ years |
We are seeking a skilled molecular or protein biologist to join our Antibody Discovery team. The Research Associate will work in a small team setting to support Adimab’s novel antibody discovery, maturation, and production platform. This role will closely interface with the Protein Analytics, High Throughput Expression, Molecular Sciences, and Computational Biology teams. Duties include: yeast propagation, mammalian cell culture, antibody library construction/selection, etc. | 4/21/2019 |
| 1038 | ABL Inc. Rockville, MD Laboratory Research Specialist BS or MS in life sciences Exp: BS: 1-2 years, MS: 0-1 years |
This position will provide extensive technical support for fulfilling contract requirements for immunological assays. Duties include: Assist in the development and qualification of new immunological assays including; but not limited to, the following:Multicolor-Flow Cytometry based assays, cytokines and other soluble biomarkers Multiplexing assays (Luminex, Aushon, MSD platforms), ELISA, ELISpot, and Neutralization Assays, among others. Responsible for organizing and ensuring efficient daily operation of the laboratory including: stocking laboratory with necessary reagents and other materials used for experiments and inventory of reagents and samples. This position will ensure the accuracy of record keeping of experimental conditions and results. Assist withdaily scientific duties in the laboratory in order to meet commercial and government contract obligations in a timely manner. Lab activities mayinvolve interaction with other functions and departments. | 4/21/2019 |
| 1039 | Biotechne Wallingford, CT Reagent Manufacturing Technician AS or BS in biology, chemistry, or related Exp: 1+ years lab experience |
This position requires the ability to function with minimal oversight and convert customer demands into finished product. The individual will execute production protocols and ensure continual operation of equipment to meet production targets, effectively and immediately communicate complications that arise during manufacturing, and be able to work across teams to establish and maintain solutions. The individual must also demonstrate a proactive mindset to manage multiple tasks and drive them to completion in a timely manner. | 4/21/2019 |
| 1040 | Biotechne Minneapolis, MN Research Associate - New Technologies/Luminex MS in chemistry, biology or related Exp: 0-2 years |
The responsibilities of this position are to assist with validation, feasibility, product development, and technical support of immunoassays. Optimize components and performance, develop manufacturing procedures, transfer product/process to production, and perform necessary troubleshooting. Work on problems of moderate scope where analysis of situation or data requires a review of identifiable factors. Perform additional duties as assigned. | 4/21/2019 |
| 1041 | B. Braun Medical Inc. Allentown, PA Associate Engineer BS in engineering Exp: 0-1 years |
Provide Engineering support toward the design, development, installation, startup, validation, and maintenance of products, processes, and equipment. Provide engineering skills within a specialty field(s). Responsibilities include: Research, develop, and prepare specifications for improvements to existing and/or new products, processes, equipment, and technology. Support projects by contributing as a team member to the development of project schedules, costs, preparing status reports, attending team meetings, and communicating issues and progress to team and management. Assist in the supervision of contract personnel and outside vendors in the performance of contracted services. | 4/21/2019 |
| 1042 | B. Braun Medical Inc. Irvine, CA Product Handler HS Diploma Exp: 0 years |
Under the direction of the Supervisor/Line Operator/Process Monitor, monitors material in order to maintain efficient flow of production. Operate hand or power trucks and other material handling equipment. Responsibilities include: Operate hand or power trucks and other material handling equipment to move materials throughout the unit. Change batteries on these material handling equipment. Delivers first (1st) pallet and subsequent pallets to staging area after verifying correct quantity of empty trays. Load product onto pallets, trays, baskets or conveyors, checking product identification to verify correct lot number, description, etc. Discard, reject and record information as needed. Sign and date the back of each tag once the pallet has been verified as having the correct amount of units and trays. | 4/21/2019 |
| 1043 | B. Braun Medical Inc. Denver, CO IV Tech I HS Diploma Exp: 1+ years in aseptic prep |
Prepares compounded sterile products and performs related activities under the direction of a pharmacist. Responsibilities include: Assists in the set up of the compounding room, equipment, and supplies for preparation of compounded sterile solutions, using aseptic technique. Performs general cleaning and maintenance duties as directed. Participates in cleanroom product introduction activities. | 4/21/2019 |
| 1044 | Affigen Austin, TX Research Associate I/II MS in biology, chemistry, or related Exp: 1+ years in pharma/biotech |
Reporting to Senior R&D Scientists, the Research Associate will be a part of our growing lab group that is responsible for generating and characterizing test materials to support manufacture process development and preclinical studies required to rapidly advance Affigen’s patient-specific monoclonal antibody therapeutics into the clinical-phase. In this role, the Research Associate is expected to take ownership of specific processes, assays or instrumentation (listed below) and act as the in-house subject matter expert in these functional areas. In addition, the Research Associate will be required to perform miscellaneous laboratory duties that may broadly traverse aspects of upstream, downstream, and analytical development and general research support. A successful candidate for this position will be performance-focused, detail-oriented, and capable of filling a multidisciplinary supporting role across multiple research and development activities through excellent communication, documentation and teamwork skills. | 4/21/2019 |
| 1045 | AGC Biologics Seattle, WA Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Principle responsibilities include: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. | 4/21/2019 |
| 1046 | AGC Biologics Seattle, WA Contract Manufacturing Associate I-IV - Upstream BS in chemistry, biology, or related Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. | 4/21/2019 |
| 1047 | Agilent Wilmington, DE R&D Electrical Engineer BS or MS in electrical engineering Exp: 0 years |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Electrical/Firmware Engineers at our site work on digital and analog PC board designs, algorithms for control of motion, flow and heated zones, intelligent systems. You will work with Real time systems, FPGA programming and robotic systems as well as thermal and pneumatic controls. One example would be a chemical sensor and circuitry to sense femtoamps of current. | 4/21/2019 |
| 1048 | Agilent Lexington, MA Inside Informatics Product Sales Specialist BS/MS in computer networking, chemistry, biology, or other sciences Exp: 0 years |
In this critical role, you will pair your experience with analytical instrumentation and our core markets, with your desire to sell, to drive growth in the Chromatography Data Systems, Data Management Systems, and Electronic Lab Notebook product lines. Responsibilities include: Act on sales leads for informatics systems, interpreting customer needs and developing solutions for these customers. Acquiring new customers and retaining and growing an existing installed base of customers.. | 4/21/2019 |
| 1049 | Agilent Wilmington, DE Analytical Instruments Technical Support BS in chemistry, biology, or related Exp: 0 years |
As an active team member, you will support customers requesting hardware, software and applications assistance with Analytical Products and Solutions and route those customers whom you can't help to the appropriate groups. Our group's organizational goal is that as part of a world-class technical support group, we provide insights to customers at their very first contact. In order to be successful, our response needs to be quick and well-informed. Direct customer contact through phone/email channels; Service Request logging in the Agilent SAP Service CRM system and request routing to the appropriate technical team for handling. | 4/21/2019 |
| 1050 | Agilent Washington DC, MD Field Service Engineer - Maryland/ Washington DC BS in chemistry, biology, or related Exp: 0 years (recent grads) |
As a field service engineer, you will work at a variety of labs, so having a solid understanding of Agilent's portfolio, and continuously learning about new instruments, software and consumables, is key. Applying your creativity, complex problem-solving skills, and can-do attitude is essential. Compliance and reporting are also important responsibilities, such as documenting and ordering components using a variety of databases. Having a natural instinct to deliver the highest-levels of customer service is vita | 4/21/2019 |
| 1051 | Agtc Alachua, FL Engineer I/II Upstream Process Development MS in bio/chemical engineering or realted Exp: 0-2 years |
The Engineer I/II in Upstream, Process Development will report directly to the Associate Director, Upstream Process Development at the Alachua, FL headquarters. Duties and responsibilities include: Plan, execute, and troubleshoot experiments for the optimization of upstream process steps in flasks and bioreactors for approved research plans. Optimize process parameters to increase virus yield from adherent & suspension cell lines. Responsible for scale up and manufacturing of viral vectors up to 200 L in bioreactor. Collect, analyze, record, and summarize data in the course of biologics production and processing Assist in maintaining laboratory supplies and equipment. | 4/22/2019 |
| 1052 | Agtc Alachua, FL Research Associate II/III/IV – Target Validation MS in biology or life sciences Exp: 0-2 years lab experience |
AGTC is seeking a highly motivated individual to support our drug development activities. They will be responsible for discovery research, implementing a scientific plan, and working independently in the lab with minimal supervision. Duties include: Target validation of candidate capsids, promoters, gene constructs, etc. Develop and qualify new assay methods. Execute routine assays and procedures. Collect, analyze, record, and summarize data. etc | 4/22/2019 |
| 1053 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant – Formulations BS in life sciences Exp: 0-2 years |
The Drug Product Formulations Manufacturing Assistant is responsible for execution of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Manufacturing Assistant will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Manufacturing Assistant will learn and demonstrate proficiency in both the technical aspects as well as the quality systems which govern cGMP manufacturing. | 4/22/2019 |
| 1054 | Ajinomoto Bio-Pharma Services San Diego, CA Document Control Assistant HS Diploma Exp: 0-2 years in GMP environment |
Ajinomoto Bio-Pharma Services is currently seeking a Document Control Assistant responsible for coordinating the review and approval of GMP documents using an electronic document management system. Responsibilities include: Coordinates document changes within an electronic document management system. Issues batch records, laboratory notebooks, and logbooks for use in GMP production and testing activities. Interfaces with document authors and reviewers to process document changes within project timelines and in accordance with established procedures. Ensures proper maintenance of document master copies and original production records. | 4/22/2019 |
| 1055 | Ajinomoto Bio-Pharma Services San Diego, CA Clean Room Monitoring Assistant - Multiple Openings HS Diploma or BS in life sciences Exp: 0-2 years |
This role is a vital role within our Quality Control group and is responsible for supporting manufacturing through collection and testing of water, surface and utility samples during various manufacturing and lab processes. As a Clean Room Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. Performs environmental monitoring within the microbiology laboratory, manufacturing suites, clean rooms, and drug product operations. Performs enumeration and gram staining of bacterial colonies. Maintains lab area including routine cleaning of benches, biosafety cabinets, shelving and floors | 4/22/2019 |
| 1056 | Akorn Decatur , IL Quality Assurance Technician HS Diploma Exp: 1+ years |
The QA Auditor I performs quality assurance duties at the assigned facility to prevent or eliminate defects in products for sterile filling operation or in final inspection and packaging operations. This individual must work in a detail-oriented, compliant manner in a high stress environment where adherence to deadlines is critical. The individual must display exemplary level of integrity at all times. The QA Auditor reports directly to the QA Supervisor or Manager of Quality Operations. Duties include: Check the production lines to make sure the right product is issued to match batch record. Monitor the production processes and ensure consistency of procedures. • Review/approve raw materials or components for use in production, etc. | 4/22/2019 |
| 1057 | Akorn Decatur , IL 2nd shift Formulation Technician I HS Diploma Exp: 0-2 years |
Formulation Technician I will be responsible for performing formulation of pharmaceutical and ophthalmic product solutions for lyophilized products. Assures proper documenting procedures and transfer of solutions to appropriate areas. Supports the development of products or processes, quality control, and proper maintenance of environmental standards. Duties include: Formulation of product solutions as well as cleaning/sanitizing solutions. Set up / Post use cleaning of formulation equipment. Transfer of product and non-product related solutions to filling areas. Following Standard Operating Procedures and Batch Record processes. Assuring proper documentation of all duties performed and material usages. | 4/22/2019 |
| 1058 | Akorn Decatur , IL Microbiologist I - NJ - 2nd shift BS or MS in biology or life sciences Exp: BS: 1-2 years, MS: 0 years |
Hours are from 3PM-11:30PM. Under limited supervision and guidance of the Microbiology management team, the Microbiologist I is responsible for the following duties: Performs routine microbiological testing of products, raw materials, components and controlled environments according to site Standard Operating Procedures and compendial methods. Documents routine procedures following laboratory and company guidelines. Issues and revises GMP documents such as SOP’s, protocols/reports, testing monographs, data sheets, etc. | 4/22/2019 |
| 1059 | Express Scripts Indianapolis, IN Pharmacy Technician- Accredo HS Diploma Exp: 0-1 years |
As a member of our fulfillment team, you’ll work in one of our pharmacy distribution facilities, which are responsible for filling and shipping over 90,000 prescriptions a day. These state-of-the-art facilities are climate controlled, well-lit, and use a wide variety of technology to help you perform at peak productivity levels. Job functions include: Process requests for new and refill prescriptions. Select and retrieve appropriate medications. Verify quantities and prepare labels for bottles. Send orders to pharmacy staff for completion and verification of prescription based programs. Select appropriate packing materials and prepare packages for shipment. | 4/11/2019 |
| 1060 | Express Scripts Tempe, AZ Patient Care Adovacate HS Diploma Exp: 0-1 years |
Handle customer service inquiries from members, providers, physicians and internal and external clients related to pharmacy benefits. Work to research and resolve problems in a timely manner. Assist members in understanding and maximizing the use of their pharmacy distribution program. Use computerized system to gather information and respond to questions. Document issues and resolutions in a common database. Escalate issues as necessary. | 4/11/2019 |
| 1061 | Express Scripts Mississauga, On Pharmacy Assistant Exp: 0-3 years in retail pharma |
The Pharmacy Assistant works closely on a daily basis with the Member Contact Centre and the Pharmacy to process member prescription requests. The Pharmacy Assistant will be responsible for processing prescription refills through Kroll and responding to and taking action on member requests as appropriate within his/her scope of practice. Duties include: Accurately process prescriptions through Kroll including third party adjudication and rescheduling of next fill. Recording and maintaining member information in the CRM system. Answering questions from patients and/or resolve customer issues according to Ontario College of Pharmacist’s regulations. | 4/11/2019 |
| 1062 | Express Scripts Tampa , FL Patient Care Adovacate HS Diploma Exp: 0-3 years |
Handle customer service inquiries from members, providers, physicians and internal and external clients related to pharmacy benefits. Work to research and resolve problems in a timely manner. Assist members in understanding and maximizing the use of their pharmacy distribution program. Use computerized system to gather information and respond to questions. Document issues and resolutions in a common database. Escalate issues as necessary. | 4/11/2019 |
| 1063 | Express Scripts St. Louis, MO Benefit Validation Analyst MS in relavent field Exp: 0-3 years |
The Testing Analyst II is responsible for the management of new and existing client testing to validate benefit set-up based on client's intent and expectation. The role analyzes client intent and creates validation and test scenarios, executes validations/tests and analyzes results. This will cover all functions necessary to implement a client, including, but may not be limited benefits, clinical, pricing, and coverage for all lines of business in scope for benefit validation (Health Plan clients, commercial clients, MedD clients, book of business projects, etc.). The role will require considerable cross-functional communication to effectively monitor the daily status of client implementations and plan changes. This role collaborates with internal partners to obtain necessary information to perform the work, request intent clarifications, identify setup issues, and bring closure to our validation/testing activity. | 4/11/2019 |
| 1064 | Express Scripts Greensboro, NC Pharmacy Technician- Accredo HS Diploma Exp: 0-1 years |
As a member of our fulfillment team, you’ll work in one of our pharmacy distribution facilities, which are responsible for filling and shipping over 90,000 prescriptions a day. These state-of-the-art facilities are climate controlled, well-lit, and use a wide variety of technology to help you perform at peak productivity levels. Job functions include: Process requests for new and refill prescriptions. Select and retrieve appropriate medications. Verify quantities and prepare labels for bottles. Send orders to pharmacy staff for completion and verification of prescription based programs. Select appropriate packing materials and prepare packages for shipment. | 4/11/2019 |
| 1065 | Unchained Labs Pleasanton, CA Lab Technician AS or BS in biochemistry, chemistry or related Exp: 1+ years |
Responsibilities as a lab technician include: Receive, document,and prepare customer samples for testing, visual inspections of samples, test plans and reports, preforming method development and validations, coordination of the maintenance/operations of lab equipment. | 4/11/2019 |
| 1066 | United Theraputics Research Triangle Park, NC QA Specialist I - Training and Documentation BS in sciences Exp: 1+ years |
The QA Specialist I – Training & Documentation assists in the execution of GXP Documentation and Training processes and the system administration of the associated Learning Management System (LMS) and electronic Document Management System (eDMS). Manages tasks associated with New Employee training and filing documents. Ensures compliance to applicable company policies, standards and regulations. Support and conduct New Employee Orientation (NEO) training and provides training support for UT and UT subsidiaries, as applicable. Controls and maintains training document and document files. Collect training records, checks for accuracy, completeness, and obtains corrections when necessary. | 4/11/2019 |
| 1067 | United Theraputics Manchester, NH Research Associate I/II - Biomaterials BS/BA in biomedical or chemical engineering Exp: 1+ years |
Support Biomaterials by performing research and development engineering in materials design, printing, cellularization, and characterization of 3D printed scaffolds. Duties include: Assist in development and characterization of 3D printing under the direct supervision of project leaders/scientists. Assist materials development to optimize cellularization of printed objects. Build and maintain an understanding of current and emerging technologies within the field of biomaterials. Assist in performing analytical techniques for material development and characterization of 3D printed scaffolds. Follow prescribed laboratory methods and protocols under GLP/GMP-conditions; laboratory safety and use of protective equipment, and handling of biohazard materials including human or animal cells and tissues | 4/11/2019 |
| 1068 | United Theraputics Manchester, NH Research Associate I/II - 3D Printing BS/BA in biomedical or chemical engineering Exp: 1+ years |
Support 3D Printing by providing expertise regarding operation and optimization of workflow. Responsibilities include: Validate pending design decisions by building and analyzing proof of concept prototypes. Design and implement test setups, relating results back to physical printer behavior and changing print parameters to optimize print quality. Assist in performing analytical techniques for material development and characterization of 3D printed scaffolds. Follow prescribed laboratory methods and protocols under GLP/GMP-conditions; laboratory safety and use of protective equipment, and handling of biohazard materials including human or animal cells and tissues | 4/11/2019 |
| 1069 | Astellas Seattle , WA Research Associate 2, Cell Differentiation MS in sciences Exp: 0-2 years |
This person will acquire further versatility in routine procedures, more technical knowledge, and more understanding of administrative operations, some troubleshooting. They will assist with more complex laboratory operation projects, and will take on more responsibility to provide content for various documents and reports. They will be able to execute protocols with some guidance, and will have ability to summarize results independently. Duties include: Culture and differentiate edited pluripotent stem cell lines into mature hematopoietic and immune cell types. Phenotype differentiated cells using flow cytometry, imaging and gene expression analyses. | 4/11/2019 |
| 1070 | Astellas Seattle , WA Quality Control Associate 2 MS in sciences Exp: 0-2 years lab experiences |
