7567 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 | 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 |
| 2 | 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 |
| 3 | 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 |
| 4 | 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 |
| 5 | 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 |
| 6 | 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 |
| 7 | 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 |
| 8 | 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 |
| 9 | 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 |
| 10 | 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 |
| 11 | 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 |
| 12 | 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 |
| 13 | 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 |
| 14 | 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 |
| 15 | 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 |
| 16 | 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 |
| 17 | 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 |
| 18 | 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 |
| 19 | 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 |
| 20 | 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 |
| 21 | 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 |
| 22 | 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 |
| 23 | 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 |
| 24 | 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 |
| 25 | 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 |
| 26 | 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 |
| 27 | 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 |
| 28 | 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 |
| 29 | 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 |
| 30 | 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 |
| 31 | 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 |
| 32 | 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 |
| 33 | 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 |
| 34 | 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 |
| 35 | 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 |
| 36 | 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 |
| 37 | 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 |
| 38 | 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 |
| 39 | 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 |
| 40 | 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 |
| 41 | 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 |
| 42 | 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 |
| 43 | 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 |
| 44 | 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 |
| 45 | 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 |
| 46 | 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 |
| 47 | 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 |
| 48 | 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 |
| 49 | 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 |
| 50 | 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 |
| 51 | 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 |
| 52 | 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 |
| 53 | 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 |
| 54 | 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 |
| 55 | 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 |
| 56 | 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 |
| 57 | 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 |
| 58 | 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 |
| 59 | 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 |
| 60 | 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 |
| 61 | 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 |
| 62 | 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 |
| 63 | 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 |
| 64 | 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 |
| 65 | 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 |
| 66 | 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 |
| 67 | 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 |
| 68 | 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 |
| 69 | 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 |
| 70 | 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 |
| 71 | 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 |
| 72 | 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 |
| 73 | 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 |
| 74 | 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 |
| 75 | 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 |
| 76 | 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 |
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| 78 | 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 |
| 79 | 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 |
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| 90 | 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 |
| 91 | 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 |
| 92 | 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 |
| 93 | 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 |
| 94 | 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 |
| 95 | 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 |
| 96 | 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 |
| 97 | 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 |
| 98 | 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 |
| 99 | 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 |
| 100 | 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 |
| 101 | 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 |
| 102 | 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 |
| 103 | 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 |
| 104 | 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 |
| 105 | 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 |
| 106 | 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 |
| 107 | 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 |
| 108 | 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 |
| 109 | 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 |
| 110 | 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 |
| 111 | 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 |
| 112 | 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 |
| 113 | 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 |
| 114 | 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 |
| 115 | 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 |
| 116 | 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 |
| 117 | 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 |
| 118 | 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 |
| 119 | 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 |
| 120 | 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 |
| 121 | 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 |
| 122 | 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 |
| 123 | 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 |
| 124 | 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 |
| 125 | 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 |
| 126 | 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 |
| 127 | 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 |
| 128 | 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 |
| 129 | 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 |
| 130 | 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 |
| 131 | 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 |
| 132 | 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 |
| 133 | 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 |
| 134 | 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 |
| 135 | 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 |
| 136 | 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 |
| 137 | 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 |
| 138 | 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 |
| 139 | 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 |
| 140 | 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 |
| 141 | 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 |
| 142 | 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 |
| 143 | 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 |
| 144 | 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 |
| 145 | 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 |
| 146 | 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 |
| 147 | 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 |
| 148 | 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 |
| 149 | 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 |
| 150 | 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 |
| 151 | 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 |
| 152 | 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 |
| 153 | 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 |
| 154 | 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 |
| 155 | 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 |
| 156 | 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 |
| 157 | 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 |
| 158 | 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 |
| 159 | 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 |
| 160 | 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 |
| 161 | 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 |
| 162 | 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 |
| 163 | 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 |
| 164 | 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 |
| 165 | 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 |
| 166 | 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 |
| 167 | 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 |
| 168 | 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 |
| 169 | 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 |
| 170 | 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 |
| 171 | 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 |
| 172 | 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 |
| 173 | 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 |
| 174 | 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 |
| 175 | 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 |
| 176 | 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 |
| 177 | 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 |
| 178 | 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 |
| 179 | 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 |
| 180 | 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 |
| 181 | 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 |
| 182 | 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 |
| 183 | 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 |
| 184 | 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 |
| 185 | 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 |
| 186 | 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 |
| 187 | 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 |
| 188 | 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 |
| 189 | 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 |
| 190 | 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 |
| 191 | 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 |
| 192 | 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 |
| 193 | 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 |
| 194 | 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 |
| 195 | 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 |
| 196 | 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 |
| 197 | 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 |
| 198 | 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 |
| 199 | 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 |
| 200 | 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 |
| 201 | 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 |
| 202 | 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 |
| 203 | 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 |
| 204 | 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 |
| 205 | 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 |
| 206 | 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 |
| 207 | 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 |
| 208 | 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 |
| 209 | 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 |
| 210 | 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 |
| 211 | 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 |
| 212 | 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 |
| 213 | 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 |
| 214 | 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 |
| 215 | 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 |
| 216 | 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 |
| 217 | 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 |
| 218 | 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 |
| 219 | 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 |
| 220 | 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 |
| 221 | 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 |
| 222 | 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 |
| 223 | 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 |
| 224 | 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 |
| 225 | 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 |
| 226 | 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 |
| 227 | 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 |
| 228 | 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 |
| 229 | 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 |
| 230 | 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 |
| 231 | 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 |
| 232 | 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 |
| 233 | 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 |
| 234 | 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 |
| 235 | 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 |
| 236 | 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 |
| 237 | 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 |
| 238 | 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 |
| 239 | 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 |
| 240 | 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 |
| 241 | 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 |
| 242 | 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 |
| 243 | 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 |
| 244 | 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 |
| 245 | 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 |
| 246 | 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 |
| 247 | 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 |
| 248 | 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 |
| 249 | 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 |
| 250 | 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 |
| 251 | 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 |
| 252 | 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 |
| 253 | 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 |
| 254 | 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 |
| 255 | 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 |
| 256 | 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 |
| 257 | 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 |
| 258 | 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 |
| 259 | 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 |
| 260 | 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 |
| 261 | 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 |
| 262 | 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 |
| 263 | 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 |
| 264 | 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 |
| 265 | 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 |
| 266 | 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 |
| 267 | 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 |
| 268 | 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 |
| 269 | 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 |
| 270 | 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 |
| 271 | 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 |
| 272 | 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 |
| 273 | 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 |
| 274 | 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 |
| 275 | 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 |
| 276 | 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 |
| 277 | 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 |
| 278 | 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 |
| 279 | 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 |
| 280 | 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 |
| 281 | 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 |
| 282 | 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 |
| 283 | 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 |
| 284 | 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 |
| 285 | 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 |
| 286 | 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 |
| 287 | 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 |
| 288 | 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 |
| 289 | 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 |
| 290 | 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 |
| 291 | 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 |
| 292 | 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 |
| 293 | 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 |
| 294 | 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 |
| 295 | 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 |
| 296 | 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 |
| 297 | 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 |
| 298 | 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 |
| 299 | 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 |
| 300 | 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 |
| 301 | 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 |
| 302 | 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 |
| 303 | 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 |
| 304 | 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 |
| 305 | 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 |
| 306 | 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 |
| 307 | 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 |
| 308 | 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 |
| 309 | 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 |
| 310 | 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 |
| 311 | 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 |
| 312 | 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 |
| 313 | 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 |
| 314 | 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 |
| 315 | 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 |
| 316 | 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 |
| 317 | 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 |
| 318 | 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 |
| 319 | 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 |
| 320 | 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 |
| 321 | 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 |
| 322 | 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 |
| 323 | 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 |
| 324 | 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 |
| 325 | 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 |
| 326 | 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 |
| 327 | 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 |
| 328 | 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 |
| 329 | 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 |
| 330 | 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 |
| 331 | 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 |
| 332 | 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 |
| 333 | 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 |
| 334 | 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 |
| 335 | 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 |
| 336 | 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 |
| 337 | 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 |
| 338 | 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 |
| 339 | 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 |
| 340 | 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 |
| 341 | 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 |
| 342 | 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 |
| 343 | 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 |
| 344 | 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 |
| 345 | 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 |
| 346 | 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 |
| 347 | 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 |
| 348 | 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 |
| 349 | 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 |
| 350 | 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 |
| 351 | 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 |
| 352 | 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 |
| 353 | 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 |
| 354 | 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 |
| 355 | 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 |
| 356 | 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 |
| 357 | 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 |
| 358 | 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 |
| 359 | 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 |
| 360 | 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 |
| 361 | 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 |
| 362 | 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 |
| 363 | 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 |
| 364 | 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 |
| 365 | 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 |
| 366 | 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 |
| 367 | 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 |
| 368 | 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 |
| 369 | 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 |
| 370 | 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 |
| 371 | 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 |
| 372 | 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 |
| 373 | 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 |
| 374 | 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 |
| 375 | 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 |
| 376 | 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 |
| 377 | 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 |
| 378 | 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 |
| 379 | 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 |
| 380 | 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 |
| 381 | 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 |
| 382 | 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 |
| 383 | 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 |
| 384 | 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 |
| 385 | 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 |
| 386 | 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 |
| 387 | 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 |
| 388 | 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 |
| 389 | 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 |
| 390 | 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 |
| 391 | 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 |
| 392 | 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 |
| 393 | 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 |
| 394 | 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 |
| 395 | 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 |
| 396 | 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 |
| 397 | 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 |
| 398 | 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 |
| 399 | 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 |
| 400 | 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 |
| 401 | 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 |
| 402 | 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 |
| 403 | 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 |
| 404 | 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 |
| 405 | 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 |
| 406 | 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 |
| 407 | 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 |
| 408 | 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 |
| 409 | 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 |
| 410 | 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 |
| 411 | 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 |
| 412 | 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 |
| 413 | 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 |
| 414 | 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 |
| 415 | 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 |
| 416 | 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 |
| 417 | 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 |
| 418 | 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 |
| 419 | 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 |
| 420 | 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 |
| 421 | 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 |
| 422 | 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 |
| 423 | 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 |
| 424 | 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 |
| 425 | 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 |
| 426 | 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 |
| 427 | 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 |
| 428 | 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 |
| 429 | 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 |
| 430 | 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 |
| 431 | 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 |
| 432 | 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 |
| 433 | 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 |
| 434 | 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 |
| 435 | 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 |
| 436 | 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 |
| 437 | 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 |
| 438 | 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 |
| 439 | 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 |
| 440 | 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 |
| 441 | 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 |
| 442 | 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 |
| 443 | 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 |
| 444 | 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 |
| 445 | 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 |
| 446 | 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 |
| 447 | 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 |
| 448 | 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 |
| 449 | 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 |
| 450 | 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 |
| 451 | 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 |
| 452 | 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 |
| 453 | 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 |
| 454 | 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 |
| 455 | 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 |
| 456 | 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 |
| 457 | 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 |
| 458 | 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 |
| 459 | 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 |
| 460 | 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 |
| 461 | 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 |
| 462 | 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 |
| 463 | 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 |
| 464 | 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 |
| 465 | 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 |
| 466 | 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 |
| 467 | 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 |
| 468 | 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 |
| 469 | 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 |
| 470 | 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 |
| 471 | 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 |
| 472 | 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 |
| 473 | 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 |
| 474 | 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 |
| 475 | 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 |
| 476 | 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 |
| 477 | 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 |
| 478 | 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 |
| 479 | 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 |
| 480 | 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 |
| 481 | 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 |
| 482 | 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 |
| 483 | 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 |
| 484 | 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 |
| 485 | 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 |
| 486 | 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 |
| 487 | 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 |
| 488 | 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 |
| 489 | 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 |
| 490 | 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 |
| 491 | 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 |
| 492 | 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 |
| 493 | 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 |
| 494 | 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 |
| 495 | 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 |
| 496 | 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 |
| 497 | 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 |
| 498 | 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 |
| 499 | 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 |
| 500 | 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 |
| 501 | 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 |
| 502 | 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 |
| 503 | 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 |
| 504 | 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 |
| 505 | 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 |
| 506 | 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 |
| 507 | 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 |
| 508 | 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 |
| 509 | 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 |
| 510 | 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 |
| 511 | 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 |
| 512 | 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 |
| 513 | 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 |
| 514 | 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 |
| 515 | 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 |
| 516 | 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 |
| 517 | 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 |
| 518 | 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 |
| 519 | 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 |
| 520 | 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 |
| 521 | 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 |
| 522 | 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 |
| 523 | 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 |
| 524 | 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 |
| 525 | 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 |
| 526 | 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 |
| 527 | 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 |
| 528 | 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 |
| 529 | 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 |
| 530 | 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 |
| 531 | 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 |
| 532 | 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 |
| 533 | 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 |
| 534 | 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 |
| 535 | 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 |
| 536 | 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 |
| 537 | 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 |
| 538 | 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 |
| 539 | 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 |
| 540 | 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 |
| 541 | 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 |
| 542 | 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 |
| 543 | 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 |
| 544 | 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 |
| 545 | 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 |
| 546 | 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 |
| 547 | 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 |
| 548 | 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 |
| 549 | 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 |
| 550 | 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 |
| 551 | 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 |
| 552 | 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 |
| 553 | 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 |
| 554 | 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 |
| 555 | 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 |
| 556 | 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 |
| 557 | 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 |
| 558 | 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 |
| 559 | 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 |
| 560 | 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 |
| 561 | 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 |
| 562 | 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 |
| 563 | 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 |
| 564 | 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 |
| 565 | 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 |
| 566 | 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 |
| 567 | 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 |
| 568 | 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 |
| 569 | 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 |
| 570 | 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 |
| 571 | 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 |
| 572 | 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 |
| 573 | 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 |
| 574 | 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 |
| 575 | 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 |
| 576 | 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 |
| 577 | 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 |
| 578 | 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 |
| 579 | 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 |
| 580 | 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 |
| 581 | 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 |
| 582 | 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 |
| 583 | 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 |
| 584 | 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 |
| 585 | 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 |
| 586 | 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 |
| 587 | 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 |
| 588 | 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 |
| 589 | 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 |
| 590 | 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 |
| 591 | 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 |
| 592 | 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 |
| 593 | 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 |
| 594 | 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 |
| 595 | 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 |
| 596 | 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 |
| 597 | 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 |
| 598 | 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 |
| 599 | 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 |
| 600 | 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 |
| 601 | 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 |
| 602 | 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 |
| 603 | 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 |
| 604 | 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 |
| 605 | 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 |
| 606 | 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 |
| 607 | 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 |
| 608 | 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 |
| 609 | 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 |
| 610 | 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 |
| 611 | 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 |
| 612 | 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 |
| 613 | 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 |
| 614 | 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 |
| 615 | 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 |
| 616 | 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 |
| 617 | 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 |
| 618 | 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 |
| 619 | 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 |
| 620 | 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 |
| 621 | 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 |
| 622 | 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 |
| 623 | 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 |
| 624 | 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 |
| 625 | 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 |
| 626 | 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 |
| 627 | 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 |
| 628 | 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 |
| 629 | 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 |
| 630 | 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 |
| 631 | 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 |
| 632 | 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 |
| 633 | 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 |
| 634 | 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 |
| 635 | 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 |
| 636 | 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 |
| 637 | 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 |
| 638 | 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 |
| 639 | 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 |
| 640 | 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 |
| 641 | 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 |
| 642 | 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 |
| 643 | 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 |
| 644 | 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 |
| 645 | 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 |
| 646 | 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 |
| 647 | 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 |
| 648 | 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 |
| 649 | 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 |
| 650 | 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 |
| 651 | 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 |
| 652 | 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 |
| 653 | 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 |
| 654 | 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 |
| 655 | 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 |
| 656 | 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 |
| 657 | 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 |
| 658 | 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 |
| 659 | 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 |
| 660 | 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 |
| 661 | 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 |
| 662 | 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 |
| 663 | 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 |
| 664 | 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 |
| 665 | 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 |
| 666 | 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 |
| 667 | 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 |
| 668 | 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 |
| 669 | 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 |
| 670 | 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 |
| 671 | 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 |
| 672 | 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 |
| 673 | 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 |
| 674 | 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 |
| 675 | 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 |
| 676 | 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 |
| 677 | 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 |
| 678 | 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 |
| 679 | 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 |
| 680 | 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 |
| 681 | 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 |
| 682 | 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 |
| 683 | 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 |