The Quality Control Associate 2 will work to provide cross-functional support for the Technical Operations team by evaluating manufacturing products for product safety and quality. Growing technical knowledge and continued understanding of quality operations with ability to troubleshoot and solve technical problems. Independently contribute to the development of new testing methods. Continues to take on more responsibility to provide content for various documents and reports. Will be able to execute protocols and summarize results with guidance. Will acquire versatility in quality control procedures, technical knowledge, understanding of administrative operations, and general troubleshooting. | 4/11/2019 |
| 1071 | Upsher-Smith Maple Grove, MN R&D Documentation Specialist MS in life sciences Exp: 0-3 years |
The R&D Documentation Specialist will be a self-motivated individual with experience in authoring regulatory submission documents as well as creation and/or revisions of manufacturing documentation in accordance with GMP standards. He/she will have: (a) demonstrated experience with authoring, editing and controlling of manufacturing batch records (MBR) and process study protocols to support pharmaceutical development activities in Research and Development (b) hands-on experience with authoring and editing of CMC submission documents for ANDAs and/or NDAs (c) experience with creation and revisions of report templates, work instructions and/or standard operating procedures (SOPs) that support R&D activities (d) demonstrated flexibility to support multiple activities within the team/department (e) ability to work closely with cross-functional R&D, Technical Services and Operations team members and mange timelines (f) excellent writing and interpersonal skills. | 4/11/2019 |
| 1072 | Vector Lab Burlingame , CA Histotechnologist/Quality Control Associate I BS/BA in biochemistry, life sciences, or related Exp: 0-2 years |
Vector Laboratories is seeking a Histotechnologist/Quality Control Associate I who will analyze in-process materials, raw materials, finished goods, and stability samples following established operating procedures. The individual may also be required to analyze samples from the research and development department using established testing procedures as per instructions. S/he may also be responsible for helping to organize and maintain laboratory reagents/supplies. The QC Associate I will operate and maintain common laboratory equipment as per instructions and will assist in inventory management as needed. Technical knowledge should include strong knowledge of general laboratory safety and practices and basic understanding of QC principles. This position works under immediate supervision and relies on instructions and established procedures to perform the functions of the job. | 4/11/2019 |
| 1073 | Concerto Health AI Memphis, TN Data Abstractor I AS or equivalent Exp: 0-2 years |
The Data Abstractor navigates electronic medical record systems and other medical databases, reviews medical records, and abstracts medical record data related to specified disease and project requirements. The Data Abstractor works under the direction of the Lead Data Abstractor. Duties include: Access electronic data systems for review of medical records and enter specific data into congruent electronic data systems. Review project specific documents, as needed, to develop familiarity with project goals and with the Abstractor tasks in each project. Use other resources as needed to gain the knowledge required to perform Abstractor work on new projects. Share medical knowledge and project-specific procedural knowledge with other Data Abstractors as needed. | 4/11/2019 |
| 1074 | Vedanta Cambridge, MA Contract - Research Associate - Molecular Biology BS or MS in biology or related Exp: 1+ years |
The research associate will work in collaboration with the Microbiology, Immunology, and Systems Biology teams to aid in the characterization of organisms from the human microbiota through the execution of molecular biology assays and next-generation sequencing. General tasks will involve DNA extraction, sequencing library preparation, PCR and PCR-product verification, qPCR, sample organization, and coordination of tasks with the microbiology and immunology teams. Additionally, the research associate will support the preparation of samples for DNA sequencing at Vedanta and off-site. | 4/12/2019 |
| 1075 | Veeva Columbus, OH QA Engineer (CRM) BS in math or computer sciences Exp: 0-5 years |
Veeva Systems is looking for an energetic and enthusiastic Engineer to join our rapidly growing team. This is a hands-on position for delivering a quality SaaS product. As part of Veeva CRM Multi Channel software QA team, you will be given an opportunity to test a high quality product that was built from scratch. Responsibilities include: Participate in product and feature designs with developers, usability specialists, user interface designers, and product managers. Build effective test cases that are used for manual and automation testing. Develop deep expertise in the product | 4/12/2019 |
| 1076 | Veeva Pleasanton, CA Associate Software Engineer, New Grad BS in computer sciences or related Exp: 0-1 years (new grad) |
You’re a front-end, back-end, or mobile software developer (including iOS and Windows Tablet) who likes to work on small teams in a fast-paced, agile environment, releasing features every four weeks. Help us design our solutions. Contribute to technical and functional design decisions, troubleshoot and provide technical product support, and be responsible for all aspects of the software development lifecycle. Drive all aspects of the software development cycle: design, implementation, tuning, testing, and monitoring of the functional areas that you will own, delivering products within the schedules and timelines. | 4/12/2019 |
| 1077 | Veeva Pleasanton, CA Associate QA Engineer, New Grad BS in applied math, information systems, or related Exp: 0-1 years (new grad) |
You’re a Quality Engineer who likes to work on small teams in a fast-paced, agile environment, releasing features every four weeks. You will help us ensure there is quality in our design implementation. You will contribute to technical and functional testing, understand the areas that need troubleshooting more than other areas, and be part for all aspects of the software development lifecycle. Drive all aspects of the software development test cycle: testing the design and the implementation of the code, driving automation and monitoring of the functional areas that you will own, delivering quality products within the schedules and timelines. | 4/12/2019 |
| 1078 | Veeva Pleasanton, CA Associate Performance Engineer, New Grad BS in computer sciences or related Exp: 0-1 years (new grad) |
The Vault Performance Engineering Team works within the Vault Development Team and participates in all phases of the SDLC. In this role you will: Collaborate with Vault team members in Product Management, Engineering Management and Quality Assurance to help design and develop performance tests. Test new features pre-production to make sure they will scale and perform. Implement and execute load tests in JMeter. Use and update Python scripts for managing test systems. | 4/12/2019 |
| 1079 | Veeva Multiple locations, Associate Consultant, New Grad BS/BA Exp: 0-1 years (new grad) |
You will work on project teams implementing Veeva’s cloud software applications. Participate in business process discovery workshops, gather requirements, configure the solution, help with testing and final deployment. Explain solutions to a variety of audiences and provide subject matter expertise on Veeva applications and technical design. | 4/12/2019 |
| 1080 | Veracyte South San Francisco, CA Laboratory Automation Engineer BS or MS in biological sciences or computer sciences Exp: 1+ years |
We are seeking a new Automation Engineer to perform technical support on our lab instrumentation in our collaborative, high-energy work environment. S/he will be responsible for supporting the installation, modification, upgrade, and validation of lab equipment. Other key aspects of the role include: Support the development, test, and implementation of automated assays to increase the operational and throughput efficiencies in the laboratory in conjunction with technical leadership, regulatory managers, and professional leadership. Work as an independent contributor, working with cross functional teams focused on the development of automated clinical assays. Collaborate with the Bioinformatics and/or Information Technology (IT) team to integrate automated laboratory solution data outputs into departmental systems such as Laboratory Information Management Systems (LIMS) | 4/12/2019 |
| 1081 | Veracyte South San Francisco, CA Lab Assistant - Accessioning AS or BS/bA in life sciences Exp: 1+ years |
The Lab Assistant - Accessioner will perform routine specimen accessioning in accordance with established protocols. The position will process specimens upon receipt in the lab. Additional responsibilities include all related clerical functions, lab maintenance and regulatory compliance tasks. You'll work alongside a highly engaged team of Lab Assistants and Clinical Lab Scientists and will collaborate with other groups across Veracyte. You'll have the opportunity for ongoing training, competency assessments and sharing ideas for continuous improvement in the lab. The work schedule is Tuesday - Saturday. | 4/12/2019 |
| 1082 | Verb Surgical Mountain View, CA Project Coordinator - Contract BS in engineering Exp: 0-5 years |
Support Senior Project Manager on program critical project. Smooth is fast, and we need to go fast. Get to see what it takes to build a surgical robot. Key accountabilities include: Update Program Milestones in a PERT and Gantt charts. Place purchase requisitions. Create graphics to communicate plans, status, risk to the team and management. | 4/12/2019 |
| 1083 | Vericel Cambridge, MA Quality Control BS/BA Exp: 1+ years in cGMP lab |
Quality Control (QC) is responsible for incoming inspection of components and raw materials, plus quality testing (e.g. analytical, microbiological) of intermediate, stability and final product samples to demonstrate that all products manufactured meet standards required for cGMP operations. Various techniques (e.g. assay transfers, validation and qualification of new instrumentation) are utilized within the Quality Control Laboratory to ensure cGMP compliance. | 4/12/2019 |
| 1084 | Veristat Remote Work, Clinical Research Associate (Oncology) BS/BA in life sciences or health care Exp: 1+ years in clinical monitoring |
As a Clinical Research Associate You Will: Manage and monitor clinical trial activity, including conduct of all monitoring visits at investigator sites and ensure all regulatory, ethics and training requirements are met. Responsible for ensuring that data will pass international quality assurance audits and regulatory inspections. Assist the project manager with the preparation of study tools, presentations and training material for investigator meetings, site qualification visits and site initiation visits as required. Work with the Management team in the development/revision and implementation of Standard Operating Procedures as required. Ensure compliance with appropriate Sponsor and Veristat SOP’s, 21CFR/ICH guidelines and applicable regulatory requirements. Ensure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Sponsor and Veristat values. Required to travel 60-80% on average | 4/12/2019 |
| 1085 | Veristat Montreal, Qu Cliniacl Research Associate BS/BA in life/health sciences Exp: 1+ years in clinical monitoring |
As a Clinical Research Associate You Will: Manage and monitor clinical trial activity, including conduct of all monitoring visits at investigator sites and ensure all regulatory, ethics and training requirements are met. Responsible for ensuring that data will pass international quality assurance audits and regulatory inspections. Assist the project manager with the preparation of study tools, presentations and training material for investigator meetings, site qualification visits and site initiation visits as required. Work with the Management team in the development/revision and implementation of Standard Operating Procedures as required. Ensure compliance with appropriate Sponsor and Veristat SOP’s, 21CFR/ICH guidelines and applicable regulatory requirements. Ensure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Sponsor and Veristat values. Required to travel 60-80% on average | 4/12/2019 |
| 1086 | Vicarious Surgical Charlestown, MA Quality Engineer BS/BA in engineering Exp: 0-4 years |
Reporting to the Director of Quality Systems, as a Quality Engineer you will help develop, maintain and enforce all aspects of the quality system from the ground level. The quality engineer will work alongside and in parallel with the product development, manufacturing and regulatory teams, improving what we already have and imagining what we don’t. We are looking for talented quality engineers who are excited to lead and assist in the development and maintenance of Vicarious Surgical’s quality system. Support ISO, and MD certification process and compliance to FDA regulations by leading and/or assisting in the development, implementation, monitoring, enforcement and improvement of the quality system. Prepare, evaluate and critique technical documentation including design justifications and rationales based on sound scientific or engineering principles. | 4/12/2019 |
| 1087 | Viracor Eurofins Lee's Summit, MO Research Scientist I BS/BA Exp: 0-3 years lab experience |
The Research Scientist is primarily responsible for conducting research, development, validation and execution of assays to meet the development requirements within corporate/client timelines and cost objectives. Learn new techniques and instrumentation, Implement research plans, designs and testing protocols , Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results , Keep accurate documentation of all research project steps according to Viracor Eurofins regulatory guidelines | 4/12/2019 |
| 1088 | Viracor Eurofins Lee's Summit, MO Quality Assurance Specialist I HS Diploma Exp: 1-2 years in regulated environment |
The position is primarily responsible for Quality Management System (QMS) activities and compliance with applicable regulatory requirements by ensuring the effectiveness of the QMS in meeting its stated goals and objectives. This position is also responsible for the management and maintenance of the electronic document management system, including training staff on document control processes and procedures. This position is also responsible for managing both paper and electronic records to ensure that controlled records are created, identified, changed, reviewed, retained, stored, and maintained in a manner that meets requirements. | 4/12/2019 |
| 1089 | Viracor Eurofins Lee's Summit, MO Laboratory Data Entry I HS Diploma Exp: 0-2 years |
The Laboratory Data Entry Associate is primarily responsible for performing duties related to accessioning and data entry with a high degree of proficiency. Duties include: Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other specimen tracking system. Examine samples for accuracy and other requirements (sample type, volume, etc.). Make appropriate internal or external contact to resolve patient demographic issues or discrepancies | 4/12/2019 |
| 1090 | Viracor Eurofins Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in sciences Exp: 1+ years lab experience |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. Duties include: Perform laboratory assays in accordance with Viracor-IBT’s standard operating procedures. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain adequate inventory of supplies, reagents and materials. | 4/12/2019 |
| 1091 | Viracor Eurofins Lee's Summit, MO Clinical Laboratory Scientist (CLS) Coordinator BS/BA in sciences Exp: 1+ years clinical lab experience |
The CLS Coordinator is primarily responsible for coordination of designated operations and/or projects within the clinical laboratory. Responsibilities include: Demonstrate outstanding competency within all trained areas of the Clinical Laboratory Scientist. Evaluate and maintain inventory to ensure continuous service to the clients without creating over-stock. Assist Supervisor or Manager in overseeing the maintenance and record keeping for all instrumentation within the section. | 4/12/2019 |
| 1092 | Viracor Eurofins Lee's Summit, MO Research Technician BS/BA in sciences Exp: 1+ years lab experience |
The Research Technician is primarily responsible for performing laboratory tests and analyses under the direction of a lab manager or research scientist. Duties include, but are not limited to, specimen management, specimen pipetting, instrument operation/maintenance, data entry, specimen storage, following Standard Operating Procedures (SOPs) and ensuring all laboratory equipment and work areas are clean, sterile, and in proper working order. Applicant may be responsible for calibration of instruments and conducts routine tasks as directed. Works under moderate supervision with some latitude for independent judgment. | 4/12/2019 |
| 1093 | Virbac St. Louis, MO Pharmaceutical Operator - Level 1 HS Diploma Exp: 1-3 years in production |
Operate filling and packaging production unit for FDA and EPA regulated and less regulated pharmaceutical products. Assignment includes: Organize activity for production, preform equipment set-ups and adjustments, preform line clearances, and monitor key lines. | 4/12/2019 |
| 1094 | Vyaire Medical Irvine, CA New College Graduate: Project Manager BS in engineering or project managemetn Exp: 0 years (new grad) |
The Project Manager function provides project support within a specialty R&D Engineering organization for new product implementation projects, improvement projects, and line extensions. The Project manager leads cross-functional team resources throughout the project life cycle and is accountable for meeting the agreed upon project scope, schedule, and budget within the directions of the Design Control Procedures. The Project Manager collaborates with internal cross functional resources and external partners (such as suppliers, vendors, testing labs and services) to properly staff their project and manage project risk. | 4/13/2019 |
| 1095 | Vyaire Medical Irvine, CA Graduate Program: Electrical Engineer BS/BA in electrical engineering Exp: 0-2 years |
We are looking for an Electrical Engineer Technician to join our Electrical Engineering team. In this role you will be responsible for sustaining activities of medical critical-care/home-care ventilator products. Duties include: Implement design updates for obsolescence of components, circuits, modules, power supplies, displays, etc. Perform root-cause analysis of production and field failures.. Ensure technical specifications meet product requirements as well as regulatory compliance and best design standards. Adhere to and improve documentation procedures in compliance with established Quality System and procedures and applicable domestic and international regulations. Perform design verification & validation. | 4/13/2019 |
| 1096 | Vyaire Medical Palm Springs, CA New College Graduate: Supply Chain - Operations BS/BA in engineering Exp: 0-2 years (new grad) |
The Graduate Program (GP) is intended to foster a pipeline of employees that deliver business critical results through outstanding performance, either as an individual contributor or as a future leader. As a member of the GP, you will have a unique opportunity to develop a broad knowledge base and skillset by working in one of the functional areas described below. GP participants will be paired with an mentor that will provide coaching and general guidance throughout the duration of the program, as well as a Functional Manager that will provide additional coaching, support and training. The functional manager will provide the goals and objectives for the position. The GP is intended to allow the graduate to learn the business and after 18 months within the program, potentially transition into another function and expand your career at Vyaire on candidate preference and organizational needs. | 4/13/2019 |
| 1097 | Vyaire Medical Irvine, CA New College Graduate: Complaint Analyst BS in engineering, chemistry, or life sciences Exp: 0-2 years (new grad) |
As a compliant analyst you will: Follow written procedures and standard work instructions to intake and process complaints. Collect basic information from customers and the knowledge gained from their specific customer experience. Forward information to appropriate internal parties as defined in written procedures, including complaint assessment based on formal flow charts, documentation and product knowledge. Prepare and submit USFDA’s MedWatch 3500A report, Health Canada’s MDPR, and/or EU’s MDV report as needed. etc. | 4/13/2019 |
| 1098 | TA Instruments New Castle, DE Manufacturing Engineer BS in mechanical engineering or related Exp: 1-3 years |
This person would be responsible for the manufacturing engineering activities of development and production programs through: the application of engineering procedures, which may involve theoretical and experimental investigation, technical direction and coordination, conception and planning of resources to support hardware requirement and; the analysis, evaluation and solution of technical problems encountered in the application of manufacturing methods, facilities, processes, materials and tooling incident to the fabrication and assembly of high technology instruments. | 4/13/2019 |
| 1099 | WAVE Life Sciences Lexington, MA Process Engineer I BS in chemical engineering Exp: 1-3 years in cGMP |
Working at the direction of the engineering leader, supports the implementation of production procedures to optimize manufacturing processes in a GMP environment. Assists with production process and/or scale-up. Assists manufacturing in problem solving with regards to equipment and systems. Collaborates with functions such as Process Development, Facilities, Quality, Supply Chain, etc. Oligonucleotide production process scale up by acting as a liaison between the Process Development and the Manufacturing teams. Support manufacturing operations and attend any equipment, process related technical issues. Troubleshoot production equipment and implement solutions. | 4/13/2019 |
| 1100 | Westat Rockville, MD Research Assistant BS in health or social sciences Exp: 1-3 years health related/research environment |
Westat is seeking a research assistant to provide patient registration support for a major National Cancer Institute contract. The primary function of this role is to set up and test patient enrollment forms in the patient registration system that enrolls patients onto oncology clinical trials. These services are provided Monday through Friday from 9:00 AM to 5:30 PM Eastern time. This position is located in our Rockville, MD office. Duties include: Setting up and testing patient enrollment forms in the patient registration system. Writing and testing logic checks. · Collaborate with the organizations leading the protocol to ensure accurate and timely availability of the forms in the system. | 4/13/2019 |
| 1101 | West-Ward Pharmaceuticals Cherry Hill, NJ Quality Lab Associate I BS/BA in microbiology or biology Exp: 0-2 years pharma experience |
Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. Responsibilities include: Ensure Environmental Monitoring (EM) of the facility’s controlled areas is performed as required. Document EM testing into the EM database prior to incubation, ensure samples are correctly incubated, and record sample results in the EM database following incubation. Compile trending data for EM testing to support investigations. Audit personnel aseptic technique in controlled areas including during process simulations (media fills). | 4/13/2019 |
| 1102 | Wright Medical Alpharetta , GA Assoc Product Development Engineer BS in mechanical or biomedical engineering Exp: 1-2 years in product development |
This entry level engineering position supports the design, development, and evaluation of new product concepts, as well as the redesign or enhancement of existing products. The position may also involve the development of assembly processes and support of equipment and fixtures. Duties include: Writing test protocols and reports. Perform product testing. Assemble prototypes for test and evaluation of new and existing medical devices. Provide technical engineering assistance and interpretation to other departments | 4/13/2019 |
| 1103 | Wright Medical Sacramento, CA Associate Sales Representative, Upper Extremities BS in related discipline Exp: 0-2 years |
This is an entry level sales position that will require you to learn our products, market and industry. This role will initially support our Hand, Wrist, Elbow and Biologics portfolio and may grow into selling the shoulder portfolio. Through determination, networking and market data, this position will seek out surgeons to educate, promote, market and sell these products in assigned geographic location. You will: Conducts regular sales calls in person to develop customer relationships and follow up on leads in order to promote, market and sell products.Prospects for new accounts and seeks opportunities to increase sales with existing customers.Listens to customer needs and suggests appropriate products/solutions. | 4/13/2019 |
| 1104 | Wright Medical Memphis , TN Assoc Global Demand Planner BS/BA in finance, supply chain, or related Exp: 0-1 years |
The Global Demand Planner will proactively analyze, recommend and challenge finished goods unit forecasts, inventory policies, and safety stock strategies based on market demands and business goals. This individual will also be responsible for facilitating proactive, cross-functional management of Global Supply Chain investments through Life Cycle Management (LCM) in the product development process. You will: Deployment of the optimum techniques to improve forecast accuracy given the demand stream characteristics observed. Identify and analyze demand trends and incorporate in forecasting, and facilitate safety stock strategies with newer brands to achieve inventory objectives for assigned products. | 4/13/2019 |
| 1105 | Wright Medical Alpharetta , GA Cartiva Quality Control Inspector HS Diploma, BS/BA Exp: 1+ years in FDA/ISO environment |
The Quality Inspector is responsible for performing inspection activities of both sterile and non-sterile products to ensure compliance to current specifications and procedures. Activities include Device History Record review, examination of supplier provided data, labeling and product acceptance, ensuring nonconforming product is identified, documented and segregated from acceptable product. Maintain control of quarantine area to ensure unintended use. This position is also responsible for handling and segregation of returned product. | 4/13/2019 |
| 1106 | WuXi AppTec St. Paul, MN Associate Quality Assurance Specialist BS/BA Exp: 0 years |
The Associate Quality Specialist is responsible for ensuring GLP studies, GMP testing, and GMP manufacturing activities are executed in accordance with the appropriate regulatory bodies and internal procedures. Responsibilities include: Ensures compliance to Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP). Perform job specific tasks in compliance with applicable Regulations, International Standards, and WuXi AppTec Policies and Standard Operating Procedures.Reviews final reports (GLP), batch records (cGMP), Certificates of Analysis (GMP), and/or other necessary documentation, as appropriate to the defined Quality Role within the applicable regulation(s). | 4/13/2019 |
| 1107 | WuXi AppTec St. Paul, MN Associate Sample Coordinator AS/AA in biosciences Exp: 1+ years lab experience |
This position is responsible for processing samples for assigned tests in compliance with GLP, GMP, and ISO standards including test sample log in and accountability. Responsibilities include: Provides operational support for Sample Preparation/Sample Receipt activities, including but not limited to media preparation, cleaning, equipment/materials staging, and use of aseptic technique. Receives incoming samples and reviews them for integrity to ensure they are sufficient for testing. Coordinates time and resources to ensure efficient processing of incoming projects. Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required. | 4/13/2019 |
| 1108 | WuXi AppTec St. Paul, MN Associate Chemistry Specialist BS/BA Exp: 0 years |
The Associate Chemistry Specialist will perform a variety of testing preparation techniques, including sample preparations/extractions, reagent preparation procedures and solvent exchange. The position will also include performing a variety of routine benchtop and analytical analysis. Responsibilities include: Perform benchtop testing, including pH, non-volatile residue, conductivity, and other entry level techniques. Extract test samples using soxhlet, submersion, and fluid path techniques. May assist scientists and other specialists with various supporting procedures, such as sample vialing, reagent preparation, and solvent exchange. | 4/13/2019 |
| 1109 | WuXi AppTec Philadelphia, PA Laboratory Technician II BS/BA in biological sciences or related Exp: 1-2 years |
Performs Cell Culture and Cell-Based assays (BSL2 and BSL2+) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Completes batch records and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs daily work activities with minimal supervision. | 4/13/2019 |
| 1110 | WuXi AppTec Philadelphia, PA Associate Warehouse Coordinator HS Diploma Exp: 1+ years |
Performs all aspects of receiving and internal deliveries to end users. Responsibilities include: Responds to receiving, delivery requests in a timely and professional manner. May help with Shipping as needed. Contacts vendors to retrieve proper quality documentation such as: Certificate of Analysis. Participates in End of Month (EOM) inventory. May participate in preparing shipping paperwork with accuracy, as well as completes shipping transaction in appropriate system (UPS etc.) as needed. | 4/13/2019 |
| 1111 | WuXi AppTec Philadelphia, PA Research Associate, Analytical Development - Molecular Biology BS/BA in biological sciences or related Exp: 1+ years |
Performs research & development activities and assay validations as required under direct supervision. Drafts test methods and clearly documents all experiments according to SOPs and cGMP guidelines. Performs laboratory maintenance duties. Works closely with Testing Operations during assay transfer and validation activities. | 4/13/2019 |
| 1112 | WuXi AppTec Plainsboro, NJ Research Associate II AS or BS/bA in life sciences Exp: 1-3 years |
WuXi AppTec is searching for a Research Associate in a growing Immuno Oncology Group. Responsibilities include: Conducting in vivo pharmacology experiments for preclinical contract research with minimal supervision. Assisting and performing efficacy and PK-PD studies and developing new in vivo/ ex vivo assays and models with minimum supervision, as needed. Help to design, optimize and execute of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. syngeneic and xenograft tumor model, acute and chronic autoimmune/inflammatory conditions, and analyses and reporting of experiments or implantation, blood/tissue collection, etc | 4/13/2019 |
| 1113 | Xbiotech USA Austin, TX Manufacturing Associate I-Downstream BS/BA in life sciences or health care Exp: 0-2 years |
Perform all activities associated with supporting downstream production of our clinical and commercial operations in a GMP manufacturing setting. One must be flexible to work multiple shifts and weekends and/or overtime as needed. Perform downstream operations including: column chromatography, sterile filtration. and viral filtration. Assist manufacturing team in final drug product processes (Formulation and Aseptic Fill). Perform setup and operation of chromatography processing equipment according to established Standard Operating Procedures (SOP’s) and/or Master Production Records (MPR’s). This equipment may include but is not limited to AKTAprocess skids. | 4/13/2019 |
| 1114 | Xellia Pharmaceuticals Raleigh, NC Production Operator I HS Diploma Exp: 1-3 years |
The incumbent will be responsible for the operation of various types of processing and test equipment in environmentally controlled areas per Standard Operating Procedures. This includes but is not limited to: steam sterilizers, vial/parts washers, dehydrogenation tunnel, formulation tanks and associated equipment, analytical balances, pumps, filter test equipment and other associated equipment. As part of these responsibilities, the Production Operator I monitor cycles and reviews data to ensure requirements have been met and completes all associated documentation. | 4/13/2019 |
| 1115 | XenoTech Kansas City, KS Research Assistant BS in chemical or biological sciences Exp: 1+ years lab experience |
The Research Assistant assists with routine laboratory functions including diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintains inventory of supplies, and various other responsibilities. These include: Design and conduct routine and atypical experiments. Maintains laboratories and equipment and performs minor repairs on equipment, with supervision. Maintains appropriate logs, records and study notebooks. Adheres to Good Laboratory Practice regulations and Sekisui XenoTech safety policies and procedures | 4/13/2019 |
| 1116 | Zimmer Biomet Palm Beach Gardens, FL Mfg Engineer BS in engineenering Exp: 0-3 years |
The manufacturing engineer is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. Duties include: Maintaining and improving controlled technical documents such as prints, procedures, bill of materials and routers. Supporting a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc. Conducting feasibility study to estimate product cost and analyze capital equipment, capacity, and capability requirements. | 4/13/2019 |
| 1117 | Zimmer Biomet Parsippany, NJ Development Engineer BS from ABET accredited school in engineering Exp: 0-3 years |
Responsible for the design, development, and processing of implants and instruments. Work is expected to encompass both the development of new products and maintenance of existing products. Position will lead development aspects of the project as a core team member. Responsibilities include: Leads the development of new products and manufacturing processes. Identifies all tasks required to complete project assignments according to Design Control procedures. Prepares work plans outlining estimated manpower requirements and development costs. Recommends project budget and schedule to carry out programs on a timely basis. | 4/13/2019 |
| 1118 | Zimmer Biomet Warsaw, IN Quality Engineer BS in engineering Exp: 0-3 years |
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Duties include: Formulates procedures, specifications, and standards for Zimmer products and processes. Develops and implements corrective/preventative action plans. Collects and analyzes data for gauge and product evaluation. Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products. | 4/13/2019 |
| 1119 | Steris St Louis, MO Entry Level Manufacturing Coordinator Vocational or AS degree Exp: Entry Level |
Responsible for knowing, understanding, and supporting the STERIS Safety Philosophy. Provides accurate and timely documentation and support to all Production Operations departments. Analyze inventory reports to assure accurate reporting of labor and materials. Compiles and reviews batch records for completeness. Identifies and corrects inaccuracies prior to forwarding to Quality Systems. Accountable for delays in release and meeting expectations for release times. Mentors plant employees and supervisors on documentation compliance and inventory accuracy. Proper execution of assigned duties has a direct impact on the efficiencies of the plant and the final customer’s satisfaction. Contributes to lean transformation by participating on rapid improvement implementation teams. Other duties assigned by Supervisor to contribute to the support of all Production Operation departments. | 4/5/2019 |
| 1120 | Steris Chicago, IL Sterile Processing Technician HS Diploma or GED Exp: 0-1 years in SPD |
Provides on-site support for the reprocessing of surgical instruments and trays to contracted facilities in compliance with the Department of Health, TJC, OSHA, CDC, AAMI and AORN standards and facilities goals and policies. Position level will be determined by previous job related experience, performance and certification requirements. | 4/5/2019 |
| 1121 | Stratos Genomics Seattle , WA Lab Assistant –Nanotechnology/ Molecular Biology BS/BA in bioengineering, biochemistry, or related Exp: 1+ years lab experience |
The laboratory assistant will have opportunities to gain experience with meaningful data analysis, thinking critically & objectively, sample preparation, SOP optimization, and experimental design. Responsibilities include: Inventory, prepare, and maintain components for the sequencing platform. Maintain a clean, safe, and organized laboratory. Perform experiments on the sequencing platform as outlined by manager. Communicate results, status updates, and SOP deviations clearly and effectively to manager. Understand the purpose of each procedural step and how it affects downstream results. | 4/5/2019 |
| 1122 | Stratos Genomics Seattle , WA Research Associate—Molecular Engineering BS/BA or MS in chemistry, chemical engineering or related Exp: 1-2 years lab experience |
Candidates will be involved in synthesizing our unique building blocks for our novel DNA sequencing technology, Sequencing by Expansion, developing and optimizing synthesis protocols as well as proposing and executing innovative experiments to push our technology forward. Functions include: Plan and execute complex projects including; communicating schedule, identifying necessary resources, implementing steps, and keeping projects on track. Design and execute well-controlled experiments. Perform data analysis and protocol development. | 4/5/2019 |
| 1123 | Stratos Genomics Seattle , WA Scientist/Research Associate, Nanotechnology/Molecular Biology BS/BA or MS in chemistry, chemical engineering or related Exp: 1-5 years lab experience |
Candidates will be involved in developing and optimizing the nanopore-based detection platform for our novel DNA sequencing technology, Sequencing by Expansion. The position primarily involves hands-on laboratory work as individual contributors and as a part of a development team. The Research Associate will work directly with founding Technical and Scientific Officers, Scientists, and Research Associates in a dynamic start-up biotech environment. Responsibilities include: Plan and execute complex projects, communicating schedule, implementation steps, and progress, Design and execute well-controlled experiments, Perform data analysis and protocol development, Identify problems and propose solutions | 4/5/2019 |
| 1124 | Stryker Portage, MI Design Engineer – Application Software - NSE BS/BA in computer sciences, engineering or related Exp: 0-5 years in design engineering |
As a Design Engineer (Application Software) is responsible for the software system design of their product or subsystem from start to finish. You will provide design creation concepts to a new product development project to ensure design alignment with overall scope. Working in a cross functional team is a guarantee. Navigating your way through technical design discussions and ensuring appropriate analysis of decisions through application of sound engineering judgment and risk analysis will be the normal. | 4/5/2019 |
| 1125 | Stryker Virtual, MN Manufacturing Engineering Technician AS or BS/BA Exp: 0-2 years |
Focus on manufacturing floor support. Also, work with Operations/Process Development teams (assembly staff, engineers, and management) to ensure that production objectives are achieved with a constant drive for continuous improvement. These objectives include: aid in the efficient implementation and analysis of processes, process flow and equipment. Work with engineers on continuous improvement opportunities for facility layout and production flow optimization. | 4/5/2019 |
| 1126 | Stryker Fort Lauderdale, FL Assembly Technician I in Fort Lauderdale HS Diploma or GED Exp: 1+ years |
Responsible for providing assembly, testing and facility support for all our production efforts. Assembly of fabricated parts and assemblies at work stations along with testing of final assemblis to meet tolerances and product specifications. Uses hand tools and power tools to assemble units according to assembly / work instructions. Relies on instructions and pre-established guidelines to perform the functions of the job. Basic skills with moderate level of proficiency. Works under minimal supervision, requires exercising some independent judgment and may be called upon to provide training to new employees | 4/5/2019 |
| 1127 | Stryker Cary, IL Marketing Product Associate BS/BA Exp: 0-3 years in marketing/sales |
The Marketing Product Associate manages product line initiatives including, sales support and communication, marketing collateral development, market research, competitive intelligence, technical support and marketing plan development. Responsibilities include: Management of current marketing platforms that support and enable our sales team. Collaborate with internal teammates from across the organization on product management initiatives such as cost savings initiatives and product enhancements. Support implementation of Sage interventions at the hospital level through on site education and sales rep support. | 4/5/2019 |
| 1128 | Stryker Kalamazoo, MI Additive Design Engineer BS in mechanical engineering or related Exp: 0-2 years |
The Additive Design Engineer is a key member of the AO Additive team, focused on developing additive-enabled product designs along with divisional R&D and AO counterparts. The Design Engineer will work as an embedded member of the divisional product development teams and work hand-in-hand on design concepts that lead to new products to be launched from the AO Additive New Product Introduction team. Key responsibilities include: Collaborate with divisional R&D and AO to understand product requirements and use additive design methodologies to improve performance of new and existing products. Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures. | 4/5/2019 |
| 1129 | Sun Pharma Billerica, MA QC Analyst I BS/BA in sciences Exp: 0-2 years |
Performs various quality control tests on raw materials, in-process and final product using established Standard Operating Procedures (SOPs) and working in accord with current Good Manufacturing Practices (cGMPs). Responsibilities include: Performs analytical quality control tests and assays for release, stability, and complaint follow-up on raw materials, in-processing and final products. Performs the quality control tests and assays and monitors equipment (i.e. water systems, environmental chambers). Maintains records of the data in manual logs. Basic training in use of Single Wavelength Ultraviolet/Visible (UV/VIS) Spectrometer, Conductivity Meter, pH meter, Dissolved Oxygen Analyzer, Karl Fischer Titrator, High temperature furnaces and oven, Fume Hoods, Stir/Hot Plates, Propane Burners, Compressed Gas Regulators and Cylinders | 4/5/2019 |
| 1130 | Surmodics Eden Prairie, MN R&D Development Technician Associates Exp: 0-10 years in medical devices |
Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. Provide technical support for catheter-based medical device design and development at SurModics, Inc. Responsibilities include: Fabricate device prototype components and assemblies to assist in the design and development of new catheter-based products. Refine processes in the development of new products while working with the engineering team. Assist with developing and troubleshooting manufacturing processes and equipment, including fixture design and equipment qualifications. | 4/5/2019 |
| 1131 | Surrozen South San Francisco, CA Research Associate, Protein Sciences Group - Molecular Biology/Protein Expression BS/BA or MS in biology, biochemistry or related Exp: 0-2 years in research |
This position is a great opportunity for both experienced associates to expand their skills to accelerate therapeutics discovery for regenerative medicine, and for energetic new graduates with passion for Biotech research in an industrial setting. Responsibiliteis include: Produce recombinant DNA clones using state-of-the-art molecular biology protocols and perform routine plasmid preps. Perform plasmid-transfection into mammalian cells for small to medium scale recombinant protein expression. Follow SOPs and perform modern purification techniques like affinity, and SEC chromatography on AKTA-FPLCs to produce a wide variety of recombinant proteins including antibodies and antibody-based constructs. | 4/5/2019 |
| 1132 | Sword Diagnositcs Chicago, IL Research AssociateI, Product Applications BS/BA in biology or related Exp: 1-3 years lab experience |
Your main responsibilities will be to perform functions in support of Product Application Scientist(s) and other individuals as needed, perform common laboratory testing (including ELISA) using established protocols, prepare buffers and other chemical solutions as needed and use proper personal protective equipment (PPE) and good aseptic technique to handle biological (including human) samples. On a day-to-day basis, you will be expected tosuggest, plan and carry out studies with guidance of supervisor, record data for evaluation, analyze results with guidance of supervisor and assist other lab personnel as needed, maintain organized records of studies performed, and other duties and responsibilities as assigned. | 4/5/2019 |
| 1133 | Syapse San Francisco, CA Associate QA Engineer - Contract BS/BA Exp: 0-1 years in software QA testing |
As an Associate QA Engineer in the System Engineering team, you will work closely with our team to validate the platform and test infrastructure that helps make the data more accessible. Duties include: Work on a System engineering team performing system testing on Syapse products. This will include manual testing and developing automation of UI/Integration tests. Documents results; offers observations or improvements after analysis of test results and overall product quality. Collaborates with the development team on bug fix verification and validation (regression testing) | 4/5/2019 |
| 1134 | Synedgen Claremont, CA Chemical Synthesis Associate BS/BA in chemistry or related Exp: 0-3 years |
Duties as a chemical synthesis associate include: Manufacture active pharmaceutical ingredients, drug products, and medical devices. Ensure compliance with the quality system, regulations, and safety procedures. Maintain instrumentation and facilities in proper operating conditions and cleanliness. Manufacture pilot stage liquid medical device products. Perform analytical testing for manufacturing, qualification, and validation activities. | 4/5/2019 |
| 1135 | Synexus Austin, TX Research Assistant/Medical Assistant BS/BA Exp: 0-1 years |