| 684 | 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 |
| 685 | 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 |
| 686 | 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 |
| 687 | 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 |
| 688 | 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 |
| 689 | 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 |
| 690 | 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 |
| 691 | 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 |
| 692 | 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 |
| 693 | 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 |
| 694 | 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 |
| 695 | 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 |
| 696 | 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 |
| 697 | 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 |
| 698 | 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 |
| 699 | 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 |
| 700 | 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 |
| 701 | 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 |
| 702 | 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 |
| 703 | 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 |
| 704 | 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 |
| 705 | 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 |
| 706 | 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 |
| 707 | 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 |
| 708 | 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 |
| 709 | 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 |
| 710 | 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 |
| 711 | 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 |
| 712 | 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 |
| 713 | 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 |
| 714 | 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 |
| 715 | 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 |
| 716 | 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 |
| 717 | 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 |
| 718 | 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 |
| 719 | 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 |
| 720 | 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 |
| 721 | 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 |
| 722 | 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 |
| 723 | 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 |
| 724 | 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 |
| 725 | 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 |
| 726 | 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 |
| 727 | 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 |
| 728 | 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 |
| 729 | 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 |
| 730 | 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 |
| 731 | 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 |
| 732 | 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 |
| 733 | 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 |
| 734 | 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 |
| 735 | 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 |
| 736 | 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 |
| 737 | 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 |
| 738 | 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 |
| 739 | 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 |
| 740 | 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 |
| 741 | 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 |
| 742 | 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 |
| 743 | 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 |
| 744 | 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 |
| 745 | 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 |
| 746 | 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 |
| 747 | 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 |
| 748 | 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 |
| 749 | 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 |
| 750 | 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 |
| 751 | 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 |
| 752 | 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 |
| 753 | 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 |
| 754 | 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 |
| 755 | 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 |
| 756 | 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 |
| 757 | 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 |
| 758 | 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 |
| 759 | 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 |
| 760 | 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 |
| 761 | 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 |
| 762 | 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 |
| 763 | 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 |
| 764 | 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 |
| 765 | 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 |
| 766 | 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 |
| 767 | 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 |
| 768 | 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 |
| 769 | 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 |
| 770 | 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 |
| 771 | 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 |
| 772 | 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 |
| 773 | 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 |
| 774 | 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 |
| 775 | 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 |
| 776 | 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 |
| 777 | 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 |
| 778 | 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 |
| 779 | 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 |
| 780 | 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 |
| 781 | 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 |
| 782 | 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 |
| 783 | 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 |
| 784 | 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 |
| 785 | 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 |
| 786 | 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 |
| 787 | 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 |
| 788 | 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 |
| 789 | 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 |
| 790 | 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 |
| 791 | 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 |
| 792 | 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 |
| 793 | 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 |
| 794 | 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 |
| 795 | 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 |
| 796 | 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 |
| 797 | 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 |
| 798 | 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 |
| 799 | 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 |
| 800 | 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 |
| 801 | 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 |
| 802 | 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 |
| 803 | 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 |
| 804 | 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 |
| 805 | 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 |
| 806 | 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 |
| 807 | 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 |
| 808 | 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 |
| 809 | 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 |
| 810 | 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 |
| 811 | 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 |
| 812 | 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 |
| 813 | 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 |
| 814 | 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 |
| 815 | 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 |
| 816 | 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 |
| 817 | 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 |
| 818 | 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 |
| 819 | 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 |
| 820 | 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 |
| 821 | 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 |
| 822 | 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 |
| 823 | 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 |
| 824 | 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 |
| 825 | 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 |
| 826 | 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 |
| 827 | 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 |
| 828 | 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 |
| 829 | 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 |
| 830 | 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 |
| 831 | 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 |
| 832 | 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 |
| 833 | 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 |
| 834 | 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 |
| 835 | 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 |
| 836 | 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 |
| 837 | 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 |
| 838 | 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 |
| 839 | 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 |
| 840 | 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 |
| 841 | 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 |
| 842 | 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 |
| 843 | 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 |
| 844 | 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 |
| 845 | 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 |
| 846 | 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 |
| 847 | 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 |
| 848 | 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 |
| 849 | Thermo Fisher Scientific Greenville, NC Formulation Technician HS Diploma Exp: 1+ years in manufacturing/productions |
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. | 3/7/2019 |
| 850 | OPKO Diagnostics Woburn, MA Research Associate, Conjugation Chemistry BS in chemistry/biochemistry Exp: 1-2 years |
OPKO Diagnostics is seeking a highly motivated Research Associate with a Bachelor's degree in Chemistry or Biochemistry and/or prior hands-on experience in bioconjugation and purification to join our research group in Woburn, Massachusetts. As a member of the R&D group, you will be working closely with in-house expert in conjugation chemistry and contribute to the development of innovative diagnostics tests on the Claros Analyzer platform. Responsibilities include: Plan, perform and document protein modification and bioconjugation experiments. Prepare, purify (e.g. HPLC, continuous gel electrophoresis) and analyze (Native and SDS PAGE) protein and antibody conjugates. Conduct experiments to improve efficiency and scalability of conjugates to support routine manufacturing. | 3/7/2019 |
| 851 | OPKO Diagnostics Woburn, MA Research Associate BS or MS in biology, chemistry or related Exp: 1+ years lab experience |
We are looking for a Research Associate with interest and experience in commercial product development for IVD immunoassays. The candidate will contribute to assay development activities on OPKO’s proprietary microfluidic cassette/platform. Responsibilities include: Design, plan, perform, and document product development activities, including immunoreagent development, immunoassay optimization, and analytical/clinical studies. Troubleshoot experiments, consult literature and actively propose/pursue solutions. Assist in the design and development of assays on the Claros platform, contribute to regulatory activities with development reports, and participate in verification / validation activities. | 3/7/2019 |
| 852 | Oranogenesis La Jolla, CA Manufacturing Associate I - DG Growth Biotech Program certification Exp: 0-1 years |
Manufacturing Technician I is responsible for completing and assisting with daily tasks associated with cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Additionally, the Technician I will be responsible for following SOPs, performing daily tasks in a clean room/cGMP environment per the current QSRs. The Manufacturing Technician I may also be responsible for the troubleshooting of manufacturing challenges. Follows established company rules, regulations and safety precautions, and maintains quality standards. | 3/7/2019 |
| 853 | Oranogenesis La Jolla, CA Lab Associate I/II BS/BA in life sciences Exp: 0-2 years lab experience |
The candidate will be involved in a variety of activities including but not limited to: working on biomaterial and cell based studies; general lab support and maintenance; materials testing; running established assays. The individual will participate in the execution of experiments in a team environment or independently post adequate training, and will support the data analysis and reporting of results as needed. | 3/7/2019 |
| 854 | Origene Rockville, MD Research Associate - Immunology BS in biology, chemistry or life sciences Exp: 1-2 years lab experience |
Responsibilities include: Involves multiple de novo R/D projects for antibodyand assay products development.Performsvalidation tests on variant sera or antibody samples. Participates other duties such as antibody production, purification and conjugation. Records experiment procedure and results in notebooks and computer accurately. etc | 3/7/2019 |
| 855 | Orthofix Lewisville, KY Design Assurance Engineer BS in mechanical engineering or related Exp: 0-2 years |
This position is responsible for providing Design Assurance support to product development activities within Orthofix supporting all new product development and selected sustaining or specials projects in Orthofix. The position will report to the Quality Director. The position must also ensure compliance with applicable product standards, governing laws and regulations, and company quality system requirements. Responsibilities include: Root cause analysis, problem solving, continuous improvement and related corrective and preventive action as they relate to complaints, non-conforming material, post-market surveillance (PMS), and other quality data, Quality Planning, Input and approval for design verification and validation testing of new designs and design changes to ensure product design quality and integrity. | 3/7/2019 |
| 856 | Orthofix Lewisville, KY Development Engineer BS in mechanical or biomedical engineer Exp: 0-2 years |
Entry level engineering position responsible for supporting projects lead by more senior engineers. Responsibilities include: developing CAD models/drawings, authoring test protocols and reports, performs product testing, etc. | 3/7/2019 |
| 857 | Osiris Columbia, MD Equipment Specialist AS/AA in biomedical technology Exp: 0-2 years |
Equipment Specialist will perform a variety of functions associated with the selection, acquisition, implementation, and qualification (FAT, IQ, OQ, and PQ) of all equipment and systems related to the laboratories, logistics, and manufacturing departments. The Equipment Specialist will assure that all equipment and systems operate in a safe and sound manner through proper calibration, maintenance, and repairs while developing and providing proper functionality training to others. Under the supervision of management, will have the oversight of contractors performing maintenance and/or service activities on equipment and systems. Will confer with management to identify equipment and systems with areas of concern and prioritize projects based on need. | 3/7/2019 |
| 858 | Osiris Columbia, MD Biotechnology, Document Control Specialist AS or BS/BA in sciences Exp: 1+ years in regulated environment |
The primary purpose of this position is to issue batch production records and product labels to manufacturing in a timely manner to meet the production schedule. Principle responsibilities include: Assignment of product lot numbers and issuance and inspection of batch records associated with each manufacturing process. Generation and inspection of complex product labelling for all products in current production, including the ability to identify minute defects on printed labels. Coordinating printing schedule based on production plan to ensure manufacturing operations are not halted through lack of batch records or product labels. Maintaining controlled area inventory, packing and verifying quality records to be sent to off-site storage. | 3/7/2019 |
| 859 | Osmotica Pharmaceuticals Marietta, GA Analytical Chemist I BS in chemistry, biochemistry or related Exp: 0-5 years |
The Analytical Chemist is responsible for testing of raw materials, in-process materials, and finished products to support release and stability programs. Perform laboratory tests such as sample extractions, set up and execution of chromatographic methods (HPLC and GC), and dissolution testing. Develops and executes UV, IR and PSD measurements and wet techniques as applied in the Pharmaceutical Analysis/Testing of products and excipients. Executes components of method validation and method transfer projects. | 3/7/2019 |
| 860 | AMRI Rensselaer, NY Research Scientist I BS or MS in chemistry or related Exp: 0-5 years in medicinal chemistry |
The Research Scientist I/II is an integral part of the AMRI team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. Responsibilities include: Synthesize compounds efficiently using literature or in-house notebook procedures. Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques. Analyze and identify compounds using a good range of modern separation and spectroscopic techniques. This will include interpretation of TLC, HPLC, polarimetry, IR, and NMR spectra of moderate complexity. | 3/7/2019 |
| 861 | AMRI Lebanon, NJ Quality Assurance Associate BS/BA in chemistry or related Exp: 0-2 years |
The Package Testing Technician is an integral part of the AMRI team, contributing to our success by performing data review, auditing laboratories, investigation/corrective action follow-up, and reviewing written procedures. Responsibilities include: Independently perform duties, both routine and non-routine, completed in a reliable and accurate manner. Endure the integrity of the final report of analysis being in compliance with all regulatory and company standards. Primary QA reviewer of all analytical data generated in the laboratory and performs weekly review of all logbooks, temperature tracking documents and any other related logs maintained in the laboratory. | 3/7/2019 |
| 862 | AMRI Alburquerque, NM Chemist I BS/BA in chemistry or related Exp: 0-2 years |
The Chemist I is responsible for support of the manufacturing department and external customers. The routine functions of the laboratory are testing of raw materials, in-process, end product, and stability samples. The Chemist I will also performs particulate testing and tests plant water for production. The chemistry department is responsible for the successful transfer of new customer products and method testing. Perform routine laboratory testing tasks using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer. Have the potential and willingness to train on new techniques | 3/7/2019 |
| 863 | AMRI West Lafayette, IN Research Scientist I BS/BA in chemistry or related Exp: 0-1 years |
The Research Scientist I is an integral part of the AMRI team, contributing to our success by performing laboratory experiments and instrumental testing in the Analytical Development group. Responsibilities include: Conduct laboratory experiments as part of development and validation of solid-state chemistry analytical methods to support drug development processes, including but not limited to preparation of solid-state mixtures and studies of solid-state attributes of materials. Perform routine instrumental testing according to study design and under the guidance of the project leader. | 3/7/2019 |
| 864 | 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. | 3/7/2019 |
| 865 | AMRI Burlington, MA Microbiologist BS in life sciences Exp: 1 year 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. Some responsibilities include: Perform microbiological testing (endotoxin, sterility and bioburden) for raw materials, in-process materials, intermediates and final product. Perform environmental monitoring of the clean rooms (under ISO and EU specifications). Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results. | 3/7/2019 |
| 866 | Pace Analytical Maplewood, MN Biochemist - Food Safety BS in biochemistry, microbio or related Exp: 1-3 years lab experience |
This candidate will perform testing as part of a product development team that deals with food safety. Responsibilities include: Perform allergen identification and measurement by ELISA and Lateral Flow Devices. Perform a wide range of general microbiology testing to include: particulate analysis, sterility testing, and microbial identification. Conduct analysis of products using traditional microbiological techniques such as serial dilution, pour plating, and filtration. Participate in general laboratory cleaning and maintenance. | 3/8/2019 |
| 867 | Pace Analytical Lenexa, KS Laboratory Technician I - Entry Level HS Diploma Exp: 0 years |
Responsibilities of a lab technician include: Washing laboratory glassware. Responsible for keeping applicable workspaces clean and safe. Assisting other lab personnel with preparing samples, analysis, data checking and, and handling simple calculations. Disposing of samples and chemicals. Providing maintenance of stock reagents and lab supplies. Following company policies and Standard Operating Procedures (SOPs). | 3/8/2019 |
| 868 | Pace Analytical Maplewood, MN Chemist - Entry-Level HPLC BS/BA in chemistry or related Exp: 0-2 years lab experience |
Candidate will perform analytical testing to support product development on inhalation devices. This is a high volume, fast-paced lab. Analytical lab experience is necessary, but fresh grads will be considered. Complete non-chromatographic tests such as: drug content, drug impurities, water content, dose content uniformity (DCU), through life testing, next generation impactor (NGI), particle size, spray pattern, microscopic appearance in support of stability, and other studies for development of an inhalation product | 3/8/2019 |
| 869 | Pace Analytical Peachtree Corners, GA Laboratory Analyst I, Wet Chemistry BS/BA in scientific field Exp: 0-2 years |
Pace Analytical Services, LLC, a leading national analytical laboratory is seeking highly motivated candidates for a Laboratory Analyst I in the Wet Chemistry department at their laboratory in Atlanta, GA. Responsibilities include: Preparing and/or analyzing environmental samples based on published methods and Pace Standard Operating Procedures. Following quality control procedures as outlined in documented procedures. Preparing standards and reagents. Entering data into Pace Laboratory Information Management System (LIMS) as applicable. | 3/8/2019 |
| 870 | Pace Analytical Peachtree Corners, GA Laboratory Technician HS Diploma Exp: <2 years |
Entry level position in laboratory services where work is closely supervised and done in accordance with well-defined standards and procedures of an uncomplicated nature. Responsibilities include: Analyzing or preparing samples in an efficient and organized manner, using approved Pace Analytical procedures. Preparing reagents and standards. Waste handling duties to include: labeling containers, understanding storage time limits, performing proper satellite accumulation, ensuring adequate space between waste containers, ensuring all waste containers are closed and incompatible materials are stored separately, understanding secondary containment, and documenting weekly inspections, if applicable. | 3/8/2019 |
| 871 | Pace Analytical Ormond Beach, FL Laboratory Analyst - Semi-Volatiles BS/BA in sciences Exp: 0-2 years |
Tuesday - Saturday, 3 PM - 11:30 PM with possible overtime and weekend hours. Responsibilities as a lab analyst includes: Preparing and/or analyzing environmental samples based on published methods and Pace Standard Operating Procedures. Following quality control procedures as outlined in documented procedures. Preparing standards and reagents. Entering data into Pace Laboratory Information Management System (LIMS) as applicable. | 3/8/2019 |
| 872 | Pacira Troy Hills, NJ QC Analyst I BS in chemistry Exp: 1+ years lab experience |
The purpose of this position is to carry out assigned laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process and final products. Other responsibilities include: Maintain organized records of tests performed and results obtained. This may include maintaining a computer accessible database for the purpose of tracking and trending analytical data. Conduct laboratory tests in compliance with established internal Standard Test Methods, compendial methods and vendor partners supplied methods. Assist in the development and improvement of written procedures. | 3/8/2019 |
| 873 | Pacira Troy Hills, NJ Research Associate II/Engineer I. BS in relevant field Exp: 1-4 years |
The purpose of this position is to assist in the scale up of manufacturing processes for new DepoFOAM formulations and the development of analytical methods to characterize materials for those efforts. Responsibilities include: Provide technical and analytical assistance to support new product development and process scale-up. Perform hands on work to set-up and execute experiments on bench-top, lab, and pilot scale manufacturing equipment. Support the technology-transfer of processes to the pilot and commercial scales to produce material for pre-clinical evaluation and clinical trials. Execute analytical methods for in-process and product material characterization, performing physical and chemical stability studies as needed. Maintain good working knowledge of the use, maintenance and repair of laboratory and manufacturing equipment. | 3/8/2019 |
| 874 | Pandion Therapeutics Cambridge , MA Associate Scientist, Immunology Research BS or MS in relavent field Exp: 0-2 years |
Responsibilities include: Developand performin vitro/ex vivo human and murine primary cell-based assays. In vivo pharmacology including test article dosing, blood collection and tissue harvesting. mmune cell isolation from whole blood and tissues, flow cytometry, cell sorting,ELISA/MSD/HTRF. | 3/8/2019 |
| 875 | Par Pharmaceuticals Rochester, MI Quality Associate II, Document Control AA/AS degree Exp: 1-2 years |
The Quality Associate II, Document Control follows the applicable Document Control SOPs and requirements in order to maintain a controlled environment within Document Control. This role, which is customer service oriented, works with various departments to either retrieve completed documents or generate new documents. Works in more complex areas of Document Control including APR documents, the Electronic Document Management System (EDMS), and management of documents during regulatory inspections. Provides guidance to the Document Control staff. Trains Quality Associate I, Document Control. Works with the team in maintaining a collaborative environment. | 3/8/2019 |
| 876 | Par Pharmaceuticals Irvine, CA Quality Associate I - 2nd Shift HS Diploma Exp: 0-1 years |
The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging. Quality activities include product sampling and inspection, area clearance to confirm process readiness, and non-conforming event support to resolve in-process issues. Communicates to multiple departments and supervision to provide timely process and issue updates. Identifies and escalates issues or problems to appropriate supervision. Participates as a team member on cross-functional teams. Participates in reviews and structured processes for continuous improvement. | 3/8/2019 |
| 877 | Paragon Bioservices Harmans, MD Quality Control Analyst I-II - Environmental Monitoring AS/AA in life sciences Exp: 0-2 years GMP clean room experience |
This role is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II/III and Commercial GMP manufacturing. Key responsibilities include but are not limited to: Perform Environmental Monitoring of Grade B-D Cleanrooms, including sampling of viable surfaces, viable air and non-viable particulates in a Phase I/II/III/Commercial GMP Manufacturing facility. Conducts routine sampling and testing of Clean Utilities such as USP water (WFI) and clean steam. Conducts bioburden testing on prepared buffers/solutions, equipment cleaning samples, in-process and release drug product samples. Ability to isolate and sub-culture microorganisms for identification. | 3/8/2019 |
| 878 | Paragon Bioservices Baltimore , MD Manufacturing Associate I - GMP Bioprocess AS/AA or BS/BA in scientific/engineering discipline Exp: 0-2 years |
The Manufacturing Associate performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. | 3/8/2019 |
| 879 | Parexel Billerica, MD Drug Safety Associate Degree in Pharmacy, nursing or life sciences Exp: 0-2 years |
The Drug Safety Specialist will provide technical and process-related support to drug safety management (clinical trials) and medical monitoring activities, ensuring compliance with relevant regulations and Standard Operating Procedures (SOPs). Daily tasks include: Triage incoming reports for completeness, legibility and validity. Electronic documentation and quality control of drug safety information. Data entry of case reports into safety database / tracking system. | 3/8/2019 |
| 880 | PBS Biotech Camarillo, CA Research Associate or Process Engineer, BioprocessR&D MS in life sciences or biotechnology Exp: 0-2 years |
This position is an invaluable opportunity to gain experience working withcutting edge technology and a variety of cell types that are significant to the rapidly emerging cell and gene therapy market. Responsibilities and tasks: Participate in research efforts for various cell culture processesbased on client needs. Prepare scientific data for external publications, abstracts, and presentations, including those atinternational conferences andtrade shows. Supportroot-cause analysis forunexpected results and provide new approachesor experimental strategiesfor problem solving | 3/8/2019 |
| 881 | PCI Pharma Services Rockford, IL Validation Analyst 1 HS Diploma Exp: 1-3 years |
The Validation Analyst I is responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities. Primary duties include: Prepares validation protocols, validation statements, reports, summaries, and master validation plans for new customer / product / system project launch and maintains existing validated processes / programs at multiple sites as well as organizing and coordinating internal and customer approvals, as needed. Ensures validation documentation completion, accuracy, and closure, including organizing and coordinating multiple approvals as required. Investigates validation deviations, documenting in formal reports, and assuring resolution of corrective action to complete project. | 3/8/2019 |
| 882 | PCI Pharma Services Philadelphia, PA Process Engineer BS in sciences or engineering Exp: 0-1 years |
The main functions of a Process Engineer are focused around two key activities of the production area: identifying and mitigating packaging issues for existing business through strong engineering and process improvement methods, and designing and supporting packaging processes for new business. Both activities are focused around technical and operational support to the production, maintenance, and support staffs in the areas of process improvement, equipment modification and optimization, safety and quality improvement, and increasing throughput. This is achieved through individual effort and facilitation of teams, tracking and analysis metrics, strong understanding and utilization of good engineering practices, project management, and the use of Lean Six Sigma techniques. | 3/8/2019 |
| 883 | PCI Pharma Services Philadelphia, PA Packaging Designer BS in related field Exp: 1-5 years |
Reporting to Package Design Manager, successful Package and Graphic Designer would utilize technical design abilities and creative insights to help develop new innovative packaging. Utilizing design software, practical packaging knowledge, graphic design abilities and hands-on assembly skills, Designer would create and prepare design solutions for PCI clients to support sales efforts as well as provide clients recommendations for optimizing existing packaging. Designer may engage clients directly in support of package creation. In addition to primary role for package design/development, Designer would support Marketing design initiatives as required. Designer supports workflows and reliability of on-site prototyping laboratory, including supplies and maintenance | 3/8/2019 |
| 884 | Penumbra Alameda, CA Quality Engineer BS/BA in engineering or scientific field Exp: 1-5 years in engineering |
As a Quality Engineer at Penumbra, you will participate in all aspects of product development, supplier development and manufacturing in order to ensure the highest level of quality in new and existing products, and their compliance to applicable regulations and standards. Responsibilities include: Represent Quality Engineering on New Product Development (NPD) cross-functional teams, interfacing among multiple departments and teams such as Manufacturing, QC, R&D, Regulatory Affairs, Operations/Planning, and Marketing. Troubleshoot, update, and improve difficult manufacturing processes for assigned product lines. | 3/8/2019 |
| 885 | Penumbra Alameda, CA Regulatory Specialist BS in sciences or engineering Exp: 1+ years in regulatory affairs |
n this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to bring our life-saving technologies to patients worldwide. Responsibilities include: Support the preparation of submissions to gain approvals for clinical research, export, and commercial distribution around the world. Support the creation, translation and review of labeling, Instructions for Use, and promotional materials. Develop a working understanding of the Quality System, biocompatibility requirements, Design Control, Medical Device Directive, Essential Requirements, ISO 13485, labeling requirements, Quality System Regulation, Canadian regulations, export requirements, and regulatory requirements of pertinent regions. | 3/8/2019 |
| 886 | Performance Validation Indianapolis, IN evel 1 Staff Validation Engineer / Specialist BS in life sciences or technical field Exp: Entry Level |
The Level 1 Validation Engineer/Specialist works within a small team environment to provide technical services to pharmaceutical or medical device manufacturers. Technical services may include interpreting drawings, manuals, or other technical information to develop requirement documents, developing testing documents that verify installation, and/or operation of the equipment, and execution /documentation of these testing documents. These documents are used by our life science customers to demonstrate compliance with USFDA regulations (or other regulatory bodies) for current Good Manufacturing Practices. | 3/8/2019 |
| 887 | PerkinElmer Thousand Oaks, CA Associate Lab Ambassador-Thousand Oaks, CA BS/BA Exp: 1+ years in customer service |
Provide high touch support for the scientist community of designated functional group(s) at designated account and general support for the on-site service engineers and technicians. Coordinate and communicate with end users regarding all aspects of OneSource Asset Management program, including service call initiation, scheduling, maintenance, inventory data integrity, escorting of vendors for “managed” activities, safety and day-today lab operations. | 3/8/2019 |
| 888 | Perrigo Covington, OH Microbiologist - 1st Shift/Rotating 2/2/3 Schedule BS in biological, or food sciences Exp: 1+ years in GMP environment |
Responsibilities include: microbiology (aerobic plate counts, probable number analysis, isolating/identifying bacterial cultures, ELISA, PCR, etc.) and routine lab functions (data entry, maintaining bacterial control cultures, instrument maintenance, etc.) | 3/8/2019 |
| 889 | Perrigo Allegan, MI Associate Packaging Engineer BS/BA in packaging engineering or other engineering Exp: 0-6 years |
Provides comprehensive package engineering support and packaging component expertise to the company through the design, development, and maintenance of packaging standards for various company and outside sub-contracting product packaging sites. Responsibilities include: Troubleshoots and resolves packaging issues associated with packaging component quality, packaging equipment, and packaging line efficiency, participates in packaging component deviation resolutions, and coordinates, conducts, and documents packaging line trials for new or improved packaging components. Works closely with other functional areas and multi-functional teams such as Operations, Sales, Marketing, Procurement, Contract Customers, Contract Packagers, Master Data, Art and Quality to launch new products/packages, develops promotions and displays, develops cost savings initiative, and troubleshoots packaging problems. | 3/8/2019 |
| 890 | Personalis Menlo Park, CA Laboratory Assistant BS in life sciences or related Exp: 0-2 years |
We are looking for a team-oriented Laboratory Assistant to join our operations team. The ideal individual must have the ability to think on their feet and troubleshoot issues. Responsibilities include: Adhere to the laboratory's quality control policies. Participate in laboratory support work as required by the team needs and at the direction of laboratory management. Following the laboratory’s procedures for specimen handling, receipt and data entry into the lab information management system (LIMS). Maintain lab equipment. Etc. | 3/8/2019 |
| 891 | Pfenex San Diego, CA Associate Scientist I MS in biology, chemistry, or related Exp: 1+ years lab experience |
Pfenex is looking to bring on a contract Associate Scientist 1 , to join the Analytical Sciences team. As a key member of the Analytical Biochemistry Group, the Associate Scientist I ,is responsible for executing analytical and biochemical characterization activities for biotherapeutic protein product development, including assay development, assay qualification, and product characterization. This position must effectively communicate timelines and issues to ensure successful manufacturing, product testing/release and data package for regulatory filings. Individual technical issue management and cross functional communication are key position attributes. The candidate will work in a team environment, collaborating with various departments to ensure that manufacturing processes are properly characterized to support process transfer, achieve project goals, and timelines. | 3/8/2019 |
| 892 | Idex Corporation Irvine, CA Mechanical Engineer BS/BA in engineering Exp: 1 year |
Responsible for mechanical design, including new product development, research and development, conceptual design, detail design, testing, validation and design for manufacture of specialized fluid handling and management systems. Duties include evaluating, quoting and releasing modifications of these existing product lines, supporting production, evaluating and process engineering changes, cost reductions and product improvement projects. | 2/27/2019 |
| 893 | Micropoint Bioscience Santa Clara, CA Quality Control Associates MS in chemistry, biology or related Exp: 0-2 years |
(Two openings) 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. Responsibilities include: Work with QA/QC manager to test, characterize and release quantitative immunoassays to meet both FDA and EU regulatory requirements for diagnostic IVD applications, Assist the R&D team in the POC product development including feasibility, verification and validation, manufacturing transfer and commercialization | 2/27/2019 |
| 894 | Micropoint Bioscience Santa Clara, CA Manufacturing Operators HS Diploma Exp: 0-2 years in manufacturing |
(Two openings)These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Responsibilities include: 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, Maintains records and documentation associated with producing cartridges in compliance with GMP and SOPs | 2/27/2019 |
| 895 | MicroVention Terumo Aliso Viejo, CA Engineer I/Engineer II BS in engineering or chemistry Exp: 0-2 years |
This 24-month rotational program is designed to train new Engineers on various aspects of MicroVention - Terumo technology, procedures, and processes. All candidates will be assigned a Mentor, as well as an Advisor to oversee their program succession, and will be provided with additional classroom training. Successful candidates will have three (3) eight-month rotations. These rotations include one (1) required rotation and two (2) optional rotation. The Engineer I (EIT) 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. Typical job duties might include: Developing new product concepts and products. Engineering design and process development. Generating intellectual property and writing invention disclosures.This 24-month rotational program is designed to train new Engineers on various aspects of MicroVention - Terumo technology, procedures, and processes. All candidates will be assigned a Mentor, as well as an Advisor to oversee their program succession, and will be provided with additional classroom training. Successful candidates will have three (3) eight-month rotations. These rotations include one (1) required rotation and two (2) optional rotation. The Engineer I (EIT) 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. Typical job duties might inc | 2/27/2019 |
| 896 | MicroVention Terumo Alajuela , Co Engineer JR BSChe, ME, EE, IE degree Exp: 1 year |
Duties and functions include: Improve, sustain, develop, and support of new and existing manufacturing processes for new and existing products, product changes and enhancements, as well as related tooling and fixtures. Investigation and testing of product processes. Manages builds for new product development in prototype and pilot production setting, including training of operators and coordination with production planning | 2/27/2019 |
| 897 | MicroVention Terumo Aliso Viejo, CA Regulatory Affairs Associate BS/BA degree Exp: 1-3 years |
The Regulatory Affairs Associate/Regulatory Affairs Specialist is in a high-visibility, high-recognition role and will be responsible for obtaining regulatory approvals, and ensures compliance to China-specific regulatory agency requirements. Job duties: Executes regulatory requirements for China. Reviews and files worldwide regulatory submissions (dossiers/ technical files / STED) to ensure MicroVention devices are commercially available in international markets based on the organization’s objectives. Reviews and files China submissions (JV & MV). Communicates with regulatory agencies on administrative and routine matters. | 2/27/2019 |
| 898 | MICR Indianapolis, IN Medical Research Study Coordinator: BS/BA and/or CCRC certification Exp: 1-3 years |
We are seeking an experienced individual who has coordinated the implementation of clinical research protocols. 1-3 years of clinical research experience and CCRC certification is preferred for this full-time position. | 2/27/2019 |
| 899 | Merck KGaA Sheboygan Falls, WI Associate Production Scientist BS/BA in chemistry, biology or related Exp: 0.5-1 years |
Essential 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). Ensure all applicable log books have been filled out completely as required by current procedures. In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. | 2/27/2019 |
| 900 | Merck KGaA Rocklin, CA Associate Scientist BS/BA in life sciences Exp: 1+ years |
Essential job functions include: Performs IHC, ELISA, and any other relevant tests as needed to conduct product development testing. Assists with establishing, maintaining, and updating the Design History Files (DHF) for new and/or existing products. Performs published literature reviews. Identifies and documents published clones, published protocols, etc as required.Provides technical support on developing new and improving existing IHC reagent processes and products. Conducts organized development testing to generate support data for new potential products or changes to current products. | 2/27/2019 |
| 901 | Merck KGaA Rockville, MD Lab Technician Analytical Chemistry/Formulations HS Diploma Exp: 1+ years |
At MilliporeSigma the Lab technician will perform a variety of tasks to support the laboratory technical staff who are required to characterize a product or material, dose formulation or bio-analytical sample for concentration, stability or other characteristics. The Lab technician will perform tasks as needed to maintain the lab and to support the assays performed in the Analytical Chemistry and Formulation labs. | 2/27/2019 |
| 902 | Merck KGaA Miamisburg, OH Production Associate AS or BS/BA in scientific field Exp: 6+ months |
Evaluate stable isotope products according to established protocols, provide technical support to others and perform operations in support of the group and department. Essential job functions include: Perform multi-disciplined, established assays and/or unit operations, involving stable isotope compounds. Ensure all applicable log books have been filled out completely as required by current procedures. Perform routine troubleshooting and miscellaneous duties or tasks as necessary. In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. | 2/27/2019 |
| 903 | Miltenyi Biotech Sunnyvale, CA Manufacturing Associate BS in biological sciences or related Exp: 1-3 years in GMP environemtn or equivalent |
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. | 2/27/2019 |
| 904 | Mission Pharmacal San Antonio, TX Product Assistant BS/BA degree Exp: 0-1 years |
Provide support managing the Samples and Marketing Materials for the Mission salesforce teams. Assist with coordinating shipment orders with the Distribution Centers on a weekly basis. Coordinate and maintain items in Sales force Ordering system on daily basis. Maintain the Sales Incentive reward program for the sales force. Provide sales reports for samples and marketing materials to the marketing teams and Outside Marketing Resources, when requested, usually monthly. Provide Sales Reports to Department Supervisor when necessary. Maintain inventory of samples and training materials for the new hire training. On a quarterly basis, pack and ship new hire training materials to and from the training location, as required. | 2/27/2019 |
| 905 | moderna Cambridge, MA (Contract) Research Associate, Formulation Design BS or MS Exp: 0-3 years in formulation or drug delivery |
This position is seeking a contract Research Associate/Sr. Research Associate who will be responsible for preparation and characterization of mRNA formulations within a dynamic and highly interdisciplinary environment. Understanding of nanoparticle preparation techniques and biophysical / chemical characterization is essential for this position. Experience with nucleic acid delivery systems is a plus. He/she will be responsible for executing lab experiments, reporting results, performing stability assessments, maintaining a high-quality lab notebook and working within a larger team of formulation scientists and associates. The successful candidate must have a foundation in pharmaceutical sciences and materials science/engineering. | 2/27/2019 |
| 906 | moderna Norwood, MA (Contract) Associate II, Quality Control BS/BA in scientific discipline Exp: 0-2 years lab experience |
The individual in this role will perform cGMP QC testing for QC Chemistry, release and stability. Also, this individual may support special projects as assigned. The shift for this role will be a 4 days a week for 10 hours a day (4X10) on either Sunday-Wednesday or Wednesday -Saturday. | 2/27/2019 |
| 907 | mpbio Solon, OH QC Technician HS Diploma Exp: 0 years |
The QC Technician is responsible for a wide variety of routine tasks in the Quality Control Department. These include: RIA and EIA bench top assay work. Inspection of incoming raw materials. Refrigerator and freezer temperature monitoring. QC document copying, collating, and filing. | 2/27/2019 |
| 908 | Charles River Spencerville, OH Formulations Technician I AA/AS or BS/BA in life sciences or related Exp: 0-1 years |
The Formulations Technician will prepare routine test article/substance dosage solutions and/or suspensions in accordance with Standard Operating Procedure (SOP) and Good Laboratory Practice (GLP) guidelines under direct supervision, and may serve as primary technician on studies that tend to be routine, less complex studies. In a typical day, you will perform standardized preparation procedures and calculations, ensure record keeping is consistent and correct, complete documentation for the use of all test articles and vehicles/reagents to ensure consistency and correctness, and receive incoming test articles/substances and reagents. You will also be expected to ensure formulations samples are collected, packaged, and shipped properly and on time, as well as ensure the test articles from assigned completed studies are returned to the sponsor or reassigned to another protocol. Additionally, you will respond to Quality Assurance (QA) audits of preparation procedures and calculations on assigned studies, ensure data sheets are complete and submit them for review, assist in reviewing data, prepare labels and samples, maintain cleanliness and general appearance of the laboratory, ensure the laboratory is stocked and assist in maintaining current inventory of reagents, test articles, vehicles, and samples, utilize appropriate Quality Control (QC) procedures/measures to help verify the accuracy and correctness of data prior to submission to internal QA, and perform all other related duties as assigned. | 2/27/2019 |
| 909 | Charles River South San Fransico, CA Research Associate BS/BA Exp: 0-3 years lab experience |
This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices. The position is hands-on, working in close cooperation with and under the guidance of more senior staff members in a fast-paced environment where a commitment to teamwork, quality data and speed is essential. | 2/27/2019 |
| 910 | Charles River Shrewbury, MA Research Technician I HS Diploma or BS in animal/life sciences Exp: 0.5-1 years in research |
The Research Technician I will 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.The Research Technician I will 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.The Research Technician I will 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. | 2/27/2019 |
| 911 | Charles River Mattawan, MI Research Technician - Reproductive Toxicology - T-Lab HS Dipolma or BA/BS or MS Exp: 0 years |
A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 2/27/2019 |
| 912 | Charles River Shrewsbury, MA Research Technician I HS Diploma or BS in animal/life sciences Exp: 0.5-1 years in research |
The Research Technician I will 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.The Research Technician I will 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.The Research Technician I will 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. | 2/27/2019 |
| 913 | Charles River Spencerville, OH Research Technician HS Diploma or BS in animal/life sciences Exp: 0.5-1 years in research |
The Research Technician will collect and record data with minimal supervision in the performance of studies. During a typical day, you can expect to perform clinical observations, sample collection, monitoring of food consumption, animal husbandry, and accurate data collection and reporting, along with the handling and restraint of animals. Additionally, you will also administer test substances by various basic methods, perform study preparation activities, read basic study protocols and extract pertinent information, review documentation of performed functions, maintain a clean work area, receive animals of all species (general health observation, sexing and identification), and perform all job functions using Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), processes, and company policies. | 2/27/2019 |
| 914 | MyoKardia South San Fransico, CA Research Associate I - Cell biology BS in physiology, pharmacology or related Exp: 1-2 years animal handling |
Essential duties and responsibilities include: Prepare isolated adult animal cardiomyocytes for contractility assays, Use pre-established experimental designs to plan, and execute myocyte contractility and Ca2+ transient assays, Propose solutions to technical issues: proactively seek out senior team member to discuss potential resolutions to problems | 2/27/2019 |
| 915 | MyoKardia South San Fransico, CA Research Associate I - Biology BS in biochemistry, biology or related Exp: 0-2 years |
Essential duties and responsibilities include: Purification of a wide variety of cardiac muscle proteins using various chromatographic techniques, Carry out multiple experiments in parallel and keep detailed, meticulous notes, Analyze and report experimental results, both in daily updates, regular database inputs, and in final reports, Execute all methods and techniques required to purify soluble and secreted proteins including the ӒKTA PURE FPLC platform, SDS-PAGE, TFF, microfluidizer, plate-based assays, spectrophotometry, and HPLC | 2/27/2019 |
| 916 | Myriad Genetic Laboratories Salt Lake City, UT Patient Advocate Triage I BS/BA in biology, science, or healthcare Exp: 1-2 years |
Triage Patient Advocate reviews all paperwork submitted with patient samples to ensure all required information for testing is received. They enter the patient’s insurance information into the database application and determine if the patient’s insurance requires additional documentation/processing for testing to be covered. The ability to focus on quality is crucial in this role. The candidate must be very detail oriented as well as be able to determine how small details will affect case completeness as a whole. | 2/27/2019 |
| 917 | NanoString Seattle, WA Automation Engineer I BS in engineering, science, or biology Exp: 1+ years |
The Automation Engineer I is responsible for maintaining existing Manufacturing systems as required. Additional duties include the development of new methods and implementation of new systems. The ideal candidate has knowledge of FDA and ISO requirements as they apply to manufacturing processes.The Automation Engineer I is responsible for maintaining existing Manufacturing systems as required. Additional duties include the development of new methods and implementation of new systems. The ideal candidate has knowledge of FDA and ISO requirements as they apply to manufacturing processes.The Automation Engineer I is responsible for maintaining existing Manufacturing systems as required. Additional duties include the development of new methods and implementation of new systems. The ideal candidate has knowledge of FDA and ISO requirements as they apply to manufacturing processes. | 2/27/2019 |
| 918 | NanoString Seattle, WA Manufacturing Research Associate I (Tuesday thru Saturday)-CodeSet Production BS in scientific discipline Exp: 0-2 years lab experience |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 2/27/2019 |
| 919 | NanoString Seattle, WA Manufacturing Research Associate I (Monday thru Friday) -Consumables Production BS in scientific discipline Exp: 0-2 years lab experience |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 2/27/2019 |
| 920 | NanoString Seattle, WA Manufacturing Research Associate I (Mon thru Fri)-CodeSet Production BS in scientific discipline Exp: 0-2 years |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 2/27/2019 |
| 921 | Natera San Carlos, CA Clinical Laboratory Associate I (Temporary) BS/BA in biological sciences Exp: 0-2 years |
Natera is currently seeking a Clinical Laboratory Associate I (Temporary) to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. Primary responsibilities include: Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors, Responsible for maintaining updated understanding and knowledge of methods performed in the lab, Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire. | 2/28/2019 |
| 922 | Natera San Carlos, CA Clinical Data Operator 1 HS Dipolma Exp: 0-1 years |
Clinical Data Entry Operator 1 accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. Primary responsibilities include: Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning, Accession samples with high accuracy and efficiency, Protect patient health information (PHI) at all times to ensure compliance with HIPAA and privacy policies. | 2/28/2019 |
| 923 | Natus Medical Chicgo, IL Engineer, Product Implementation BS/BA Exp: 0-2 years |
Natus is seeking a Product Implementation Engineer for our Midwest region. This position is responsible for working with customers on Neuro product line site-specific server planning for SQL, Citrix, and HL7; server implementations, and post-installation support. The qualified individual will provide input to product development teams on such products and train technical support as required to support such products and may be called on to visit customer sites for the installation, in-service, and repair of the company's supplied equipment. | 2/28/2019 |
| 924 | Navitor Pharmaceuticals Cambridge, MA Research Associate BS/BA or MS in biology or related Exp: BS: 1-2 years, MS: 0-2 years |
We are seeking highly motivated, energetic and committed individuals to join our interdisciplinary team and actively contribute to advancing our drug discovery programs from discovery to proof-of-concept. You will build your experience in early discovery projects using cell-based and biochemical/biophysical approaches to support small-molecule discovery activities and advance our cutting-edge programs that target the mTORC1 pathway | 2/28/2019 |
| 925 | Nektar Biologics Huntsville, AL Process Technician II BS in chemistry, biochemistry, chemical engineering or related Exp: 0-2 years |
Operates production equipment. Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities. May help in validating processes and equipment that are directly related to filtration, cleaning and sterilization. Maintains records and clean room environment to comply with regulatory requirements, good manufacturing practices and standard operating procedures. Works on projects that are moderately complex in nature. Exercises judgment in resolving problems and making some routine recommendations. Provide Lab Support for manufacturing suites. Learn how to run equipment, read and understand SOPs. Support processing by adhering to SOPs. Follow HazMat procedures, for movement of Raw Material used in chemical processes. Support investigations Review SOPs. Troubleshoot and offer ideas on improvements. Interact with other departments to share information. Performs other duties as assigned. |
2/28/2019 |
| 926 | Nelson Laboratories Salt Lake City, UT Lab Analyst - Sun - Thurs, 9am-5:30pm BS/BA in relevant sciences Exp: 0-2 years |
he Laboratory Analyst conducts testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 2/28/2019 |
| 927 | NemaMetrix Eugene , OR Laboratory Technician I, Biology BS in biology or related Exp: 1 year |
This is a collaborative, team‐based role with the responsibility to perform Molecular Biology and C. elegans screening tasks for R&D discovery and development projects. Responsibilities include: Perform molecular biology assays including PCR, qPCR, and gel electrophoresis. C. elegans culture and maintenance. Working knowledge of basic laboratory equipment and protocols, including solution preparation and dilution series.This is a collaborative, team‐based role with the responsibility to perform Molecular Biology and C. elegans screening tasks for R&D discovery and development projects. Responsibilities include: Perform molecular biology assays including PCR, qPCR, and gel electrophoresis. C. elegans culture and maintenance. Working knowledge of basic laboratory equipment and protocols, including solution preparation and dilution series. | 2/28/2019 |
| 928 | Neogen Lansing, MI QC Technician I AS/AA in sciences Exp: 1+ years |
The QC technician I position requires the candidate to perform routine biological and chemical assays daily. Other responsibilities include assisting supervisors with improving procedures, participating in troubleshooting and meeting goals and objectives. The ideal candidate would have laboratory experience at a college or industrial setting. | 2/28/2019 |
| 929 | Neogen Lexington, KY Diagnostic Production Technician I HS Dipolma Exp: 0-2 years |
The Diagnostic Production Department for Neogen Corporation is seeking candidates for a technician position responsible for manufacturing, packaging, and assembly of diagnostic test kit components. The ideal candidate will be reliable, possess attention to detail, and able to work in a fast-paced environment. Responsibilities include: Sets up, adjusts, and operates laboratory equipment and instruments including, but not limited to: balances, microplate dispensing equipment, reagent dispensing equipment, bottle cap tightener, and labeling equipment. Cleans and maintains work areas and equipment used in daily manufacturing duties. Produces and packages plates approved by QC Department. | 2/28/2019 |
| 930 | Neogen Lansing, MI Production Chemist BS/BA in biology, science, or food sciences Exp: 1-3 years |
Formulate batch reagents needed to meet production schedule using standardized manufacturing documents. Assist in establishing protocol for manufacturing new products. Essential Duties and Responsibilities include the following. Other duties may be assigned. Formulate chemical reagents from stock with direction from the appropriate Standard Manufacturing Procedure (SMP) or Standard Operating Procedure (SOP). Conduct chemical (immunological) reactions for development of reagents with direction from the appropriate Standard Manufacturing Procedure (SMP) or Standard Operating Procedure (SOP). Assist in process transfer from R&D to Manufacturing Department with direction from the appropriate Standard Manufacturing Procedure (SMP) or Standard Operating Procedure (SOP). | 2/28/2019 |
| 931 | Neogen Lansing, MI Lateral Flow Chemist BS/BA in chemistry, biochemistry, or related Exp: 1+ years |
The Food Safety Division is currently seeking a candidate for a Lateral Flow Chemist position. The selected candidate would be responsible for formulating reagents and preparation of some components used in the assembly of Diagnostics and Dairy Antibiotics Lateral Flow products. Other duties would include testing and documenting results following ISO and GMP procedures. The ideal candidate should have the ability to perform basic mathematical operations, follow and document all manufacturing procedures, be capable of identifying and resolving problems in a timely manner and be able to work both independently, as well in a group setting. The selected candidate will be responsible for preparing buffers, solutions, and reagents according to Standard Manufacturing Procedures (SMP’s) and Work Orders, while maintaining an accurate inventory of chemicals and supplies. | 2/28/2019 |
| 932 | Neogen Lincoln , NE Lab Technician - Processing BS/BA in scientific discipline Exp: 0-2 years |
Performs laboratory tests and services to support customer data generation within the platform specific processing lab, through a variety of scientific techniques, instrumentation, and disciplines by performing the following duties: Gain and maintain the ability to operate all electronic and robotic equipment essential to primary platform processing. This includes all hand held electronic repeaters, multichannel pipettes along with liquid handling robots. Maintain consistency and quality in lab techniques and procedures within an ever changing and fluid work environment. Accurate record keeping which includes but is not limited to laboratory notebooks, lot record tracking, sample archives, LIMS and/or repository as necessary. | 2/28/2019 |
| 933 | Nephron Pharmaceuticals West Columbia, SC Quality Assurance OnlineEvening 12 hour Shift ONLY HS Dipolma Exp: 1+ years |
Performs Weight Check and Quality Attributes Inspection of the product through the filling and packaging process in compliance with company policies / procedures, FDA and cGMP regulations. Ensures the accuracy and completeness of batch records. Monitors and perform start up, in-process and finished product inspections including weighing. Monitor all production areas and personnel for adherence to all cGMP, SOP’s and safety regulations. | 2/28/2019 |
| 934 | Nephron Pharmaceuticals West Columbia, SC Micro Analyst I BS in biology or related life sciences Exp: 1+ years |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Apply quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures. Demonstrate ability to understand and interpret test results in relation to acceptance or rejection of lot tested. Report, initiate documentation and assist in excursions and investigations of OOS and OOT reports. | 2/28/2019 |
| 935 | NeuroPace Mountain View , CA Manufacturing Engineer BS in mechanical or industrial engineering Exp: 0-4 years |
Maintain quality standards in and around manufacturing areas, ensuring a safe work environment for all personnel and helps to develop a culture of accountability, continuous improvement, and collaboration. Responsibilities includes: Write, review, and improve manufacturing procedures and forms in compliance with the quality system, ensuring accuracy and consistency. Collaborate with Manufacturing and Development Engineers to create, review, and maintain manufacturing routers. Including verifying manufacturing labor times are properly calculated. Support departmental responsibilities associated with training and qualifying manufacturing assemblers. | 2/28/2019 |
| 936 | NGM Biopharmaceuticals South San Fransico, CA Research Associate I BS in life sciences Exp: 0-2 years |
he primary responsibilities will include planning and execution of experiments focused on novel target discovery and validation using a wide range cutting edge in vitro and in vivo techniques. The new team member is expected to work within a cross-functional team generating high quality biological data fueling NGM’s drug discovery engine. Design and execute experiments for target identification and validation including utilization of in vitro cell-based assays and in vivo disease animal models. | 2/28/2019 |
| 937 | Avecia Milford, MA Research Associate MS in chemistry or life sciences Exp: 1+ years |
The Research Scientist I is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides. Provide technical leadership in analytical project meetings. Communicate with clients and contributes to department objectives for continuous improvement and technical excellence. | 2/28/2019 |
| 938 | Nkarta South San Fransico, CA Research Associate/Senior/Process Engineer MS in biology related discipline Exp: 1-6 years |
Job duties and responsibilities include: support process development of phase appropriate cell therapy production processes. Evaluate raw materials and culture systems for use in cell therapy manufacturing processes. Support process optimization efforts to increase process robustness, reduce costs and improve yield. Design and execute experiments independently; accurately record, analyze and communicate data to senior staff and team members. | 2/28/2019 |
| 939 | Nordson Sunnyvale, CA Manufacturing Engineer I, Nordson MEDICAL BS/BA in mechanical engineering Exp: 1-2 years |
This individual will possess a broad range of medical device manufacturing engineering skills and experience, as well as depth of knowledge with assembly processes, equipment, and tooling. The ideal candidate is a self-motivated individual who is comfortable rolling up their sleeves and working hands-on in the process. Job duties include: Develop R&D pilot lines for new products and ensure design for manufacturability (DFM) through concurrent engineering practices. Establish robust assembly processes for both new products developed at Nordson Medical and those transferred into Nordson Medical. | 2/28/2019 |
| 940 | Nordson Amherst, OH Test Engineer (Electrical) BS in electrical or computer engineering Exp: 0-2 years |
Job duties and responsibilities include: Electrical and mechanical aptitude with the ability to design, fabricate and wire electrical control panels and test fixtures. Write comprehensive documentation on tester hardware and software designs. Provide troubleshooting support to engineering and assembly teams on products and processes | 2/28/2019 |
| 941 | Nordson Amherst, OH Process/ Product Support Engineer BS in mechanical or electrical engineering Exp: 1-3 years |
Responsible for supporting both pre-sales and post-sales activities including customer process development, product engineering and demonstrations, material evaluation, on-site installation, servicing and repair of complex equipment and systems for all products and markets. Also serves as company liaison with customers on administrative and technical matters and be assigned to specific customer accounts as the primary technical support contact. | 2/28/2019 |
| 942 | Nordson Concord, CA Associate Engineer, Mechanical BS/BA Exp: 0-2 years |
Responsible for designing, defining, implementing system requirements, analyzing and/or testing Asymtek products. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained. Receives specific and detailed instructions as to required activities and expected results. Performs a variety of routine tasks, which should provide experience and familiarization with the engineering staff, methods, practices and programs of the company. | 2/28/2019 |
| 943 | Norwich Pharma Norwich , NY Chemist I BS in chemistry, biology, or related Exp: 0-3 years |
Duties and functions include: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 2/28/2019 |
| 944 | Novartis Lake Forest, CA Mechanical Engineer BS/BA Exp: 0-4 years |
In this role, the incumbent conducts process research, process development and process upscaling for new medical device products. She/He also investigates and evaluates existing technology and designs new methodology, materials, machines and/or processes as needed for medical device development. Responsible for leading, participating in or supporting the product development activities such as prototyping/testing, pilot builds, verification & validation testing, risk assessment and production tooling validation. Generates detailed fabrication drawings, appropriate product requirements and technical file documents and leads design reviews. Responsible for the design and development of mechanical components, systems, and products using PTC Creo | 3/2/2019 |
| 945 | Novavax Rockville, MD Bioprocess Associate I BS/BA Exp: 1-2 years in lab or cGMP |
We are seeking a highly detail-oriented and organized individual to support Process Development with the manufacture of buffers and media. Additionally, this individual would be responsible for managing the PD inventory program. Main function will be to perform the day to day activities in the Solutions Preparation Area: preparation of buffers, preparation of cell culture media/feeds, calibration of pH and conductivity meters/probes, transport of glassware, scheduling equipment maintenance, etc., to support all of process development. | 3/2/2019 |
| 946 | Novavax Gaithersburg, MD Lab Support I Degree in scientific discipline Exp: 0-2 years in cGMP lab |
Individual is responsible for ordering lab supplies by inventorying stock; placing orders; verifying receipt, restocking lab and discarding expired reagents. Individual will track critical reagent supplies and notify affected personnel when supplies are low. Individual will maintain laboratory equipment by following standard operating procedures; maintain equipment related supplies, record and maintain equipment temperature logs. Individual will be responsible for performing daily/weekly and monthly equipment (Biosafety cabinets, incubators, water baths, plate washers, refrigerators, freezers etc) cleaning as per laboratory schedule. | 3/2/2019 |
| 947 | Novodiax Hayward, CA Innovation Scientist BS degree in biology or related Exp: 0-2 years lab experience |
Candidate will be responsible for development and optimization of tissue-based assays. Individuals will have a background in biology or a related discipline and laboratory experience in human and animal tissue preparation, histological staining, and immunohistochemistry (IHC). Individuals must be self-motivated and detail-oriented, exhibit excellent organizational and communication skills, as well as demonstrate the ability to work under defined timeframe, thrive with a high degree of independence and be a team-player. | 3/2/2019 |
| 948 | Novozymes Houston, TX Lab Technician HS Dipolma Exp: 1+ years |
The Lab Technician will inoculate spores from a stock culture onto petri plate medium for growth and manually harvest spores after growth into sterile carrier. This position will also maintain accurate records of inoculation and harvest plates. We are looking for someone who can follow directions carefully and accurately, proven initiative, communication skills and ability to gain respect and cooperation of others throughout the organization. | 3/2/2019 |
| 949 | Novum Fargo, ND Entry Level Technicians HS Dipoma Exp: 0-1 years |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 3/2/2019 |
| 950 | Novum Las Vegas, NV Research Technician Hs Dipolma Exp: 3+ months |
The entry level Research Technician will be responsible for supporting study progression according to study protocol and Standard Operating Procedures. Responsible for obtaining vital signs, performing EKGs, and drug/pregnancy testing from study participants as required by the protocol. Observes, obtains and processes all laboratory specimens. Performs service oriented duties along with stocking supplies and general support to all phases of screening process. | 3/2/2019 |
| 951 | Novum Pittsburgh, PA Data Coordinator BS/BA Exp: 0-2 years |
The Data Coordinator will be responsible for assisting in the design, implementation and delivery of high quality clinical data within project timelines. Will execute data queries; perform medical coding, data reconciliation for study databases, and tracks data clarifications. Assists in the design of study start up documents i.e. Data Management Plan, eCRF, spec design, and edit check specs | 3/2/2019 |
| 952 | Kantar Warren, NJ Graduate Development Program BS/BA, 3.0 GPA or higher Exp: 0 years |
This is a graduate development program that will provide skill training in areas such as data, client management, leadership, business acumen, and project management over a two-year program. | 2/19/2019 |
| 953 | Kantar West Chester, PA Custom Product Development Specialist I BS/BA in math, computer sciences, information systems, or realted Exp: 1-3 years |
We are looking for a Jr.-level applications developer to design, build, modify, deploy, and support custom applications to complement existing syndicated applications per our client’s needs. | 2/19/2019 |
| 954 | Kantar New York, NY Associate, Program Leadership BS/BA in marketing, psychology, or economics Exp: 1+ years market research is plus |
As a member of the Program Leadership team, you will be responsible for executing research projects for existing publisher, agency and advertiser clients. In this role, you will be responsible for project excellence from the point of project sale through final data delivery; acting as the point person between all operational and sales teams to ensure efficient and successful project execution for our clients. | 2/19/2019 |
| 955 | Kashiv BioSciences Bridgewater, NJ Scientist I - AR&D MS in analytical chemistry, biochemistry, or related Exp: 0-2 years |
A Scientist will be a key technical resource responsible for independently developing methods, generating reliable and interpreting data, using analytical instrument that include HPLC, UPLC, GC, UV/Vis, Mass spectrometer, dissolution apparatus and particle analyzer. This position is also responsible for designing experiments, writing method validation protocols, conducting method validation, and processing and interpreting the analytical data. | 2/19/2019 |
| 956 | Kashiv BioSciences Bridgewater, NJ Facilities Engineer BS/BA or MS in engineering Exp: 1-3 years |
The Facility Engineer will ensure that all safety standards are followed. Maintenance and inspections will be done to guarantee those cGMP standards are being followed. Performs routine inspections of the equipment. Monitoring of the BMS system and coordinating the PM schedule and maintenance activity. Generate engineering documents for equipment, Facility and utilities and execute the same, Support Project Execution and Vendor Development. Maintain and coordinate to have the updated floor plans and P&ID of the equipment’s and facility. | 2/19/2019 |
| 957 | KBI Biopharma Durham, NC Research Associate BS/BA or MS in chemistry, biochemistry, or related Exp: 0+ years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Understands experiments and conducts troubleshooting analysis. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. | 2/19/2019 |
| 958 | KBI Biopharma Boulder, CO Research Associate BS/BA in chemistry, biochemistry, or related Exp: 0-3 years |
Temporary position. Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Conducts laboratory experiments in support of biopharmaceutical development and process development including running electrophoresis gels, HPLC’s, etc. and preparing buffers. Maintains and updates knowledge and instrumentation and maintenance. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. | 2/19/2019 |
| 959 | KCAS Shawnee, KS Analyst I BS/bA in sciences Exp: 0-2 years |
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. | 2/19/2019 |
| 960 | KCAS Shawnee, KS Quality Specialist II HS Diploma Exp: 1+ QA experience |
The Quality Specialist II performs activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements, including document review, audits, inspections, and consulting on quality and compliance issues. Provide training assistance in routine quality and compliance topics. Provides consultation on quality and compliance topics in areas of expertise and assists with quality improvement initiatives as needed. | 2/19/2019 |
| 961 | Kinovate Life Sciences Oceanside, CA Production Specalist (Chemist) BS/BA in chemsitry or relavent Exp: 1-2 years |
The incumbent in this position is responsible for all production activities at KLS. Directly reporting to the Production Manager and working with the QA/QC analysts, this position will also ensure all production process are documented and executed accurately according to established SOPs. The ideal candidate is a chemist with at a minimum of one year of experience in production of chemical compounds, preferably in a GMP environment. | 2/19/2019 |
| 962 | KSQ Therapeutics Cambridge, MA Associate Scientist/Scientist, Biotherapeutics Drug Discovery BS or MS in biology or related Exp: 1-5 years |
The successful applicant will work with internal functional groups to help design and execute screening strategies for therapeutic antibody discovery campaigns – including biochemical, molecular, and/or cellular assays for the testing of biotherapeutics from discovery to lead-optimization. Work with internal functional groups to develop, optimize and execute high throughput binding assays (ELISA, Octet, FACS) and cell-based assays (functional, phenotypic, reporter etc.) for screening panels of therapeutic antibody candidates | 2/19/2019 |
| 963 | KSQ Therapeutics Cambridge, MA Associate Scientist/Scientist, Autoimmunity BS Exp: 0-3 years |
Responsibilities as an associate scientist include querying novel pathways/mechanisms for therapuetic intervention with CRISPR technologies, work as part of an interdisciplinary team to contribute to the design and execution of experiments that support our research activities and project goals, and design, plan, and execute high-quality and well-controlled immunological assays to provide insight into potency and mechanism-of-action . | 2/19/2019 |
| 964 | LabCorp New York, NY Specimen Processing Specialist (Laboratory Associate) HS Diploma Exp: 1+ years lab experience |
Prepares laboratory specimens for analysis and testing. Spinning samples, pouring urine tubes and creating frozen samples. Picking up and delivering samples to clients/hospitals. Unpacks and routes specimens to their respective staging areas. Accurately Identify and label specimens. Pack and ship specimens to proper testing facilities. | 2/20/2019 |
| 965 | 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. | 2/20/2019 |
| 966 | LabCorp Greenville, NC Specimen Accessioner 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. | 2/20/2019 |
| 967 | LabCorp Phoenix, AZ QA Analyst BS/BA in medical technology Exp: 1-2 years |
Provides leadership in the areas of quality assurance, quality control, quality related training, and standardization compliance within the laboratory. This position is also responsible for project management activities as they relate to identified areas within the laboratory requiring standardization to improve the quality and/or efficiency of operations. | 2/20/2019 |
| 968 | Lake Pharma Hayward, CA Lab Assistant, Process Development AS or BS in biology or related Exp: 0-2 years |
Responsibilities include but are not limited to: Maintain laboratory instruments, follow SOPs for mammalian cell culture and protein/antibody purification, conduct data input, analysis, and interpretation, think critically and creatively to determine appropriate resources for resolution of problems, recognize and trouble shoot anomalous and inconsistent experimental results. | 2/20/2019 |
| 969 | AI Therapeutics Guilford, CT Post-Baccalaureate Researcher BS in life sciences Exp: 1+ years |
We are looking for a talented post-baccalaureate researcher with applied experience in molecular and cell biology. Work alongside other experimental biologists, deep learning scientists, computational biologists and a world-class leadership team to help progress a new platform for precision medicine applications. Responsibilities include: Maintain cell lines and primary cultures. Perform in vitro cellular assays to support drug development efforts. Perform biochemical assays to support mechanism of action studies. Perform NGS assays to assay expression signatures and mutations in cell lines and primary tumors. | 2/20/2019 |
| 970 | Lampire Everette, PA Molecular Biologist BS/BA in biology or related Exp: 1-3 years |
Seeking a highly motivated Research Associate I/II with a background in Molecular Biology to assist in the development of new technologies including CRISPR genome engineering and recombinant antibody generation. The successful candidate will be responsible for learning, researching and implementing recombinant DNA approaches to support research team needs, as well as designing work-flows, and assay development. | 2/20/2019 |
| 971 | Latitude San Diego, CA Research Associate BS in chemistry, pharmaceutical sciences, or related Exp: 1-5 years |
A successful candidate will possess proficiency in a variety of analytical chemistry techniques including HPLC. The position of Research Associate will report to a Formulation Scientist. Responsibilities include: assist the supervising Formulation Scientist to complete individual formulation development projects, assist in the design, execution and interpretation of formulation development based on the defined deliverables, as well as in the planning of activities to meet the project timelines, and prepare presentations of data and progress and assist in regular presentations to external clients during formulation development projects | 2/20/2019 |
| 972 | LifeMine Cambridge, MA Research Associate/Senior Research Associate, Synthetic Biology BS in biology, or chemistry Exp: 1-2 years |
We are seeking a Research Assistant with expertise in the use of molecular biology tools such as RNA/DNA extraction, PCR/qPCR, RT-qPCR, plasmid miniprep, and DNA restriction and electrophoresis. Experience in molecular cloning (traditional and seamless aka Gibson), designing constructs, analyzing sequencing data etc. Role will likely evolve to support our effort to engineer and manipulate fungal secondary metabolite clusters to increase the titers of natural product production and establish LifeMine’s fungal genomically-enabled drug discovery platform. | 2/20/2019 |
| 973 | LifeSensors Malvern, PA Entry Level Scientist BS or MS in biology or related Exp: 0-2 years |