Assists the Clinical Research Coordinators in their responsibilities by doing the following: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Perform basic lab procedures, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; and Utilizes universal precautions when in contact with possible contaminants, obtains and maintains certification for the handling of potential infectious fluids and maintains safety for self, patient and others around them; | 4/5/2019 |
| 1136 | Synteracts Morrisville, NC Biostatistician MS in statistics, math or related Exp: 0-2 years |
The Biostatistician performs the data analysis with supervision for assigned clinical studies. Works closely with the clinical team, project Sponsor, clinical data manager, other statisticians and programmers to analyze and present the data based on Sponsor specifications. He/she develops, creates, verifies/validates and maintains the programs for assigned projects in compliance with standard operating procedures. Maintains the full-scope of responsibility for assigned projects: ensures on-time delivery, communicates the status of projects to internal teams and project Sponsors, executes quality assurance procedures on work produced by others and ensures statistical analysis is being done according to specifications. | 4/5/2019 |
| 1137 | Synthego Redwood City, CA Laboratory Associate, Night shift AA in chemistry or biology Exp: 1-3 years |
. As a Lab Associate at Synthego, you will join our growing operations team and have direct responsibility for the synthesis and purification of our gRNA products. This role requires a strong attention to detail, a desire to learn and adapt to new processes, and familiarity with safe laboratory practices. This role will combine hands-on laboratory protocols with advanced automation to ensure the timely delivery of high quality products to our customers. Duties include: Synthesize oligonucleotides by following established SOP’s . Practice continuous improvement by contributing ideas and suggestions to new and existing processes. Operate complex robotic systems to manage liquid product through a highly automated workflow | 4/5/2019 |
| 1138 | System1 Biosciences San Francisco, CA Research Associate BS in biological sciences Exp: 0-1 years |
We are seeking a highly motivated and responsible technician to join our team under a full time or part-time contract. Responsibilities would include: Preparation of biological reagents to support cell culture. Sterilization of culture vessels and associated components. Maintenance and troubleshooting of automation equipment. Must be available for limited and compensated work on weekends. | 4/5/2019 |
| 1139 | System1 Biosciences San Francisco, CA Lab Aid BS in biological sciences Exp: 0-1 years |
We are seeking a highly motivated and responsible Lab Aid to join our team under a full time or part-time contract. Responsibilities include: Ordering lab consumables and reagents. Organizing shipping and receiving of consumables and biological samples. Stocking and managing lab inventory. Managing outside vendors for a range of different services (e.g., LN2, CO2, dry ice, lab coat laundry). | 4/5/2019 |
| 1140 | Taconic Germantown, NY Animal Care Technician HS Diploma or GED Exp: 0 years |
The Animal Care Technician 1 will be responsible for providing general support to animal care technicians in a barrier by completing tasks related to supply import, export, general barrier cleaning and basic animal husbandry. Responsibilities include: Ensuring high standards of animal welfare are met. Reporting inhumane treatment regarding animal care, use or abuse. Documenting work performed according to SOP’s. Ordering supplies, loading and unloading containers or supply cylinders. | 4/5/2019 |
| 1141 | Takeda Thousand Oaks, CA Utility Technician HS Diploma or GED Exp: 0-3 years in biotech maintenance or manufacturing |
Under general to minimal supervision, the Utilities Technician will be a skilled craftsperson responsible for performing installation, troubleshooting, maintenance, repair, testing, monitoring and documentation/logs of a wide variety of office, utility and facility equipment/systems used in manufacturing plants, utility plants, analytical labs, and office areas. The Utility Technician will be responsible for completing various quality system and safety documentation. All work must be completed in a safe (in accordance to HRA, JHA, etc), timely manner according to planning and predefined schedules with minimal impact to production while complying with GMP, SOP, CFR and company regulations. | 4/5/2019 |
| 1142 | Takeda Thousand Oaks, CA Manufacturing Associate I HS Diploma or GED Exp: 0-2 years |
Key responsibilities include: Employee maybe required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include: Identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. Responsible for Room sanitization, wrapping up components, operating autoclave, performing CIP/SIP of tanks, small parts washing. Visual inspection of lyophilized product vials, Visual inspection of empty vials for glass defects, Visual inspection of empty vials for washout defects, visual inspection of rubber stoppers for defects. Record bioreactor, chart recorder readings, alarm response related to the bioreactor, skid performance, inoculums and emergency response during blackouts. etc. | 4/5/2019 |
| 1143 | Takeda Brooklyn Park, MN Laboratory Technician AS in life sciences w/lab coursework Exp: 1-2 years |
Objectives in this position include: Perform supportive activities for general laboratory operations, laboratory equipment preventative maintenance, sample pull, receipt and delivery. Support the Technical Operations group by performing routine laboratory tasks to facilitate the experiments performed by the associates and scientists. Assist in the general organization of the laboratory and perform some basic administrative tasks such as photocopying/scanning and organizing documents and files. | 4/5/2019 |
| 1144 | Takeda Los Angeles, CA Manufacturing Technician II HS Diploma/GED, or AS Exp: HS: 1+ years, AS: 0 years |
This position reports to Weekend Grave (E) shift. This position is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. He/She is expected to fully participate in both departmental projects and any quality working teams which may be applicable. Under the general direction of the manufacturing lead operator and the overall direction of the supervisor, this position shall be responsible for the hands on execution of all activities in the production area. Activities include manual tasks and operation of automated equipment. He/She has sufficient technical and administrative competence to initiate minor revisions to existing documents, to troubleshoot simple existing procedures, and to contribute to continuous improvement initiatives. | 4/5/2019 |
| 1145 | Takeda Thousand Oaks, CA Quality Analyst I AS in sciences Exp: 0-3 years |
The selected candidate is responsible for performing the day-to-day quality operations for the Quality Assurance (QA) department within the Quality organization, including batch record review on the floor and quality inspection activities associated with BAXJECT III processes. Perform the final review of QA Inspection documentation to support Filled Unlabeled Vial (FUV) and Final Drug Product (FDP) release. Identify and assess quality risks in activities and processes according to regulatory agency requirements and guidelines and Takeda quality practices. Initiate and complete event investigations to identify why a deviation occurred and to minimize/eliminate reoccurrence. Revise documents to drive continuous improvement including streamlining processes and maintaining GMP compliance. Support departmental projects and any quality working teams when required. | 4/5/2019 |
| 1146 | Takeda San Diego, CA Research Associate, Antibody Discovery MS in biology, chemistry, or related Exp: 0-2 years |
The candidate will perform complex research assignments and will be responsible for the discovery and engineering of therapeutic biologics including antibodies, fusions and other platforms. The candidate will communicate results within the Biotherapeutic Engineering team and with cross functional project team members. Responsibilities include: Under minimal supervision, execute discovery and lead optimization projects using display platform technologies with high quality and efficiency. Handle large data sets and analyze the data. Identify hits based on affinity, specificity and potency. Isolate DNA/RNA, analyzing sequencing data. Apply knowledge of antibody function and characterization, conduct repertoire analysis, and V region classification | 4/5/2019 |
| 1147 | Talis Menlo Park, CA Research Associate MS in biology or related Exp: 0-3 years |
The candidate will join the Assay Development group in the R&D division where focus is on molecular assays development such as nucleic acid isolation, purification, amplification and labeling technologies. We are seeking talented, motivated individuals to join a collaborative effort to enable development of rapid diagnostic tests of several pathogens from various clinical specimens. | 4/5/2019 |
| 1148 | Talis Menlo Park, CA Firmware QA Engineer I BS or MS in computer science or engineering Exp: 0-2 years |
Candidate will work closely will with firmware engineers to execute and write test cases for qualifying new firmware and software builds. Candidate will perform root cause analysis on test failures and write detailed bug reports. Create test scripts for automation framework for unit, integration, and life cycle test, preferably in Python, is a plus. Experience in ARM, RTOS, I2c, SPI, UART or CAN preferred. | 4/5/2019 |
| 1149 | Tanvex San Diego, CA QC Associate, BioAssay BS in biology, chemistry, or related Exp: 0-2 years in quality control |
The QC Associate is responsible for routine and non-routine product testing using biochemical methods such. Additional responsibilities include assisting with transferring analytical methods from development into the QC laboratory and test method validation; generating test results and reporting results for the assigned GMP testing in a timely and compliant manner; sample coordination, lab equipment maintenance, QC document management and review. Knowledge of performing cell-based assay, immuno-assays, and/or QPCR assays in a GMP environment is essential. | 4/5/2019 |
| 1150 | TE Connectivity Minneapolis, MN Operations Engineering Manufacturing Proesses Rotation Associate BS in manufacturing or mechanical engineering Exp: 0-2 years |
The program consists of four six month rotations in multiple areas where this core process is utilized and accompanied by a robust technical and leadership curriculum. At the conclusion of the two year program, participants will be candidates for leading technical or management roles across the company in this core manufacturing process. Responsibilities may include: Shadowing, assisting and learning from the global leaders of the Compounding Extrusion, and Finishing Center of Excellence (CoE) and the Digital Factory Center of Excellence (CoE). Learning how to connect processes to our digital factory network, extract digital process information, and build improvement plans to act on what the data shows. Learning the Wire and Tubing Extrusion core manufacturing process and being an advocate of sharing best practices from one plant to another. | 4/5/2019 |
| 1151 | TE Connectivity San Jose, CA R&D/PRODUCT DVL ENGINEER I BS in engineering or mechanical field of study Exp: 1-3 years in mechanical design |
R&D Product Development Engineer is responsible for the development and introduction of new medical interventional products. The R&D Engineer will champion the execution of new products that deliver an exceptional customer experience. Additionally, the R&D Engineer will be responsible for managing project costs, issuing quotes to customers, procuring material quotes and interacting with customers. This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS).TE Connectivity’s R&D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. | 4/5/2019 |
| 1152 | TE Connectivity Wilsonville, OR PRODUCTION OPERATOR (FINISHING OPERATOR) HS Diploma Exp: 1-3 years |
TE Connectivity's Manufacturing/Production Teams transform raw materials into finished goods and ensure component flow. They perform changeovers and setups according to production schedule, perform quality checks according to established processes and document the results as required by our quality procedures. Every team member is responsible for maintaining housekeeping and organization of the work area as well as following TE Connectivity's EH&S policies and procedures. | 4/5/2019 |
| 1153 | Tedor Pharma Cumberland, RI Production Technician HS Diploma Exp: 1-2 years production environment |
The Production Technician position performs all tasks involved in the pharmaceutical process following cGMP’s and SOP’s such as wet granulation, dry granulation, tablet compression, encapsulation, tablet coating, packaging and finished product, put product on stability. The position follows standard work methods and practices safe work habits to ensure production is as efficient and safe as possible. Perform hands on R&D process/product scale up and production studies on specifically assigned products and projects. Perform cleanings to rooms and equipment, major and minor cleaning, swabs equipment, cleaning verification, confined space entry, lockout tag out. | 4/5/2019 |
| 1154 | Teligent Buena, NJ QC Chemist I BS in chemistry Exp: 0-3 years in pharma or lab experience |
Provide accurate and timely testing of raw materials, finished product and/or stability samples as assigned. Ensure the safety and reliability of products produced in compliance with quality and regulatory requirements. Essential responsibilities include: Perform quality control testing on raw materials, finished product, pre-approval and commercial stability samples as assigned by the supervisor. Wet and Physical chemistry techniques including but not limited to: Karl Fisher, Viscosity, Microscopy, pH, specific gravity, IR, Specific Rotation and wet chemistry. | 4/5/2019 |
| 1155 | Tempus New York, NY Jr. Clinical Data Abstractor BS or MS in genetics Exp: 0-3 years |
We are looking for Jr. Data Abstractors (JDAs) to join our rapidly growing clinical data team. JDAs will be responsible for reviewing clinical records, structuring key data elements and helping to ensure that clinicians who treat cancer patients have access to meaningful data and insights. Responsibilities include: Extract, structure and analyze data to construct the foundation of a cancer genomics database, Work with multiple data sources to extract information to pull into various reports, Maintain highest quality standards through rigorous QA process to identify and correct mistakes and inconsistencies in abstracted data | 4/5/2019 |
| 1156 | Tempus Chicago, IL QA Coordinator BS/BA Exp: 0-2 years |
As a QA coordinator, your responsibilities include: Report significant investigation/deviation issues and system deficiencies to management, as appropriate. Coordinate the internal document control system of standard operating procedures (SOPs) and other quality documentation. Collaborate closely with those assigned to document control duties in specific departments, as applicable. Perform administrative duties to generate documents as necessary, with inputs from subject matter experts. Proof reads all change documents for proper formatting, correct spelling, punctuation and general accuracy. | 4/5/2019 |
| 1157 | Tempus Chicago, IL Jr. Clinical Trials Data Specialist BS or MS in genetics, or related Exp: 0-2 years |
We are looking for a Jr. Clinical Trials Data Analyst who will work with our clinical and computational biology team on reports for clinical and research use. Responsibilities include: Works collaboratively within cross-functional teams at Tempus (including but not limited to scientists, pathologists, product development) to create customized clinical reports. Analyze patient clinical records and molecular testing results to identify potential clinical trials. Perform critical quality control functions in clinical report workflow. Support ongoing and future projects within the team. | 4/5/2019 |
| 1158 | Tempus Chicago, IL Product Designer (Entry Level) BS/BA Exp: 0-3 years of product design for web applications |
As a Product Designer, you will be responsible for defining the experience of our products. You will be supporting and collaborating with the lead designer on this project and future endeavors. Support user-centered design projects with internal and external stakeholders, including physicians. Define and prototype your solutions, iterating quickly with your cross-functional team of engineers, computational biologists, data scientists, and other designers. Manage timelines in an agile environment to deliver enterprise-grade product | 4/5/2019 |
| 1159 | Tempus Chicago, IL Clinical Molecular Technologist - PM Shift BS or MS in medical technologies, chemistry, or biological sciences Exp: 0-2 years |
As a clinical molecular technologist, you will be responsible for: Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory. Utilize automation and robotics to standardize the discovery pipeline from sample acquisition to sequencing output. Maintain quality metrics and data generation for next-generation sequencing platforms. Work to maintain CLIA/CAP compliance in a novel field | 4/5/2019 |
| 1160 | Tergus Pharma Durham, NC Scientist I, IVRT BS in pharma sciences, chemistry, biology, or related Exp: 1-2 years lab experience |
Responsibilities include: Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP lab, Performs In Vitro Release Testing (IVRT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs. Prepares solutions for IVRT and High Performance Liquid Chromatography (HPLC) analysis such as Mobile Phase and buffer. | 4/5/2019 |
| 1161 | Teva Elizabeth, NJ Quality Analyst I BS/BA in sciences Exp: 1-3 years in QA |
The Quality Analyst I (QA Specialist: Complaint Investigation Support) is responsible for the general oversight of Customer Complaints, Complaint Deviations & CAPAs, and Documentation Change Request/Revision (Protocols, SOPs, Lists, Forms, APR attachments, etc.) associated with departmental procedures. Essential duties include: Receive complaints through the designated software system in a timely manner. In accordance with applicable standard operating procedures (SOPs) categorize the complaint, make appropriate contact with the complainant to obtain information required to properly investigate the complaint and complete the applicable fields in the system to document the activities. Request the return of samples, when required, and determine the necessary actions required to thoroughly investigate the complaint, including but not limited to documenting the information received through interviews with parties impacted by the complaint submission, documenting the information received from submitted documentation and field samples, submitting samples to the Quality Control laboratory for analysis, sending samples out to outside vendors for analysis, requesting information for various departments to support the complaint investigation and coordinating the complaint investigation with impacted departments, including other Actavis sites and contract vendors. | 4/5/2019 |
| 1162 | Teva Salt Lake City, UT Laboratory Tech I HS Diploma Exp: 1+ years in manufacturing lab |
Under close supervision, performs limited or routine testing of raw materials, components and finished products, prepares standard and sample solutions, and maintains appropriate sample testing documentation. Duties include: Learns to perform sampling and in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). Learns to conduct routine analysis of raw materials (identification and assay) using Ultra violet/infrared (UV/IR), thin layer chromatography (TLC) and automatic titration. Learns to dispose of acid waste and organic solvent waste according to Environmental Protection Agency (EPA) regulations, and transfers gas cylinders as instructed by management. | 4/5/2019 |
| 1163 | Teva Salt Lake City, UT Quality Control Analyst I BS/BA in sciences Exp: 1+ years lab experience |
Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments. Duties include: Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus, particle size analyzer, Instron, Densitometer, Rheometer, viscometer (LV/RV/Cone and Plate), pH meter and analytical balance. Prepares standard, sample, and buffer solutions as required by test methods and performs all necessary calculations associated. Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by SOPs. Cleans, maintains and calibrates laboratory equipment to ensure compliance with current Good Manufacturing Procedures (cGMP). | 4/5/2019 |
| 1164 | Teva Salt Lake City, UT QC Planner-Quality Lab Planner BS/BA in chemistry or related Exp: 1+ years in QC Lab |
Responsible for prioritizing and coordinating testing of raw material, in-process, bulk product, packaged finished product, stability samples, micro samples, and/or water samples for analysts, as needed to support manufacturing. Assist in the checking/auditing of raw data and various logs generated by analysts. | 4/5/2019 |
| 1165 | Teva West Chester, PA Biological Researcher I BS or MS in related field Exp: BS: 1-2 years, MS: 0-1 years |
Responsible for Operations fo GLP Fill-Finish manufacturing facility for parental DP's. Perform all activities supporting the production of sterile DP, including but not limited to: operation of the filling line, filter integrity testing, preparation of components and supplies including use of the autoclave, documentation (batch records, logbooks, etc.), routine in-process analytical testing, visual inspection, and cleaning of critical process equipment. Support supply chain logistics to enable early Toxicology and Clinical DP manufacturing including materials movement, change controls, relevant documentation readiness through interface with internal or external CMO sites. | 4/5/2019 |
| 1166 | Teva West Chester, PA Research Associate BS or MS in biology or related Exp: BS: 1-2 years, MS: 0-1 years |
Perform research laboratory tasks and experiments, making detailed observations, and analyzing data under the supervision of a supervisor. Responsible for performance of assays for validation of test methods according to pre-approved validation plans and acceptance criteria and in accordance with relevant method SOPs and most recent regulatory guidelines. Responsible for sample handling and performs sample analysis from pre-clinical or clinical studies in accordance with the approved method SOPs. Maintains laboratory equipment and inventory levels for laboratory supplies. May also write summaries, reports, and protocols regarding experiments. | 4/5/2019 |
| 1167 | Teva Cincinnati, OH Quality Analyst I BS/BA in sciences Exp: 1-3 years in pharma or manufacturing |
Responsible for reviewing documentation for batches that are manufactured and packaged. Assure compliance with cGMP before being released for further processing, packaging or commercial market. Review completed manufacturing and packaging documents, as well as laboratory test specification sheets. Ensure all pertinent information is compiled, reviewed and approved prior to any product disposition. Identifies improvements/new procedures/ compliance gaps based on applicable regulations. Assign QA status (Release/Reject/Quarantine/Impound) to work-in-process and finished product. Investigates and troubleshoots all routine problems which occur during work assignments. | 4/5/2019 |
| 1168 | Thermo Fisher Florence, SC Scientist 1 -PRD BS/BA in chemistry or sciences Exp: 0-3 years |