We are seeking individuals who arepassionate about research, bringout of the box thinking and take bold steps todevelopinnovativetechnologies with applications in the ubiquitin research field.Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with, protein expression andpurification and cloning. Knowledge of the ubiquitin proteasome pathwayis desired. | 2/20/2019 |
| 974 | Lonza Hayward, CA QC Analyst I BS/BA in chemistry or biological sciences Exp: 0-2 years |
This position is responsible for performing biological, chemical and physical analyses on pharmaceutical products through all stages of the manufacturing process from incoming raw materials, in-process, stability and final products. Perform biological, chemical assays for raw materials, initial, in-process, stability and final products.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. | 2/20/2019 |
| 975 | Lubrizol Corporation Gastonia, NC Chemical Operator HS Diploma Exp: 0 years |
Filtering finished latex from reactors to storage, including: the verification that latex is within all specifications, calculation of correct storage tank capacity, proper sampling and record keeping (valve placement sheets, shift log, filing charts, etc.). Manufacture, packaging and shipment of customer bulk orders, including: the calculation of correct tanker outage/inage, inspection of tanker, proper sampling, completion of weight ticket and bill of lading. Manufacture, packaging and shipment of customer drum orders, including: proper sampling and labeling, completion of packing list and bill of lading and the proper use of forklift. | 2/20/2019 |
| 976 | Lubrizol Corporation Deer Park, TX QA Lab Technician BS/BA Exp: 0-3 years |
We currently have a challenging and rewarding position for a Lab Technician at our Deer Park, Texas facility. Responsibilities include: Performs test on all in coming raw materials prior to their use in the process, maintains all lab related data systems, including computer and hardcopy formats. Responsible for data systems, including computer and hardcopy formats, and performs regularly scheduled and unanticipated analytical testing on all in-process product and communicates the results to production units. | 2/20/2019 |
| 977 | Lucigen Middleton, WI International Sales Coordinator BS/BA in business or marketing Exp: 1-2 years |
The International Sales Coordinator provides administrative and management support to LGC, Biosearch Technologies' distribution network, both domestic and international, as well as support to international customers. This position requires excellent customer interaction with both internal and external customers. Responsibilities include: Respond to distributors' inquiries regarding pricing, marketing tools, re-direct technical questions, or special projects such as logistics planning & preparations for distributor meetings, Capture marketing and sales announcements, or corporate updates to develop monthly newsletter for distributors and distribute the newsletter in electronic format to entire distribution network, etc. | 2/20/2019 |
| 978 | American Regent New Albany , OH R&D Analytical Chemist I BS in chemistry Exp: 1+ years |
This R&D position will be responsible for testing of raw materials, finished products, and stability samples using existing analytical methods and wet chemistry. Perform routine analytical testing of raw materials, finished product, stability samples and lab batch samples. Record and report all lab data as per approved procedures and regulatory requirements. | 2/21/2019 |
| 979 | Luminex Associate Scientist II, IL ASSOCIATE SCIENTIST II BS/BA in science, chemistry or biomedical sciences Exp: 1-3 years |
Manufacturing oligonucleotides used in Luminex’s diagnostic tests. (The oligonucleotides are used to prepare a variety of chemical reagents that are filled into assay consumables such as trays or cartridges). The oligonucleotide manufacturing process is a manual, multi-step wet chemistry process. The operation of specialized computer controlled instrumentation such as synthesizers and purification equipment used in the manufacture of defined sequence oligonucleotides. | 2/21/2019 |
| 980 | United Therapeutics Research Triangle Park, NC Research Associate - Tissue Engineering BS/BA or MA in science, engineering or biological sciences Exp: 1-2 years |
Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. Prepare lung scaffolds for tissue engineering experiments, cannulate and load scaffolds into bioreactor chambers, and seed scaffolds with pulmonary cells. Perform maintenance, cleaning, sterilization, and set-up of bioreactors for tissue engineering studies. Follow proper procedures regarding laboratory safety, use of personal protective equipment, and handling of biohazard materials, including human or animal cells and tissues Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. Prepare lung scaffolds for tissue engineering experiments, cannulate and load scaffolds into bioreactor chambers, and seed scaffolds with pulmonary cells. Perform maintenance, cleaning, sterilization, and set-up of bioreactors for tissue engineering studies. Follow proper procedures regarding laboratory safety, use of personal protective equipment, and handling of biohazard materials, including human or animal cells and tissues Conduct and assist in research efforts to develop tissue-based regenerative medicine products for the treatment of pulmonary hypertension and other lung diseases. Prepare lung scaffolds for tissue engineering experiments, cannulate and load scaffolds into bioreactor chambers, and seed scaffolds with pulmonary cells. Perform maintenance, cleaning, sterilization, and set-up of bioreactors for tissue engineering studies. Follow proper procedures regarding laboratory safety, use of personal protective equipment, and handling of biohazard materials, including human or animal cells and tissues | 2/21/2019 |
| 981 | LSNE Madison, WI QC Microbiology Technician BS Exp: 0-2 years |
Job summary: Conducts sampling of incoming raw materials, production environments, and/or facility clean utilities, as per approved procedures and submits these samples to the appropriate testing facility for documented and controlled results. Applies material / system status labels, as indicative of testing status and/or results obtained. Assists with lab maintenance and inventory. | 2/21/2019 |
| 982 | Machaon Diagnostics Oakland, CA Clinical Laboratory Assistant BS/BA in chemistry, biology, or related Exp: 6 months |
Demonstrate proficiency and understanding of standard clinical laboratory practices. Review requisitions, orders tests and processes specimens in preparation for laboratory procedures. Perform general laboratory maintenance tasks including preparing reagents, re-stocking consumables and washing glassware. Assist with quality control and quality assurance paperwork. Assist with clinical trials including completion of Institutional Review Board documentation, subject recruitment, screening, and management, and performance of research related testing. Design and revise forms and protocols. Adhere to Machaon policies and procedures as directed by the supervisor, manager or medical director. Interact with patients, subjects, visitors, physicians, and coworkers in a professional and courteous manner. | 2/21/2019 |
| 983 | Mammoth Biosciences San Francisco, CA Resaerch Associate BS/BA in chemistry, biology, or related Exp: 1+ years |
Mammoth is seeking a Research Associate experienced in protein and nucleic acid biochemistry techniques to work with our CRISPR development team. The ideal candidate will have experience with protein engineering, molecular biology, protein purification and bioinformatics. Further, the candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. The Research Technician will report directly to a Scientist. | 2/21/2019 |
| 984 | Manus Bio Cambridge, MA Research Assistant, Molecular Biology BS or MS in bioengineering, biology, or biochemistry Exp: 1+ years lab experience |
Responsibilities include but are not limited to: Construct and validate gene and plasmid constructs, Express metabolic pathways in microbial systems, Test expression and activity of enzymes in a variety of assays, Ferment bacterial cultures, Perform analytical assays to identify and quantify metabolites | 2/21/2019 |
| 985 | Masy Bioservices Pepperell, MA Inventory Technician I HS Diploma Exp: 1-2 years |
This position is responsible for ensuring all incoming customer product is correctly inspected, inventoried and accurately entered into the electronic inventory system. This includes initially entering data and being a secondary reviewer. Duties include abiding by area work instructions and ensuring that customer product is stored at appropriate conditions during inventory to ensure compliance. Communicate with appropriate personnel to determine all pertinent information that needs to be captured | 2/21/2019 |
| 986 | MedImmune Gaithersburg, MA Researc Associate MS Exp: 1-2 years lab experience |
his is a hands-on laboratory-based position to support pre-clinical research to further our understanding of the disease-driving mechanisms and to develop new medicines for respiratory diseases such as COPD, asthma, and pulmonary fibrosis. The candidate will assist in study design, execution and data analysis of complex and technically demanding in vitro and in vivo experiments using a variety of cellular and molecular techniques. The candidate will develop close working relationships within a highly collaborative environment using strong interpersonal and communication skills to advance team goals. his is a hands-on laboratory-based position to support pre-clinical research to further our understanding of the disease-driving mechanisms and to develop new medicines for respiratory diseases such as COPD, asthma, and pulmonary fibrosis. The candidate will assist in study design, execution and data analysis of complex and technically demanding in vitro and in vivo experiments using a variety of cellular and molecular techniques. The candidate will develop close working relationships within a highly collaborative environment using strong interpersonal and communication skills to advance team goals. | 2/21/2019 |
| 987 | MedImmune Gaithersburg, MA Rsearch Associate II MS in biology or related Exp: 0-2 years |
Major responsibilities include planning and executing experiments related to developing protein engineering platforms for therapeutic antibody generation and optimization. She/he will work with scientists to create research plans, execute experiments, analyze and interpret data and present results to the group and the department. She/he is expected to have a strong work ethic, excellent organizational skills and keep good records. Strong team-based communication and presentation skills will be required. | 2/21/2019 |
| 988 | MedImmune Gaithersburg, MA R&D Associate II - BPD MS in mechanical or biomedical engineering Exp: 0-2 years |
This role will contribute in the development of product requirements, generate and evaluate device concepts, conduct engineering analyses, develop detailed engineering specifications, create device designs, and perform design verification/validation testing in a cross-functional team to ensure successful development and launch of mechanical and electro-mechanical medical devices. This role requires excellent technical writing skills and good understanding of design control process. | 2/21/2019 |
| 989 | MedImmune Gaithersburg, MA Engineer I/II BS or MS Exp: BS: 0-2 years for Engineer I, MS: 1+ years for Engineer II |
This position reports to the Associate Director of Engineering Technical Services supporting GMP clinical biomanufacturing. Responsible for maintaining reliable equipment performance for one or more manufacturing systems at MedImmune’s Gaithersburg Clinical Manufacturing facilities including cell culture, purification, and support systems. Monitors equipment performance. Identifies equipment issues and develops technical solutions | 2/21/2019 |
| 990 | MedImmune Gaithersburg, MA R&D Associate II MS in biology or related Exp: 0-2 years |
The successful candidate will carry out bioanalytical cell based assay testing of recombinant protein therapeutics under cGMP. The ideal candidate will make detailed observations, analyze data, interpret results, and exercise appropriate technical discretion in the design, execution, and interpretation of experiments in an independent manner.This person may be involved in the qualification and validation of cell-based bioassays for biological characterization and testing of biopharmaceutical products, and assist in assay investigations and troubleshooting. He/She will perform cell culture, maintain cell lines and perform routine lab equipment maintenance. The candidate will be expected to prepare technical reports, SOPs and technical summaries for meeting presentation. The candidate will be expected to assist/lead investigation for non-conformances and coordinate equipment validation with different departments. | 2/21/2019 |
| 991 | Medpace Cinncinnati, OH Vender Management Associate BS/BA Exp: 1+ years |
Review third party contracts for business implications and acceptable predefined legal terms; Utilize governance, risk, and compliance (GRC) software to contribute to contract management and third party information; Employ risk analysis processes in the performance of third party due diligence; Apply understanding of policies and procedures associated with purchase contracts such as indemnification and amendments; Review third party performance ensuring that contract KPI’s are achieved and develop relevant improvement plans in collaboration with the operations teams; Analyze financials to assist in negotiation of agreements; Prepare and coordinate third party requests for proposals; and May be responsible for other projects and responsibilities as assigned. Review third party contracts for business implications and acceptable predefined legal terms; Utilize governance, risk, and compliance (GRC) software to contribute to contract management and third party information; Employ risk analysis processes in the performance of third party due diligence; Apply understanding of policies and procedures associated with purchase contracts such as indemnification and amendments; Review third party performance ensuring that contract KPI’s are achieved and develop relevant improvement plans in collaboration with the operations teams; Analyze financials to assist in negotiation of agreements; Prepare and coordinate third party requests for proposals; and May be responsible for other projects and responsibilities as assigned. | 2/21/2019 |
| 992 | Viant Orchard Park, NY Design Engineer BS/BA in related field Exp: 0-3 years |
Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications. | 2/21/2019 |
| 993 | Medtronic Miami Lakes, FL Associate Supplier Quality Engineer BS/BA in engineering or sciences Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. 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. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. 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. Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. 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.Responsibilities may include the following and other duties may be assigned. 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. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. 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. Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. 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. | 2/21/2019 |
| 994 | Medtronic Davers, MA Associate Microbiologist BS/BA or MS in biology, biomedical engineering, or technical discipline Exp: 0 years |
Reviews sterile load cycle data and performs sterile load release for finished product lots manufactured by Medtronic Danvers or contract manufacturers. Administers the Environmental Monitoring Program for the Danvers manufacturing areas including viable and non-viable particulate counts, product bio-burden, water and surface microbial levels, etc. to ensure an appropriately controlled environment meeting regulatory expectations and industry standards. Communicates detailed information regarding monitoring results and trends to Manufacturing and Quality; recommends revisions to monitoring program and/or manufacturing process controls and ensures effective corrective actions are implemented, where necessary. | 2/21/2019 |
| 995 | Medtronic Boulder , CO Associate R&D Engineer BS/BA in engineering or sciences Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. • Works as part of a team, providing technical support on New Product Development and Sustaining Project Initiatives, ensuring medical devices are designed with the utmost regards to safety, reliability and quality. • Designs, develops, analyzes, troubleshoots and provides technical skills during legacy product remediation and new product development. • May be involved in product research and development, including assessing user needs and product requirements • Reviews existing and generates new Technical Documentation to ensure Medical Devices comply with all applicable standards. Includes generating and executing verification test protocols. • Translates research discoveries into usable and marketable products.Responsibilities may include the following and other duties may be assigned. • Works as part of a team, providing technical support on New Product Development and Sustaining Project Initiatives, ensuring medical devices are designed with the utmost regards to safety, reliability and quality. • Designs, develops, analyzes, troubleshoots and provides technical skills during legacy product remediation and new product development. • May be involved in product research and development, including assessing user needs and product requirements • Reviews existing and generates new Technical Documentation to ensure Medical Devices comply with all applicable standards. Includes generating and executing verification test protocols. • Translates research discoveries into usable and marketable products. | 2/21/2019 |
| 996 | Medtronic North Haven, CT Quality Engineer - Manufacutring Operations MS in engineering or sciences Exp: 0 years |
esponsibilities may include the following and other duties may be assigned. 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. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality. Provide Quality Engineering support as a Process Validation team member and lead/execute Test Method Validations and Measurement Systems Analysis (MSA).esponsibilities may include the following and other duties may be assigned. 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. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality. Provide Quality Engineering support as a Process Validation team member and lead/execute Test Method Valida | 2/21/2019 |
| 997 | Merck Elkton, VA Associate Specialist Engineering, Bulk Manufacturing BS in engineering Exp: 0.5-1 years |
The role encompasses technical services support in the areas of equipment and automation systems, validation, deviation management and product franchise. Specific assignments may be focused in one area or span across multiple areas of focus. Candidates will be responsible for: Provide on-the-floor support of operational and technical issues; collaborating with the shop floor to provide immediate responses to deviations and potential deviations. Performing deviation investigations aimed to prevent deviation re-occurrence, including determining the root cause, identifying corrective/preventative actions, identifying event scope, and conducting a product impact assessment. Where applicable, complete investigational test protocols to determine root cause, product impact, event scope, etc | 2/22/2019 |
| 998 | Merck West Point, PA Scientist/Engineer, Bio-Process Development MS in chemical engineering or biological sciences Exp: 1+ year |
The primary job responsibility will be to deliver on specific assigned objectives related to development of robust and scalable processes for the manufacture of clinical supplies and subsequent technical transfer of such processes to GMP operations. The successful candidate will have a strong working knowledge of chromatography, membrane filtration, and centrifugation technologies and be able to apply this understand towards process development challenges. Experience in programming (e.g. Visual Basic, Python) and statistical & data visualization software (e.g. Excel, Spotfire, JMP, Design Expert) will be considered as a positive factors. In addition to the core responsibilities outlined above, the individual is expected to have an understanding of the regulatory guidelines governing cGMP manufacture, keep careful notes, comply with all required training, and maintain a focused attention on laboratory safety. | 2/22/2019 |
| 999 | Merck Durham, NC Process Engineer – Merck Manufacturing Division BS in engineering or sciences Exp: 0 years |
The successful candidate will be expected to be a first responder to requests from the manufacturing areas when support is needed. The well-qualified candidate must have analytical, problem-solving, and communication skills. In this role, the candidate will provide support for the manufacturing of aseptic products. | 2/22/2019 |
| 1000 | Merck West Point, PA BS/BA Exp: 1+ years internship/coop experience |
This individual will be involved in streamlining and optimizing system operations while working with the Command Center System Engineer. The Operations Support Engineer will also be heavily involved in troubleshooting and resolving issues related to systems and programs used in the Commend Center. This role is highly visible and will need to work very efficiently with other departments on the plant site, as well as, contract personnel and external agencies. This is a multi-tasking position and requires strong attention to detail. Develops and maintains comprehensive knowledge of West Point facilities, operations, and personnel. Utilizes available resources to ensure continuous smooth operation of the site. | 2/22/2019 |
| 1001 | Meridian Cincinnati, OH Lot Release Associate I BS in biology or related Exp: 0-1 years |
The Lot Release Associate I is responsible for ensuring product quality assurance requirements are satisfied and fully documented. They will participate in the review of quality documentation, review of production and documentation, and any other associated activities to ensure product compliance prior to release of product. Responsibilities include: Maintain departmental trend information. Set up, completed and maintain all Lot Release log sheets. Ensure that all Lot Release records are appropriately stores, maintained and retrievable. etc | 2/22/2019 |
| 1002 | Meridian Research Bradenton, FL Clinical Research Coordinator AA/AS or higher Exp: 0-2 years |
Responsibilities and Duties include: Coordinate Clinical Studies adhering to the principles of Good Clinical Practice Collect initial medical background from patients and other appropriate sources Work as a cohesive team member coordinating assigned studies and backing up other studies on location Educate and provide information to patients, families, and community groups regarding clinical drug trials Assist and support Recruitment Team with prescreen activities and other activities related to subject recruitment | 2/22/2019 |
| 1003 | Merieux NutriSciences Madison, WI Microbiologist BS/BA Exp: 1-2 years |
The incumbent is responsible for the testing of food samples using various microbiological analyses. Job responsibilities include: Follow appropriate methods and SOPS when conducting sample preparation. Maintain quality control records. Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities. Pipette sample solution into tubes or plates according to the analysis process being performed. Pour the agar into plates or tubes to begin the growth process. Perform confirmation tests on suspect plates or tubes to identify the strain of bacteria. | 2/22/2019 |
| 1004 | Merit Medica South Jordan, UT Product Manager I BS/BA in marketing or related Exp: 1+ years |
Responsible for providing routine product marketing and analysis support. Essential functions include: Works with product users to increase the ability of Merit to improve products to meet specific customer needs, Works with customers in coordinating Market Research Trials, Evaluates new product potential, Serves on product decision making teams to assist in product development and identifying marketing opportunities, etc. | 2/22/2019 |
| 1005 | Merit Medica Malvern, PA R&D Engineer II MS in science or engineering Exp: 1+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. Essential duties include: Independently evaluates, selects, and applies standard technical techniques, procedures, and criteria, using judgement in making minor adaptations and modifications. Investigates a moderate number of technical variables in completing assignments that have clear and defined objectives. Performs work which involves conventional types of plans, investigations, surveys, structures, or equipment with relatively few complex features for which there are precedents. | 2/22/2019 |
| 1006 | Merit Medica Malvern, PA R&D Engineer BS/BA or MS in engineering or sciences Exp: 0-1 years |
Performs routine technical work such as the design, manufacture and operation of structures, machines and systems under general supervision and guidelines. Essential duties include: 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. | 2/22/2019 |
| 1007 | Merit Medica South Jordan, UT Manufacturing Lab Engineer I BS/BA or MS in mechanical or manufacturing engineering Exp: 0-2 years |
Our Manufacturing Lab Engineer performs testing on equipment and parts in a manufacturing lab environment. Performs routine technical work such as the design, manufacture and operation of structures, machines and systems under general supervision and guidelines. Prepares and tests specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks. | 2/22/2019 |
| 1008 | Merit Medica Malvern, PA Quality Assurance Inspector - 1st Shift HS Diploma Exp: 6 months |
This position operates, maintains and troubleshoots clippers, stretchers, and testing equipment. Operations are performed per written SOPs, including CGMP guidelines. Perform inspection of extruded products such as braided shafts, non-braided tubes, tips, etc. Completes the inspection steps of clipping and stretching to ensure smooth product flow. Complete paperwork associated with work orders being processed. Interacts with material handling for checking orders into stock. | 2/22/2019 |
| 1009 | Merz Mesa, AZ Regulatory Affrs Assoc BS/BA in scientific or healthcare discipline Exp: 1+ years |
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. Support preparation and coordination of submissions in accordance with the current regulations and guidance’s. Ensure submissions support company objectives and strategy. Identify and communicate regulatory risks and project issues. Make recommendations to team and regulatory management. | 2/22/2019 |
| 1010 | Method Sense Marrisville, NC Quality Assurance Associate BS Exp: 1-3 years |
We are seeking a Quality Assurance Associate to work closely with the MethodSense Executive Team and Project Managers to assist with the maintenance of client’s Quality Management Systems, supporting client Regulatory solutions, and the implementation and maintenance of client technology solutions on a contract basis. | 2/22/2019 |
| 1011 | MQA Concord, CA Microbiology Lab Tech I AS in biology or related Exp: 0-1 years |
The lab tech performs or supports testing such as microbial load estimation by different methods, MIC, MBC, disinfectant studies, antimicrobial assays, bacteria and mold identification, PCR, water chemical analysis, endotoxin test, virology assays, SDS PAGE, BCA, Cytotoxicity assays, cell banks and collects air, surface and water samples at MQA or client facilities. Testing is performed in accordance with standard operating procedures. Monitors and checks operation, calibration, and service condition of laboratory equipment along with monitoring and maintaining laboratory supplies. Complies with procedures and adhere to documentation practices in accordance with MQA policies. Perform data entries into computer databases, along with reporting adverse or unusual events to management. Participates in process improvement activities as needed. Prepare SOPs as needed. | 2/22/2019 |
| 1012 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in engineering, or chemical engineering Exp: 1/2 years or more |
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. 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. | 2/13/2019 |
| 1013 | Hovione East Windsor, NJ Associate Quality Assurance Specialist BS in engineering, or chemical engineering Exp: 1/2 years or more |
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). | 2/13/2019 |
| 1014 | Human Longevity San Diego, CA Oncology Bioinformatics Laboratory Scientist BS or MS in computer science, bioinformatics or related Exp: 0-2 years |
The Oncology Bioinformatics Laboratory Scientist will work closely with the Oncology R&D team to provide informatics support across multiple applications of somatic variant calling using next-generation sequencing technologies. An ideal candidate will have experience developing/implementing somatic variant calling analysis tools in a CLIA/CAP NGS laboratory. This role will be required to participate in the design and execution of validation studies to support the key objectives of the Oncology division. | 2/13/2019 |
| 1015 | ICUmedical San Clemente, CA R&D Engineer BS in mechanical or engineering discipline Exp: 0-2 years |
The R&D Engineer is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. The key responsibility of this position is the design, development, and improvement of product lines to ensure their efficiency and reliability. The incumbent will be heavily involved with plastics, polymers, molding, medical disposables, plastics engineering, and solid modeling. The R&D Engineer will be expected to interface with customers and suppliers on high-volume disposable medical device design. | 2/13/2019 |
| 1016 | ICUmedical Salt Lake City, UT Production Planner BS/BA Exp: 0-2 years |
As a production planner you will analyze, plans and prepares production schedules for manufactured products within the production facility to meet customer demand. Draws up production schedules to establish sequence and lead time of each operation to meet shipping dates according to sales forecasts and/or customer orders. Analyzes production specifications and plant capacity data and performs mathematical calculations to help determine manufacturing processes, tools, and human resource requirements. Gathers performance data and assesses whether or not departments are performing according to production schedules. Produces reports that evaluate plant capacity and identify areas where improvements can be implemented. | 2/13/2019 |
| 1017 | Idexx Westbrook, ME Lab Associate - Infectious Disease R&D Lab Operations HS Diploma or AS Exp: 0-2 years |
You will be joining the cross-functional R&D Lab Operations team responsible for building research and development SNAP devices, supporting acquisition of diagnostic samples for R&D product testing, and supporting general laboratory operations. The successful candidate will be a self-starter, motivated and excels in a highly collaborative laboratory environment. | 2/13/2019 |
| 1018 | iFyber Ithaca, NY Micro/MolecularResearch Associate BS/BA in biological sciences Exp: 1+ years research experience |
iFyber is seeking aresearch associateto assist with R&D projects at the interface between chemistry, biology, and material science. iFyber serves clients in the medical device, diagnostics, and antimicrobial industries. The person in this position will support a variety of programs that will require experience and/or the ability to pick up bench skills related to microbiology. Responsibilities include: Conduct microbiologyexperimentsboth independently and in a collaborative fashion, Plan tasks for successful completion of experiments based on requirements set by senior staff, Follow established protocols and work with senior staff to adapt or design new protocols | 2/13/2019 |
| 1019 | Imbed Bio Fitchburg, WI Production Technician BS/BA in sciences Exp: 1-4 years work in lab/production environment |
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. | 2/13/2019 |
| 1020 | Illumina Bay Area, CA Systems Engineer 1 BS/BA in eletrical, biomedical, mechanical, or chemical engineering Exp: 1-3 years in product development, experience in programing |
We are seeking a Systems Engineer 1 to help us build the next generation of clinical diagnostic tests. This position work with external and internal partners in Operations, R&D, and Software Development to develop new laboratory automation and diagnostic equipment. This engineer will focus on development and system testing activities for our sample preparation systems. Responsibilities include: Participate in development of consumables, assay automation processes to accomplish development and product goals. Conduct screening and troubleshooting experiments to assess the technical capability and performance of assay, robotic, fluidic, sensor, and instrumentation sub-systems and systems, collaborating with senior engineers and scientists. | 2/13/2019 |
| 1021 | Immatics Houston, TX Laboratory Support Assistant AS degree in biological sciences Exp: 1+ years |
The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. The primary purpose of the Laboratory Support Assistant position is to provide support to the research and manufacturing teams to assist in laboratory maintenance and logistics coordination. In addition, provide support to the clinical team in support of adoptive cellular therapy (ACT) clinical trials. This position will report to the Director QA/QC. | 2/13/2019 |
| 1022 | Immatics Houston, TX Research Associate - CMC BS/BA or MA in biological sciences Exp: 1-3 years |
The primary purpose of the research associate position is to perform complex, highly specialized and time sensitive technical cell manipulation and testing procedures to perform experiments pertaining to process, product, or assay development of cell and gene therapy products. Responsibilities include: Performs aseptic cell growth and manipulation procedures such as cell isolation or enrichment, sorting, culture, cellular product cryopreservation, and cell product thaw/wash. Performs and handles human peripheral blood for processing and product manufacture. Perform cell-based studies or assays for product development, assay development, or product characterization. | 2/13/2019 |
| 1023 | Immucor Norcross, GA Red Blood Cell Processing Technician BS/BA in life sciences Exp: 1-3 years |
As a Red Blood Cell Processing Technician, you will perform production tasks in a clean-room environment. In addition, it will be your responsibility to ensure that your work is consistently in compliance with Good Manufacturing Practices and Good Documentation Practices. Additional duties include: Performing blood processing operations according to corporate policies, operating procedures, specifications, and verbal work instructions. Ensuring that blood products are transported, processed and stored in a manner that prevents contamination.Following appropriate control measures to prevent mixing of dissimilar production components in compliance with Good Manufacturing Practices | 2/13/2019 |
| 1024 | Immunogen Waltham, MA RESEARCH ASSOCIATE I MS in life sciences Exp: 1 year |
Develop and troubleshoot LC/MS assays (pharmacokinetic analysis of free payload and antibody, metabolite profiling, drug-antibody ratio measurement) using TTOF 6600, 5500 Triple Quad, Sciex OptiFlow, and Versette instrumentations to support pre-clinical and clinical studies. Test pre-clinical samples to support candidate identification for early development phases. Analyze and interpret data; communicate results and interpretation. Plan experiments, troubleshoot when needed, summarize results, write and review technical reports. Collaborate with project team leaders to organize timelines for assays needs and sample testing. Summarize and present results in internal meetings. | 2/13/2019 |
| 1025 | Immunomedics Morris Plains, NJ Cell Culture Technologist, Upstream Process & Manufacturing BS/BA in biology or related Exp: 1-3 years |
The Cell Culture Technologist, Upstream Process and Manufacturing Sciences is responsible for participating in the operation of mammalian cell culture processes under cGLP conditions. Responsibilities include: Prepares and maintain cGLP research cell banks. Performs cell culture expansion under cGLP for cell culture in benchtop bioreactors and shake-flasks.Strong aseptic techniques and demonstrated ability in documentation and knowledge of cGMP/cGLP cell culture development. | 2/14/2019 |
| 1026 | Immunomedics Morris Plains, NJ QC Analyst, Raw Materials BS/BA in biology, chemistry, or related Exp: 1-3 years |
The QC Analyst, Raw Materials is responsible for release testing of incoming raw materials and utilities (water and gas) samples testing. The incumbent will be supporting testing and method validation activities either inhouse or at a third-party provider. The responsibilities may also include receiving, inspection and sampling of incoming raw materials as assigned. This position also includes responsibility for authoring technical reports, specifications for incoming raw materials and evaluation of change notifications, as directed. | 2/14/2019 |
| 1027 | Impel Seattle , WA Pharmaceutical Formulation Technician BS/BA in chemistry, pharmaceutical sciences or related Exp: 0-5 years |
The Pharmaceutical Formulation Technician will conduct formulation and process development for powder and liquid nasal dosage forms under the supervision of the Pharmaceutical Formulation Scientist. Responsibilities include: Conduct laboratory experiments under the supervision of the formulation scientist. Assist technical staff in the development of Impel’s drug formulations. | 2/14/2019 |
| 1028 | In Cube Labs San Jose, CA Mechanical Engineer I BS/BA in mecahnical engineering or related Exp: 1+ years |
The ideal candidate is expected to play a pivotal role in our R & D team. The candidate must have a background in mechanical engineering. Experience with design, fabricating and assembling medical products is highly desired. Responsibilities include: creating/updating/releasing engineering designs, designing tools for manufacturing, working with outside vendors, develop test protocols and reports. | 2/14/2019 |
| 1029 | Inova Diagnostics San Diego, CA Chemist I - Bioflash Manufacturing BS/BA in biological sciences Exp: 1-2 years lab exerience |
Participates in the preparation of autoimmune diagnostic products, utilizing the Bioflash technology platform, following established procedures. Major duties include Bioflash bead and reagent preparation activities and the preparation of controls and conjugates for the Bioflash product lines. | 2/14/2019 |
| 1030 | Inova Diagnostics San Diego, CA Chemist I- Research & Development BS/BA in biological sciences Exp: 1-2 years lab exerience |
Assists with the development of new or improved autoimmune diagnostic assays according to established procedures. Major research and development duties include assistance with reagent formulation and optimization of existing formulations. Additional duties involving organizing and facilitating timely progress and completion of projects will be assigned. | 2/14/2019 |
| 1031 | Inovio Pharmaceuticals San Diego, CA Laboratory Assistant (Logistical Operations) AS degree in biological sciences Exp: 0-1 years |
The Laboratory Assistant provides assistance with lab management functions to support all aspects of research within the company. The position interfaces with multiple departments (R&D, engineering, accounting, quality) and performs general lab maintenance duties and recordkeeping. | 2/14/2019 |
| 1032 | Inovio Pharmaceuticals Plymouth Meeting, PA Clinical Trials Associate BS/BA Exp: 0-2 years |
The Assistant, Clinical Trials (CTA) is responsible for supporting, under the direct supervision of the supervisor/Clinical Project Lead (CPL), clinical trial execution, externally sponsored research and program level activities as assigned within Clinical Operations at Inovio. This position assists in various tasks and projects related to clinical trials as well as basic, administrative duties such as ordering drugs and devices, maintaining milestone trackers and filing of essential documents of externally sponsored trials. | 2/14/2019 |
| 1033 | Insmed Bridgewater, NJ Complaint Associate, Quality Asurance BS in engineering or life sciences Exp: 1-2 years |
Reporting to the Associate Director, Quality Assurance - GMP, the QA Complaint Associate, will play a key role in the complaint process and related customer interactions. This role has a critical interface with the commercial Patient Support Program and will work directly with the team on a daily basis to manage product complaints, device inquiries and support. Specific areas of responsibility include: Complaint intake/entry into Veeva, ensuring accurate and thorough complaint intake information, Preliminary assessment of all complaints within 24 hours for regulatory escalation and replacement need, trouble-shooting with complainant, maintaining work instructions, patient follow-ups as needed, etc. | 2/14/2019 |
| 1034 | Omnipod Acton, MA Regulatory Affairs Assocaite - LAF BS preferred Exp: 0-2 years |
The position of Regulatory Affairs Associate will be responsible to provide immediate administrative regulatory support to ensure timely introduction of advertising and promotion content in the U.S, as well as opportunity in the future to support new products subject to medical device regulations in both the U.S. and global regions. Provide regulatory support to marketed products and ensure company’s regulatory compliance status. Responsibilities include: Manage regulatory databases and administer regulatory processes, primarily advertising and promotional content, which includes activities such as data management and verification, Support the development and implementation of regulatory processes, procedures, and standards as assigned. | 2/14/2019 |
| 1035 | Omnipod Los Angeles, CA Clinical Services Specialist - West BS/BA Exp: 0-2 years |
The Clinical Services Specialist (CSS) is primarily responsible for meeting required sales quota and all clinical initiative expectations. This responsibility will require extensive travel and extended stays in a field based territory to support open territory needs. The CSS will provide product sales, training, downloading and technical support in accordance with company policy. They will also in-service physicians, mid-level staff, CDE’s, and ancillary staff on the OmniPod Insulin Management System, build relationships with our customers, and bec skilled at selling and using the OmniPod Insulin Management System. | 2/14/2019 |
| 1036 | Integer Chaska, MN Supplier Quality Engineer I BS/BA in related field Exp: 0-2 years |
The primary purpose of this position is to develop the risk-based supplier management process, lead the critical supplier-related projects, and support daily supplier non-conformances and requests for change. This position will also be responsible for performing GMP/ISO audits on suppliers, proposing improvements to their quality system and tracking the closure of any audit related non-conformance. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. The primary purpose of this position is to develop the risk-based supplier management process, lead the critical supplier-related projects, and support daily supplier non-conformances and requests for change. This position will also be responsible for performing GMP/ISO audits on suppliers, proposing improvements to their quality system and tracking the closure of any audit related non-conformance. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. The primary purpose of this position is to develop the risk-based supplier management process, lead the critical supplier-related projects, and support daily supplier non-conformances and requests for change. This position will also be responsible for performing GMP/ISO audits on suppliers, proposing improvements to their quality system and tracking the closure of any audit related non-conformance. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. | 2/14/2019 |
| 1037 | Integer Plymouth, MN Associate Prototype Technician - 2 AS degree or above Exp: 0-3 years |
The primary purpose of this role is to perform assembly and inspection operations over a range of new products and/or processes. Will support non-cyclical work which may include prototypes and pre-production lots in preparation for validation, clinical trials or transfers. Will also support multiple builds within the facility including lab and cleanroom environments. With guidance from Engineering on projects and using work procedures, this role provides support to the Engineering teams to meet various deadlines. May provide support to other team members or provide input to the Engineers on assembly, processes, and build/quality documentation. | 2/14/2019 |
| 1038 | Integra Plainsboro, NJ Quality Control Analyst I BS/BA in biological or chemical sciences Exp: 0-3 years |
The Quality Control Analyst I will be responsible for executing laboratory testing and data analysis, as well as, assist with test methods development, validation development and implementation. Tests and inspects raw materials, work-in-process (WIP), and finished goods at various stages of production process. Selects random samples for tests at specified stages such as incoming or in production process, and tests products for variety of qualities, such as dimensions, performance, appearance, correct assembly, and other testing outputs. Records test data, applying statistical quality control procedures. Works collaboratively with Manufacturing, Engineering, Quality Assurance, and other functional experts to support all daily operational activities. Consults with management to resolve quality, production, and efficiency problems. Functions in conjunction with manager and functional experts on special department projects. Works with internal departments to ensure implementation, maintenance, and improvement of the quality management system. Performs the essential duties and responsibilities as listed in section below. | 2/14/2019 |
| 1039 | Integra Plainsboro, NJ Microbiologist I HS Diploma, BS/BA in biology preferred Exp: 0-3 years |
As a Microbiologist I, duties include: Ensure compliance with all company policies and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive. Perform and document in-house microbiological testing on all in-process and finished products to comply with acceptance requirements. Perform LAL, water analysis, growth promotion, gram staining, identification of microorganisms and other microbiological testing. Perform and document environmental monitoring in compliance with Standard Operating Procedures. Report any equipment and testing deviations to the Supervisor. Submit samples for shipment to third party labs when necessary. Maintain GMP/GLP laboratory notebooks and documentation relevant to the duties and responsibilities assigned. | 2/14/2019 |
| 1040 | Integral Molecular Philadelphia, PA Research Associate I BS/BA in biology, bioengineering, or related Exp: 1-2 years lab exerience |
As a research associate, responsibilities include: 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, prform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry) | 2/14/2019 |
| 1041 | IDT Coralville, IA Synthesis Scientist I - Main Production Nights BS/BA in sciences Exp: 0-2 years |
The Synthesis Scientist I synthesizes custom oligonucleotides according to the customer’s order. This generally includes synthesis, cleavage, deprotection and QC sampling of the products being made. Other responsibilities include adherence to lab SOPs, maintaining lab equipment/stock, keeps record of specalized processes for oligo, etc. | 2/14/2019 |
| 1042 | IDT Coralville, IA Custom Quality Control Analyst I - SAG Group BS/BA in biological or chemical sciences Exp: 0-2 years |
The Custom Quality Control Analyst I ensures the quality of processes and products in support of all manufacturing areas within Integrated DNA Technologies. Essential functions include: analyze data for quality/consistency/accuracy, handels samples for preperation fore assays, understands ISO requirements, etc. | 2/14/2019 |
| 1043 | IDT Coralville, IA Manufacturing Chemist BS/BA in biological or chemical sciences Exp: 0-2 years |
The Manufacturing Chemist efficiently produces high quality materials for use in IDT’s production labs. Essential Functions include: monitoring inventory, follows processes for manufacturing/storage/transportation, gathers/interprets/analyzes oligo data, maintains accurate/detailed product/process, intstrument and training. | 2/14/2019 |
| 1044 | Integrity Bio Camarillo, CA Research Associate BS/BA in biochemistry, chemistry, biology, or related Exp: 1-5 years |
Duties and functions include: assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision, set up/perform HPLC as well as other assays to characterize protein/peptide molecules, analyzes data, etc. | 2/14/2019 |
| 1045 | Integrity Bio Camarillo, CA Project Management Associate BS/BA in biochemistry, chemistry, biology, or related Exp: 0-5 years |
Duties and functions include: Schedule and attend meetings, draft agendas, lead discussions, author meeting minutes, and follow up on action items, Assist in designing client studies and generateproposals outlining scope, material requirements, schedule, and budget, Coordinate execution of projects with IBI project teams, put together study timelines, oversee submission of data, and respond to client inquires | 2/14/2019 |
| 1046 | Intuitive Multiple Locations, Field Service Engineer AA degreen in electornics or engineering Exp: 1-3 years |
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. Pre site verifications to prepare site for system installation. Assist in coordination of system delivery (e.g. confirming site readiness). Perform system installations. Install system upgrades. Provide technical and clinical support to end-users and other ISI employees. Train customer on new features or enhancements made to existing features. 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. Pre site verifications to prepare site for system installation. Assist in coordination of system delivery (e.g. confirming site readiness). Perform system installations. Install system upgrades. Provide technical and clinical support to end-users and other ISI employees. Train customer on new features or enhancements made to existing features. | 2/14/2019 |
| 1047 | Intuitive Milford, CT Mechanicl Design Engineer - Advanced Energy Insturments BS or MS in mechanical engineering Exp: 0-3 years |
The Mechanical Design Engineer will help develop new Advanced Energy instruments while addressing performance, cost, and reliability requirements and completing the development, documentation, and verification of those designs. The successful candidate will have both the technical depth to resolve complex mechanical, materials and manufacturing design issues and the ability to work in an interdisciplinary team to troubleshoot to root cause higher level system issues. A strong sense of shared responsibility and shared reward is required as well as a commitment to high product quality. | 2/14/2019 |
| 1048 | Invitae San Francisco, CA BS/BA in biological sciences Exp: 1+ years |
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. | 2/14/2019 |
| 1049 | Thermo Fisher Scientific Florence, SC Scientist I - R&D BS/BA in chemistry or sciences Exp: 0-2 years |
This is an exceptional entry-level opportunity to assist with the R&D efforts at the Florence, SC facility by conducting important experiments that support our customers with pharma development. Duties include: Conduct chemical experiments and/or analysis 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 | 2/16/2019 |
| 1050 | Thermo Fisher Scientific Mississauga, Ca Complicance Associate (Contract) BS/BA in sciences Exp: 1-2 years |
In this one-year contract position you will support and ensure adherence to established Standard Operating Procedures (SOPs) for conducting and generating the Annual Product Review report. You will act as a liaison between several internal departments with the intent to gather relevant data. Additionally, you will support the compilation of product data for the review period with the objective of verifying the consistency of existing process, the appropriateness of current specifications, highlighting any trends and identifying both product and process improvements for the drug product. Performs administrative tasks of data entry, generates trending reports and statistical data analysis for Annual Product Reports. | 2/16/2019 |
| 1051 | Thermo Fisher Scientific Eugene, OR Scientist, Production (entry level) BS/BA in biology, chemistry, or related Exp: 0-2 years |
As a Scientist I you will work in a manufacturing environment and be responsible for performing protein and dye conjugations while following quality and safety standards. You will follow written procedures, and be technically capable of performing production processes. Responsibilities include: produce/analyze protein products, maintain inventory in lab, analyze and present data. | 2/16/2019 |
| 1052 | Thermo Fisher Scientific Pittsburg, PA Pricing Coordinator I AS degree in business Exp: 0+ years |
Coordinates and administers accurate pricing on ~2000 customer contracts with sales of over $200 Million using Thermo Fisher’s complex pricing systems. Key responsibilities include: Nice price agreement, pricing maintenance, troubleshooting, customer service, and supplier rebates. | 2/16/2019 |
| 1053 | Invivoscribe San Diego, Ca Manufacturing Associate II BS/BA in scientific discipline Exp: 1+ years |
The Manufacturing Associate II contributes to the drafting and reviewing of new documents, including Standard Operating Procedures, Batch Records, Validations, work instructions and Purchasing Specifications. Assists with all aspects of manufacturing, including the production of master mixes, controls and assay kits. Manufactures products adhering to Quality System Regulations and are accompanied by appropriate documentation. | 2/16/2019 |
| 1054 | IQVIA Durham , NC Laboratory Associate 1 BS/BA in scientific discipline Exp: 0-2 years |
Perform routine analysis and laboratory testing procedures to obtain data from client specimens. Provide routine documentation and review of work performed in a timely manner. Responsibilities include: Complete and prepare documentation in compliance with regulatory and corporate guidelines. Perform and document all specimen test procedures with accuracy, consistency and timeliness in accordance with current standard operating procedures (SOPs) and regulatory guidelines. Exercise good judgment in assessing whether test procedure is proceeding according to expectations and that the results are within acceptable tolerances. | 2/16/2019 |
| 1055 | IQVIA Marietta , GA Entry Level Clinical Trial Project Coordinator BS/BA in management, life science or related Exp: 0-2 years |
The Project Coordinator provides support to the Project Manager and related team members by performing generic procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. startup, maintenance and close-out); Ensure work is conducted in line with standard operating procedures, policies and good practices. Using monitoring tools, pro-actively identify trends and provide feedback to internal departments and/or client on performance of both the Investigator and the Q2 Solutions services to ensure timely service delivery. Examples may include: | 2/16/2019 |
| 1056 | IQVIA Durham , NC Lab Associate - Nucleic Acid Isolations and Initial QC BS/BA in scientific discipline Exp: 0-2 years |
Perform routine analysis and laboratory testing procedures to obtain data from client specimens. Provide routine documentation and review of work performed in a timely manner. Perform and document all specimen test procedures with accuracy, consistency and timeliness in accordance with current standard operating procedures (SOPs) and regulatory guidelines. Identify abnormal progress of test procedure, potential QC failures, or otherwise unusual results and escalate to senior lab personnel immediately. | 2/16/2019 |
| 1057 | IQVIA Durham , NC Statistical Programmer - Entry Level BS/BA or MS in mathmatics, biostatistics, or public health Exp: 0-1 years |
Statistical Programming projects vary, your typical responsibilities and opportunities might include: Programming all aspects of a clinical trial, from files to tables, listings and figures Using SAS in a quality control and production capacity Programming from scratch as well as updating existing programs Developing specifications for analysis files and annotating output shells for programming instruction and documentation Working and communicating effectively in a team environmentStatistical Programming projects vary, your typical responsibilities and opportunities might include: Programming all aspects of a clinical trial, from files to tables, listings and figures Using SAS in a quality control and production capacity Programming from scratch as well as updating existing programs Developing specifications for analysis files and annotating output shells for programming instruction and documentation Working and communicating effectively in a team environment | 2/16/2019 |
| 1058 | IQVIA Durham , NC Biostatistician - Entry Level MS in math, statistics, public health Exp: 0-1 years |
Biostatisticians projects vary, your typical responsibilities and opportunities might include: Develop analysis plans, table shells, programming and table specifications; produce tables, listings and figures; perform data review and statistical analysis. Programming aspects of a clinical trial, from files to tables and listings. Assist with protocol development and protocol and case report form (CRF) review. Advise data management staff on database design and critical data. May advise on validation checks. Assist in writing statistical sections of integrated reports. Assist project lead in fulfilling project responsibilities. | 2/16/2019 |
| 1059 | Irvine Scientific Santa Ana, CA Quality Control Microbiologist Level II BS/BA in microbiology Exp: 1-2 years |
We are seeking an individual to perform applicable testing on raw, in-process, and final products to insure material quality as well as to perform tests for monitoring environmental conditions and water quality. Responsibilities include: testing raw, in-process and finished products. Testing environmental conditions, testing water systems, calibrating and maintaining instrumentation, etc. | 2/16/2019 |
| 1060 | McNeil Consumer Healthcare Guelph, Ca Assistant Scientist, Analytical testing- 12 month contract BS/BA in biochemistry, chemistry, biology, or related Exp: 1+ years lab experience |
Under limited supervision and in accordance with all applicable federal, provincial, and local laws/regulations, the Companies’ policies, procedures and guidelines, you will be responsible for: Performing assigned scientific experiments and routine tasks according to established procedures. Coordinating and/or executing: method validations and/or transfers; chemical and physical testing of stability samples; sampling and testing of process validation batches. Assisting in laboratory investigations. Reviewing data and documents. Collating, analyzing, and processing data. Keeping accurate records and supporting the development of technical documentation. | 2/16/2019 |
| 1061 | Jounce Therapeutics Cambridge, MA Research Associate/Associate Scientist BS or MS in biological sciences Exp: 0-2 years |
We are looking for a creative and highly motivated research associate/associate scientist to join the Translational Genomics department at Jounce Therapeutics. The successful candidate will be an integral team member supporting the translational science efforts that help transition novel immune-oncology biologics from bench to bedside. Primary responsibilities include the design and execution of gene expression and genomics-based experiments. In addition, the candidate will work with other lab members to harness and implement new technology within the genomics space. Job responsibilities include careful design and execution of experiments, data analysis and interpretation, thorough documentation of work, and clear communication of results both in group settings and in written reports. | 2/16/2019 |
| 1062 | Jubilant Life Sciences Spokane, WA Associate, Regulatory Affairs BS/BA Exp: 1-2 years |
TheRegulatory Affairs & Pharmacovigilance Associatesupports the regulatory compliance and pharmacovigilance programs by coordinating the scheduled activities of state and federal reporting, as well as medical complaint handling, ensuring compliance with US and International regulatory agencies. This individual evaluates both the compliance and medical complaint report information in order to plan appropriately, request information, and maintain schedule adherence. Responsibilities also include eSubmissions and the assurance that assigned departmental procedures are developed and maintained in accordance with US and/or global regulatory requirements as well as enhancing regulatory compliance systems and strategies. | 2/16/2019 |
| 1063 | Catalent Madison, WI Associate, Quality Assurance Validation BS/BA in technical discipline Exp: 0-2 years |
The Quality Assurance Validation, Associate supports ongoing validation efforts and quality systems responsibilities in support of the manufacturing, testing, and release of formulated drug substance. This role contributes to the development of concepts and techniques specific to validation and risk management. The Quality Assurance Validation, Associate serves as the quality contact for quality projects and continuous improvement efforts regarding Validation and Quality Risk Management. | 2/16/2019 |
| 1064 | Catalent Madison, WI Associate Scientist, Analytical Development MS in chemistry/biochemistry Exp: 1+ years |
The Associate Scientist, Analytical Development is responsible for developing new analytical methods independently and transferring the methods internally or from/to clients. Duties include: Executes all activities related to the analysis of proteins from mammalian cell culture ranging from SDS-PAGE analysis, ELISA analysis, various HPLC based methods, cIEF and product binding assays. The position requires strong documentation skills and the ability to follow SOPs. Independently develops/optimizes analytical methods to characterize protein/antibody, including, but not limited, to RP-HPLC, SEC, cIEF, and CE | 2/16/2019 |
| 1065 | Catalent Madison, WI Associate Quality Assurance Systems, Document Control BS/BA in biology, biotech, or engineering 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. | 2/16/2019 |
| 1066 | Catalent Strathroy , Ca Documentation Associate HS Diploma or GED Exp: 1-3 years in documentation |
The Documentation Associate will support the creation, review, and processing of general documents and batch records. The Documentation Associate is also responsible for issuing, distributing, and reviewing documents in a timely and efficient manner. Responsibilities include: Creating and updating master documents, issuing a copy of the current approved master documents for packaging or manufacturing; Compiling, summarizing and reporting information from the batch records as required; Accurately controlling the electronic and paper versions of all documents such as Standard Operating Procedures, Master Forms, Packaging Instructions and Production Batch Records; | 2/16/2019 |
| 1067 | Celegene San Diego , CA Catalent MS in Organic chemistry Exp: 1-5 years |
This position is responsible for activities associated with the development of small molecule active pharmaceutical ingredient (API) within Celgene and in contract development and manufacturing organization (CDMO). The individual would be expected to investigate and execute syntheses of complex molecule, develop scalable chemical manufacturing processes, and assist with technology transfers to CDMOs. He/ She will also serve as a resource of scientific and technical expertise and assume some departmental responsibilities for assigned projects and equipment. | 2/16/2019 |
| 1068 | Celegene Warren, NJ Associate Scientist, CAR T Product Sciences MS in biology, immunology, or biomedical engineering Exp: 1-3 years |
As part of the Product Sciences group, the energetic and motivated scientist will design, perform and interpret complex experiments related to the development of novel analytical tools and characterization of the final product and process intermediates for CAR-T products. This role will support the activities related to the identification of product critical quality attributes, in collaboration with Process/Analytical Development, Translational Development, Clinical and Immuno-Oncology research functions. | 2/16/2019 |
| 1069 | Just Biotherapeutics Seattle , WA Associate Scientist, Analytical BS Exp: 0-3 years |
Just is seeking a motivated and creative scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional testing of large molecule therapeutics and analysis of process impurities. The successful candidate will have some experience with DNA purification, PCR and ELISA assays. The candidate should possess strong written and verbal communication skills, strong organizational skills, a desire to learn new scientific concepts, the ability to multitask and an ability to work directly with scientific staff across multiple disciplines. | 2/16/2019 |
| 1070 | Just Biotherapeutics Seattle , WA Associate Scientist, Functional Biocharacterization BS Exp: 0-5 years |
Just is seeking a motivated and creative scientist who desires a significant opportunity to improve worldwide access to biotherapeutics. In this position, you will work with a multidisciplinary team for the analytical and functional biocharacterization of large molecule therapeutics and analysis of process impurities. Experience with HPLC and CE methods, DNA extraction, PCR and ELISA binding assays preferred. Cell-based and ligand-receptor binding assays, as well as high-throughput methods and liquid handling robotics beneficial. The successful candidate has strong written and verbal communication skills and is interested in ways to improve technology. The ability to multitask and to work both independently and in teams in a fast-paced collaborative environment is necessary. | 2/16/2019 |
| 1071 | Just Biotherapeutics Seattle , WA Process Engineer I, Purification BS Exp: 0-3 years |
Just is seeking a highly motivated entry-level manufacturing Process Engineer(s) that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible for the manufacture of mammalian cell-based biotherapeutics for clinical use under cGMP conditions. Under direct/moderate supervision, job responsibilities include set-up, operation, and maintenance of disposable-based manufacturing equipment; execution of manufacturing process operations; and assist in general lab operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. | 2/16/2019 |
| 1072 | FibroGen San Francisco, CA Regulatory Affiars Associate (Temporary) BA/BS in biological science Exp: 0-1 years |
As regulatory representative for assigned clinical studies, provides representation for study-level regulatory activities and updates in study team management meetings, supports clinical trial application activities, reviews and approves investigator document packages including FDA and ex-US submissions, and manages other regulatory aspects of study as directed. | 2/5/2019 |
| 1073 | FibroGen San Francisco, CA Research Associate (Temporary) BA/BS in biological science Exp: 1+ years |
Duties include preparation of biological samples (plasma, urine, etc. and tissue hydrolysates), quantiative analysis of small moleculars by HPLC-MS/MS. | 2/5/2019 |
| 1074 | IDEX Corporation Rochester, NY Mechanical Engineer BS in Mechanical Engineering Exp: 1-3 years |
As a mechanical engineer, individual duties include: develope/execute new product plan in accordance with Pulsafeeder processes, works with marketing to generate product specifications, designs reliable and cost-effective products, etc. | 2/5/2019 |
| 1075 | Fluidda West Hollywood, CA Research Engineer MS in engineering or industral sciences Exp: 0 years |
he research engineer produces specifications for, designs, develops, tests and optimizes the FRI technology. A person in this function performs research on new methodologies needed to address investigative questions. The research engineer combines these with medical science insights and data analysis strategies to come up with an optimal solution for every problem. | 2/5/2019 |
| 1076 | Fluke Everette, WA Mechanical Engineer BS in mechanical engineering Exp: 0-2 years |
As a member of the IG Engineering NPI team, the candidate will be responsible for contributing to the development of mechanical components used in the manufacture of handheld/bench top product enclosures. This includes component and overall system designs that meet Design For Manufacturability (DFM) , compliance to industry standards and Fluke defined product robustness requirements. The role requires a person who is able to interact with a diverse and very skilled team of engineers, collaborate on work tasks across sites and functions, and manage high ambiguity | 2/5/2019 |
| 1077 | Fog Pharma Cambridge, MA RA/SRA, Chemistry BS or MS in chemistry or related Exp: 0-3 years |
We are seeking a highly motivated Research Associate or Senior Research Associate with Peptide Chemistry experience to join our peptide medicinal chemistry team. The individual should have experience in peptide synthesis and purification, peptide libraries, and the optimization of drug like properties with leading molecules. Primary job responsibilities include: Synthesis, purification and analytical characterization of peptides, small proteins and chemically-modified analogs using state-of-the-art synthesis and purification techniques. Program and operate instrumentation such as automated parallel peptide synthesizers, semi-preparative and preparative HPLCs, and an analytical LC/MS | 2/5/2019 |
| 1078 | Pall Life Sciences Cortland, NY R&D Leadership Program BS/BA or MS in engineering or science Exp: 0-2 years |
You will receive both on-the-job training and also specialized learning on key Danaher Business Systems tools like the Problem Solving Process, Kaizen and Visual Project Management. These, plus personal mentoring by senior managers and engineers, will enable you to develop the skills required for key positions within the future organisation. Upon graduation from the program, you will progress to the next stage in your Journey with Pall by moving into a “permanent” role and entering our funnel for future talent. | 2/5/2019 |
| 1079 | Foundation Medicine Cambridge, MA Pathology Research Assistant BS/BA in biology or biochemistry Exp: 0-2 years |
This is a great opportunity for a dedicated, recent graduate looking to gain more experience in molecular genetics as well as the broader functionality of a genomics laboratory committed to advancing the field of precision medicine. As you prepare for the next steps in your career, you will work directly with the pathology team and will assume the following duties: Participate in research projects, led by either the pathologist or yourself, focusing on various aspects of cancer genomics and immunohistochemistry through data gathering, data analysis, figure creation and writing manuscripts. Participate in projects, led by either the pathologist or yourself, focusing on quality improvement/quality assurance of laboratory operations and workflow through team collaboration with data gathering, data analysis, generation of metrics, internal presentations and/or manuscript synthesis and submission. | 2/5/2019 |
| 1080 | Micro Medicine Waltham, MA Research Associate BA/BS in biological science or related Exp: 1-3 years research experience |
This opportunity, you will report to the Director of R&D and work with the Research and Product Development teams to both support existing applications and assist in the development of new applications in diagnostic, therapeutic, and research markets. Duties include processing clinical samples, including blood and blood products, employing safe, accurate, and repeatable methods, gathering data and information to identify best methods, materials, and technologies for cell and molecular assays, etc. | 2/5/2019 |
| 1081 | Frontage Exton, PA Associate Scientist-Product Development- CMC MS in Pharm. Sciences, polymer chem, microbiology, or chemical engineering Exp: 0-4 years |
Responsibilities as an associate scientist-product development include: Perform assigned tasks per procedures compliant with cGMPs and participate in the clinical manufacturing of parenteral, ophthalmic, and other sterile dosage forms, Assist with manufacturing area maintenance such as area monitoring and qualification, purchase of gowning supplies, purchase of equipment and room cleaning supplies, microbiological monitoring supplies, Execute product development studies under the guidance of supervisor or lead project scientist to support formulation development (R&D), and clinical drug product manufacturing | 2/5/2019 |
| 1082 | FujiFilm College Station, TX Associate Scientist – Downstream Process Development MS in chemistry, biology, or related Exp: 1+ years |
Essential functions as an associate scientist include: Assist in the development, optimization, and scale-up of chromatography processes (including affinity, IEX, HIC, etc.) and filtration processes (including UF/DF, depth filtration, and sterile filtration, etc.), Operation of chromatographic systems (GE AKTA, and other Unicorn based equipment), and Maintaining detailed laboratory notebooks following FDBT procedures. | 2/5/2019 |
| 1083 | FujiFilm Morrisville, NC Scientist I, Downstream Process Development MS Exp: 1+ years |
The successful candidate assists in the planning of, conducting, evaluating, and interpreting routine laboratory experiments. The individual monitors on going experiments and identifies and resolves or suggests alternates or solutions to complex occurrences. The individual understands and applies use of equipment, technology and materials associated with area of expertise and related studies and projects. The individual takes a more active role in non-routine analytical or process development activities. | 2/5/2019 |
| 1084 | FujiFilm College Station, TX Quality Control Chemist I BS/BA in chemistry, biochemistry, or related Exp: 0-1 years |
The Quality Control Chemist I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory. Essential functions include: Assist in quality control testing of samples provided to the QC laboratory (SDS Page, western blot, ph/conductivity), Assist with preparing and executing test qualification and validation of QC test methods, and Assist with writing Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation. | 2/5/2019 |
| 1085 | FujiFilm Durham, NC Manufacturing Process Engineer I BS/BA in science, engineering or related Exp: 1-3 years |
The ideal candidate works independently and with colleagues to provide assistance for the design, development, standardization and maintenance of an operational biotechnology utilized in the manufacture of proteins and drug substances. This person would become familiar with a variety of core manufacturing and operational technologies including equipment used in: Fermentation, Cell Culture/Single Use Technology, Filtration, Centrifugation and Chromatography, Mixing and Buffer Preparation, Parts washing and Sterilization, and Homogenization | 2/5/2019 |
| 1086 | FujiFilm College Station, TX Associate Scientist - Upstream Process Development MS in chemistry, biology, or related Exp: 1+ years |
The Associate Scientist - Upstream Process Development will assist in the development and execution of experiments for the development, optimization, and characterization of cell-based and viral vaccine processes and will be involved in experimental design, data analysis, and interpretation. This individual will assist the Process and Analytical Development Teams to drive processes towards robust Phase I and Phase II GMP manufacturing processes for multiple viral projects and provide technical support for associated regulatory filings. The individual should have familiarity with a range of cell-based and viral vaccine production technologies, including cell and virus expansion, infection, scale-up, harvest and filtration technologies.The successful candidat will also be experienced in basic laboratory analytical techniques (SDS-PAGE, Western blots, spectroscopy, pH/conductivity meters, etc.) | 2/5/2019 |
| 1087 | Fulcrum Therapeutics Cambridge, MA Bioinformatics Engineer BA/BS in engineering or life sciences Exp: 1+ years |
Fulcrum is seeking a Bioinformatics Engineer to (1) implement and manage lab informatics software applications utilized across research teams and (2) build and sustain custom software in the Computational Biology group. Lab informatics includes applications such as GeneData, Dotmatics, LIMS-biorepository systems, cheminformatics tools, and relational databases. Working closely with the IT/Operations and Molecular Sciences groups at Fulcrum, this individual will manage these applications on the cloud in a secure manner, serve as the point of contact with application vendors, organize training, and operate on an efficient budget. Custom software development within Computational Biology will be focused on, but not limited to, molecular profiling pipelines. | 2/5/2019 |
| 1088 | Gene Dx Gaithersburg, MD DNA Sequencing Lab Technician BS/BA in biology or biochemistry Exp: 0-2 years |
This position is for an entry level DNA technician position in our laboratory. The job involves following basic protocols for PCR, gel electrophoresis, and Sanger sequencing. The Technician will be trained to use the various robots and instruments used to automate our PCR and sequencing workflows. At times technicians will be working as part of a team but would also be responsible for a good amount of individual work. Our work is clinical in nature and is repetitive, so this position absolutely requires someone who is very focused, meticulous, and willing to see that there are small things to learn every day. Implement the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping | 2/5/2019 |
| 1089 | Gene Dx Elmwood Park, NJ Marketing Product Associate BS/BA in science or MS in biological sciences Exp: 0-2 years |
The GeneDx Marketing Product Associate plans and coordinates product test development, launch, and marketing functions. Primary duties include: Helps identify and analyze, in conjunction with marketing and test development groups, promising areas of research or technology that address unmet needs and have large potential markets, Builds processes for transitioning products form test development to marketing, and Works closely with the clinical and design teams on materials such as scientific posters, presentations and publications | 2/5/2019 |
| 1090 | Gene Dx Gaithersburg, MD Cytogenetics Lab Technician BS/BA in biology, biochemistry, or life sciences Exp: 0-2 years |
The Laboratory Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease, using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. Responsibilities include: Implements standard operating procedures for specimen handling and processing, Assess and process prenatal specimens for DNA extraction and sendout testing | 2/5/2019 |
| 1091 | Genewiz Research Triangle Park, NC Laboratory Technician I, Genetic Analysis HS Diploma, or AAS Exp: 1+ years |
Quality driven processers. When our customers send us samples for sequencing, they help to prepare and process these samples as quickly and as awesomely as possible, while maintaining the highest quality standards in the industry. They prepare DNA templates which include preparation, amplification and PCR purification and load these samples onto the sequencers. They also work to prepare buffers and other related solutions. Customer focused. Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. They understand our customer needs with empathy and know that everything they do is making a difference. | 2/5/2019 |
| 1092 | Genewiz San Diego, CA Sales Associate I BS/BA degree in biology or life sciences Exp: 1 year |
Responsibilities as a sales associate include: Achieve annual sales goals within defined territory/accounts through the development, maintenance, and enhancement of customer accounts, Retain current business baseline revenue by managing relationships with customers and other account contacts by collaborating with business leaders and the customer interface teams and, Drive the marketing process for the territory by creating a marketing plan, registering/planning/ attending local vendor shows, and working with Marketing to follow up on leads from email campaigns | 2/5/2019 |
| 1093 | Genewiz South Plainfield, NJ Sample Management Coordinator, Logistics HS Diploma or BS/BA in biological sciences Exp: 0-1 years |
A Sample Management Coordinator is: A multi-tasker while keeping in mind the details. They help us to carry-out shipment, receipt, tracking and handling of samples. They partner with the sample management team to troubleshoot and resolve sample related issues. They communicate with internal and external customers via email and/or phone and manage project tracking logs. They use online tools for sample submission and data uploading. They manage internal/external storage and shipping of samples. They address, record and track communication related to project samples. They work to manage tasks related to sample management for numerous customer accounts. They help to provide administrative, internal and external support for distribution. | 2/5/2019 |
| 1094 | GenMark Diagnostics Carlsbad, CA Research Associate II MS in biological sciences Exp: 1+ years |
Essential Duties and Responsibilities: Responsible for day to day running of experiments and data analysis, conducts general molecular biology tasks, including nucleic acid purification, quantification, amplification and analysis on multiple platforms, prepares reagents and solutions as needed, using appropriate procedural and documentation methods, maintains stockroom supplies and inventory, prepares documents meeting company standards, including data summaries, reports, SOPs and procedures, presents work at meetings as required, and proposes new strategies and methods to address immediate and upcoming technical issues | 2/5/2019 |
| 1095 | EuroFins Rahway, NJ Entry Level HPLC/UPLC Scientist BS or MS in chemistry, biochemistry, or related Exp: 0-2 years |
HPLC / UPLC Scientist responsibilities include, but are not limited to, the following: Conducts analysis and experimentation on formulated pharmaceutical materials in the laboratory with minimal supervision and using prescribed procedures, conducting independent chemical analyses of candidate formulations and working closely with formulators to streamline drug product development, evaluating “Fit For Purpose” analytical methods and working closely with the analytical method development team to streamline analytical method development, general knowledge of separations science and hands-on experience in chromatographic analysis, data interpretation and processing | 2/5/2019 |
| 1096 | EuroFins Kalamazoo, MI Biological Development Scientist BS/bA in biology, microbiology, or related biological sciences Exp: 1-2 years |
As a biological developmental scientist, individual responsibilities will include: Quantitate antigens using antibody-based assays including ELISA and Western blot, Generate recombinant DNA constructs using techniques including nucleic acid extraction, PCR, gel electrophoresis, plasmid DNA cloning, and bacterial transformation, Maintain cell cultures and perform transfection for transient protein expression | 2/5/2019 |
| 1097 | Genomatica San Diego, CA Fermentation Associate I/II BS/BA in life sciences Exp: 1-3 years |
Genomatica is seeking a highly motivated Research Associate, Molecular Biology to join the Strain Engineering team. This team is responsible for construction, characterization, evolution and fermentation of host strains. The successful candidate will utilize her/his knowledge of molecular biology for cloning of relevant genes into various single-gene and multi-gene DNA constructs using a high-throughput, automated platform. | 2/5/2019 |
| 1098 | Genome DX Biosciences San Diego, CA Sample Processor I BS/BA Exp: 1+ years lab experience |
The Sample Processer’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the GenomeDx internal and external customers in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 2/5/2019 |
| 1099 | Neo Genomics Aliso Viejo, CA Associate Project Manager AS or equivalent Exp: 1+ years |