This is an entry-level opportunity to support the Process R&D efforts at the Florence, SC facility. Responsibilities include: Conduct chemical experiments in laboratory as instructed by a senior staff supervisor. Accurately record and report experiments and scientific findings per assigned departmental standards in a timely manner to meet project objectives. Maintain a clean and safe work environment within the framework of OSHA, cGMP, safety regulations and Thermo Fisher SOPs | 4/6/2019 |
| 1169 | Tmunity East Norriton, PA Associate Process Development Scientist BS or MS in biochemical engineering, chemical engineering, or biotechnology Exp: 0-3 years lab experience or process development |
The Associate Process Development Scientist will perform studies to develop and optimize the manufacturing process of gene-modified cellular products to support the company’s development programs. Under the supervision of Sr. Scientist: Perform development studies including optimization of cell isolation, cell culture, cell transduction and cell cryopreservation processes. Evaluate innovative manufacturing & analytical technologies for engineered T cell manufacturing to improve process efficiency. Author technical and scientific documents including but not limited to SOPs, Master Batch Records, study protocols and reports. | 4/6/2019 |
| 1170 | Tocagen San Diego, CA QA Associate - Document Control BS/BA in life sciences Exp: 1-3 years |
The Quality Assurance Associate is responsible for handling tasks associated with Document Control, including processing, archival, filing, scanning, indexing and formatting new and existing documents within the framework of Veeva Vault Quality Docs software. This position involves familiarity and experience with cGMP Quality System processes and supports all functional areas with needs related to QMS documentation. | 4/6/2019 |
| 1171 | Tolmar Fort Collins, CO Research Assocate I BS/BA in chemistry, biochemistry, or related Exp: 0+ years lab experience |
Under direct supervision, perform sample analysis, data and document review, and method development and validation. Essential duties include: Develop and validate analytical methods to current ICH and USP guidelines. Accurately analyze formulation, drug, or product samples and assist other departments in analyzing samples as requested. Perform routine sample analyses in support of GLP or R&D stability protocols. Assist the Quality Control laboratory in troubleshooting method issues. Exercise technical discretion in the design, execution and interpretation of experiments that contribute to project strategies. Write and review technical reports, summaries, protocols, test methods, standard operating procedures, and other documents for use in the company or for submission to governmental agencies. | 4/6/2019 |
| 1172 | Tolmar Windsor, CO Stability Associate I BS/BA in chemistry Exp: 1+ years |
Responsible for maintaining the following systems and/or databases: Stability System II Software, stability database, stability variances, stability environmental chambers, stability reports, data entry, data auditing and stability records. Other responsibilities include: Requisition, label and place stability samples into appropriate storage conditions according to approved protocols. Enter new lots into the Stability System II Software and stability databases, and audit study start documentation. Pull samples at appropriate time points and deliver to the QC, AD and Microbiology Labs, as appropriate. | 4/6/2019 |
| 1173 | Toxikon Bedford, MA Research Associate, Medical Device Extraction BS/BA in sciences Exp: 0-1 years |
The successful candidate will work hand in hand with our study directors, quality assurance and sponsors/clients to ensure all medical device preparation aspects are performed per scientific and regulatory standards. Responsibilities include: Review the nature and composition of medical devices and determine sample requirements for testing. Medical devices are prepared for testing using geometrical calculations and therefore skill in routine mathematic principles is required. | 4/6/2019 |
| 1174 | Translate Bio Lexington, MA Associate Scientist BS or MS in chemistry or related Exp: 0-6 years |
We are seeking a highly motivated and scientifically rigorous individual to join the Research and Process Development team as an Associate Scientist. The position will report to the Director of the group and will focus on developing novel lipid nanoparticle (LNP) formulations for mRNA delivery. Responsibilities include: Provide formulations and perform characterization assays /data analysis with focus on in vivo studies, drug carrier design/development, assay development etc. Support formulation development activities related to formulation optimization with focus on potency and tolerability. Develop novel formulations for different ROAs. | 4/6/2019 |
| 1175 | Tris Pharma Monmouth Junction, NJ Production Development/Formulation Scientist I MS in pharma sciences Exp: 1+ years in pharma lab |
Product Development R&D Scientists perform preformulation and formulation development activities, prepares formulation batches for compatibility studies, stability studies, Pilot batches and Pivotal batches, perform maintenance of Research and Development (R&D) equipment/instruments. | 4/6/2019 |
| 1176 | Tris Pharma Monmouth Junction, NJ Scientist – Method Validation MS in chemistry Exp: 1+ years |
We have a unique opportunity for an entry level to intermediate Scientist to perform laboratory analyses in the testing of raw materials for release, in process (IP), finished products (FP) during process validation and stability (ST) samples of test batches and to carry out laboratory work to support method validation activities. This position is located at our Monmouth Junction, NJ facility. Responsibilities include: Operates general analytical instruments during raw material, in process and finished product testing such as HPLC, GC, UV/Vis, automatic titration, IR, AA, TLC and dissolution apparatus. Performs wet chemistry tests such as LOD, pH, and titration; prepares standard and sample solutions as required by the test methods; and performs all necessary calculations associated with the test analyses. | 4/6/2019 |
| 1177 | Tunnell Boston, MA Research Associate BS/BA Exp: 0-3 years |
Responsible for the execution and analysis of experiments and analytical procedures. Displays an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures. Investigates basic technical problems and performs routine scientific procedures and experiments under general supervision. Plans and prioritizes concurrent experimental procedures. Integrates, complies, and tabulates data and assists supervisor in the analysis and interpretation of the results. May provide oral presentations on results to other department members. Works under active supervision. Follows established procedures. Work is reviewed for soundness of technical judgment and overall adequacy and accuracy. Contributes to the completion of milestones associated with specific projects. Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources. Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters. Experience: 0 to 3 years. | 4/6/2019 |
| 1178 | Tunnell King of Prussia, PA Analyst BS/BA in engineering Exp: 0-4 years |
As an analyst, you will be part of teams that work across the entire spectrum of our offerings and our clients. We are working with some of the most innovative companies, who are providing the latest in critically needed therapies. | 4/6/2019 |
| 1179 | Regis Technologies Chicago, IL PRODUCTION OPERATOR HS Diploma Exp: 0-2 years |
North suburban Chicago contract pharmaceutical manufacturing company needs a Reactor Operator to operate and clean equipment used in the production of bulk chemicals. Responsibilities include: Operation of all plant equipment. Cleaning of all plant equipment. Staging of raw materials in production areas. Unloading of intermediates and products from equipment | 3/31/2019 |
| 1180 | Regis Technologies Chicago, IL PRODUCTION CHEMIST BS/BA in science or engineering Exp: 0-2 years |
North suburban Chicago contract pharmaceutical manufacturing company needs a Production Chemist to operate and clean equipment used in the production of bulk chemicals. Responsibilities include: Operation of all plant equipment. Cleaning of all plant equipment. Interaction with clients and sales team. Directing operators and technician | 3/31/2019 |
| 1181 | Zygo Middlefield, CT Associate Software Engineer BS in computer sciences Exp: Entry Level |
The selected candidate will develop, code, test, and debug new software and enhancements to existing software under the direction of senior developers. Our development approach fosters communication and collaboration across multiple scientific disciplines and provides all members of our team’s opportunities to contribute creatively to our projects. This position supports Zygo’s growing workload in application development for the Metrology and High-Precision Optical Fabrication markets. | 3/31/2019 |
| 1182 | Relay Cambridge, MA Research Associate - Compound Management AS or higher in life sciences Exp: 0-2 years |
You will lead fulfillment of dry and solution-based compound sample requests for scientific teams. Our Compound Management group is highly automated and in this role you can expect to operate laboratory robotics on the reg, while interfacing with web-based software tools. You will also be responsible for processing new samples into the archive inventory, which also includes accurate sample weighing and dissolution. | 3/31/2019 |
| 1183 | REMD Biotherapeutics Camarillo, CA Associate Scientist BS/BA in cell or molecular biology Exp: 0-2 years lab experience |
REMD Biotherapeutics is seeking exceptionally motivated scientists with strong background and proven track records in molecular and cellular biology to join our Drug Discovery team located in Camarillo, CA. Responsibilities in this role include: Design and perform cutting-edge research that utilizes genetic engineering to create novel therapeutic proteins and the cell-based assays needed to assess their biological activity. Work independently and collaboratively to develop and execute novel physical and biological assays required to evaluate new antibody-derived therapeutic proteins. Organize, analyze and present complex data generated on novel proteins in a scientifically rigorous manner for the purpose of advancing clinical candidates. | 3/31/2019 |
| 1184 | Revance Newark, CA QC Analyst I (Contract) BS/BA Exp: 0-2 years lab experience |
Conduct routine and non-routine analysis of in-process and finished products. Perform biochemical and/or chemical analyses of product to ensure stability. Compile data for documentation of test procedures that may include biochemical and chemical assays, initial lot release and stability testing and formulation studies. Revise and update standard operating procedures as needed. May participate in special projects as method validation or method transfer on analytical department. | 3/31/2019 |
| 1185 | Revance Newark, CA Clinical Trial Associate BS/BA in life sciences or related Exp: 0-2 years |
Acts as the primary liaison between Clinical Program Leads and Clinical Research Organizations (CROs). Supports Clinical Program Leads in operational and logistical tasks of pre-start up, start up and start up activities related to clinical trials performed according to regulatory, GCP ICH requirements, operational best practices and quality standards (ICH GCP / country and local requirements / company SOPs). Provide support across the Clinical department and partner with Clinical Program Leads and Medical Affairs on specific tasks involved in support of running clinical trials, from start- up through completion. | 3/31/2019 |
| 1186 | Rheonix Ithaca, NY System Integration Engineer BS in mechanical, systems or biomedical engineering Exp: 0-2 years |
The Systems Integration Engineer is responsible for integrating new biology and engineering developments into the product line and transferring to manufacturing. In this role he/she will work closely with the engineering and biology teams to develop and perform optimization and characterization experiments. He/she will also provide external customer support for system installations, maintenance and repair. | 3/31/2019 |
| 1187 | Rho Chapel Hill, NC Business Development Associate BS/BA Exp: 0-2 years |
The Business Development Associate will support the Business Development team in their efforts to achieve territory and corporate sales goals as well as assist in creating and executing a successful sales strategy. The ideal candidate will be adept at client-specific research and will provide active support in generating business leads. Responsibilities include: Perform outreach (phone, mail, email) to potential leads to generate interest in Rho’s services with provided text and scripts. Schedule telephone, face-to-face, and web meeting appointments for Rho business development professionals. Ensure a high level of communication and customer service | 3/31/2019 |
| 1188 | Purdue Wilson, NC Pharmaceutical Technician HS Diploma Exp: 0-5 years in pharma |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Responsibilities include: Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials, blends, and bulk accountability throughout manufacturing processes. Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. | 3/31/2019 |
| 1189 | Roivant New York, NY Tech Analyst, Roivant Analyst Program BS/BA or MS Exp: 0 years |
The two-year tech rotational program at Roivant begins summer 2019 and will give you experience across a variety of functions within Roivant and our subsidiary companies. Throughout our businesses, analysts will look for ways to integrate modern technology and will have the opportunity to develop Roivant’s innovative health and pharmaceutical companies in their early stages. As an analyst, you will have the opportunity to rotate through the following teams: Digital innovation, Digital Product, Devops, Data Architecture | 3/31/2019 |
| 1190 | Roivant New York, NY Accounting Analyst (Roivant Analyst Program) BS/BA or MS Exp: 0 years |
Roivant offers a two-year analyst program, beginning in summer 2019, with three tracks – general, tech, and accounting. Within the accounting track, analysts will focus on the different functions of our Accounting and Finance teams. In each area, analysts will work side-by-side with experienced professionals and senior management to improve overall department efficiency, company controls, procedures, as well as provide general departmental support. | 3/31/2019 |
| 1191 | Sabbio Therapeutics Sioux Falls, SD Research Associate (VAC) BS/BA in relevant field Exp: 1-5 years lab experience |
We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smooth operation and timely lab activities.We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smooth operation and timely lab activities.We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smooth operation and timely lab activities.We're seeking a Research Associate to perform experiments, immunoassays and other technical procedures in addition to writing research protocol and reporting experimental data. Essential duties: • Conduct routine laboratory procedures, assays, and experiments according to protocols. • Complete training and submit records on established protocols, assays and procedures. • Collect, evaluate, interpret and document research data according to scientific objectives. • Log, store and maintain samples with accurate records for research and production projects. • Maintain laboratory to ensure smo | 3/31/2019 |
| 1192 | Santa Cruz Biotechnologies Paso Robles, CA Research Assistant BS in biology or related Exp: 0-2 years (entry level) |
This is a full time position with career advancement opportunities within the company. Responsibilities include: Ability to perform standard analytical and preparative procedures required for the development and analysis of monoclonal antibodies. Ability to characterize antibodies by designing and optimizing experiments, interpreting data, and selecting the best possible products to develop. Capacity to utilize established, routine procedures and follows instructions from supervisor. Strong scientific background and business communication skills. | 3/31/2019 |
| 1193 | Sarepta Therapeutics Andover, MS Associate I BS in chemical engineering, process chemistry, or related Exp: 1+ years organic lab experience |
The Associate I, Oligonucleotide Chemistry will work on a rapidly growing team focused on supporting internal Research and Discovery, Analytical Development, Pre-clinical, and Toxicology groups. This role will perform high throughput synthesis, purification, and isolation of Sarepta’s phosphorodiamidate morpholino oligomers (PMOs). The Research Manufacturing Oligonucleotide Chemistry group synthesizes PMOs for lead-candidate screening, Analytical standards, and commercialization support. | 3/31/2019 |
| 1194 | Sarepta Therapeutics Andover, MS Associate I, Nucleoside Manufacturing BS in chemical engineering, process chemistry, or related Exp: 0-1 years |
The Associate I, Nucleoside Manufacturing will focus on support of our Contract Nucleoside Manufacturing sites including oversight of both routine manufacturing and tech transfer of new/improved processes to the sites. Nucleoside manufacturing ensures uninterrupted supply of API and sterile drug product in support of Sarepta’s manufacturing organization. The position is responsible for manufacturing trending, interaction with Sarepta process development, and production planning and execution with contract manufacturing organizations (CMOs). | 3/31/2019 |
| 1195 | Sarepta Therapeutics Columbus , OH Research Support/ Animal Technician HS Diploma Exp: 1-2 years |
Follows standard operating procedures and maintains recordkeeping pertaining to equipment operation, animal and supply inventories in accordance with federal and state guidelines and regulations. Handle, transfer, and distribute mice, supplies and waste as needed to and from work area(s). Coordinate with vendors and supervisors on operational, administrative and technical responsibilities . Monitor the daily health and welfare of the animals according to IACUC guidelines | 3/31/2019 |
| 1196 | Scholar Rock Cambridge, MA Laboratory Operations Assistant HS Diploma or BS in life sciences Exp: 0-1 years |
The Laboratory Operations Assistant will support laboratory scientists in the pursuit of new therapeutics with the potential to change patients’ lives. The candidate will be an essential part of maintaining a highly functional research lab in the biotech industry. Responsibilities include: Assist scientists and facilities team in conducting laboratory support tasks as needed. Stock and control inventory for the research lab. Perform routine maintenance lab maintenance including daily, weekly, monthly and as needed equipment maintenance . | 3/31/2019 |
| 1197 | Scholar Rock Cambridge, MA Associate Scientist / Senior Associate Scientist, Protein Sciences (multiple openings) BS or MS in biology or related Exp: 1-5 years |
Candidate will join the Protein Sciences group to express and manufacture antigens, antibodies, and proteins to support multiple Discovery Programs. Responsibilities include: Purification and characterization of antigens and antibodies to support the Discovery Research team at both small and large scale amounts. Generate and provide protein reagents in a timely manner to colleagues to support Discovery Research. Participate in cross-functional teams as Protein Sciences representative and/or subject matter expert . | 3/31/2019 |
| 1198 | Seattle Genetics Bothell , WA QC Analyst I BS/BA in sciences Exp: 0-3 years |
This position is located within the Quality Control department and is responsible for performing potency/binding assays (cellular bioassays and ELISA) and other related Quality Control methods for release and stability testing. Additional responsibilities include: preparation of solutions for potency assays, perform routine preventative maintenance on lab equipment, lab stocking, and performing cell passages. | 3/31/2019 |
| 1199 | Seattle Genetics Bothell , WA The Analytical Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate with experience in release and characterization met BS/BA in analytical chemistry, biochem, or related Exp: 0-2 years |
The Analytical Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate with experience in release and characterization method development for monoclonal antibodies and antibody drug conjugates. His/her responsibilities will include development and qualification of chromatographic and electrophoretic methods to support process development, quality control and physicochemical characterization of therapeutic antibodies and antibody drug conjugates. The candidate will (1) Conduct experiments to support method development and qualifications for mAbs and ADCs (2) Generate and interpret high quality data and technical reports to support various regulatory submissions including IND, BLA, IMPD, etc., and | 3/31/2019 |
| 1200 | Seattle Genetics Bothell , WA Research Associate I, BioProcess Development BS/BA in chemistry, engineering, biology, or related Exp: 0-2 years |
The BioProcess Development Department at Seattle Genetics is seeking a Research Associate to participate in the purification development efforts to support process development for our antibody and antibody-drug conjugate programs. Responsibilities include: Perform bench-scale chromatography and filtration development and characterization studies. Conduct platform fit assessments for early phase programs. | 3/31/2019 |
| 1201 | Seattle Genetics Bothell , WA Research Associate I, Analytical Sciences - MS Core Group BS in analytical chemistry, biochemistry, or related Exp: 0-2 years |
The Analytical Sciences Group at Seattle Genetics is seeking a highly motivated Research Associate to join the mass spectrometry (MS) core group. The ideal candidate will possess hands-on experience with protein mass spectrometry methods and data analysis. Primary responsibilities will include generation and interpretation of MS-based characterization data for monoclonal antibodies (mAbs) and Antibody drug conjugates (ADCs) in support of clinical and commercial programs. Responsibilities include: Conduct experiments aimed at characterizing posttranslationally modified mAbs and ADCs. Generate and interpret high quality data and technical reports to support various regulatory submissions including IND, BLA, IMPD, etc.. | 3/31/2019 |
| 1202 | Seattle Genetics Bothell , WA Shipping & Receiving Associate I HS Diploma or AS or BS Exp: 0-2 years in shipping/receiving |
Responsible for receipt, storage, and delivery of laboratory supplies & equipment, office supplies and other products such as break room supplies. Shipping & Receiving Associates I must demonstrate meticulous attention to detail, flexibility and a willingness to perform a wide variety of tasks while adhering to defined procedures. The position will work directly with the Purchasing, Research & Development, and Finance departments to accurately track, record, deliver and maintain the correct amount of supplies and equipment to the correct locations at all times. | 3/31/2019 |
| 1203 | Sebela Rosewell, GA QC Chemist BS in chemistry or related Exp: 0-2 years in cGMP environment |
Laboratory Bench Position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. Principle duties include: Perform testing of raw materials and products. Perform instrument qualification and maintenance. Perform test method validation/verification. Review analytical data for completeness, accuracy, and compliance | 3/31/2019 |
| 1204 | Sedia Biosciences Portland, OR QC TECHNICIAN AS in technical field Exp: 1+ years lab experience |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. | 3/31/2019 |
| 1205 | Sedia Biosciences Portland, OR MANUFACTURING TECHNICIAN AS in technical field Exp: 1+ years lab experience |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. | 3/31/2019 |
| 1206 | Sedia Biosciences Portland, OR Associate/Assistant Protein Scientist (R&D) BS in biochemistry, biology, or related Exp: 1-3 years |
The ideal candidate will assist in the development, expression, and scale up recombinant proteins from bacterial or other vectors, purify proteins and perform subsequent validation and quality assessments. The selected candidate will have demonstrated experience in most of the technical skillsets and be able to work in a small group of individuals, in a highly cross-functional environment. | 3/31/2019 |
| 1207 | Sedia Biosciences Portland, OR SCIENTIST/ASSOCIATE SCIENTIST (R&D-Product Development) MS in biology, chemistry or related Exp: 1-3 years lab experience |
This position would be a full-time exempt position (40 hours per week) at our primary laboratory facility in Northeast Portland. The successful candidate will be responsible for running laboratory tests, recording data, performing some degree of data analysis, drafting protocols, and communicating with managers from R&D and other departments. They will also be asked to participate in production of prototype products, and assist in transition of those procedures (through training and/or record-keeping) to our manufacturing department. Workflow is approximately 50-70% laboratory work, with the remainder being office work. The nature of our work requires the candidate to be capable of working comfortably in a BSL 2 laboratory | 3/31/2019 |
| 1208 | Sekisui Charlottetown, CA Research Associate BS in science or technical discipline Exp: 0-2 years |
The Research Associate will be responsible for designing, executing and interpreting experiments and analytical procedures under general supervision. Initiates, directs and executes pre-clinical scientific research and/or development strategies in research and/or development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. May participate in development of patent applications. Interfaces with various departments. | 3/31/2019 |
| 1209 | LabCorp Birmingham, AL Histotechnologist AS degree Exp: 1-3 years in histology |
Performs all technical duties related to the production of histo-pathological slides including embedding, microtomy, special stains, and IHC staining. 2nd shift. | 3/31/2019 |
| 1210 | LabCorp Burlington, NC Specimen Processing Specialist (Microbiology) HS Diploma Exp: 1-3 years in clinical lab |
This is a multi-discipline position with 3 primary components: specimen accessioning, sample splitting/sorting and data entry. Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing and routes specimens by type to various staging areas. Performs all paperwork, technical and non-technical procedures required to process and submit specimens. Assigns specific computer generated identification numbers, checks for accuracy and records all items processed. Operates data entry terminals and automated data systems, follows standard sequences/coding when entering data and corrects, edits, and/or verifies data entered into automated systems. Must be able to perform eSIS audits to resolve any outstanding problems. 3rd shift | 3/31/2019 |
| 1211 | LabCorp Rapid City, SD Lab Technician AS in medical lab technology Exp: 1-3 years |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in a designated technical department. nterprets results, subject to verification by Technologist/Supervisor, and providing allowance by State regulations. | 3/31/2019 |
| 1212 | LabCorp Tustin, CA Medical Data Entry/Accessioning HS Diploma Exp: 1-2 years |
Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing. Unpacks specimens from branches or ports and routes specimens by type to various staging areas. Prepares all specimens received for testing in designated laboratory departments or locations such as staging of specimens, centrifuge, separate serum, and blood smears. Aliquots sample for departments. Prepares excess specimen samples for storage and resolves and document problem specimens. 2nd shift | 3/31/2019 |
| 1213 | LabCorp Seattle, WA Phlebotomist HS Diploma w/ WA Medical Assistant Phlebotomy cert Exp: 1+ years |
PST meets minimum requirements and experience for client office and roving (with limited locations) positions, and patient service centers offering minimal services. Skill and comprehension level required for this category: Phlebotomy certification (where required) from an accredited agency, completion of an approved phlebotomy training course, or a minimum of one year verifiable phlebotomy experience. Exhibit proficiency in blood collection by venipuncture and capillary technique from patients of all age groups, and urine drug screen collections. Able to grasp a firm understanding of the importance of compliance and safety as outlined during new hire orientation and annual training. | 3/31/2019 |
| 1214 | LabCorp Phoenix, AZ Lab Assistant HS Diploma Exp: 1-2 years |
Performs all paperwork, technical, and non-technical procedures required to process and submit specimens. Assigns specific computer generated identification numbers, checks for accuracy, and records all items processed. Forwards accessioned specimens to designated laboratory location(s); and locating and correcting any discrepancies. Learns and keeps familiar with lab procedures and location of stored specimens. Locates specimens and pulls from various departments as requested. | 3/31/2019 |
| 1215 | SeraCare Milford, MA Research Associate II MS in biochemistry or biology Exp: 0-1 years |
Support includes independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material. Perform general molecular techniques such as plasmid purification, gel-electrophoresis, RNA transcription, and bacterial culturing. Perform nucleic acid analysis (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results. Work with supervisor to plan and execute new projects as assigned according to the timelines and ensure documentation meets GLP/GMP requirements. | 3/31/2019 |
| 1216 | Merck KGaA St. Louis, MO Technical Service Scientist BS/BA Exp: 1+ years |
The candidate will be a key member of an entry level, interactive technical service team that acts as the front line of communications between customers and our technical service specialists. This team is focused on providing best-in-class customer support via telephone, email and internet. The candidate is responsible for fielding basic technical inquiries on MilliporeSigma's products and navigating more advanced technical inquiries to the appropriate specialist within the organization. Our customer base includes Pharmaceutical and Biotech companies, Universities, Hospitals and Government agencies. Professional communication and schedule flexibility are imperative. | 3/31/2019 |
| 1217 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, chemical enginering or related Exp: 0-4 years |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Shift: Wednesday - Saturday, 4:00 pm - 2-20 am. Job functions include: Safely perform operations to meet quality expectations. Ensure quality throughout the process. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). | 3/31/2019 |
| 1218 | Merck KGaA Rocklin, CA Production Associate HS Diploma Exp: 1+ years |
Under close supervision, the Production Associate participates in entry-level production duties such as filling, labeling, packaging, shipping and other duties as assigned in a laboratory/manufacturing environment. Essential duties include: filling, labeling, packaging, etc. | 3/31/2019 |
| 1219 | Merck KGaA Milwaukee, WI Associate Production Scientist- Flow BS/BA in chemistry , biology or related Exp: 0-4 years |
While working 2nd shift (3:30 pm to 12:00am), continuously manufacture products according to established flow protocols, provide technical support to others and perform operations in support of the group and department. Essential job duties include: Safely perform operations to meet quality expectations. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. Participate in process improvements under the guidance of a Supervisor or Scientist. | 3/31/2019 |
| 1220 | Merck KGaA Billerica, MA QC Research Associate - Protein Science BS/BA in biology or related Exp: 1+ years lab experience |
The Protein Science / Buffer-media prep and QC group is a core function of the Protein and Cell Sciences (PCS) department that supports both early and late stage discovery projects and seeking a QC Research Associate. Responsible for small to large scale media and buffer production, as well as QC analytics supporting GLP tox drug substance production. Responsible for media / buffer preparation, equipment maintenance and calibration, data analysis, electronic lab notebook and batch record documentation. Responsible for media and buffer preparation to meet GLP tox protein production and reference run schedules, which includes raw material and chemical procurement and inventory control. | 3/31/2019 |
| 1221 | Sinclair Research Auxvasse, MO Formulations Technician MS in chemistry Exp: 0-2 years |
You will set up and manage the analytical laboratory and instrumentation including being responsible for SOP development, analytical software validation, dose formulation preparation, dose analysis and reporting in compliance with relevant regulations including GLP. Additionally, you may monitor analytical equipment performance and perform required routine maintenance procedures. As the member of the Lab Team at a Pre-Clinical CRO, it is also important to ensure we closely monitor laboratory supplies and cleanliness to provide a clean and regulatory compliant laboratory. | 3/31/2019 |
| 1222 | Singota Solutions Bloomington, IN Associate Quality Control Analyst BS in chemistry or related Exp: 1+ years |
Supportthe Quality Control function with respect to raw material, in-process, release and stability testing. Collaboratively participates in Development functionsfor the company including pre-formulation, formulation, process and analytical development activities. Specifically: Operate various lab instruments and equipment including (but not limited to): Karl Fisher, pH, HPLC, FTIR, UV-VIS, DSC, TOC, Lab-ware washers, Autoclave, Laminar Flow Hoods, Bio-Hazard Hood, Microbalances, and other diverse lab equipment and various wet chemistry techniques. Perform quality control analyses on a variety of equipment following formal written documentation, including SOPs, client methods, and compendialrequirements | 3/31/2019 |
| 1223 | Siolta Therapeutics San Francisco, CA Research Technician – Microbiology MS in microbiology or related Exp: 0-2 years |
Siolta Therapeutics is seeking a highly motivated and talented technical staff scientist to provide support for the company’s therapeutic development program focused on prevention/treatment of airway inflammation through manipulation of the gut microbiome. The successful candidate will work closely with other team members on preclinical studies of a rationally designed microbial therapeutic. The successful candidate will be technically proficient in microbial culture and molecular techniques. | 3/31/2019 |
| 1224 | Smith&Nephew Andover, MA Test Engineer I BS or equivalent Exp: 0-2 years |
Role is a Test Engineer, an individual contributor responsible for development and design of test fixtures, software and verification and feasibility testing as it relates to R&D development activities for capital devices. Follow FDA guidelines for Design Controls and internal quality processes. Interact with suppliers to ensure proper process controls on the parts we design into our products. Work cross functionally with marketing, quality, manufacturing and sustainability to ensure the customer experience is the best we can make it. | 3/31/2019 |
| 1225 | Smith&Nephew Mansfield, MA Quality Engineer 1 BS in engineering Exp: 0-3 years |
Position functions include: Develops and works with area teams to implement continuous quality improvement programs/productivity projects which may include: vendor certification for ship to stock; design of experiments to identify and thus control process variables; evaluation of lot inspection and initiation of process audit activities; and installation of statistical and non-statistical process controls; simplification of forms. Lead the review, disposition, and corrective action activities associated with discrepant components, materials, sub-assemblies and finished products. Develops and administers an inspection, test, and/or audit program to assure that incoming, in-process, and finished product meets functional specifications and quality standards. | 3/31/2019 |
| 1226 | Solid Biosciences Cambridge, MA Associate Process Engineer, Upstream Manufacturing Science & Technology BS/BA in life sciences, engineering, or related Exp: 0-2 years |
This position will provide engineering support in the upstream process for tech transfers to contract manufacturing organizations as well as technical support for ongoing manufacturing operations through process monitoring, troubleshooting, and process improvements. Key duties include: Support scale-up, process optimization, technology transfer, and start-up activities. Includes onsite presence at our contract manufacturing organizations. Support the development of new processes and technologies to improve yields, product quality, and process robustness. | 4/1/2019 |
| 1227 | Sorrento Therapeutics San Diego, CA Manufacutring Associate BS/BA in biology, biomedical sciences, chemical engineering or related Exp: 0-2 years |
A Manufacturing Associate who will be responsible for manufacturing CAR-T cells per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Responsibilities include: Weigh and measures in-process materials to ensure proper quantities are added/removed. Adheres to the production schedule ensuring on-time, internal production logistics. | 4/1/2019 |
| 1228 | Sorrento Therapeutics San Diego, CA CAR-T Process Development Positions MS in biology or related Exp: 1-2 years |
The individual must have good understanding of primary cell immunology and tumor biology. Previous experience in related areas is preferred but not required. Responsibilities include: Planning and executing human T cell studies focused on optimizing processes for manufacturing CAR-T cells at pilot and GMP scale. Coordinating experiments and projects collaboratively with R&D team and manufacture team. Maintain detailed documentation records and author reports, SOPs, batch records and other materials to facilitate tech transfer, manufacturing and regulatory submissions | 4/1/2019 |
| 1229 | Sorrento Therapeutics San Diego, CA RESEARCH ASSOCIATE, ANALYTICAL DEVELOPMENT BS in analytical chemistry, biochemistry, or related Exp: 0-4 years |
We are seeking a highly motivated individual to join our analytical development and quality control team. The position offers a unique opportunity for the candidate to work on a variety of projects using various techniques to assess analytes. The position’s focus will be on therapeutic protein drugs development with analytical methods development and validation, characterization and release testing of drug substance and drug product, and stability testing in a GMP- and GLP-compliant environment. | 4/1/2019 |
| 1230 | Sotera San Diego, CA Firmware Verification Engineer BS in computer sciences or related Exp: 1+ years software verification |
The Firmware Verification Engineer of Sotera Wireless will develop, implement, perform, and document both automated and manual software verification tests for the company’s proprietary embedded software. The verification engineer will be required to collaborate with all product development teams: embedded software, systems software, hardware, data science, and software quality assurance. | 4/1/2019 |
| 1231 | Spherotech Lake Forest, IL Quality Control Associate BS in chemistry or related Exp: 1+ years |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. This | 4/1/2019 |
| 1232 | Sprint PNS System Cleveland, OH Clinical Research Associate I BS in life sciences Exp: 1-2 years in research |
Primary responsibilities include: Coordinates and implements clinical study activities for product development projects. Works directly with the clinical, research, and regulatory staff to execute clinical studies. Trains clinical site staff on study protocols, good clinical practices and use of investigational devices. Coordinates and monitors clinical studies to ensure compliance with study protocols, regulatory requirements and Good Clinical Practices. | 4/1/2019 |
| 1233 | Springfield Clinic Springfield, IL Patient Access Specialist - Plastic Surgery HS Diploma Exp: 1+ years in medical office |
Under the direct supervision of the Operations Manager, the Patient Access Specialist is responsible for facilitating patient access services by managing incoming calls, assisting clinic customers at first point of contact, and streamlining clinic-wide communications. Also responsible for the daily work schedule for a group of physicians/staff by answering the phones, obtaining records, verifying patient information, scheduling appointments, entering charges and collecting payments. | 4/1/2019 |
| 1234 | Starkey Hearing Technologies Eden Prairie, MN Research Audiologist I MS+ in audiology Exp: 1+ year |
We are looking for a Research Audiologist that will be responsible for research, subject and data management related to activities pertaining to Alpha and Beta product evaluations, pilot testing, and hearing aid fitting methods. This position will assist in determining the direction of product development. Work will be collaborative with other researchers and personnel in Minnesota. | 4/1/2019 |
| 1235 | Starkey Hearing Technologies Eden Prairie, MN Regulatory Affairs Engineer II BS/BA in sciences or engineering Exp: 1+ years |
We are seeking to add a Regulatory Affairs Engineer II that will be responsible for supporting all Regulatory affairs for medical devices and hearing related products. This position will work with various departments across the organization such as Sales and Marketing to the Product Development group with guidance from senior regulatory personnel throughout the product life cycle. You would support activities that keeps Starkey current with changes to medical device regulations. This position is also responsible for creating and maintaining the technical files for all medical devices and hearing related products. | 4/1/2019 |
| 1236 | Stellartech Milpitas, CA R&D Technician HS Diploma or BS in life sciences Exp: 1+ years |
Primary responsibilities include: Provide general technical assistance to engineering and manufacturing operations. Design and develop 3D machined, formed and molded parts in Solidworks or other 3D modeling program. Assemble electromechanical medical devices. Build prototype circuits and enclosures. | 4/1/2019 |
| 1237 | Stellartech Milpitas, CA Quality Engineer II BS Exp: 1-3 years |
Perform quality engineering development activities for new product designs by assisting Engineering in the preparation of design and development plans, Design History File documentation, and Design History File preparation. Review and approve Device Master Record documentation for new product design and maintenance, including: bills of material, assembly procedures, manufacturing operations, assembly diagrams, test procedures, component specifications, labeling, and operator’s manuals. Perform ongoing quality engineering activities on current products to improve product designs and/or manufacturing processes including participation in NCM, Complaint, and CAPA investigations and actions as necessary. Assist in maintenance and improvement of the Quality System with guidance of QA Management, including internal audits, external audits, and quality improvement activities. | 4/1/2019 |
| 1238 | Pfizer Morrisville, NC Associate Scientist, Analytical R&D BS in biology, chemistry or related Exp: 0-2 years |
The qualified individual will be responsible for becoming proficient in a breadth of analytical methodologies including real-time PCR, HPLC, cell-based assays, and other relevant biochemical analysis methods. The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team. The candidate must thrive in a fast-paced, matrixed environment. Attention to detail, strong organizational skills, and effective interpersonal and communication skills are required. Ability to document analytical results in regulated systems and technical reports is also required. | 3/14/2019 |
| 1239 | Pfizer Collegeville, PA Stistical Programmer (Associate) BS or MS in statistics, biological sciences, or related Exp: 1+ years SAS programing |
This role is a hands on statistical programmer supporting study and asset teams in the delivery of less complex statistical programming deliverables. Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures, and qc work for which they are responsible. Ensures adherence to high quality programming standards in their daily work. Accountable for their assigned work in the programming space supporting the programming leads for a particular study or asset deliverable. | 3/14/2019 |
| 1240 | Pharmacyclics Sunnyvale, CA Clinical Project Assistant BS/BA in science, RN or related Exp: 1+ years in pharma, biotech or healthcare setting |
The Clinical Project Assistant (CPA) provides support to the clinical study teams in the execution of clinical trials. Under the direction of the Clinical Project Associate, CTM or Study Lead, the CPA’s primary responsibilities include maintaining Trial Master File (TMF) and Clinical Trial Management System (CTMS) in an inspection-ready state, assisting with site management, initiating collection of and reviewing and tracking essential documents throughout the life of the trial. This role contributes to the production and distribution of study materials and site/study communications. | 3/14/2019 |
| 1241 | Pharm-Olam Raleigh , NC SAS Programmer BS in related field Exp: 1-3 years in research |
To help design analysis data set specifications. Manage and manipulate multiple large SAS data sets, including defining populations and variables, performing calculations and summarizations. Prepare specific analytic deliverables, combining multiple programming outputs to create cohesive reports. Key responsibilities include: Responsible for creating specifications for generation of analysis datasets per ADaM/Pharm-Olam/Sponsor requirements, or as mentioned in SAP. Responsible for writing programming in order to generate tables and listings for clinical data on assigned projects for Production/Validation as assigned by Line Manager. Responsible for assisting in the development of programming procedures for the department. | 3/14/2019 |
| 1242 | Pharm-Olam Houston, TX SAS Programmer BS in related field Exp: 1-3 years in research |
To help design analysis data set specifications. Manage and manipulate multiple large SAS data sets, including defining populations and variables, performing calculations and summarizations. Prepare specific analytic deliverables, combining multiple programming outputs to create cohesive reports. Key responsibilities include: Responsible for creating specifications for generation of analysis datasets per ADaM/Pharm-Olam/Sponsor requirements, or as mentioned in SAP. Ensure SAS programs adhere to specifications/Mock Shells and Pharm-Olam programming standards. Responsible for writing programming in order to generate tables and listings for clinical data on assigned projects for Production/Validation as assigned by Line Manager. | 3/14/2019 |