The Pharma Services Associate Project Manager performs tasks for multiple projects as part of project teams. Projects are usually sponsored by pharmaceutical, medical device, or diagnostic testing companies. This role works on projects involving biology, bioinformatics, engineering, software, and other technical disciplines. You will work under the supervision of the responsible Project Manager, Senior Project Manager, or Director. | 2/5/2019 |
| 1100 | Neo Genomics Aliso Viejo, CA Clinical Laboratory Technologist I or II BS in cytogenetics or biological sciences Exp: 1+ years |
In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. | 2/5/2019 |
| 1101 | GigaGen South San Francisco, CA Research Assistant BS/BA Exp: 1-3 years research experience |
GigaGen seeks a talented, highly motivated Research Assistant to work alongside PhD-level scientists on research. This project involves high-throughput discovery and development of therapeutic antibody drug candidates from human and mouse immune repertoires. The work involves significant cell culture work, including a bioreactor and flow cytometry. | 2/7/2019 |
| 1102 | Gilead Foster City, CA Process Engineer II - Solid Dose Manufacturing MS in science field Exp: 0 years |
As a process engineer you will be responsible for: determining functions most critical to departmental success/supports priorities accordingly, manages processes across functions/teams, manages budget for pharmaceutical/packing engineering-related projects. etc. | 2/7/2019 |
| 1103 | Ginkgo Bioworks Boston , MA Research Associate - NGS BS/MS in biology, bioengineering, biochemistry, or related Exp: 1+ years |
As a research associate you will operate high-throughput semi-automated NGS processes, monitor and report on process and perform analysis, suggest and validate process improvements using knowledge of molecular and microbiology | 2/7/2019 |
| 1104 | Ginkgo Bioworks Boston , MA Research Associate - Protein Engineering BS/MS in biology, bioengineering, biochemistry, or related Exp: 1+ years |
We are looking for someone who is excited about the field of synthetic biology and loves a challenge. Responsibilities include enzyme purification and characterization. We want a person who is eager to learn and has a desire to utilize automation to work more efficiently. Our ideal candidate will elevate our team through creative solutions while working closely with other foundry groups. | 2/7/2019 |
| 1105 | Glaukos San Clement, CA Engineer, Research and Development BS/MS in mechnical engineering, or MBA Exp: 0-2 years |
The Engineer, I will perform a variety of mechanical engineering activities on the ocular related products including product design, concept prototyping, concept testing, and early development, clinical builds, manufacturing scale up development and sustaining activities. Responsibilities include developing creative solutions to design and manufacturing problems, ensuring the proper engineering deliverables are accurately generated, generation of 3D CAD models, 2D CAD drawings, test procedures, etc, project management/ leadership, maintaining schedule and product release plans. This individual will may lead project teams with other engineers, designers, and manufacturing staff with a focus on meeting product specifications with technically strong, high quality, cost effective designs following Glaukos’s defined development process. Further, all duties shall be performed in a professional way with attention to detail while supporting Glaukos’ Quality Policy and the appropriated regulatory agencies, including FDA Quality System Regulations (21 CFR 820), ISO Standards (EN ISO 13485) and Risk Management (EN ISO 14971). | 2/7/2019 |
| 1106 | GSK Rockville, MD Associate Biochemist BA/BS in chemistry, biochemistry, molecular biology, or related Exp: 0-2 years |
Responsibilities as an associate biochemist include: coordinating routine in-process biopharmaceutical materials, bulk bio-pharmaceutical ingredients, finish bio-pharmaceutical products/stability sample testing. Conduct/document routine compendial, chemistry, immunology and molecular biology analytical testing for in-process, release and stability samples per SOP. Operate/aintain QC lab equipment. | 2/7/2019 |
| 1107 | GSK Rockville, MD Biopharmaceutical Manufacturing Associate II BS/BA in related field Exp: 0 years |
A Bio-pharmaceutical manufacturing Associate II performs all production operations in the area of assignment within the Rockville Manufacturing facilities. Support Start-up/changeovers/tech transfer activities and perform production operations in areas assigned. Duties include: preparation of buffers and medias and other solutions, following written procedures and batch records. Operate process equipment such as tanks, CIP/SIP skids, agitators, filtration devices, integrity testing and other small equipment following a high standard of GMP compliance and SOP and BRs as written. | 2/7/2019 |
| 1108 | GSK Upper Providenc, PA Associate Scientist / Scientist, Biopharmaceutical Product Sciences BS or MS in pharmacuetics, biology, chemistry, or related Exp: 1+ years lab experience |
The successful candidate will join a Product Development Team within the Biopharmaceutical Product Sciences (BPS) department of the Biopharm Product Development & Supply organization within GSK R&D. The candidate will focus on developing protein formulations, assessing product stability, implementing biopharmaceutical drug product manufacturing processes, and when applicable, coordinating with Device Engineering for implementation of drug delivery devices. The scientist in this role may be expected to contribute to cross-functional initiatives and/or rotate between other BPDS departments to support a flexible product development initiative. | 2/7/2019 |
| 1109 | GSK King of Prussia, PA Biopharmaceutical Manufacturing Associate II BS/BA in science/engineering Exp: 0-1 years |
Under the direction of senior personnel, performs production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. | 2/7/2019 |
| 1110 | GSK Hamilton, MT Manfacturing Associate BS/BA in related field Exp: 1-2 years |
As Value Stream Manufacturing Associate you will manage/lead/be responsible for performing duties as assigned with respect to quality, timeliness, quantity and cost. Work individually and as a team to deliver cGMP compliant product. Adhere to GSK policies, procedures and support site goals. Complete documentation in line with regulatory, GSK, and departmental requirements. Work and communicate closely with other departments both inside and outside of the Value Stream. | 2/7/2019 |
| 1111 | Global Pharma Tek Edison, NJ Pharmacovigilance Scientist BS/BA in science or engineering Exp: 0-2 years |
Pharmacovigilance Scientist. Jobs located in Edison, NJ. Review non-serious and serious AEs and aggregate AE listings. Prepare signaling meeting presentations in collaboration with the team, including a review of events of interest, initial trending of AEs, set thresholds for escalation, and preparation of meeting minutes. Monitor the safety profile of assigned compounds to identify any safety signals and support execution of plans for signal evaluation. | 2/7/2019 |
| 1112 | Global Pharma Tek Edison, NJ Process/Validation Engineer BS/BA in pharmacy, life sciences or related Exp: 1-2 years |
Reviews standard operating procedures which are related to each equipment according to 21 CFR part 11.Uploads developed protocols in the company’s record website by following the procedures.Prepares riboflavin solution in biological quality lab by following the procedure and uses on vial washer and puck washer to test spray coverage test on filling lines.Prepares biological samples to verify the sterility of the heating and cooling zones in depyrogenation tunnel.Witnesses’ vendor SAT (Site Acceptance Test) protocol and execution of all equipment associated with each filling lines.Calculates particle count at the equipment on the Abboject and Ampoule filling lines to verify if rooms are maintaining Grade A aseptic conditions.Performs smoke studies to verify the laminar flow hoods are working consistently throughout in Grade A aseptic conditions. | 2/7/2019 |
| 1113 | Global Pharma Tek Edison, NJ Drug Safety Associate BS/BA in Pharmaceutical science or related Exp: 1-2 years |
Global PharmaTek, LLC has job openings for Drug Safety Associate.Jobs located in Edison, NJ and various unanticipated locations throughout the U.S.Receives clinical study SAE reports, review for medical/regulatory content and assure accuracy per protocol requirements, obtaining follow up as needed; ensure that all SAE’s are complete prior to database closure Process and distributes clinical study SAE reports as per the company SOPs Completes AE/SAE reconciliation prior to clinical trial database closure Receives, processes, and distributes spontaneous adverse event reports for marketed products, both serious and non-serious, as per the company’s SOP’s .Processes all types of adverse event reports utilizing the ARIS safety database Assists with preparing and/or reviewing safety summaries for Investigator Brochures and annual reports, safety submissions for marketed products, and other safety reports as needed or requested | 2/7/2019 |
| 1114 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Manager BS in biology or physical sciences Exp: 1-2 years cell culture experience |
ssists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. Responsible for the execution of a Manufacturing Batch Records (MBR) for specific projects to manufacture cell derived biopharmaceuticals in compliance with cGMP guidelines and regulations. Activities include cell culture in various cell culture vessels including preparation of inocula for bioreactor production, and operation of various bioreactors. Department responsibilities also include cell culture process development activities, consisting of cell line characterization, media formulation evaluation, and inoculum process development. ssists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. Responsible for the execution of a Manufacturing Batch Records (MBR) for specific projects to manufacture cell derived biopharmaceuticals in compliance with cGMP guidelines and regulations. Activities include cell culture in various cell culture vessels including preparation of inocula for bioreactor production, and operation of various bioreactors. Department responsibilities also include cell culture process development activities, consisting of cell line characterization, media formulation evaluation, and inoculum process development. | 2/7/2019 |
| 1115 | Gore Flagstaff, AZ Industrial Engineer BS in supply chain, industrial engineering, or related Exp: 1+ years lab experience |
As an industiral engineer you will be responsible for: leading cross functional operation projects, drive financial analysis, ensure execution of quantitative project management deliverables within projects such as project cost benefit analysis and metrics of project success, etc. | 2/7/2019 |
| 1116 | Grand River Aseptic Manufacturing Grand Rapids, MI Aseptic Manufacturing Associate HS Diploma, BA/BS preferred Exp: 0-1 years |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Candidates must be willing to work 2nd or 3rd shift. | 2/7/2019 |
| 1117 | Halo Pharma Whippany, NJ Inspector Quality Assurance HS Diploma Exp: 1-2 years |
The Inspector Quality Assurance (2nd shift) is responsible for performing duties related to but not limited to In-coming materials (i.e. sampling , review specification and release materials in SAP and any other related electronic database), Line Inspections in SDF, Santyl and Packaging lines, review batch records when required, perform all quality assurance activities in accordance with cGMP and standard operating procedure. | 2/7/2019 |
| 1118 | Halozyme San Diego, CA Research Associate 1, Analytical Testing Support - Contract BS/BA in related field Exp: 1+ years lab experience |
The Research Associate will be a member of the Product Development team at Halozyme and will be responsible for performing analytical testing support, method development, and qualification for in process, drug substance and drug product samples from a variety of drug development programs. Analysis will cover a wide array of analytical techniques such as UV/Vis, ELISA, potency, HPLC, CE, icIEF and wet-chemistry. This individual will also be involved with data verification of laboratory notebooks, protocols, reports, and regulatory filings to ensure the accuracy of the record and to meet critical timelines. | 2/7/2019 |
| 1119 | Auris Health Redwood City, CA Mechanical Engineer BSME or similar Exp: 0-3 years |
Auris is looking for a Mechanical Engineer who will support the design and development of robotic systems for medical applications. This Mechanical Engineer will work closely with engineers from other teams to design and develop robotic equipment that meets clinical, user, and safety requirements. Responsibilities include: design/create electromechanical prototypes, provides hands-on troubleshooting, process and manufacturing support as well as designing implementing, integrating and testing hardware solutions, create design solutions, utilizing engineering methods, etc. | 2/7/2019 |
| 1120 | Harpoon Therapuetics South San Francisco, CA Research Assistant/Associate, Protein Science – Formulation and Analytics BS/BA in biology, biochemistry, or life sciences Exp: 1-2 years |
Harpoon Therapeutics is a startup clinical stage biotechnology company located in South San Francisco, CA. We are focused on the development of novel immune cell engaging therapeutics for oncology indications. We are looking for a motivated, flexible, highly-productive individual who seeks to work in a cross-functional collaborative research environment. As an integral member of the Protein Science group, this individual will partner with the New Technologies, Biology Research, and Translational Medicine groups to develop our proprietary platforms. This position is lab based with the successful candidate primarily engaged in protein formulation and analytics. | 2/7/2019 |
| 1121 | Medtronic Mounds View, MN Component Engineer MS in engineering or science Exp: 0-2 years |
In this exciting role as a Component Engineer you will have responsibility for driving component qualification through effective partnership with external suppliers and internal design and development teams to assure that our products exceed the requirements and expectations of patients, physicians, regulatory agencies and the business. | 2/7/2019 |
| 1122 | Medtronic Irvine, CA Manufacturing Engineer MS in engineering or science Exp: 0-2 years |
We are seeking a hands-on Manufacturing Engineer to work closely with R&D, Operations and Quality in the development of new processes necessary to produce Catheters/Delivery Systems/Stents for a lean manufacturing environment. Manage development builds, develop new manufacturing processes, implement and qualify production equipment and methods, generate testing protocols and reports, and work with minimal direction for NPI. | 2/8/2019 |
| 1123 | Medtronic Boulder, CO FPGA DEVELOPMENT ENGINEER MS in electrical engineering or computer science Exp: 0-2 years |
The FPGA Development Engineer will be a member of the Medtronic R&D team working on development and support of electrosurgery generator products. FPGA Engineers can apply their education and talents in FPGA development for embedded systems, including the understanding of how software interacts with hardware. The position is a hands-on development role with a dynamic set of responsibilities in design and verification of embedded systems including RTL coding, simulation, and laboratory testing. | 2/8/2019 |
| 1124 | Medtronic North Haven, CT Associate Chemist (Quality Dept.) BS/BA Exp: 0 years |
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. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality Performs chemical evaluations of new and existing products and processes. | 2/8/2019 |
| 1125 | High Point Clinical Trials Center High Point, NC Lab Supervisor HS Diploma required, BS/BA preferred Exp: 1+ years |
We need a self-motivated laboratory leader to oversee the required specimen processing laboratory which supports safety testing conducted at our growing clinical trial center. 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. | 2/8/2019 |
| 1126 | Hikma Columbus, OH Project Manager - R&D BS/BA in scientific/technical discipline Exp: 1-3 years |
Manage the ideas to launch process and NPD Project Management Team with an approach focused on cross-functional team coordination. Support CSO with general process and budget management for the R&D function. Responsibilities include portfolio management, managing team, planning/reporting projects, and creating timelines. | 2/8/2019 |
| 1127 | Hikma Cherry Hill, NJ Quality Lab Associate I, Env. Monitoring BS/BA in microbiology or biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. | 2/8/2019 |
| 1128 | Hikma Columbus, OH Scientist I, QC Aero Star 2nd Shift BS in chemistry or related Exp: 1+ years lab experience |
To perform routine, work-flow processes within the quality control laboratory to meet customer requirements by supporting the testing of raw materials and finished products while ensuring regulatory compliance standards and release times are met. | 2/8/2019 |
| 1129 | Hill-Rom Skaneateles Falls, NY Service Engineer BS/BE in engineering, ID, electronics or computer science Exp: 0-5 years |
As a Service Engineer, you will work closely with domestic and international cross functional teams to provide service strategy guidance and deliver product service standard work solutions. You will provide hands-on expertise and technical support during the design and post surveillance phase of products and services including network based and stand-alone medical monitoring systems and devices. | 2/8/2019 |
| 1130 | Hill-Rom Cary, NC Quality Analyst BS/BA in business administration, management or engineering Exp: 1-3 years |
Coordinates documentation and facilitates communications regarding the required documentation of pending, in progress and completed installations of Clinical Workflow Solutions products. Reviews all documents related to the CWS Device History Records prior to submission to document control in accordance with FDA acceptance activities standards. Responsible for reviewing and processing certification documents associated with CWS implementation and service work orders. Daily interfaces with field service personnel, project management and document control to complete required tasks. | 2/8/2019 |
| 1131 | Hologic San Diego, CA Research Associate BA/BS in molecular biology, chemistry or related, or MS Exp: BS: 1-3 years, MS: 1+ years |
Hologic is seeking a Research Associate responsible for designing and performing experiments while collaborating and communicating effectively. Duties & Responsibilities: Performs moderately complex experiments with input from supervisor. Understands experimental goal and exhibits critical thinking skills when evaluating data. Able to summarize related groups of experiments. Provides input to the experimental design. Is able to analyze experimental data with minimal input from supervisor. | 2/8/2019 |
| 1132 | CSL Canton, OH General Supervisor of Quality (Management Trainee) BS or AS Exp: 0-1 years |
General Supervisor of Quality will act as lead supervisor in ensuring the day-to-day activities of quality operations are compliant with Standard Operating Procedures (SOPs) and applicable federal and local regulations as well as HR policies. Advise management of ER issues or escalated quality issues. Maintain clean efficient work environment, and ensure sufficient operating supplies and forms are available. Comply with all Health Safety and Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. May conduct routine internal procedures and documentation audits. Promote safety in all actions. | 1/30/2019 |
| 1133 | Hologic Marlborough, MA Associate Product Manager BS or AS Exp: 1-3 years in marketing |
The Associate Product Manager will support the Brand and Integrated Marketing teams for the Hologic Surgical Division through collateral and campaign development, daily product management needs, and through the creation and management of small digital marketing campaigns. This role's responsibilities include: Support brand leads throughout the supply chain process, ensuring consistent communication to internal and external stakeholders as needed. Contribute to marketing activities, including collateral creation and promotion/campaign assistance related to the promotion of the Office access tools business, as well as MyoSure and NovaSure as needed | 1/30/2019 |
| 1134 | Hologic San Diego, CA Analytical Chemist BS in Chemistry or related Exp: 1+ years in analytical chemistry |
We are currently seeking an Analytical Chemist in Quality Control responsible for analysis of raw materials, oligonucleotides and in-process samples. Essential Duties and Responsibilities include: Performs routine analytical testing using GMP/GLP practices. Performs data analysis and results interpretations comparing to specifications, validity criteria, alert limits. Responsible for maintaining product and QC material inventories. 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. | 1/30/2019 |
| 1135 | Hologic San Diego, CA Research Associate 1 BS/BA in molecular biology, chemistry, biochem, or related Exp: 0-2 years lab experience |
Hologic is seeking a Research Associate 1 responsible for designing and performing experiments while collaborating and communicating effectively. Duties & Responsibilities: Performs minimally complex experiments with input from supervisor. Understands experimental goal and may provide input to the experimental design. Analyzes data from individual experiment with input from supervisor and documents work in laboratory notebook or report. Able to summarize a group of experiments. Effectively communicates with peers and supervisor. May present data in group meetings. | 1/30/2019 |
| 1136 | Cyprotex Watertown, MA Associate Scientist BS in relevant bio disciplin Exp: 1-2 years |
Cyprotex US is looking for an Associate Scientist based in Watertown, MA to assume responsiblity for the routine screening of compounds in various in vitro toxicology assays and reporting to the Associate Director or Senior Scientist. There will be no direct reports. Responsibilities include cell culture experiments, toxicology screens, validation/investigative assays, and experimental troubleshooting. | 1/30/2019 |
| 1137 | Cytek Biosciences Chicago, IL Flow Cytometry Field Service Engineer 4-year degree in life sciences, engeineering, or technical military service Exp: 0 years |
Install, troubleshoot and repair flow cytometers and Cytek Upgrade products in a professional and timely manner. Perform job with absolute best customer service; work well with scientists. Identify customer needs and contribute to improvements in Cytek products. Manage your own schedule, complete paperwork and reports in a timely manner, work well as part of a small but growing team of engineers. | 1/30/2019 |
| 1138 | Cytovance Biologics Oklahoma City, OK QA Associate I BS in science/life science Exp: 1-2 years in quality systems |
QA Operations Associate I is responsible for maintaining quality oversight of operational areas by working closely with Operation’s personnel and performing various checks during manufacturing processes to ensure that current Good Manufacturing Practices (cGMP’s) are followed. The QA Operations Associate I also assess regulatory and quality risks in activities and processes according to GMP and Cytovance Standard Operating Procedures. Duties include record reviewing, process audis, room releases, interfacing with various functional groups (manufacturing, QC, etc.), and support CAPA systems. | 1/30/2019 |
| 1139 | Cytovance Biologics Oklahoma City, OK Solution Prep Associate I High School/GED or AS in life sciences Exp: 1-2 years in CGMP manufacturing preferred |
This position is accountable for producing and delivering large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. Duties include batching/delivering media and buffer batches, assisting in reviewing/creation of operation documents, etc. | 1/30/2019 |
| 1140 | Cytovance Biologics Oklahoma City, OK PD Associate I BS in life sciences, chemistry, chemical engineering or related Exp: 0-3 years |
The Process Development Associate I conducts laboratory experiments in a productive manner with consistent quality and timely outputs, under supervision. Duties includes monitoring/executing experiments, keeping detailed written records in accordance with GDPs, and function independently in an lab environment. | 1/30/2019 |
| 1141 | Dexcom Mesa, AZ Quality Inspector 1 HS diploma/GED Exp: 6 months QC inspector experience |
The incumbent is responsible for performing a variety of quality control (QC) related work functions that include performing visual, functional and dimensional inspection and testing of raw materials, component piece parts, in-process materials, and review of lot history records in accordance with documented specifications and/or procedures. Prepares accurate documentation of QC inspection results including accepted and non-conforming materials. Scanning and archiving of Receiving Inspection Reports for the department. | 1/30/2019 |
| 1142 | Dexcom San Diego, CA Clinical Research Associate 2 BS/BA in life science/health related field Exp: 0-2 years |
As a clinical research associate, individual will: implement and monitor clinical studies at participating study sites according to the FDA Code of Federal Regulations (CFR), Good Clinical Practices (GCP), and ICH Guidelines. Works with other CRAs and Clinical Affairs management to assist in the conduct of Dexcom-sponsored clinical studies (including In-House studies). Responsible for conducting site visits, monitoring, and performing all ancillary requirements in executing clinical studies to ensure proper data collection and write-up for documentation or submission of clinical study data. | 1/30/2019 |
| 1143 | Dexcom San Diego, CA Engineer 1 - R&D BS in bioengineering/chemical engineering, mechanical engineering Exp: 0-1 years |
As a member of the R&D Advanced Technology team, this Engineer will work closely with product designers from all technology areas (sensor, transmitter, software, etc.) to take the product through preclinical in-vivo feasibility. This role will support the planning, development, and execution of pre-clinical models to evaluate prototype product. This role will work closely with other engineers to determine the appropriate study design to evaluate the product, and this role will analyze/report study results. Additionally, this role may also facilitate additional activities to support the product to begin testing in human clinical studies | 1/30/2019 |
| 1144 | Dexcom San Diego, CA Clinical Research Associate 1 BS/BA Exp: 0-2 years |
As a clinical research associate, individual will: implement and monitor clinical studies at participating study sites according to the FDA Code of Federal Regulations (CFR), Good Clinical Practices (GCP), and ICH Guidelines. Works with other CRAs and Clinical Affairs management to assist in the conduct of Dexcom-sponsored clinical studies (including In-House studies). Responsible for conducting site visits, monitoring, and performing all ancillary requirements in executing clinical studies to ensure proper data collection and write-up for documentation or submission of clinical study data. Nursing/diabetes experience desirable | 1/30/2019 |
| 1145 | Diagenode Denville, NJ Regulatory Affairs Officer MS in life sciences Exp: 1-3 years |
The Regulatory Affairs officer is in charge of meeting regulatory expectations and ensuring compliance of In Vitro Diagnostic (IVD) products with national and international regulatory requirements. Key responsibilities include advising/assisting other departments (research and development, production, quality, marketing, sales, ...) with the various regulatory aspects related to IVD products, and to prepare regulatory applications: assessment of regulatory requirements according to the countries in which the product will be submitted: collection and compilation of information/data in collaboration with the other departments, redaction of submission files and management of shipments for the placing on the market of the product | 1/30/2019 |
| 1146 | Dicerna Cambridge, MA Research Associate, RNAi Pharmacology BS or MS in biology, pharmacology, or related Exp: 1+ years |
As a resaerch associate, individual will include rodent dosing, ampling, necropsy, and in vivo experimentation, cross function collaboration, performing aboratory assays according to SOPs, troubleshooting as needed; assay development. Generating data using both standard and novel molecular technologies, and carefully maintaing appropriate documentation | 1/30/2019 |
| 1147 | Dicerna Cambridge, MA Research Associate 2019A, RNAi Discovery BS/MS 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 in vivo (mouse) and in vitro methodologies. | 1/30/2019 |
| 1148 | Mylan Morgantown, WV Chemist BS/BA Exp: 0-2 years |
As a chemist one will be responsible for performing pharmaceutical testing (HPLC, GC, TLC, UV, IR Spectroscopy, etc), develop/validate analytical test methods for pharmaceutical products, and write technical analytical reports. | 1/30/2019 |
| 1149 | Dr. Reddy's Shreveport, LA Formulation Scientist BS in pharaceutical sciences Exp: 0-2 years |
This critical position will be responsible for the successful development of robust formulae and processing of selected products from laboratory batches through scale up and commercialization. Responsibilities include: Identify the Quality Target Product Profile, Critical Quality Attributes, Critical Material Attributes and Critical Process Parameters to arrive at robust formulation strategy. Develop stable product formulations that meet or exceed requirements within specified timelines. Work with Biopharmaceutics and analytical teams to design predictive in vitro methods. Travel to CMO (internal DRL sites or external) for the execution of pilot bio-batches, scale up batches and exhibit batches. | 1/30/2019 |
| 1150 | Dr. Reddy's Shreveport, LA Technical Services Associate BS/BA in chemistry, physics, engineering, or pharmaceutics Exp: 0-2 years |
Duties as a tehcnical service associate include: project management (project plan, tracking of activities, material tracking, review scheduling), process validation activities (review/approve protocols, update manufacturing records), and continuous process verfication (protocol verification, data collection). | 1/30/2019 |
| 1151 | Dynosense San Jose, CA QA Engineer BS in CS or engineering Exp: 0-2 years |
As a QA Engineer you will be responsible for the planning/coordinating of testing activities, develop/test/plan test cases, test scenarios based on user stories and product's design description to meet business requirments/technical specifications, and identify software defects. | 1/30/2019 |
| 1152 | EAG Laboratories Syracuse, NY Sample Prep Technician AS preferred Exp: 0-2 years |
EAG Laboratories is looking for a Technician to join our team in Syracuse, NY. The Materials Laboratory Technician will be responsible for supporting Project Managers and Analyst activities. In this position, the individual will be using manufacturing, test, development, or diagnostic equipment, operate and maintain sample preparation related equipment. Also, prepare samples and equipment for analyses, including but not limited to, machining, mounting, and polishing, using techniques. | 1/30/2019 |
| 1153 | Editas Cambridge, MA Research Associate I/II – In Vivo Pharmacology BS or MS in biology or related Exp: 1-2 years |
Editas is seeking a highly motivated Research Associate I/II to join our in vivo pharmacology group. 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. The successful candidate will be part of a dynamic team and will interact with the discovery, platform, process development groups, as well as contract research organizations. | 1/30/2019 |
| 1154 | Editas Cambridge, MA Process Development Associate BS or MS in biology or related Exp: 1-3 years |
This new role on the Technical Development and Manufacturing team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to perform experiments that generate data to guide development of processing methods and standard operating procedures (SOPs) for the preparation of cellular therapies for translational clinical studies. 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.). | 1/30/2019 |
| 1155 | Editas Cambridge, MA Research Associate I/II, Immunotherapy BS or MS in biology or related Exp: 1-3 years |
In this role, you will contribute to the pre-clinical development of gene-edited cell products for oncology indications. An ideal candidate should have a background in immunology, cancer biology, and a strong interest in genome editing. Duties include basic molecular biology work, develop/perform immune cell activation, cytoxicity and other cellular/ELISA-based assays, and conducting cell based experiments. The successful candidate will be part of a dynamic team and will interact with the discovery, platform, process development groups, as well as contract research organizations. | 1/30/2019 |
| 1156 | Edwards Draper, UT Manufacturing Engineer II, THV Metals MS in engineering Exp: 0-2 years with industry relevant internships/projects/thesis |
As a manufacturing engineer, individual will apply knowledge of technical principles and Edwards systems/procedures to optimize manufacturing processes. Daily responsibilities include supporting day-to-day manufacturing operations, collaborating with R&D to establish manufacuturing procedures/practices, and identify opertunities to optimize manufacturing. | 1/30/2019 |
| 1157 | Edwards Baltimore, MD R&D Engineer II - Surgical Structural Heart MS in engineering Exp: 0-2 years with industry relevant internships/projects/thesis |
This R&D engineering position is responsible for design and development experience in new medical device and product development. The R&D Engineer II supports new technology development by creating CAD models, prototyping new technologies, and executing performance testing. An Engineer II works through complex challenges and problems, communicates clearly, and works well in a team. | 1/30/2019 |
| 1158 | Eisai Baltimore, MD Manufacturing Tech I AS or BS/BA Exp: 0-2 years |
This position will be responsible for GMP complicance/documentation management and manufacture product according to SOPs and batch record instructions. Daily duties include: set-up, dismantling and maintenance of equipment and assures equipment is ready for production operations. Performs routine sanitization of areas, completes cleaning, autoclaving & depyrogenating of equipment, reviews and edits SOPs, batch records, and other documentation, participates in trending of processes and/or processing parameters and provide initial evaluation of the data – notifying Manufacturing Manager of trends, etc. | 1/30/2019 |
| 1159 | Eli Lilly Clinton, IN Electrical Engineer BS in Electrical Engineering Exp: 1 year |
The Electrical Engineering will provide project management support for the Clinton Laboratories plant site. Primary responsibilities include ownership, support and/or troubleshooting for the power distribution system, various control systems, energy initiatives, electrical safety programs, design and execution of small projects and participation in proactive asset maintenance reliability efforts for electrical equipment | 1/30/2019 |
| 1160 | MilliporeSigma Madison, WI Assistant Analytical Scientist, R&D BS in Chemistry or related Exp: 0-2 years |
This is a laboratory position in the API R&D organization. The primary activities for this position will involve assisting with the development of analytical methods, performing sample testing during R&D, and then transferring the newly developed methods to Quality Control for manufacturing. Essential job functions include assisting with the development of test methods for R&D products/intermediates/materials, perform lab testing as needed (HPLC, GC, DSC, TGA, etc.), and to report data/analysis in timely manner. | 1/31/2019 |
| 1161 | MilliporeSigma Sheboygan Falls, WI Associate Production Scientist QC BS or BA in chemistry, chem engineering, or related Exp: 0-1 years |
In this role, you are to perform trace metals analysis on raw materials, in-process and final product samples in support of all business needs. Perform routine analysis using ICP-OES and ICP-MS. Collect and prepar samples to generate analysis reports. Conduc routine instrument maintenance and troubleshooting minor instrument issues; assisting management with prioritizing samples for analysis, supporting method development and data documentation. This role is on 2nd shift: Monday - Friday, 3:00 p,m - 11:30 pm (Availability to occasionally work on extended hours and weekends is required). | 1/31/2019 |
| 1162 | MilliporeSigma Milwaukee , WI Associate Production Scientist BS or BA in chemistry, chem engineering, or related Exp: 0-1 years |
In this role you will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Essential job functions include performing safty operations, ensuring quality, performing routine assays, processes and/or unit operations, ensure proper documentation, and participate in quality audits. This job is a 24/7, 2.2.3.2 Rotating 12 hour shift 6:00 PM- 6:30 AM - 3 day weekend, every other weekend. | 1/31/2019 |
| 1163 | MilliporeSigma St. Louis, MO Associate scientist BS/BA degree in chemistry, chemical engineering or related life science. Exp: 6+ months lab experience |
Perform Quality Control activities in support of GMP products, including routine testing and peer review of raw materials, intermediate and final products, and stability samples. Essential job functions include ensuring quality through adherence to GMP requirements. Assure adequately trained to perform tasks/assignments. Perform routine assays in accordance to applicable GMP requirements, processes and/or unit operations. Clean-up equipment and working areas during and after operations. Provide complete and accurate records consistent with quality guidelines and GDP requirements. | 1/31/2019 |
| 1164 | Emergent BioSolutions Baltimore, MD Analyst I, Quality Assurance BS/BA Exp: 0-3 years |
Job Summary: Provide oversight and support of document and records management in Document Control using company procedures and regulations. Provide support for Global Document Management System project (Veeva). This position is a key role to ensure product documentation meets defined quality standards and provides guidance to users of the document control processes. Demonstrate good judgment in selecting method and techniques for obtaining solutions. Resolves a wide range of issues in creative ways. Defines appropriate actions and requirements for resolution of issues. Communicates effectively with management project status, issues and mitigations | 1/31/2019 |
| 1165 | Emergent BioSolutions Rockville, MD Manufacturing Associate BS/BA in biology, chemistry, or related Exp: 0-2 years |
Job activities include the preparation of equipment and components for aseptic filling operations, performing visual inspection of filled vials, vial labeling, vial packaging and distribution of filled vials as per GMP regulations. Execute daily tasks according to standard operating procedures in support of filling operations such as washing, cleaning and sterilizing equipment and components. Qualifies as an aseptic operator for the participation of filling activities using isolator technology. | 1/31/2019 |
| 1166 | Enable Injections Cincinnati, OH Quality Associate I AS or BS/BA Exp: 0-3 years |
Under the direction of the Quality Assurance Manager, the Quality Associate I will support Document Control activities and Records Center management. Provide support to Design Control Teams by establishing and managing Design History Files (DHF). Provide support for tracking and trending of key metrics for the document control program. This position will also support external audits and other Quality related activities as required. Responsible for the continuous improvement and implementation of the Document Control and Document Management Quality Systems in a regulated environment. Ensures product safety, regulatory compliance, and compliance through proper management of quality documents and quality records | 1/31/2019 |
| 1167 | Endo Pharmaceuticals Inc Horsham, PA QC Analyst l - Chemistry BS in biological sciences or related Exp: 0-3 years |
The QC Analyst I - Chemistry will provide bioanalytical expertise for the Quality Control department. Key areas of focus are development and implementation of the quality aspects of late stage or marketed product strategy. This role is also responsible for maintaining sample traceability via QC logbooks. Responsibilities include: Testing responsibilities may include RP-HPLC, SEC, KF, FT-IR, SDS-PAGE, and UV-Vis. Assists with preparing new SOPs / test methods or revising of existing documentation. | 1/31/2019 |
| 1168 | Endo Pharmaceuticals Inc Horsham, PA Associate Quality Engineer BS in Engineering, science or equivalent Exp: 0-1 years |
The Associate Quality Engineer is responsible for supporting and assisting with review and oversight of validation and qualification activities, performing various types of analysis and assisting with internal investigations, CAPA, and change controls. Responsibilities include: Supports validation and qualification activities at the site including process validation, computer validation (URS), IQ, OQ and PQ. With guidance, provides support for investigations, corrective actions, continuous improvement projects, and process capability improvements (FMEA, root cause analysis, process mapping, Six Sigma, SPC, DOE, etc.). | 1/31/2019 |
| 1169 | Endo Pharmaceuticals Inc Horsham, PA Manufacturing Associate l DSP HS Degree/GED Exp: 0-3 years |
Works in a hands-on capacity in the cGMP purification and production support areas to manufacture bulk drug substances. Supports necessary purification and production activities, including validation and development work as needed. Works in hands-on capacity to operate chromatography systems, ÄKTA chromatography controllers, UF/DF skids, perform sterile filtrations, prepare production buffers, and clean equipment as required. | 1/31/2019 |
| 1170 | Endo Pharmaceuticals Inc Columbus , OH Sales Professional - Columbus BA/BS Exp: 0-3 years |