| 1243 | Stryker Redmond, WA Associate Customer Quality Engineer BS in engineering Exp: 1+ years |
Responsible for continuous product and process quality improvements. Conducts investigations into NCs and CAPAs stemming from the products in the field. Leads root cause activities and Identifies potential failure modes and risks and resolves customer issues appropriately. Knows and applies the fundamental concepts, practices, and procedures of the general Quality and Regulatory post-market environment. Responsibilities include: Gather and analyze Post Market trending data (e.g. Q, service reports, complaints, MDR/MDV) to identify opportunities for quality improvements. Communicate with Customers, members of Field Service and Sales organizations to gather information necessary to carry out investigations. | 3/14/2019 |
| 1244 | PMI Biopharma Solutions Nashville, TN Analytical Chemist, Analytical Development BS in biology, chemistry or related Exp: 1-2 years in pharma |
The Analytical Chemist III position, reporting to the Director, Analytical Development, will operate under moderate supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development. | 3/14/2019 |
| 1245 | PolarityTE Salt Lake City, UT Research Trials Assistant BS in science or technical discipline Exp: 1+ years in clinical research |
PolarityTE is seeking a motivated, responsible, and self-sufficient individual to help support the everyday tasks of the Clinical Trials department. Responsibilities will span multiple trials and indications. Key responsibilities include: Manage the organization of trial files and critical documents. Support clinical trials team with shipments, equipment tracking and management, and supply inventory. Maintain clinical trial metrics and patient enrollment activities for weekly and monthly meetings. etc. | 3/14/2019 |
| 1246 | PolyPeptide Laboratories Group San Diego, CA Production Chemist I BS/BA in chemistry or related Exp: 1-3 years in chromatographic purification |
Job duties include: Responsible for the synthesis and purification of peptides under Good Manufacturing Practices (cGMP). Participates in the development and scale-up of synthesis and purification processes. | 3/14/2019 |
| 1247 | Poseida Therapeutics San Diego, CA Process Development Associate MS in biology Exp: 1+ years |
The Development Associate will be a key member of a dynamic team that develops and implements characterization strategies to support and enable process and clinical development of gene-engineered cell products. This is a lab-based position that will involve hands-on development of clinical manufacturing processes for selecting, gene-modifying and growing T cell subsets. This position will interface with our Research and Development team as well as with outside Contract Manufacturing Organizations. The ideal candidate will be skilled in T cell culture techniques, flow cytometry and have experience working in or supporting cGMP manufacturing projects. The candidate will have good oral and written communication skills, and will work with minimal supervision to design experiments, manage projects, collect data, and prepare reports. | 3/14/2019 |
| 1248 | PPD Middleton, WI Associate QC Reviewer BS in related field Exp: 0-2 years |
As associate QC reviewer you will be responsible for: Ensures the quality of laboratory data and reports. Reviews chromatographic data and related notebooks as specified by Standard Operating Procedures (SOPs). Evaluates data to ensure compliance with analytical methods, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) | 3/14/2019 |
| 1249 | PPD Middleton, WI Assoc Scientist BS in related field Exp: 1+ years |
Responsibilities include: Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/14/2019 |
| 1250 | PPD Richmond, VA Associate / QA Auditor I - Vaccines BS/BA in life science or related Exp: 1+ years in clinical research |
Responsibilities include: Audits laboratory data for compliance with methods and standard operating procedures and report findings. Audits sample result tables and analytical reports for completeness and accurate representation of the data and report findings. Assists in the preparation of audit findings and/or other related information. Serves as a resource to operational departments on audit or quality assurance subject matter | 3/14/2019 |
| 1251 | PPD Richmond, VA Entry Level Scientist - Immunochemistry BS/BA in relevant field Exp: 0-2 years |
Responsibilities as a Entry Level Scientist include: Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/14/2019 |
| 1252 | PPD Middleton, WI Assistant Scientist- HPLC, GC BS/BA in relevant field Exp: 0-2 years |
Responsibilities as an Assistnat Scientist - HPLC include: Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. | 3/14/2019 |
| 1253 | PPD Middleton, WI Assstant Scientist BS/BA in relevant field Exp: 0-2 years |
Responsibilities as a assistant scientist include: Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/14/2019 |
| 1254 | PPD Austin, TX Med Tech I BS/BA in medical technology or NCA Exp: 0-2 years |
The Medical Technologist independently and without technical supervision performs low, moderate, and high complexity clinical laboratory testing as a generalist, with assignment in some or all of the following disciplines: urinalysis, coagulation, hematology, chemistry, special chemistry, and immunology. The Med Tech also troubleshoots laboratory equipment and methods and provides technical supervision of others as required. | 3/14/2019 |
| 1255 | PRA Health Sciences Chicago, IL Associate Regulatry Labeling Specialist BS/BA in science or health related field Exp: 0 years for associate level |
Responsibilities include: Provdies regulatory expertise/guidance for development and submission of US labeling components. Controls consistency of US labeling content through alignmnet with the core documents across product families and with all applicable best practicies. Must have a basic understanding of the drug development process and knowledge of the pertaining regulations | 3/14/2019 |
| 1256 | PRA Health Sciences Phoenix, AZ Application Developer - Health Data Services MS in computer sciences or related Exp: 1-2 years |
Candidate will be involved in developing and maintaining a portfolio of customer-facing solutions and applications. These projects will mainly include front end web and mobile developments, backend applications, and mobile content synchronization processes. Must have experience with ASP.Net, Python, Java and Javascript. | 3/14/2019 |
| 1257 | PRA Health Sciences Lenexa, KS Entry Level Clinical Trial Specialist BS/BA in science or health related field Exp: Entry Level |
As a clinical trials specialist, you are the primary point of contact/liaison for the sites. Sponsor internal stakeholders during study life cycle. Preform investigative site recruitment/feasibility, essential document collection and review, maintenance and close-out in-house site management activities in accordance with the Sponsor and/or PRA protocol. In addition, you will create and distribute meeting agendas and take meeting minutes during internal and sponsor calls, roll out training plans to team members and provide access to project systems. | 3/14/2019 |
| 1258 | PRA Health Sciences Los Angeles, CA Clinical Research Associate BS/BA in clinical, health or science related field Exp: 1+ years of clinical monitoring |
The Clinical Research Associate will monitor the progress of linical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and the reported in accordance with the protocol, SOPs, ICH-GCP, and other regulatory requirements. | 3/14/2019 |
| 1259 | PRA Health Sciences Salt Lake City, UT Lab Associate PRN BS/BA in medical, lab or life sciences Exp: 1-2 years in lab |
The Lab Associate is part of the operational team within the sample preparation alb. The Lab Associate ensure the appropriate collection, processing, storage and shipment of samples. Daily tasks may inolve maintenance of equipment, processing and shipment of samples. The Lab Associate is part of the study team that is responsible for the execution of the study. \ | 3/14/2019 |
| 1260 | PRA Health Sciences Lenexa, KS Medical Resaerch Associate/ Phlebotomist PT HS Diploma Exp: 1-2 years in medical or clinical field |
Duties include: Perform study specific clinical procedures, collect and record study data on CRF/SDs and interact with subjects during confinement and outpatient periods of clinical studies. Performs basic medical procedures according to protocol for specified study participants, include but not limited to informed consent, vital signs, Height/weight/BMI measurments, meals, water fast, phlebotomy, finger stick blood sugar, ECGS, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment, etc. | 3/14/2019 |
| 1261 | Precision BioSciences Durham, NC Research Associate, Bioanalytics MS in cell biology/immunology Exp: 1+ years in biopharma |
The Research Associate, Cell Therapy Bioanalytics works within the Cell Therapy Development Team and participates in providing bioanalytical support for Cell Therapy Process Development projects. The position will contribute to Bioanalytics development efforts for CART-cell projects by providing sample preparation and analysis in a timely manner. This position is lab-based and will share facilities and resources with the Cell Therapy teams. Daily responsibilities include: Execute bioanalytical methods for in-process sample analysis and cell product testing, Analyze generated data according to established SOPs and report results of analysis to Cell Therapy Team Leaders in a timely manner, Coordinate with Scientists, Research Assistants, and Research Associates to plan and carry out experiments for developing T Cell Therapies. | 3/14/2019 |
| 1262 | Precision Health Economics Los Angeles, CA Associate Research Scientist-Health Policy MS Exp: 1+ year conducting health economic research |
Collaborating across a broad portfolio of sophisticated health economic and health policy research projects. Performing a wide range of activities including: literature reviews; regression analysis; preparing content for reports and manuscripts, slide decks and meeting notes; quality assurance/review; and other activities. | 3/14/2019 |
| 1263 | Precision Health Economics New York, NY Associate Research Scientist - HEOR MS Exp: 1+ year conducting health economic research |
You will collaborate across a broad portfolio of sophisticated health economic and health policy research projects. You will perform a wide range of activities including: literature reviews; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. | 3/14/2019 |
| 1264 | Precision Health Economics Oakland, CA Associate Research Scientist-HEOR MS Exp: 1+ year conducting health economic research |
As an Associate Research Scientist/Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. | 3/14/2019 |
| 1265 | Precision Health Economics Boston, MA Associate Research Scientist-HEOR MS Exp: 1+ year conducting health economic research |
As an Associate Research Scientist/Research Scientist, you will responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects as a member of a project team. You will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming) and will execute a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance/review; and other activities, under the direction and supervision of a project leader. | 3/14/2019 |
| 1266 | Precision Medicine Group New York, NY Scientific Associate - Medical Writer MS in life sciences Exp: 1-2 years in medical communications |
Scientific Associates develop and write medical content for assigned client account(s) and work in conjunction with all internal teams to ensure that the client vision is achieved and content is medically accurate. Responsibilities include: Developing and writing medical content for multiple and wide-ranging therapeutic areas and appropriate audiences. Ensuring project quality and outcomes by demonstrating in‑depth technical expertise of assigned therapeutic category and/or managed care areas. Developing strategic content for full range of medical content (slide presentations, advisory boards, strategy guides, monographs, discussion guides, training resources, etc.) | 3/15/2019 |
| 1267 | Precision Medicine Group Houston, TX Flow Cytometry Technologist BS/BA in life sciences or related Exp: 0-1 years in flow cytometry |
Day to day tasks as a technologist include: Performing simple and complex processing of blood and body fluids (routine and non-routine procedures). Setting up instrumentation and running calibration samples. Running quality control samples, clinical samples and generating data. Work with QA to perform good documentation and ensure the lab is operating under CLIA, GLP and GCP standards. | 3/15/2019 |
| 1268 | Profusa South San Francisco, CA Electrical Engineer MS in electrical or computer engineering Exp: 0-5 years |
We seek an experienced electrical engineer with digital/analog circuit design skills to lead the electrical design of these devices. Major responsibilities include: Develop breadboard systems for testing feasibility of optical detection concepts. building miniaturized PCB’s from broad user requirements following design control by gathering and writing engineering requirements, designing the circuit, laying out the PCB, overseeing its fabrication and assembly, powering up and testing the circuit with embedded developer’s help. Interface with vendors to oversee design transfer and manufacturing scale-up. Test electrical functionality of devices | 3/17/2019 |
| 1269 | Progenra Malvern , PA Scientist, Medicinal Chemistry BS or MS in organic/medicinal chemistry Exp: 0-10 years |
As a medicinal chemist you will apply state of the art synthetic chemistry, structural and computational approaches to discover and synthesize novel medicines for a variety of diseases including immuno-oncology, inflammation and neurodegenerative diseases. Research Scientist will independently plan and implement efficient synthetic routes for target compounds and apply state of the art purification and characterization techniques, conduct research with the drug discovery team to develop SAR, analyze the data and write laboratory reports. Position provides opportunities to grow, write papers and patents, and present data at internal, national and international meetings. | 3/17/2019 |
| 1270 | Progenra Malvern , PA Research Associates BS or MS in life sciences Exp: 1-10 years |
Research associates will be expected to apply focused expertise to projects supporting the development of screening assays, and to the discovery and evaluation of compounds active in the various screens. Candidates should have demonstrated proficiency in molecular biology or biochemistry and be willing to contribute to the company product and intellectual property development as exemplified by scientific articles, patents, and internal publications. Research associates are, in addition, expected to present their data in company settings and, if appropriate, at external meetings and in the literature. | 3/17/2019 |
| 1271 | Mission Pharmacal Boerne, TX Compounding Technician HS Diploma Exp: 1+ years |
Responsibilities as a compounding technician include: Mixing chemicals/ingredients and operating all mixing related equipment in a way that meets safety, quality/compliance and productivity objectives. Following and enforcing safety rules, regulations and procedures. Checking all raw materials against MBR ingredients list, recognizes errors and notifies lead personnel as required. Compound/blend all routine formulations and follow MBR as written. | 3/17/2019 |
| 1272 | Protein Simple San Jose, CA Research Associate BS in biochemistry, chemistry, or related Exp: 1-3 years |
The Research Associate will be an integral member developing new technologies for protein analysis. This will position will report in to the R&D Science group and support product development (Consumables/Reagents and Instruments) from conceptualization to commercialization. Key responsibilities include: Assist product development by performing experiments and in-depth data analysis. Design and execute experimental plans independently. Observe and meticulously record all details during product development | 3/17/2019 |
| 1273 | ProTrials Research San Jose, CA Clinical Trials Associate RN or Bachelor Exp: 0-2 years |
Essential duties include: Obtains, reviews, processes, and tracks study related documents (CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc.). Maintains and disseminates basic study tracking information including, but not limited to: Visit Reports, Regulatory Documents, Site Contact Lists, Team Contact Lists, Vendor Lists, and Budget Disbursements. Manages and tracks Investigational Product supplies for study centers; receives and prepares requests, ships and returns Investigational Product supplies. | 3/17/2019 |
| 1274 | PSC Biotech Pomona, CA Entry Level CSV Engineer BS in chemical or biomedical engineering Exp: Entry Level |
We are looking for an Entry-Level Computer System Validation Engineer to support our PSC Software Team in Pomona, CA. Job responsibilities include: Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards.Collaborate with project stakeholders and the information systems team to define needs and achievable solutions and/or justifications to system requirements. Initiate/update GxP and Risk Assessments on system. | 3/17/2019 |
| 1275 | Pulmatrix Lexington, MA Engineering Associate BS/BA or MS in chemical, biomedical engineering Exp: 1-5 years in biotech/pharma R&D |
We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. Responsibilities include: Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying. Perform physicochemical property and aerosol performance characterization of solid-based inhalation dosage forms. | 3/17/2019 |
| 1276 | Purdue Wilson, NC Pharmaceutical Technician HS Diploma Exp: 1-5 years |
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing and/or packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary responsibilities include: Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing and/or packaging equipment (oral solid dose manufacturing and packaging may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.). Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.). | 3/17/2019 |
| 1277 | Purdue Coventry, RI Lab Technician BS in chemistr Exp: 1-2 years in cGMP,FDA, DEA environments |
This position will also be responsible for providing escort for equipment qualification with vendors, witnessing controlled substance receiving and dispensing, coordinating laboratory waste disposal and pickup, as well as performing and/or facilitating equipment calibrations. This role may perform other related assignments and duties as required. This position will primarily provide hands on support in manufacturing finished product dosage forms – tablets, capsules, liquids and semi-solids. This position will be responsible for equipment set up, product manufacturing and cleaning as per EHS, DEA and FDA regulations. In addition to assisting the product development scientists in manufacturing finished product prototypes, general support of the laboratory is required. Support activities will include managing inventories for raw materials, personal protection equipment, supplies, etc. | 3/17/2019 |
| 1278 | Purdue Coventry, RI Associate Scientist BS/BA or MS in chemistry or related Exp: 1+ years |
The position responsibilities will include both routine and non-routine stability analysis in accordance with cGMP guidelines. These responsibilities will consist of, but are not be limited to, coordinating stability programs, writing stability protocols, SOPs, test methods and final reports. Additional responsibilities include ensuring all laboratory equipment and instrumentation are maintained in compliant condition, to assist in coordinating equipment qualifications, reviewing notebooks/experimental data, trouble shooting and training junior staff. | 3/17/2019 |
| 1279 | Purdue Coventry, RI Process Engineer BS/BA in chemical engineering or chemistry Exp: 1-2 years in manufacturing or engineering |
The Shift Process Engineer performs all manufacturing tasks required for the safe production of active pharmaceutical ingredients in compliance with FDA, DEA, OSHA, Federal, State, and Local regulations. The primary objective of this position is to ensure that all manufacturing operations are conducted in a safe manner with a high regard for all applicable cGMP’s and DEA requirements. Working flexibility across a broad range of chemical operations and participation on self-managed work teams is required. Training for and participation on Emergency Response Team is required. Availability for overtime and shift work (including rotating shifts and seven-day operation) is also required. | 3/17/2019 |
| 1280 | Qiagen Waltham, MD Contract Data Analyst Associate BS/BA in biomedical, electrial, or computer engineering Exp: 1-3 years |
QIAGEN is seeking candidates who will assist in the analysis and interpretation of experimental data generated during the development of the GeneReader sequencer, QIAGEN’s next generation massively parallel DNA sequencing platform (NGS). The successful candidate will play a key role within the GeneReader development team by providing data reduction, interpretation, and visualization of NGS data and associated platform metadata to drive hypothesis-driven research. Data processing and interpretation will be performed using a combination of existing research and development tools and new software development to enhance existing capabilities as needed to support the team. | 3/17/2019 |
| 1281 | Qiagen Waltham, MD Contract Research Associate BS/BA in engineering or sciences Exp: 1+ years |
QIAGEN is seeking candidates who will assist in the development, implementation and optimization of sequencing protocols on the sequencer, QIAGEN’s next generation massively parallel DNA sequencing platform. The successful candidate will be an integral part of the sequencing development team and will be responsible for maintenance and operation of instruments, preparation of reagents according to SOPs as well as executing complex laboratory experiments. | 3/17/2019 |
| 1282 | Qiagen Waltham, MD Associate Bioinformatics Engineer BS in bioinformatics with computer science minor OR MS in bioinformatics Exp: 0-2 years |
You would be working in our clinical implementation team and participate in different projects related to implementation and integration of our QCI Interpret product lines. Responsibilities include: Data engineering supporting QCI Interpret and IVA customers with their bioinformatics data needs. QCI Interpret onboarding including test product, API and report configuration. Participate in other bioinformatics projects within the R&D and Service organization. | 3/17/2019 |
| 1283 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diploma Exp: 1-3 years |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. Responsible for Manual production and assembly procedures in compliance with relevant regulations and Standard Operation Procedures. Adhere to and accurately complete all production-related documentation. Responsible for set up, trouble shooting and operation of production related equipment within the assembly area. | 3/17/2019 |
| 1284 | Qiagen Germantown, MD Technical Associate HS Diploma Exp: 1-4 years |