Entry-level Sales Professional role that executes a selling process and has developed basic knowledge of customers’ organization/staff and the ability to uncover their primary issues regarding their business and patients. The Sales Professional can articulate the core strengths and limitations of assigned Endo products and competitor products. The Sales Professional is always in the process of building relationships and ongoing interactions to establish trust and deliver value with all relevant contacts at the customer. Plans and executes annual plans to achieve account objectives and sales goals. Some responsibilities include: Develop and execute an individual prescriber plan of action for maximum selling opportunity as developed through territory business plan. Incorporate and execute on all expectations regarding adherence to all FDA, PDMA, HPPA, and Endo established Policies on all interactions with Healthcare Professionals. Maintain up-to-date database to document sales call information, trends, future call objectives, sampling data and overall territory performance. | 1/31/2019 |
| 1171 | Endotronix Lisle, IL Manufacturing Engineer BS/BE in mechanical or biomedical engineering Exp: 1-3 years medical device engineering |
Endotronix, Inc. seeks a Manufacturing Engineer to join its Manufacturing team to assist with activities related to the development, manufacturing and validation of wireless implantable sensor products in Lisle, IL. Responsibilities include: Develop manufacturing processes including laser processing, dispensing, soldering, assembly processes and automated electrical testing, working to improve cost, manufacturability and lead time, and creating manufacturing documentation (Item Specifications/drawings, routers Manufacturing Process Instructions, Standard Test Methods, etc.) | 1/31/2019 |
| 1172 | Envigo Indianapolis, IN Purchasing Associate AS Exp: 0-5 years |
This opportunity will be responsible for performing routine assignments associated to purchasing. This would include placing orders, entering orders, filing and other activities, manage the operations and tactical procurement of goods and services in multiple categories, and approve purchase requisitions for supplier, equipment and services according to departmental procedures. This position is contract/temporary | 2/1/2019 |
| 1173 | Enzo Ann Arbor, MI Manufacturing Assistant I AS or BS/BA in chemistry or life sciences Exp: 1+ years |
This position is responsible for accurately and efficiently assembling in-house and OEM manufactured products, and providing support to the Production department to ensure timely production, product quality, and accurate maintenance of inventory. Responsibilities include: Fill and label kit components. Assemble immunoassay kits, chemicals, and other products. Perform OEM-related duties, including product re-labeling, assembly, and receiving. Operate automated filling machines and equipment. etc. | 2/1/2019 |
| 1174 | Enzo Ann Arbor, MI Associate Manufacturing Scientist BS/BA in chemistry, biochemistry, biology or related Exp: 1-3 years |
This position is responsible for the planning, implementation, and maintenance of Small Molecule QC methods, processes, and operations for current and new chemicals in the Small Molecule Portfolio with assistance from senior scientists or management. In this role this scientist will also be expected to contribute to the improvement of QC methods and processes with a focus on adhering to strict product lot release deadlines. The Associate Manufacturing Scientist is also responsible for understanding small molecule product specifications, troubleshooting technical problems, and for developing new methods for optimizing the current QC testing/manufacturing/packaging of small molecules. This position is responsible for the planning, implementation, and maintenance of Small Molecule QC methods, processes, and operations for current and new chemicals in the Small Molecule Portfolio with assistance from senior scientists or management. In this role this scientist will also be expected to contribute to the improvement of QC methods and processes with a focus on adhering to strict product lot release deadlines. The Associate Manufacturing Scientist is also responsible for understanding small molecule product specifications, troubleshooting technical problems, and for developing new methods for optimizing the current QC testing/manufacturing/packaging of small molecules. | 2/1/2019 |
| 1175 | EpiVax Providence, RI Project Coordinator BS/BA in life sciences Exp: 1+ years |
Project Coordinator assists in daily project management, including grant production, project schedual development, project budgets, project communication, and status reporting. Specific responsibilities include: identifying private/federal funding opportunities, establishing/maintaining grant submission processes, initiating inter-interstutional agreements, preparing letters of intent/support/CLs for PI, consultants, subcontractors, etc. | 2/1/2019 |
| 1176 | ERT Rochester, NY Associate Biostatistician MS in statistics Exp: 1+ years |
Essential duties/responsibilities as an associate biostatistician include: Develop SAS and R programs for statistical analysis in conjunction with the Senior Biostatistician. Test, maintain, and execute SAS and R programs to perform statistical analysis including central tendency analysis, categorical analysis, and concentration-QTc analysis for data from both TQT studies and early clinical studies, in close consultation with the Senior Biostatistician. Prepare tables, figures, and listings for statistical analysis as outlined in the statistical analysis plan. Assist in post-processing data activities including data QC, completing IIRV reports, and cardiologist consistency checks. | 2/1/2019 |
| 1177 | ERT Boston, MA Translations Coordinator BS/BA or equivalent Exp: 1-3 years project management/coordination experirence |
The Clinical Systems Translations Coordinator is responsible for facilitating the language translation process for products that are deployed globally and must work closely with 3rd party translations vendors to translate product solutions. Responsibilities include: Work with ERT’s Project Management team to schedule and scope translations projects, and drive completion of translations-related milestones per the schedule. Utilize the technical process required to implement translations into devices, and use technical troubleshooting skills. Review the work product of the translation agency for completeness and escalate and mitigate quality of delivery issues. | 2/1/2019 |
| 1178 | Eurofins La Jolla, CA Associate Formulations Scientist BS or MS in chemistry or related Exp: 1-3 years |
Duties as an associate formulations scientist include: Preparation of prototype formulations (solutions, suspensions, tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids) for exploratory studies in in-vitro and in-vivo models. Development of oral, topical and intravenous (sterile) dosage forms for feasibility studies and small scale manufacturing operations. Assessment of the chemical and physical stability of prototype formulations, as well as the performance of prototype formulations using in-vitro tests (non-sink dissolution, precipitation, etc.) | 2/1/2019 |
| 1179 | Eurofins Lancaster, PA Associate Bio/Pharmaceutical Project Management Specialist BS/BA in science, business or related Exp: 0-2 years |
Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for an Associate Specialist to support our Bio/Pharmaceutical Project Management group in Lancaster, PA. Associate Specialist responsibilities include, but are not limited to, the following : Serve as the primary communication link between the client and laboratory operations. Provide sample log-in information and instruction to Sample Administration and ensure appropriate study materials are available to lab operations per project plan. Perform a full auditing review of sample submissions in the Laboratory Information Management System (LIMS) including a review of all associated documents (methods, specifications, protocols) prior to making samples available to the laboratory. | 2/1/2019 |
| 1180 | Eurofins Petaluma, CA Associate Analyst I BS/BA Exp: 1-4 years |
Eurofins Scientific is searching for an Associate Analyst I in Petaluma, CA. Title responsibilities include, but are not limited to, the following: ·Understand and follow Quality System documents relevant to responsibilities, e.g., Quality Manual, SOPs, and Methods. ·Adhere to, and assist laboratory staff in adhering to, appropriate quality measures to meet or exceed the standards set by ISO/IEC 17025, government regulatory (cGMP, GLP), and company requirements relevant to assigned duties. ·Adhere to all health, safety, and environmental regulations relative to assigned analyticl work; maintain and assist others in maintaining a clean, safe work environment. ·Perform timely and accurate analysis of samples to meet customer commitments, including but not limited to, preparing samples for analysis, using appropriate analysis methods and techniques, applying appropriate data review and reduction, and providing data interpretation and opinion. | 2/1/2019 |
| 1181 | Eurofins West Point, PA Upstream Process Development Spectrophotometry Scientist BS or MS in chemsitry, biochemistry, chem engineering or related Exp: 0-2 years |
Upstream Process Development Spectrophotometry Scientist responsibilities include, but are not limited to, the following: In-line light scattering studies to support the tech transfer of sterile drug product processes between manufacturing sites. Develop lab based methods for the real time determination of formulation homogeneity during the filling process of The client’s alum adjuvant vaccine products Ready instrumentation for use in the field at manufacturing facilities Scope may include transfer of manufacturing processes from The client facilities to external third party manufacturing organizations, both domestic and international Work with engineering groups at the manufacturing facilities to ensure the instrumentation can be effectively coupled to the process equipmen | 2/1/2019 |
| 1182 | Eurofins Bothell, WA Trace Metals Scientist BS/BA in science or chemistry Exp: 1 year analytical chemistry |
This position is an entry level analytical preparation position. The Associate Scientist performs a majority of sample preparation and light analysis of dietary supplement and environmental samples for trace metals determinations. The associate scientist interprets and manages data using LIMS, Access and Excel, ensuring that data meets all established QA/QC criteria and is made available to the Project Manager within specified time frames. | 2/1/2019 |
| 1183 | Eurofins Rahway, NJ Chemical Engineer BS in chemical, mechanical engineering or related Exp: 1+ years |
The Chemical Engineer responsibilities include, but are not limited to, the following: Design, develop, and test approaches to improve containment (e.g., limiting potential operator exposure through equipment modification and engineering controls) for pilot plant scale pharmaceutical product development unit operations associated with long acting implants and respiratory products. This work will involve direct interaction with equipment manufacturers, third party machine shops, as well as safety and industrial hygiene experts. | 2/1/2019 |
| 1184 | Eurofins Durham, NC Sterility Microbiologist BS/BA in biology, chemistry, or related Exp: 1-3 years lab experience |
Microbiologist responsibilities include, but are not limited to, the following : Performs laboratory testing on a variety of product samples, including bulk vaccine, filled vaccine, and media. Will initially be assigned to support the microbiology testing laboratories. o The emphasis is on microbiological methods, such as sterility, bacteriostasis/fungistasis, Neomycin potency, Mycoplasma, and Mycobacteria. o Cell culture propagation and maintenance procedures, and/or microbiological laboratory procedures o Authors standard operating procedures (SOPs) for the performance of laboratory methods | 2/1/2019 |
| 1185 | Heraeus Dayton, OH Process Development Technician AS in Chemistry Exp: 1+ years |
As a process development technician you will be responsible for production of products and to support the scale-up process of new products meeting customer specifications and performance requirements. Projects involve establishing standard operating procedures for new products or product modifications. Additional responsibilities include: Control or operate equipment in which chemical changes or reactions take place during the processing of products and pilot scale evaluations, interpret process data trends, developmental results, and statistical analysis, and draw samples of products for the Analytical Department at specified stages so that analyses can be performed for specific chemical characteristics such as pH levels, concentrations, or viscosities. | 2/1/2019 |
| 1186 | Evonik Hopewell, VA QC Lab Technician I AS orBS/BA in chemistry Exp: 2< years |
As a QC Lab Technician you will provide basic laboratory test analyses, inventory lab supplies, and verify functionality of laboratory equipment. Responsibilities include: Perform Quality Control Tests on all raw material, in-process and finished samples brought to the lab per SOP’s and sample testing plans. Complete associated paperwork. Provide minimal guidance to Operations on corrections to batches to meet specification. Inventory laboratory supplies for all materials necessary to perform QC tests. | 2/1/2019 |
| 1187 | Evonik Lafayette, IN Process Engineer BA/BS in chemical engineering or related Exp: 0-2 years |
Apply process engineering knowledge and skills to support the synthesis of starting materials pharmaceutical intermediates and final bulk products in a safe, efficient and environmentally responsible manner. Specifically, the process engineer is responsible for demonstrating process understanding, monitoring, and managing process performance. Responsibilities include: Provide process engineering support for established processes. Analyze data and initiate continuous improvement. Design, implement and support scale-ups or process modifications. | 2/1/2019 |
| 1188 | Evonik Wallingford, CT Lab Technician BS in Chemistry or related Exp: 1-5 years |
As a lab technician you will: Prevent release of material not meeting specifications and acceptance of raw materials not in specifications. Maintain inspection, measuring, and test equipment and perform verifications/calibrations in accordance with the plant quality system. Must also be aware of the regulatory requirements and must implement those standards as specified in the standards and regulatory requirements in this work assignment. Maintain a clean lab that promotes safe, accurate, and efficient completion of quality tasks. Assure material is of acceptable quality by performing necessary lab tests/inspections. Review the analytical results to determine if they are meaningful, accurate, and completed in compliance with the established Control Plan. | 2/1/2019 |
| 1189 | Exagen Vista, CA clinical laboratory scientist BS/BA in biology, chemistry, or related, CLS certified Exp: 0-2 years |
The Clinical Lab Scientist (CLS) will work in Flow Cytometry area and performs testing. Performs and document quality control and preventative maintenance. Follow good laboratory practices and procedures for compliance. Primary duties include the following. Other duties may be assigned: Independently perform clinical laboratory testing procedures. Follow quality control procedure to assure accuracy of test systems. | 2/1/2019 |
| 1190 | Exosome DX Waltham, MA Scientific Associate, Business Development BS/BA in life sciences Exp: 1-2 years |
The Scientific Associate, Business Development will play a vital role supporting the Business Development/CDx Team. This position will report jointly to the Scientific Manager of the Business Development Team and to the Business Development Manager. Key accountabilities include handling logistical aspects of Pharma/CDx projects, developing and/or enhancing Scientific documents (SOWs, SOPs, presentations), Regulatory documents and Business Documents in support of Pharma/CDx projects in support the successful execution of CDx projects. Activities also include drafting and editing scientific and business presentations and marketing documents with the pharma audience in mind, assisting in CDx associated project management and oversight activities. | 2/1/2019 |
| 1191 | Exosome DX Waltham, MA Laboratory Technologist BS or MS in biological sciences Exp: 0-2 years |
The ideal candidate will have a good understanding of CLIA requirements, will assist in the development and validation of Laboratory Developed Tests (LDTs) for diagnostic and clinical trials testing, and will be responsible for performing testing for a variety of biomarkers. Responsibilities include: Perform complex molecular biology procedures at the Cambridge facility under the supervision of the Clinical Laboratory Director. Contribute to laboratory test development optimization, validation and verification using cell and molecular biology techniques such as RNA/DNA extraction, PR-PCR, and Nucleic acid sequencing. | 2/1/2019 |
| 1192 | Celegene Seattle, WA Research Associate, Analytical Technologies BS or MS in biology, bioengineering, or related Exp: BS: 1-3 years lab, MS: 1+ years lab experience |
In this individual contributor, lab-based role, the Research Associate will work in a collaborative environment to perform process analytics testing to support Celgene’s development programs. This position will report to the head of Cell-Based Assay Group, joining a subgroup within Analytical Core. The incumbent will join an analytical testing group that values data quality, high productivity and teamwork. Key responsibilities include: Execution of multiplexed cell-based assays (killing assays, mixed lymphocyte reactions, ELISA, Luminex etc.), Execution of multiparameter Flow cytometry (Phenotypic, functional assays, etc.), Data analysis and reporting with an emphasis on high-quality data and quick turnaround, and Improve current methods and processes to increase throughput and efficiency within the analytical core group | 1/22/2019 |
| 1193 | Celegene Bothell, WA Manufacturing Associate I BS in science or engineering Exp: 0-2 years in cGMP manufacturing |
The primary focus of the role will be cellular therapeutic manufacturing at JuMP during process transfers, routine production, and technology improvements. The key deliverables for this role are (1) helping to establish the JuMP manufacturing operations and (2) completing production assignments with a high quality and timely output. | 1/22/2019 |
| 1194 | Celegene Warren, NJ Associate Bioengineer II BS or MS in biochemical, chemical, or biomedical engineering or cell biology Exp: BS: 1-3 years, MS: 0-2 years |
With minimal supervision, design and execute/implement characterization experiments of moderate complexity Critically analyze and interpret data using statistical methods. Apply fundamental scientific knowledge to projects and problems in a positive manner. Perform data analysis and summarize experimental results Interact with Process Development and Analytical Development teams to advance projects Author technical documents for interdepartmental use. Organize, record and maintain experimental data Convey data analysis and interpretation to supervisor and colleagues with clarity and high level of accuracy. Ensure proper operation and perform routine maintenance of all laboratory equipment Assist other staff to complete all laboratory tasks as necessary Maintain a safe workplace in accordance with company and OSHA policies/procedures | 1/22/2019 |
| 1195 | Cell Signaling Technologies Beverly, MA Research Associate - Antibody Manufacturing Core BS in biological sciences Exp: 1+ years lab experience |
We are seeking an entry-level Research Associate to join our fast-paced, highly collaborative team. The Research Associate will work as part of the Antibody Manufacturing Core to produce and purify antibodies for development. The Antibody Manufacturing Core is responsible for upstream processes to produce monoclonal antibodies in cell culture. | 1/22/2019 |
| 1196 | Celldex Needham, MA Associate Scientist BS in biological sciences Exp: 1-3 years mammalian cell culture |
The Associate Scientist is part of a team working to develop mammalian cell culture (CHO) for the manufacture of recombinant proteins (transient and stable expression). The Associate Scientist will be responsible for maintaining mammalian cell lines for the production of research and pre-clinical products and ensuring scale-up to pilot plant manufacturing under cGMP. | 1/22/2019 |
| 1197 | Cellectis New York, NY Research Associate, Immuno-Oncology BS/MS in biology or related Exp: 1+ years lab experience |
Cellectis is seeking a highly self-motivated Research Associate to join its Immuno-Oncology (IO) group focused in the development of innovative cellular therapies for cancer treatment. Ideal candidates are self-driven, dynamic, and preferably skilled in the following techniques: cell culture (cell lines and primary cultures), cell-based and immunological assays (cytotoxicity, ELISA, Antigen-dependent proliferation), lentiviral transduction, multicolor flow cytometry. Candidates must be able to keep detailed documentation of daily experiments and should be able to perform data analysis with minimal supervision. The successful candidate should be able to excel in a fast-moving, goal-oriented environment aiming to make a change in immunotherapy. | 1/22/2019 |
| 1198 | Corning Wilmington, NC Process Engineer BS or MS in chemical, material, electrical, or ceramic engineering Exp: 0-3 years |
Purpose of the position is to lead and/or participate on project teams to develop new manufacturing technology for the purposes of reducing cost, increasing capacity and/or improving product. Provide engineering-level production support to manufacturing operation and actively engage in plant safety initiatives and projects. Develop and maintain systems to monitor and proactively address equipment/process performance, including trend analysis and implementation plans. | 1/22/2019 |
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| 1200 | Champions Oncology Rockville, MD Formulation Technician I BS in chemistry, pharmacology or related Exp: 1+ years |
Duties and responsibilities include: collecting and documenting 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. Additionally, technician must prepare and dispose of test materials, vehicles, and reagents according to study protocols and SOPs, prepare labels and related documentation of study procedures, and maintain inventory of drugs, reagents, and lab supplies including costing and ordering. | 1/22/2019 |
| 1201 | Champions Oncology Rockville, MD Cell Culture Assistant BS in biological sciences Exp: 1+ years |
Duties and responsibilities include: preparing passaged and primary cells for use by in vivo and in vitro technicians as directed, performing related general duties such as inventorying supplies and reagents, general lab housekeeping, and maintaining safety records. Individual must be able to work effectively and productively in a team-oriented environment while maintaining a strong sense of accountability, integrity and confidentiality. | 1/22/2019 |
| 1202 | Champions Oncology Rockville, MD Research Technician I, Surgical Services BS in biological sciences Exp: 1+ years |
Duties and responsibilities include: handling and care of animals, animal observation, characterize and orthotopically/heterotopically surgically implant tissue samples, preform preperation activities for blood collection, processing and storage. Requires experience in preclinical in vivo pharmacology, in vivo experimentation, to work effectively and productively in a team-oriented environment while maintaining a strong sense of accountability, integrity and confidentiality. | 1/22/2019 |
| 1203 | Champions Oncology Rockville, MD Research Technician II, Study Services BS/MS in biology or related Exp: 0-3 years |
Primary objectives include supporting in vivo oncology studies in mice as a member of the Study Services Team. Individual should have experience conducting preclinical in vivo experintation in mice . | 1/22/2019 |
| 1204 | Charles River Boston, MA Veterinary Technician Surgical Services 1 BS in animal science or veterinary technology Exp: 1+ year animal care/handling |
The position will report to the Associate Director, Surgical Services and will be responsible for overseeing animal health, care and welfare for the large animal Surgical Services Program at Children’s Hospital. The individual will contribute to and participate in the facility animal health care program, as well as peri and post-procedure animal care. The veterinary technician will contribute to the documentation of animal health and communicate with research staff. The individual will provide training to both research and animal facility staff, and serve as an information and technical resource for the institutional animal research community. The individual will maintain performance levels consistent with and according to Children’s Hospital professional standards and requirements. | 1/22/2019 |
| 1205 | Charles River Mattawan, MI Laboratory Specimen Assistant - Pathology Services - Post Life Setups HS/GED, BS, or Masters Exp: BS/MS: 0 years |
The Laboratory Specimen Assistant is responsible for managing specimen containers, data, and communications for accurate and timely tracking and disposition of specimens within the necropsy, trimming, and histology laboratories. Individuals in this role use effective communication and interpersonal skills in a collaborative team environment. | 1/22/2019 |
| 1206 | Charles River Mattawan, MI Research Technician - Neurobehavioral Sciences HS/GED, BS, or Masters Exp: BS/MS: 0 years |
A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 1/22/2019 |
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| 1208 | 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. | 1/23/2019 |
| 1209 | Circassia Multiple Locations, NA Sales Representative-Device Bachelors Exp: 1-2 years sales |
The Sales Professional will lead a device territory base business and growth by promoting, selling, and supporting a Circassia Respiratory device product specifically across the Respiratory Specialty and Institutional space. This person will be tasked with successfully partnering cross-functionally with internal business partners in order to drive growth with current customers/accounts as well as develop new business with customers/accounts of high potential within the outlined geography. | 1/23/2019 |
| 1210 | Circassia Multiple Locations, NA Sales Representative-Pharmaceutical Bachelors Exp: 1-2 years sales |
The Sales Professional will lead territory base business and growth by promoting, selling, and supporting a Circassia Respiratory pharmaceutical product specifically across the Respiratory Specialty and Primary Care Physician (PCP) space. This person will be tasked with successfully partnering cross-functionally with internal business partners in order to drive growth with current customers/accounts as well as develop new business with customers/accounts of high potential within the outlined geography. | 1/23/2019 |
| 1211 | Clinipace Morrisville, NC Pharmacovigilance Specalist BS in life science, nursing/pharmacy Exp: 1-2 years |
The Pharmacovigilance Specialist (PVS) primary responsibility is SAE case management. This includes but is not limited to: initial case disposition, confirmation of case disposition with Medical Monitor (MM)/Safety Physician PV (SP PV), MM, receipt of adverse event data, data entry, source document data extraction, draft narrative development, follow-up management and reporting according to regulatory requirements. All activities will be in accordance with Clinipace and/or client SOPs, ICH Guidelines and local regulatory requirements. | 1/23/2019 |
| 1212 | Clinipace Morrisville, NC Clinical Trial Associate Bachelors in health care/life science Exp: 0-2 years |
The Clinical Trial Associate will support and work closely with the global project team including internal and external customers and suppliers through all phases of the study. Duties may include coordination, participation in study meetings, minute taking or ADI Log maintenance, study and site binder creation, data entry, tracking, scanning, copying, creating, maintaining and QC of essential documents and Trial Master Files. Coordinates and distributes study supplies. Meets defined chargeability expectations for position. | 1/23/2019 |
| 1213 | ClinSmart Newtown, PA Clinicla Research Associate (contract) BS in science or registered nursing degree Exp: 2 years as field clinical research monitor |
The CRA may be involved in all stages of the clinical trial, including identifying an investigational site, training investigators, and setting up, initiating, monitoring and closing down the trial. | 1/23/2019 |
| 1214 | Coating Place Verona, WI QC Analytical Chemist BS in chemistry or related Exp: 0-2 years lab experience |
The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. | 1/23/2019 |
| 1215 | Coda South San Francisco, CA Research Associate, Neurobiology BS in neuroscience, or biological sciences Exp: 1-2 years research experience |
We are looking for a highly motivated and dynamic candidate for the role of Research Associate, Cell Biology / Electrophysiology. This individual will work under the guidance of a scientist to support characterization of our engineered ligand-gated ion channels using electrophysiology assays in the lab. The ideal candidate is open-minded, trainable, and enthusiastic about research. Responsibilities include cell culture, solution preparation, data analysis and presentation, and general lab maintience | 1/23/2019 |
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| 1217 | , Exp: |
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| 1218 | Cogent Cincinnati, OH Analytical Chemist BS in life science Exp: 0-2 years |
This is a clinical research position, assisting a study Principal. Individual should have some experience working in regulated labs, troubleshooting LC-MS bioanalytica assay performaces, and generating/reporting analytical data. | 1/23/2019 |
| 1219 | Cogent Indianapolis, IN Process Engineer BS or MS in chemical or biochemical engineering Exp: 1+ years |
This position will provide key engineering and validation support and project coordination primarily to the manufacturing process side of plant operations. Additionally, technical support for process and product investigations will be offered. Major responsibilities include: Provide technical support for the manufacturing processes, including process investigations, process changes, and technical transfer and scale up of new product introductions. Coordinate and execute tech transfer projects in support of new clinical and commercial products and contract manufacturing opportunities. In addition to project management responsibilities described above, individual will be required to interface with external clients and contractors in support of contract manufacturing opportunities. ect. | 1/23/2019 |
| 1220 | , Exp: |
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| 1221 | , Exp: |
Cogent Professionals is searching for two (2) organic synthesis chemists for one of our Indianapolis, IN area pharmaceutical laboratories. Responsibilities include the ability to prepare multi-step organic syntheses reactions, bench chemistry, documentation, and ability to maintain high level of productivity in lab settings. | 1/23/2019 |
| 1222 | , Exp: |
Under the direction of the Senior Manufacturing Quality Engineer, the Manufacturing Quality Engineer I will be assigned product accounts and be responsible for collaborating with Program Managers, Manufacturing Engineers and other departments to analyze customer ECO’s and ensure effective implementation to the production floor through proper use of the Cogmedix ECO process. As part of the ECO Process and new proposal review, support the management of the customer BOM structure, creation of part numbers and structuring of Supplier Relationships and costs. Define PP/PA/Phantom, Commodity codes, documentation packages commodity and Work Instruction evaluation. Promptly respond to manufacturing floor issues, taking appropriate action within the Cogmedix Quality System and continually building strong rapport with customers and suppliers. Generate process validation/qualification documentation (e.g., validation protocols, IQ/OQ/PQ) and implement protocols and completion of reports. | 1/23/2019 |
| 1223 | , Exp: |
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| 1224 | Cold Genesys Santa Ana, CA Clinical Trial Associate AS or higher in biological sciences Exp: 1+ years in lab/clinical trial work |
Cold Genesys, Inc. is a biopharmaceutical company focused on the development of cancer immunotherapies to combat cancer. We are currently conducting a Phase III oncolytic virotherapy clinical trial across the US. Our company is rapidly expanding our clinical development efforts and would like to onboard a Clinical Trial Associate to assist us in monitoring our ongoing Phase I-III clinical trials in the US and overseas. Responsibilities include: Coordinating with investigator sites to ensure compliance with protocol and maintenance of patient safety, performing clinical on-site monitoring at various site locations across the United States, may include initiation visits, and functioning as a liaison between third party contractors and the investigator sites. | 1/23/2019 |
| 1225 | Compugen South San Francisco, CA Research Associate BS or MS in biology, bioengineering, or related Exp: 1-3 years mammalian cell culture |
This is an opportunity to discover therapeutic antibodies for immuno-oncology applications. In this role, the successful candidate will participate in projects to select therapeutic leads by screening and characterizing antibodies from initial discovery using various assays and antibody production. This is a critical role that enables therapeutic lead selection and requires strong organization, attention to detail, generation of experimental data, troubleshooting skills, and presentation of work to project teams. | 1/24/2019 |
| 1226 | Conagen Bedford, MA Automation Associate – Synthetic Biology Automation BS or MS in biology, bioengineering, or related Exp: 0-2 years |
We are looking for budding bioengineers excited about our mission and the idea of developing automated solutions for genetic engineering of industrial microbes. You will bring your bench biology chops and an eagerness to learn and apply lab automation to organism engineering challenges. From the start you will be applying robotics to enhance our workflows, with the goal of learning and becoming independent operators and programmers of this equipment. The candidate must have bench biology experience. Prior experience with automated lab equipment or high-throughput screening is highly desirable. Strong organizational and communication skills are essential. | 1/24/2019 |
| 1227 | Conagen Bedford, MA Fermentation Research Associate BS or MS in biochemistry, chemical engineering, or industrial biotechnology Exp: BS: 1+ years, MS: 0 years |
The Process Development Group provides support through the development and optimization of production processes. We work with our R&D and manufacturing colleagues. We are seeking a Research Associate to join our Fermentation Process Development team. This individual will collaborate with Scientists and Process Engineers to design experiments, record and analyze results, and participate in scale-up/scale-down activities. Responsibilities include performing media, buffer, and stock solution preparation, small scale studies, operating and monitoring fermentation processes, and routine sampling processing. | 1/24/2019 |
| 1228 | Conformis Wilmington, MA Buyer/Planner I No degree listd Exp: 1+ years in purchasing/planning capacities |
Buyer/Planner I is responsible for securing materials and equipment necessary to produce ConforMIS products to meet the Company’s Sales & Operations Plans and Quality Objectives. Responsible for planning, expediting, scheduling, and the organizing of all activities pertaining to the logistical support of customer orders. Buyer/Planner I is responsible for securing materials and equipment necessary to produce ConforMIS products to meet the Company’s Sales & Operations Plans and Quality Objectives. Responsible for planning, expediting, scheduling, and the organizing of all activities pertaining to the logistical support of customer orders. | 1/24/2019 |
| 1229 | Conformis Wilmington, MA Product Quality Engineer BS in science or engineering Exp: 1-3 years in quality |
The Product Quality Engineer will be responsible for product quality engineering/ quality assurance activities. This includes interpretation and implementation of quality standards to routine manufacturing, continuous improvement, and product release activities. Essential duties include developing/maintaining working relationships across the company, performing quality testing of CER/water system, administer bioburden/endotoxin testing, implement/maintaining quality system in accordance to regulatory requirments, developing/upgrading procedures for quality system, etc. | 1/24/2019 |
| 1230 | Conformis Wilmington, MA Manufacturing Engineer I BS or MS in engineering Exp: 1-3 years in manufacturing |
The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments. Responsibilities include optimization of manufacturing processes for Lean Manufacturing, developing/updating preventative maintenance programs, conducting time studies/process flow mapping, etc. | 1/24/2019 |
| 1231 | Conmed Utica, NY Quality Assurance Lab Technician I AAS in science Exp: 0-3 years in lab |
Decontaminate and evaluate returned Customer Complain Products by performing visual, functional, electrical, mechanical, and chemical testing, when appropriate. Provide evaluation results/reports for complaint files per procedural requirements. | 1/24/2019 |
| 1232 | Conmed Largo, FL Manufacturing Engineer I BS in engineering or equivalent Exp: 1-3 years in manufacturing environment |
Under supervision perform a variety of engineering work in planning and design of tools, equipment, machinery, processes, etc. and oversee the installation, operation, maintenance of such equipment, etc. Implement changes, alterations, modifications and repair based on engineering project requests, etc. Perform process validations and qualify vendors, suppliers, components, etc. | 1/24/2019 |
| 1233 | Conmed Utica, NY Packaging Engineer I BS in packaging engineering/package science preferred Exp: 0-2 years |
This engineer will have immediate opportunities to contribute to ongoing sustaining, and new product packaging initiatives working alongside other experienced Packaging Engineers, as well as cross-functionally with manufacturing, project management, R&D, procurement, regulatory, marketing, quality and operations team members. Duties include designing/implementing packaging designs and operation processes for mechanical function, manufacturability, and efficiency, perform in-process packing systems engineering tasks, prepare equipment validations protocols and reports, etc. | 1/24/2019 |
| 1234 | Constellation Cambridge , MA Research Associate - Translational Biology BS/MS in life sciences Exp: 1-3 years |
Constellation's Translational Biology department is seeking an experienced Research Associate to conduct oncology target validation and mechanism of action studies in a highly collaborative, goal-oriented team environment. The position requires excellent hands-on experience with commonly used techniques in cancer cell biology and/or chromatin biology. | 1/24/2019 |
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| 1236 | Core RX Clearwater, FL Project Logistics Associate Bachelor's Degree Exp: 1-2 years in customer service/technical support |
Work closely with project management and clients to establish required specifications for manufacturing materials from approved vendors and ensure sourced materials are available when required. Ensure materials are sampled by Quality Control and tested per the approved specifications. Work closely with the Quality Unit to ensure results for material testing are completed and submitted for approval in order to release for use in manufacturing. Support projects by locating sources and completing purchase orders as per the established internal processes and procedures.. Assist Purchasing with vendor management; factoring in costs, customer service, availability of materials and assessing reliability | 1/24/2019 |
| 1237 | Corium Grand Rapids, MI Contract Associate Quality Assurance Specialist BS in science Exp: 1+ years in GMP |
QA Operations: Uses technical, regulatory, and cGMP knowledge to provide oversight for both commercial and development projects. Responsibilities include: Review executed records. Identify and report any errors or omissions. Provide troubleshooting and guidance to employees on quality issues. Review documentation and release raw materials, WIP, and finished goods to next processing stage. Participates as a team member in investigations (DEV, CA/PA and customer complaints). Assemble and issue batch records to Manufacturing. QA Operations: Uses technical, regulatory, and cGMP knowledge to provide oversight for both commercial and development projects. Responsibilities include: Review executed records. Identify and report any errors or omissions. Provide troubleshooting and guidance to employees on quality issues. Review documentation and release raw materials, WIP, and finished goods to next processing stage. Participates as a team member in investigations (DEV, CA/PA and customer complaints). Assemble and issue batch records to Manufacturing. | 1/24/2019 |
| 1238 | Myriad RBM Austin, TX RBM Research Associate (manufacturing) BS or AS Exp: 0-5 years |
Myriad RBM is looking for a self-motivated individual to fill a Research Associate-Manufacturing position in our Austin facility. In this position you will be responsible for planning, performing, and evaluating the process of manufacturing reagents and propose experiments within a project(s) to provide valid and needed information. Conduct assigned experiments and assists in their designs. Manufacture reagents required for the testing of samples, including but not limited to coupling of antibody to beads, biotinylation of antibody for detection, testing of minipool and simplex reagents, batching and qualification of new lots of batched reagents, and troubleshooting problematic reagents. | 1/24/2019 |
| 1239 | Covance Leeds, Un Research Tech I Science based education Exp: 0-1 years clinical research experience |