Responsible for the vialing of bulk material, capping, labeling, plate coating and the assembly of kits in compliance with QSR, ISO, OSHA, IVDD, MDD regulations and relevant Standard Operating Procedures. Manual Vialing and coating of components under general supervision as well as using automation (large and small scale) in the production of finished product. Participate in the initiation/change of Quality documentation (i.e. MMRs, SOPs, NRs Variances) as well as ERP (Routers, BOMs, labor and production sheets) related documentation. Employees will be expected to contribute to process improvement initiatives, maintain departmental SOPs and Bluelines and maintain inventory of lab supplies. | 3/17/2019 |
| 1285 | QPS LLC Newark, DE Associate Scientist I - Protein Binding BS/BA in chemistry, analytical chemistry or biochemistry Exp: 0-2 years |
Whether their focus is on small molecules, proteins, antibodies, vaccines or oligonucleotides, QPS provides our clients with a full range of services to support the entire spectrum from early discovery, to IND-enabling ADME, to clinical studies. An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. | 3/17/2019 |
| 1286 | QPS LLC Newark, DE Associate Scientist I - Biotransformation BS/BA in chemistry, analytical chemistry or biochemistry Exp: 0-2 years |
An Associate Scientist in our DMPK department will be a fully-supervised trainee, responsible for formulations, and sample processing and analysis to support preclinical drug discovery and development. Responsibilities include: Assist with quantitative and qualitative bio-analytical studies by conducting sample preparation with various analytical chemistry methodologies. Perform routine lab operations, such as sample extraction, preparing reagents, pipette, weigh, monitor, record, label tubes, order and maintain inventory of supplies, and timely disposal of study samples, in a neat/clean manner. | 3/17/2019 |
| 1287 | Bio-Techne Minneapolis, MN Production Assistant 1 HS Diploma Exp: 0-2 years lab experience |
As a Production Assistant 1, you will be responsible for the processing of raw biological material for use in product manufacturing. You will also perform maintenance and cleaning of production equipment and containers to ensure safety and compliance, as well as completing required paperwork. | 3/17/2019 |
| 1288 | Bio-Techne Minneapolis, MN Research Associate BS/BA in biological sciences Exp: 0-2 years lab experience |
As a Research Associate, you will assist in production of insect-derived RUO and GMP recombinant proteins in various bioreactor systems as well as various human cell lines for CAP Survey, media and supplement preparation, and all other duties as assigned. In this position, your scheduled work-week is Tuesday through Saturday. | 3/17/2019 |
| 1289 | Bio-Techne Newark, CA Associate Scientist BS/BA or MS in biology or chemistry Exp: 1-2 years |
Key responsibilities include: Perform manual and automated RNAscope assays to evaluate client-provided tissue samples. Perform digital slide scanning, imaging, and fluorescent microscopy to acquire data. Generate and create custom reports to deliver to clients. Participate in editing custom reports from other projects. | 3/17/2019 |
| 1290 | Reata Pharmaceuticals Irving, TX Research Associate BS or MS in biological sciences Exp: 1-3 years lab experience |
The Research Associate is an entry-level position that is responsible for the execution and analysis of cell-based, molecular biology, and biochemical assays in support of Reata’s drug discovery and development programs. The ideal candidate will be a dynamic member of the research team who can reliably generate data using validated assays. The Research Associate is expected to work both independently and in collaboration with team members. In addition, the Research Associate must thrive in an environment that demands frequent reprioritization of projects and goals. Key responsibilities include: Execute cell and molecular biology experiments to support drug discovery and development. | 3/17/2019 |
| 1291 | RB Hillsborough, NJ Packaging Operator HS Diploma Exp: 1+ year in manufacturing environment |
The Packaging Operator is responsible for providing the Technical and Operational Skills needed to deliver world class results in the key areas of Line Efficiencies, Quality, and Cost while meeting our high standards of Safety, Customer Service, and Teamwork. Key responsibilities include: Operation of Packaging Line and related equipment including startup, clearing jams, manual operations and shutdown. Follows all applicable waste, scrap reduction and recycling guidelines. Assists in changeovers, wash outs and preventative maintenance. | 3/17/2019 |
| 1292 | Recro Gainesville, FL Manufacturing Associate I - 1st/2nd Shift HS Diploma Exp: 6 months |
The Manufacturing Associate I is responsible for the processing of commercial products at the Gainesville Site. This includes receiving order instructions (Batch Records), weighing and staging of materials, solution preparation, solution application (coating beads), drying, screening, machine set-up, sampling, packaging, and storing of the products. | 3/17/2019 |
| 1293 | RefleXion Hayward, CA Firmware Engineer MS in electrical or computer engineering Exp: 1+ years |
This position has responsibility and authority for delivering top quality firmware solution required to meet overall radiotherapy product requirements. This includes: Prototype, design, implement, test, debug and maintain firmware (device drivers, BSPs and Hardware Abstraction Layer library) that serve as the bridge between hardware resources and application software. Participate in completing test cases, conduct embedded systems verification and generating test reports to support a 510(k) submission and FDA clearance. Participate in cross-functional project teams with scientists, technical support and other engineers to resolve software issues. | 3/17/2019 |
| 1294 | Regeneron Tarrytown, NY R&D Associate, Inflammation & Immunology BS/BA Exp: 1-4 years |
Seeking a motivated Research Associate with at least 1-4 years of experience working on inflammation, asthma allergy, autoimmunity or mouse models of human disease to join a highly interactive immunology team. Conducts experiments, predominantly of basic immunology and basic lab techniques. Troubleshoots methodological and technical issues, interprets experimental data and literature, and communicates results to supervisor, department, or project team. Helps create a safe, effective, and efficient working environment. | 3/17/2019 |
| 1295 | Regeneron Tarrytown, NY R&D Associate, Infectious Diseases MS Exp: 0-4 years in lab |
Regeneron is seeking a highly qualified candidate for a R&D Associate for infectious disease target discovery, assay development and monoclonal antibody evaluation and selection. Responsibilities include: Design, execute and control experiments based on protocols. Perform advanced laboratory calculations and manipulations along with the analysis and interpretation of data with little to no supervision. Communicates experimental results, conclusions and ideas directly to supervisor, project team members and management in quality presentation form. Develop new methods or technologies and troubleshoot protocols. | 3/17/2019 |
| 1296 | Regeneron Tarrytown, NY R&D Associate (Non-Clinical Bioanalysis) BS/BA Exp: 0-2 years |
This is an entry level associate position. R&D Associates at this level are required to closely follow instructions regarding the execution of experiments. They are expected to have a basic understanding of general laboratory techniques, such as pipetting and making solutions, in addition to limited experience performing immunoassays. All work is conducted under direct supervision. The associate has minimal decision making capability and requires direct supervision on work assigned. Possesses a knowledge of the basic principles of ELISA obtained through academic training or relevant industry experience. | 3/17/2019 |
| 1297 | Regeneron Tarrytown, NY R&D Associate (Formulation Process Development) BS or MS in biomedical or chemical engineering Exp: 0-3 years |
R&D Associate in the Formulation Development Group (FDG) will work in a state-of-the-art drug product (DP) laboratory developing processes and unit operations for protein-based drug products. The Associate will work closely with FDG leads/scientists to support development activities across multiple programs and will ensure a seamless technology transfer to the manufacturing team. The Associate will also support full functionality of DP process laboratory including setup and maintenance, procurement of tools, as well as equipment installation and operation. Additionally, the position will independently execute process development and analytical characterization studies, and will document the same in electronic notebooks and reports. | 3/17/2019 |
| 1298 | Nurx Syracuse, NY Pharmacy Technician HS Diploma or BS Exp: 1+ years as pharmacy technician |
Weekend and On-Call Position. Responsibilities and duties include: Process and key-in prescriptions with accuracy, attention to detail, and efficiency. Correctly input sensitive prescription information into computer system, dispense correct medication, and verify information before releasing prescriptions. Demonstrate knowledge of Third Party insurances and billing procedures. Proactively partner with the Pharmacy, Operations and Engineering teams to address issues and achieve high quality and throughput in fast-growing, technology-empowered pharmacy. | 3/7/2019 |
| 1299 | NuVasive San Diego, CA Assoc Test Engineer, Validation MS in computer science, engineering or related Exp: 1+ years |
As the Validation Engineer, you will ensure the quality of the medical device software and hardware meets the design requirements and that they are testable. You will also develop, implement and maintain test plans, protocols, test scripts and traceability matrix for design verification & validation. Essential responsibilities include: Execute protocols/test scripts and document results. Generate and/or update summary reports. Ensure compliance with FDA device regulatory requirements, including DHF and 510(k). Communicate with Hardware and Software Development, Marketing, Technical Services, and other project team members to ensure schedules and requirements are consistent with project expectations. etc. | 3/7/2019 |
| 1300 | NuVasive Richmond, VA Associate Neurophysiologist BS or CNIM Elgible Exp: 0-1 years |
Health care professional responsible for real time data collection and monitoring of a patient’s nervous system throughout surgery. In addition, he/she must establish and maintain open cooperation and communication with the surgical team, which includes interaction with the surgeon. Additional responsibilities include pre-operative patient assessments and post-operative billing uploads. Responsibilities: Consult with surgeon regarding structures at risk and modalities to be monitored. Interact with patient, when applicable, to obtain a detailed history and clearly explain the neurophysiological tests to be performed. Display and label waveforms for marking, measuring and calculating information such as latencies, amplitudes and conduction times following established guidelines and protocols. Communicate with the surgeon and surgical team throughout the case to relay monitoring information. | 3/7/2019 |
| 1301 | NuVasive West Carrolton, OH Manufacturing Engineer BS in technial engineering discipline Exp: 1+ years |
As the manufacturing engineer, candidate will be responsible for: Coordinate cross-functional teams to execute and document the manufacturing launch of new/legacy products. Determine manufacturing processes required to accurately and efficiently make spinal implants, from raw material to final cleaning and shipment. Develop and complete manufacturing documentation (pFMEA, control plan, process flow, work instructions, and inspection plans). Perform research, design, and development of manufacturing processes including production flow, assembly methods, and production equipment. Perform product/process analysis and troubleshooting for cost reduction, quality improvement, and improved efficiency. Design, develop, test, source, and cost-justify various tools, machinery, and equipment for recommended manufacturing methods. | 3/7/2019 |
| 1302 | NuVasive Memphis, TN Associate Sterile Processing Tech HS Diploma Exp: 1+ years |
Initiates, maintains, and compiles records associated with ordering, receiving, storing, issuing, and shipping materials, supplies, and equipment by performing the following duties. Compares nomenclature, stock numbers, and other listed information on packing slips to verify the accuracy of purchase orders and shipping orders. Compiles data from sources such as contracts, purchase orders, invoices, requisitions, and accounting reports and writes, types, or enters information into computer to maintain inventory, purchasing, shipping, and other records. Verifies inventory computations against physical count of stock and adjusts errors and reports documenting reasons for discrepancies with proposed corrective action. etc. | 3/7/2019 |
| 1303 | NxStage Lawrence, MA Test Engineer I BS in engineering Exp: 1-3 years |
The individual in this position will support product development and lead test-related activities related to the development of NxStage Medical’s equipment and disposable products. Responsibilities include: Work closely with all engineering disciplines, including Systems, Electrical, Mechanical, Disposables, and Software Engineering, as well as Project Management and Quality personnel, to verify and validate product designs. Participate in the planning and lead the execution of Validation & Verification (V&V) testing activities in support of regulatory filings for Class II medical devices. Specify, design, and develop test systems (hardware & software); ensure that all test systems and equipment are appropriately validated and controlled. Manage V&V documentation, including derivation of Test Procedures from System and Sub-System Specifications, validation of Test Procedures and Test Fixtures, and generation of test reports. | 3/7/2019 |
| 1304 | Ology Bioservices Alachua, FL Downstream BioManufacturing Process Associate BS/BA in science or engineering Exp: 0-2 years in biologic based GMP |
This position will assist production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). Responsibilities include: Perform and/or assist with downstream related activities including Chromatography purification, Centrifugation and Ultracentrifugation, Ultrafiltration/Diafiltration, Viral Clearance. Draft Standard Operation Procedures, Change Control, Deviations. Properly disinfect and stage materials into production rooms before the production campaigns. Assist with equipment ordering, installation, qualification and routine maintenance. Perform activities to support production campaign such as preparation of tubing assemblies, autoclave, material request and transfer into production room. | 3/7/2019 |
| 1305 | Ology Bioservices Alachua, FL Upstream Biomanufacturing Process Associate I BS in biology, chemistry ore equivalent Exp: 0-2 years |
This position will assist production related activities in the cGMP Manufacturing Core according to established procedures at the Medical Counter Measures (MCMs) Advanced Development and Manufacturing Facility in Alachua (Florida). Responsibilities include: Perform and/or assist with upstream related activities including Cell culture at small and large scale, Cell transfection, Media and buffer preparation, Bioreactor and Fermentor based production. Draft Standard Operation Procedures, Change Control, Deviations. Write raw material specifications, research, source and order material and lab wares. Perform activities to support production campaign such as preparation of tubing assemblies, autoclave, material request and transfer into production room. | 3/7/2019 |
| 1306 | Olympus Richmond, WA Research Scientist I BS in biomedical engineering or related Exp: 0-1 years |
The Research Scientist I assists and participates in biomedical, pre-clinical and clinical research and development projects, experiments, and investigations relevant to the Company’s product strategy or services, disseminating findings through internal reports. This is an entry level research position. Job duties include: Support the design and implementation of research and/or engineering development projects. This may include but is not limited to, support of in-vivo (animal) and ex-vivo testing. Collaborate with other functional groups including product development, clinical and regulatory to fulfill project deliverables. Assist with the execution of clinical research investigations and product evaluations. Create and maintain files related to the pre-clinical and clinical activities. | 3/7/2019 |
| 1307 | Olympus Waltham, MA Mechanical Engineer II (Document Control) BS in engineering or equivalent experience Exp: 1+ years with design drafting in manufacturing |
As a Mechanical Engineer II on the Engineering Services team, you will be empowered and inspired to do your best work. You will contribute to our mission by helping to support new product introduction and improve existing and new XRF and XRD products that help make the world a safer place. In your role, you will help to improve efficiencies on the production floor by working with Production Engineering in the design and documentation of production fixtures and tooling. In a typical day, you will: Design production fixtures and tooling. Translate concepts to final designs and documentation complete with Bills of Material. Resolve product/process problems, support development of new products/processes, initiate technical investigations, and prepare design specifications, analyses, and make recommendations for presentation and approval. | 3/7/2019 |
| 1308 | Olympus Richmond Hill, Ca Endoscope Technician I - Recovery HS Diploma Exp: 1+ years in technical repairs |
The Endoscope Technician must understand and accept the responsibility to ensure the safety of all Olympus products that are repaired by strictly following established processes and procedures. Under the direction of the Manager, the incumbent shall evaluate, troubleshoot, disassemble, assemble, repair and inspect Endoscopes, Electronics, or Microscopy products to meet company product standards and ensure full and proper functioning of the repaired product. Level I Technician: Assignments are semi-routine difficulty level. Requires daily supervision, detailed instruction on new assignments. | 3/7/2019 |
| 1309 | Olympus Waltham, MA Production Test Technician II HS Diploma Exp: 1+ years in technical repairs |
The Production Test Technician II will perform the set-up, calibration, testing and troubleshooting of circuits, components, instruments and mechanical assemblies. Follow methods and procedures from drawings, diagrams and test plans. May complete rework on assemblies and / or systems as a result of testing. Job duties include: Adhere to policy and procedures to maintain a safe and clean work environment. Apply acquired job skills, company policies and procedures to complete assigned tasks and adherence to production plan schedules while producing high quality products to standards. Advise management of adverse manufacturing and/or equipment conditions and issues that are affecting production and /or safety. | 3/7/2019 |
| 1310 | Olympus Multiple Locations, na Field Service Engineer I AS or BS/BA in electrical, biomedical, or computer sciences Exp: 1+ years of servicing/reparing electronics |
As a Field Service Engineer I working on the Field Service team, you will be empowered and inspired to do your best work. You will contribute to our mission by providing our customers with the best support and repair solutions, assisting our field sales teams with installations and maintenance of equipment and contributing to the growth of the division. Duties will incude: Performing new equipment installations, upgrades, post installation testing, troubleshooting and all other aspects of technical support for all endoscope, mechanical, electronic, video, computer, LAN and network products. Troubleshooting, diagnosing, and repairing the entire line of medical electronic, video, computer and network products on customer premises, at Olympus repair facilities, and when necessary via telephone. Escalating support issues when customer satisfaction is jeopardized and report all product non-conformance and safety concerns. | 3/7/2019 |
| 1311 | Oncotherapy Solutions LLC Seattle, WA Research Associate I MS in biological sciences Exp: 1+ years |
Oncotherapy Solutions LLC is seeking a highly motivated and creative research associate to characterize and test drug conjugates in-vitro as well as analyze tissue and blood samples from outsourced in-vivo studies. Responsibilities include: Perform solubility and in-vitro stability assays as well as formulation of drug conjugates. Conduct viability and apoptosis in-vitro assays using cancer cell lines, normal cells and immortalized non-tumorigenic cell lines. Extract and purify nucleic acids and proteins from cells, tumor and normal tissues as well as perform RT-PCR, PAGE, western blotting and ELIZA. | 3/7/2019 |
| 1312 | Thermo Fisher Scientific Saint Louis , MO Scientist I, Analytical and Formulation Sciences BS in biology, chemistry ore equivalent Exp: 0-2 years |
Perform various chromatography assays including reverse phase, size exclusion, affinity and ion exchange chromatography. Participate in analytical studies to support method and formulation development, structural characterization, comparability, forced degradation, and other development activities of biopharmaceuticals at all stages of clinical development. Conducts routine tasks and sample analyses to support process development. Executes, records, and evaluates experimental data appropriately, including the writing and revising of process development reports and technology transfer protocols as needed. | 3/7/2019 |
| 1313 | Thermo Fisher Scientific Cincinnati, OH Research & Development/Manufacturing Scientist I BS/BA in science or engineering Exp: 0-2 years in metrology support |
Provides Metrology support in a laboratory environment by following standard practices. Performs laboratory instrument calibrations, qualifications, preventative maintenance, and repairs as assigned. Makes detailed observations and reviews, documents, and communicates test results. Essential functions include: Executes test methods for instrumentation including, but not limited to; LC, GC, dissolution, spectroscopy, pH meters, thermometers, and balances. Recognizes and reports out-of-specification or unexpected results and non-routine instrument mechanical performance problems. Supports routine instrument preventative maintenance and troubleshoots unplanned mechanical repairs. | 3/7/2019 |
| 1314 | Thermo Fisher Scientific Cincinnati, OH Research & Development/Manufacturing Scientist I BS/BA in science or engineering Exp: 0-2 years in metrology support |
Provides Metrology support in a laboratory environment by following standard practices. Performs laboratory instrument calibrations, qualifications, preventative maintenance, and repairs as assigned. Makes detailed observations and reviews, documents, and communicates test results. Essential functions include: Executes test methods for instrumentation including, but not limited to; LC, GC, dissolution, spectroscopy, pH meters, thermometers, and balances. Recognizes and reports out-of-specification or unexpe |