Duties and responsibilities include: Accurately performs blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings. Preparation and accurate recording of ECGs/Holters. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Monitors meals to ensure dietary compliance by research participants. Assists in the preparation of rooms and medical equipment. Assists with screening procedures as needed. Maintains a clean, safe and efficient working and study environment. Fosters respectful relationships with study participants | 1/24/2019 |
| 1240 | Covance Indianapolis, IN Histotech I BS in biological sciences w/wo ASCP HT certification Exp: 1+ year in histotech |
Duties include: trim wet tissues, embed tissues into paraffin, tissue staining, microtomy, necropsy, and other basic histological duties | 1/24/2019 |
| 1241 | Covance Indianapolis, IN Research Asst II BioA BS/BA Exp: 1-2 years |
Research Assistant II BioA will be responsible for organizing and conducting routine analysis in compliance with applicable methods, protocols, SOPs, and regulatory agencies. Set up, operate, and perform routine/non-routine maintenence on equipment. Assists in setting up and performing method developmenet and validation of varies analytes in a variety of matricies. | 1/24/2019 |
| 1242 | Covance York, Un QC Laboratory Analyst Scientific deree in biochemistry, chemistry, bioogy, or related Exp: 0 years |
The QC analyst will join the Large Molecule team in the CMC division and will be responsible for performing analytical testing on large protein molecules (e.g. monoclonal antibodies, ADCC, biosimilars etc). This testing will be performed to support characterization, method validation, batch release and stability across pre-clinical, clinical and commercial release. | 1/24/2019 |
| 1243 | Covance Wilmington, NC Contracts Specalist I Bachelors or university-level law degree (UK/EU) Exp: 0-2 years |
Perform the following, with occasional guidance from line management or more experienced colleagues: daily tracking, negotiation and approval of Site Agreements and Site Agreement templates (as applicable) for clinical study teams; timely updating of the departmental Site Agreement Management System (“SAMS”) or any other system required for use on a particular study. Manage assigned studies with careful compliance with internal processes and procedures, or otherwise according to specified Sponsor requirements. Performs contract administration functions including: assisting with obtaining approvals on authorization forms as required; maintaining a contract tracking system to report contract status updates and signing status; providing notice of all executed contracts to the appropriate team members along with contract values; and scanning and filing executed contracts in the shared electronic storage area in a timely manner for access by other staff members. | 1/24/2019 |
| 1244 | Covance Leeds, Un Project Coordinator I (Project Management Academy) University/college degree related to health profession/sciences Exp: 0 years |
Project expertise for CTMS reporting, study metrics, risk management regarding communication, coordination, and eTMF quality. Able to co-ordinate and manage support across large global study. Applies therapeutic knowledge to daily activities of the clinical trial, brings new knowledge to the team, drives best practices in coordination, communication and documentation. Primary responsibility for the coordination and completion of all administrative functions in support of the project manager. | 1/24/2019 |
| 1245 | Myriad AutoImmune Salt Lake City, UT Patiente Advocate BS or BA in biology, science, or healthcare Exp: 1-2 years |
Myriad Autoimmune has a Patient Advocate position will be responsible for handling incoming calls from medical professionals, patients and field staff. They will be responsible for supporting the sales team by developing and maintaining positive customer relations, which can substantially affect service and/or product revenue(s). Responds to customer product inquiries and escalates satisfaction issues as appropriate. Respond to inquiries from customers, patients and field staff in a professional and timely manner | 1/25/2019 |
| 1246 | Crinetics Pharmaceuticals San Diego, CA Research Associate, Biology BS or MS in life sciences Exp: 0-5 years |
We are seeking a highly motivated Research Associate to join the Biology group at Crinetics. You will work within a highly collaborative group focused on GPCR targets linked to unmet needs in endocrine disease. The successful candidate will participate in discovery and translational efforts aimed at identifying and characterizing novel therapeutic targets. You will investigate the mechanisms of action of new molecules and define optimal drug profiles in vitro. You will work in a dynamic environment to help advance programs from discovery into development as part of a multidisciplinary team. | 1/25/2019 |
| 1247 | , Exp: |
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| 1248 | CrownBio San Diego, CA Research Associate - In Vivo (I or II) BS in science Exp: 1-2 years in pharma/toxicology preferred |
Crown Bioscience has an immediate opening for a full-time or part-time Research Associate in our In Vivo department. Responsibilities of the position include the handling, treatment, and monitoring of tumor-bearing mice. | 1/25/2019 |
| 1249 | CrownBio San Diego, CA Research Associate I – Flow Cytometry BS in science Exp: 1-3 years |
Crown Bioscience has an immediate opening for a full-time Research Associate in our BDT department. Responsibilities and duties of the position include designing/performing multicolor flow cytometry for preclinical projects, analyzing of data for immunophenotyping/biomarker research, and preperation of samples, reports, and summaries. | 1/25/2019 |
| 1250 | CryoLife Kennesaw, GA Quality Assurance Speacialist I BS in life sciences or related Exp: 1+ years preferred |
Establish and maintain Quality Systems that comply with regulations and standards. Review all records associated with the production of medical device products. Reduce waste and variability in processes. Ensure that all areas identified as “Principal Responsibilities” are accomplished in an efficient and professional manner. | 1/25/2019 |
| 1251 | CSBio Menlo Park, CA Chemist, GMP Manufacturing BS/BA in chemistry, biochemistry, or related Exp: 1+ years |
We are seeking qualified individuals to join us as GMP Manufacturing Chemists at our Menlo Park facility. This position will be responsible for the synthesis and cleavage of peptides or the purification and lyophilization of peptides in our GMP manufacturing areas. Core duties and responsibilities include the following: Execute batch production records or protocols for synthesis and cleavage processes with minimal supervision in a timely and efficient manner, Analyze organic and inorganic compounds to determine chemical and physical properties, Operate laboratory equipment and instruments including: HPLCs, centrifuges, freeze dryers, stir plates, lab balance, mass spectrometers, sonicators, vacuum ovens, N2 tanks, etc. | 1/25/2019 |
| 1252 | , Exp: |
We are seeking a qualified individual to join us as a Validation Engineer at our Menlo Park facility. This position will support and coordinate Validation activities which may include manufacturing equipment, utility systems, facilities, laboratory instruments, and software within the company's GMP facility. Job responsibilities include the following: Perform commissioning, qualification, and validation activities for facility, utility, equipment, and software; including developing project plans, preparing protocols, addressing discrepancies, and developing technical reports, Author and execute IQ, OQ, and PQ qualifications and summary reports, Develop and/or participate in generating validation lifecycle documentations, such as impact assessments, URS, FS, TM, etc. Work with Quality, Operations, Manufacturing and Quality Control to establish, develop, communicate, and maintain all GMP equipment in validated state; this includes but is not limited to manufacturing equipment, facilities, computer systems, and laboratory instrumentation. | 1/25/2019 |
| 1253 | , Exp: |
The Clinical Research Associate will perform all types of site visits including Site Selection, Initiation, Monitoring, and Close-out, as well as drug accountability and other monitor activities to assure adherence to Good Clinical Practices (ICH GCP), SOPs, and study protocols. As the Clinical Research Associate you will ensure selected study sites have adequate qualification resources and facilities/equipment, have provided eligible subjects and qualified investigators. | 1/17/2019 |
| 1254 | Merck Milwaukee, MI QA Assurance Associate BS in chemistry, biology, or related science Exp: 1+ years of quality/customer contact work |
The Quality Assurance Associate works within the Teutonia QA team to ensure that the site meets customer and Life Science quality requirements. Responsibilities will include reviewing/updating procedures, providing training on quality-related topics, performing self-assessments and internal audits, assist with/or lead investigations/root cause analyses/CAPAs for customer complaints or other internally identified issues. Ensure that all aspects of product release meet analytical, production, packaging and labeling specification in accordance with established quality systems. Support the maintenance, development and improvement of GMP and/or ISO-9000 quality systems, such as auditing (internal, supplier, and customer), training, change control, complaint handling, and documentation control. | 1/17/2019 |
| 1255 | Merck St. Louis, MO Associate Production Scientist BS in chemistry, biology, or related science Exp: 0-1 years |
Manufacture products according to established protocols, provide technical support to others and perform operations in support of the group and department. Responsibilities include preforming production operations, communicate/document status of processes, products, and equipment, perform and interpret analytical evaluations of products and intermediates, and preform daily production operations. | 1/17/2019 |
| 1256 | Merck Burlington, VT Associate Scientist, Downstream Process Development Exp: 1-3 years in biopharmaceutical industry |
Within the Biodevelopment Process Development group, will execute projects including developing purification processes and analytical methods for a variety of therapeutic candidate proteins including monoclonal antibodies and Fc fusion proteins. The scope of work includes protein purification, biochemical and biophysical characterization, as well as to develop, validate and transfer robust analytical methods required for successful drug development and manufacturing. Compile and analyze experimental data to generate process knowledge and decide on next experimental steps. Write development and validation reports and ensure their timely delivery. Prepare and present project updates to global project team and to upper management. Execute client projects according to budget and timelines given to the project team. | 1/17/2019 |
| 1257 | Merck Bedford, MI GOglobal Marketing Bioprocessingn 2019 MBA or MS in business Exp: 0 years |
In the course of an individual rotation plan you will get to know the multiple aspects of Marketing in our Life Science Biopharmaceutical Processing business area (e.g. Product Management, Digital Marketing, Strategy, Pricing) for various product areas, such as Single Use, Upstream, Downstream or Integrated Systems. After a first assignment at our home base in Bedford, US, you will be going international to one of our subsidiaries for a second assignment. In the third assignment, you will get the chance to broaden your perspective and experience a different functional scope or business area in your home location. | 1/17/2019 |
| 1258 | Brooks Chelmsford, MA Quality Assurance Engineer BS in technical field Exp: 0 years |
The Quality Engineer leads investigation of product and process problems and develops dispositions, modifications, and corrective actions for recurring or non-recurring discrepancies. A leader and a key cross-functional facilitator interfacing with manufacturing, engineering, customer, vendor and contract manufacturers to ensure requirements are met. Skilled at developing and implementing quality plans, programs, and procedures using quality control statistics, lean manufacturing concepts, and analyses. Ensures product quality conforms to established company, customer and regulatory requirements. Reviews, analyzes and reports on quality discrepancies related to assemblies and processes. Responsibility may include planning and implementing process quality plans for new product introductions. | 1/17/2019 |
| 1259 | Biotechne Woburn, MA Product Engineer BS or MS in chemical engineer, material science or related Exp: 1-3 years |
As part of the Process Development team, this position will support optimizing production condition and characterization of CloudzTM hydrogel particles for research and clinical use. The role will focus on formulating new hydrogel formulations and identifying optimal particle formation conditions to deliver scalable, repeatable and functional product for a variety of internal and external customer projects. Additionally, the Product Engineer will contribute to developing new chemical, imaging and physical particle analysis tools with opportunity to collaborate with technical groups across Bio-Techne. | 1/17/2019 |
| 1260 | Biotechne San Jose, CA Process Engineering Technician BS in science or engineering Exp: 2+ years in manufacturing |
The successful applicant for the Process Engineering Technician position will support and engage with members of the San Jose Consumables Manufacturing/ Production team, as well as a multidisciplinary team of engineers and scientists, to sustain and improve reagent finishing processes including liquid handling and automated dispense equipment. | 1/17/2019 |
| 1261 | Biotechne Centennial, CO SRM/Content Management Associate BS in biological sciences Exp: 0 years |
The Content Management Associate will manage scientific product data displayed on the Novusbio.com website. (S)he will help to create content that effectively markets scientific products on Novusbio.com. (S)he must have a basic back ground in science as well as being technically savvy in Excel. The Content Management Associate must be able to communicate with all areas of the company including Marketing, IT, Customer and Technical Service. | 1/17/2019 |
| 1262 | Biotechne Minneapolis, MN Research Associate, Diagnostics Division Research BS in Engineering or biological sciences Exp: 0-2 years |
The individual in this position will work in a team environment. Their primary responsibilities include supporting feasibility studies and product development of Hematology controls. They assist with the optimization and testing of components, develop manufacturing procedures, and perform necessary troubleshooting. The individual is trained and follows standard practices and procedures to ensure a safe working environment. | 1/17/2019 |
| 1263 | , Exp: |
Individual will use lentiviral vectors to genetically modify freshly isolated T lymphocytes, expand modified T cell cultures, and characterize cultures using standard immunological assays including flow cytometry. Data from experiments will be compiled and presented to functional teams, and used to inform future experiment/project design. | 1/18/2019 |
| 1264 | , Exp: |
bluebird bio’s Oncology Discovery Team is looking to add an Associate Scientist to its Research and Discovery group. This group identifies and develops novel strategies that enhance anti-tumor T cell activity through synthetic biology and genetic engineering. This new position will serve a critical function by providing laboratory level support to project leads with a focus on cellular and molecular immunology. As a team member, the successful candidate will use their proficiency in several immunological techniques (e.g. FACS, ELISA, western blot, qPCR, etc.) to help drive exploratory science, make recommendations on next steps and facilitate the transition to drug product. | 1/18/2019 |
| 1265 | Bluebird bio Cambridge, MA Associate Scientist, CPD BS or MS in cell biology, immunology, or related Exp: BS: 2+ years, MS: 0 years |
The focus of this position is to provide support for the testing and development of new assays for characterization clinical samples. We are looking for a motivated associate scientist with the experience and drive to take ownership of important development and characterization projects. Responsibilities include supporting studies on CD34+ recovery, mammalian cell culture, and molecular biology based experiments. | 1/18/2019 |
| 1266 | Bluebird bio Durham, NC Manufacturing Associate BS in science or engineering Exp: 0-15 years |
You will have responsibilities for executing all process steps in the manufacture of lentiviral vector (LVV), a critical starting material in our gene therapy platform. This role will focus on both the facility startup, new product technology transfers and routine (clinical and commercial) manufacturing. As part of new facility design, construction, startup, and transition to routine operations, this individual will work with the cross-functional bluebird team, including Quality Assurance, Quality Control, Facilities, Manufacturing Sciences & Technology, and Process Development to lead day-to-day operations. We seek candidates with proven ability to work in a GMP environment. Specifically, we are looking for team members with track records of building a safety culture, driving the highest standards of a quality mindset, and ensuring uninterrupted supply for patients. | 1/18/2019 |
| 1267 | Bluebird bio Cambridge, MA Associate Scientist, Vector Characterization BS in biological sciences Exp: 1-3 years |
The candidate’s primary responsibilities will be to perform analytical testing to advance product quality understanding and support development of next-generation analytical technologies. Primary responsibilities include execution of lentiviral experiments, generation, analysis and presentation of data, and general lab management. | 1/18/2019 |
| 1268 | , Exp: |
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| 1269 | Boehringer Ingelheim aint Joseph, MO Technician IV Bio QC BS in life sciences Exp: 0 years |
Performs bio-analytical methods (immunological, in vivo, microbiological, molecular biological, or virological) for various Bio QC tests on raw materials, in-process, release or stability samples in compliance with 9CFR, EU and VICH regulatory guidelines, Outlines of Production and Special Outlines. Initiates, executes and completes assays as per validated procedures and within Quality and Compliance guidelines and communicates testing, compliance and/or scheduling issues to supervisors. | 1/18/2019 |
| 1270 | Brammer Bio Alachua, FL Scientist I Bachelors Exp: 0-1 years |
This position will work in the GMP compliant QC Laboratories to develop, qualify, and conduct cell-based, nucleic acid-based, protein-based, and chemistry-based assays that support quality control of biopharmaceutical products being developed and manufactured. Will perform routine assays and testing including PCR, real time PCR, agarose gel electrophoresis, SDS-PAGE, immuno blotting, ELISAs, immunocytochemistry, and infectivity and reporter gene based cell assays using insect or mammalian cell lines. This position will also troubleshoot and optimize assays under the supervision of the GMP QC Manager. Functions also involve maintenance of cell lines used in the QC laboratories, maintenance (routine and preventive operation) of equipment, and preparation and purification of commonly used biological reagent and chemical supplies. Will be expected to technically interpret, write controlled documents and reports, and review data produced by self and participate in laboratory investigations. | 1/18/2019 |
| 1271 | Brammer Bio Cambridge, MA QA Associate AS or BS in science or engineering Exp: AS: 2+ years, BS: 0 years |
The Quality Assurance Compliance Associate performs activities in support of dispositioning product and/or raw materials while ensuring clarity and compliance Brammer Bio policies and procedures, customer requirements, and regulatory standards. Responsibilities include but not limited to: Review and approval of all documentation related to late phase and commercial manufacturing to ensure timely review and disposition of client batches/lots. Review and approval includes manufacturing batch record reviews, internal records, client records, and master batch records. Support conditional and final GMP release activities for disposition of bulk drug substance and drug product. | 1/18/2019 |
| 1272 | Brammer Bio Lexington, MA Manufacturing Associate III, Drug Product/Fill Finish BS Exp: 1-3 years |
Responsible for cGMP manufacturing operations at the Brammer Cambridge site Drug Product (DP) Fill/Finish operations. Acitivities include performing basic to complex activities on fill finish line for drug product, performing critical downstream activities, documentation of all activities, monitoring of automated production systems, and daily aseptic processing. | 1/18/2019 |
| 1273 | Brammer Bio Alachua, FL Lab Technician, Quality Control BS preferred Exp: 0-1 years lab work experience |
The Laboratory Technician will work in the QC cGMP compliant Laboratories to develop, qualify, and conduct cell-based, nucleic acid-based, protein-based, and chemistry-based assays that support quality control of biopharmaceutical products being developed and manufactured at Brammer Bio under contract. Duties include performing routine assays and testing including but not limited to PCR, quantitative PCR, agarose gel electrophoresis, SDS-PAGE, immuno blotting, ELISAs, immunocytochemistry, and infectivity and reporter gene based cell assays using insect or mammalian cell lines. The Laboratory Technician will also troubleshoot and optimize assays under the supervision of the GMP QC Manager/ Research Coordinator. Functions also involve maintenance of cell lines used in the QC laboratories, maintenance (routine and preventive operation) of equipment, and preparation and purification of commonly used biological reagent and chemical supplies. The Laboratory Technician will be expected to technically interpret and review data produced from the assays they run. | 1/18/2019 |
| 1274 | Brammer Bio Cambridge, MA Associate, Process Sciences BS or advanced degree in biochemical, chemical engineering or related Exp: BS: 0-2 years |
The primary responsibility is to support the process establishment and process characterization for the manufacturing of viral vectors. This position requires close interaction with the Process Sciences (PS) colleagues, Manufacturing Science & Technology, Manufacturing, Process Development, and other departments. This role will focus on defining and characterizing robust, scalable and efficient manufacturing processes to produce late-phase human clinical trial and commercial viral vector products. | 1/18/2019 |
| 1275 | Bristol-Myers Squibb Devens, MA Associate, QC Chemistry BS Exp: 1-2 years in GMP QC Lab or equivalent |
To perform QC analytical testing in support of biologics bulk drug substance manufacturing using defined methods in a cGMP compliant laboratory. Assures test results are accurately recorded and abnormal data or equipment/instrument malfunctions are promptly reported to his/her supervisor | 1/18/2019 |
| 1276 | Bristol-Myers Squibb Redwood City , CA Associate Research Scientist MS Exp: 1+ years of lab experience |
The qualified candidate is a highly motivated, interactive, and creative individual that possesses the ability to support early stage drug discovery programs by preclinical model development and target validation. The candidate will be expected to effectively collaborate with colleagues in the oncology, immunology and bioinformatics groups. The successful candidate will demonstrate clear understanding of principals of target identification, professional verbal and written communication skills, capable of presenting scientific results to multidisciplinary teams and key stakeholders. The primary responsibilities for this role include target validation by engineering isogenic cell lines and characterization of downstream molecular pathways | 1/18/2019 |
| 1277 | Bristol-Myers Squibb Redwood City , CA Associate Research Scientist, NGS Scientist BS or MS in molecular biology or related Exp: BS: 2+ years, MS: 0 years |
The Associate Research Scientist will join the Mechanistic Disease Discovery Research team at Bristol-Myers Squibb in Redwood City, CA and aide in the advancement of early stage therapeutic targets. This position will support day-to-day operation of a next generation sequencing lab. Experience in sequencing of primary human samples, both tumor and immune-derived, as well as mouse samples will be key to successfully fulfilling the requirements. The position will require the individual to be highly collaborative and work closely with and support an array of project teams and scientists within the Discovery Research organization. | 1/18/2019 |
| 1278 | Bristol-Myers Squibb Devens, MA Assistant Automation Engineer BS in engineering or equivalent Exp: 0-2 years |
Major duties and responsibilities include participation in control system initiatives such as change/project implimentation, incident/issue investigation, CAPA & safety related corrective actions, and manufacturing support. Other duties include system modifications, troubleshooting, and collaborative investigation of automation software/hardware problems. | 1/18/2019 |
| 1279 | Bristol-Myers Squibb Devens, MA Associate, QC Microbioloist BS in biological sciences Exp: 0-2 years |
Perform routine environmental monitoring and clean utilities sampling and testing in accordance with SOPs, safety, and cGMP guidelines to support qualification of new facility. Monitor critical operating parameters for equipment and instrumentation to ensure standard operation. Recognize, report, and document deviations from test methodologies, specifications, and alert limits Develops working knowledge of cGMP, learn specific job related SOPs and develop proficiency in laboratory techniques. | 1/18/2019 |
| 1280 | C3J Therapeutics Los Angeles, CA Research Associate I/II BS in molecular biology, genetics, virology or related Exp: 1+ year lab experience |
C3J Therapeutics is seeking a Research Associate I/II to work with the R&D team. The candidate will support the overall program goals and strategy of the group which include significant laboratory activities, such as phage engineering and characterization, protein expression and preclinical evaluation of phage therapy efficacy in relevant animal models. The candidate will have broad molecular and cell biology experience. Previous experience with virology and viral vector construction (phage or mammalian viruses) will be considered a plus. Excellent verbal, presentation, and written communication skills are essential and the capability to effectively work in a team environment is required | 1/18/2019 |
| 1281 | , Exp: |
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| 1282 | Cambrex Charles City, IA Process Support Chemist II BS in chemistry Exp: 0-2 years lab experience |
Reporting to the Process Support Supervisor, the Process Support Group – Chemist II will be responsible for daily laboratory testing of in process materials, environmental testing, validation transfer support and other various laboratory support. | 1/18/2019 |
| 1283 | , Exp: |
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| 1284 | Caribou Berkeley, CA In-vivo Pharmacology Research Associate BS in life sciences Exp: 1+ years experience working with rodents |
Caribou is seeking an experienced Research Associate to join its R&D team at its facility in South San Francisco, CA. The candidate must be motivated, enthusiastic, professional and committed to working as a team player. The ideal candidate enlists confidence, comfort and a working knowledge of laboratory animals, with a background in animal husbandry, restraint and handling. In addition, experience with injection and blood draw techniques, along with rodent surgery and anesthesia experience is desirable. The candidate must have the ability to effectively communicate with coworkers, take direction from supervisors, and be accountable for their actions. They must possess a strong attention to detail and always strive to perform quality work. This is an excellent opportunity to utilize and advance the ideal candidate’s laboratory animal skills in a progressive, state-of-the-art and diverse facility. | 1/19/2019 |
| 1285 | , Exp: |
We are seeking a Process Development Associate to contribute to our newly created Process Development group in Berkeley. The ideal candidate will participate in the Process Development efforts and interact closely with functional group leaders, scientists and research associates to transfer the technology from discovery to pre-clinical development. This hands-on role will involve design and execution of the experiments for process development, optimization, scale-up, and tech transfer, and will help manage the technology transfer to a CMO/CRO. | 1/19/2019 |
| 1286 | , Exp: |
We are seeking a Research Associate to join our Immune Cell Engineering team in Berkeley. The ideal candidate will interact closely with functional group leaders, scientists and research associates to drive discovery and development of new therapeutics in pre-clinical development. Responsibilities include mammalian cell culturing, immune cell biology based assay development and implementation, and coordinating experiments with other researchers | 1/19/2019 |
| 1287 | Zeiss Bay Area, CA Field Support Engineer I BS in engineering, electronics, cs, or related Exp: 0-3 years in technical 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. | 1/19/2019 |
| 1288 | Casebia Therapeutics Cambridge, MA Process Development Engineering Associate BS in biological sciences Exp: 1+ years |
Our ideal candidate will have hands-on technical experience with both upstream and downstream process development for the manufacture of biologics and will have a solid understanding of bioprocess engineering principles. The position will be responsible for supplying recombinant virus to research, process development and analytical development teams throughout the organization. The individual will develop and optimize Casebia’s reagent-grade recombinant virus production process and will be a key member of the team developing expression and purification strategies for novel gene editing/gene therapy vectors. | 1/19/2019 |
| 1289 | Casma Cambridge, MA Research Associate, Biology MS in biology or related Exp: 1-3 years |
We are seeking a highly motivated, Research Associate to participate in drug discovery programs that lead to the identification of new targets and drug candidates for clinical development. The individual should possess strong core competencies in cell biology, molecular biology, assay development. | 1/19/2019 |
| 1290 | Catalent Madison , WI Assistant Scientist, Analytical Development - Formulation BS or MS in biotechnology or related Exp: BS: 1-3 years, MS: 0 years |
The Assistant Scientist, Analytical Development - Formulation position will perform a variety of laboratory procedures to support Analytical Development. The Assistant Scientist, Analytical Development - Formulation will perform daily work assignments accurately and in a timely and safe manner. The Assistant Scientist, Analytical Development - Formulation will independently evaluate, select and apply standardized scientific and techniques; assignments have clear and specified objectives, and require the investigation of a limited number of variables. This position relies on limited experience and exercises judgment within defined procedures and practices in making minor adaptations and modifications. | 1/19/2019 |
| 1291 | Cato San Diego, CA Project Coordinator Trainee-Entry Level Position BS in science or engineering Exp: 0 years |
Works with the project manager coordinating all aspects of communication and activities related to a project. Prepares for, attends, and does follow-up for sponsor meetings; compiles documents for submission to the regulatory agencies or to the sponsor; coordinates the document review process; works with the clinical trial manager on the conduct of a clinical trial; creates and monitors project budgets; manages the project files; prepares project activity tracking reports and attends project review. | 1/19/2019 |
| 1292 | , Exp: |
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| 1293 | , Exp: |
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| 1294 | Astellas Seattle, WA Research Associate 2, Cell Engineering MS in scientific discipline Exp: 0-2 years |
We are seeking a highly-motivated and energetic Research Associate to join our R&D team to precisely edit and differentiate human pluripotent stem cells and perform phenotypic assays to guide choices for future clinical-grade therapeutic products. This person will acquire further versatility in routine procedures, more technical knowledge, and more understanding of administrative operations, some troubleshooting. This person will assist with more complex laboratory operation projects, and will take on more responsibility to provide content for various documents and reports. This person will be able to execute protocols with some guidance, and will have ability to summarize results independently.We are seeking a highly-motivated and energetic Research Associate to join our R&D team to precisely edit and differentiate human pluripotent stem cells and perform phenotypic assays to guide choices for future clinical-grade therapeutic products. This person will acquire further versatility in routine procedures, more technical knowledge, and more understanding of administrative operations, some troubleshooting. This person will assist with more complex laboratory operation projects, and will take on more responsibility to provide content for various documents and reports. This person will be able to execute protocols with some guidance, and will have ability to summarize results independently.We are seeking a highly-motivated and energetic Research Associate to join our R&D team to precisely edit and differentiate human pluripotent stem cells and perform phenotypic assays to guide choices for future clinical-grade therapeutic products. This person will acquire further versatility in routine procedures, more technical knowledge, and more understanding of administrative operations, some troubleshooting. This person will assist with more complex laboratory operation projects, and will take on more responsibility to provide content for various documents and reports. This person will be able to execute protocols with some guidance, and will have ability to summarize results independently. | 1/7/2019 |
| 1295 | Asuragen Austin , TX Scientist I, Product Development MS in scientific discipline Exp: 1+ years |
Asuragen is seeking an outstanding scientist to work as part of a product development team to develop, launch and maintain molecular diagnostic products for inherited genetic disease and cancer testing. The successful candidate will contribute to new product initiatives through requirements definition, prototype design, optimization, verification, validation and troubleshooting of assays under FDA and ISO Design Control regulations. A significant focus will be on process and specification development across multiple PCR-based assay formats and technologies, including NGS, PCR/CE and qPCR. | 1/7/2019 |
| 1296 | Atreca Redwood City, CA Research Associate, Protein Biochemistry BS/BA or MS in molecular biology, biochemistry, or related Exp: 1-6 years |
In this position, the successful candidate will apply her/his skills and expertise in protein biochemistry to assist in purifying protein targets bound by Atreca antibodies so that they may be identified using protein sequencing techniques. These methods include immunoprecipitation, chromatography and other protein biochemistry techniques. | 1/7/2019 |
| 1297 | Arthrex Naples, FL QA Rotational Engineer BS in engineering Exp: 0-2 years |
This is a rotational program for the Global QA and RA departments. The scope of the rotation is limited to Florida, to include Arthrex INC, AMI, and ALC. The associate is responsible for supporting the QA/RA Departments with quality related support for improving and maintaining the Arthrex global Quality Management System (QMS) to ensure compliance to FDA QSR, ISO 13485, and all other applicable regulatory requirements. This is to be accomplished developmentally by working in various sectors of QA/RA, to include Product Surveillance, Quality Systems and Regulatory Compliance, Pre-Production Quality, Supplier Quality, Regulatory Affairs, and Manufacturing Quality Engineering. | 1/7/2019 |
| 1298 | Avid Bioservices Tustin, CA Sr. Research Associate/Research Associate, Upstream Cell Culture Process Development BS or MS in biological sciences Exp: BS: 2-4 years, MS: 1-2 years |
We are seeking a Research Associate/Sr. Associate, Process Development who is interested in pursuing a career in developing biologics and pharmaceutical agents. The Research Associate/Sr. ("RA") will assist process development in developing and optimizing scalable processes with improved product yield and reduced costs for manufacturing systems. In addition, the Sr. RA may assist with the maintenance of production equipment and may research and implement new methods and technologies to enhance process operations. | 1/7/2019 |
| 1299 | Azzur Great Boston Area, MA Engineer II BS in engineering or other applied scientific discipline Exp: 1-4 years |
The following is a short list of the typical responsibilities and deliverables of any given project. The level of knowledge expected will be commensurate with level of incoming experience: Development and editing of SOP, validation test procedures, and project plans. Thermal mapping of temperature controlled chambers, warehouses, and SIP processes, tehnical report writing and presentations, and data analysis. | 1/7/2019 |
| 1300 | Bausch Health Bothell, WA Electrical Engineer I, Energy-Based BS in EE required Exp: 1-2 years |
The successful candidate will implement conceptual/product designs for performance, innovation, reliability, and cost. S/He will not only conceptualize solutions, but follow through with detailed design supervision, prototyping, testing, supplier management, and documentation. S/He should have strong written and verbal communication skills and openness to working in a team environment. Specifically, to assist the Energy-Based Devices department in the R&D of current/future devices, which are based on electromagnetic and mechanical energy (i.e. RF, Optical, Lasers, and Ultrasound). | 1/8/2019 |
| 1301 | Baxter Opelika, AL Quality Lab Technician I BS in Chemistry or biological sciences Exp: 0-2 years |
This position is intended to perform Quality Control Testing to support acceptance of raw materials and finished product. This position will cross-train to perform all laboratory tests to support dialyzer manufacturing. These tests will include microbiological, chemical, and performance tests. Performs required tests in the performance, microbiological, and chemical labs on finished dialyzers and raw materials to support product acceptance. This includes performing analyses, calibrations and maintenance on multiple lab equipment/instruments and entering results in the Guardus system. May assist with environmental and process media monitoring by taking samples and testing as required by defined procedure. Maintains cleanliness of labs and lab instruments | 1/8/2019 |
| 1302 | Baxter Round Lake , IL Engineer II BS or MS in Engineering Exp: BS: 2-4 years, MS: 1-3 years |
Individual will be expected to review individual complaints and associated service data to determine risk level and complete investigation into the “As Determined” problem and cause coding for each complaint. Code selected based upon the overall understanding of electro-mechanical device design file and associated risk files. From this, they will recommend, and/or support projects for process improvements to the quality system as approved by management. | 1/8/2019 |
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| 1304 | Sea-Bird Electornics Bellevue , WA Production Engineering Technician I BS or AS in Electrical engineering or related Exp: New college grads encouraged to apply |
This position reports directly to the Production Engineering Manager. A Production Engineer Technician is accountable for the following: Electronic hardware debugging and troubleshooting to the components level, use electronic test equipment including bench top power supplies, DMM, oscilloscope, etc., maintain software for internal company use that supports automation and efficiency (LabView, Python), and design software applications to improve efficiency on the production floor | 1/8/2019 |
| 1305 | Bard (BD) Covington, GA Quality Engineer I BS in engineering or science Exp: 1+ year experience with FDA regulated industry |
This position performs tasks to remediate technical files ensuring compliance to EU MDR and various quality-engineering functions. This includes working to support Design Control projects as well as other duties in support of the Quality System, Design Control System, Document Control, Manufacturing, and the R&D / Product Development departments. | 1/8/2019 |
| 1306 | BD Covington, GA Quality Engineer I BS in engineering or science Exp: 0-2 years |
This position will assist with complaint investigations, quality management remediation efforts and other quality engineering activities as required. Assist with Monthly Reporting Related to Post Market Surveillance. Assist with Engineering representation on Product Development Teams. Develop physical and functional test methods to ensure specifications are met. Develop processes validation requirements (IQ, OQ, PQ) and equipment qualifications. Perform process improvement, control and monitoring on manufacturing processes. | 1/8/2019 |
| 1307 | BD Vernon Hills, IL R&D Engineer BS in engineering or science Exp: 1 internship |
Research and Development Engineering is responsible for developing and implementing new products and product improvements through adherence to established design control processes and good engineering / documentation practices. Works with Business Unit Management and the PPA project team to identify, design, implement and sustain new products/processes. Provides a sound working knowledge of engineering principals, concepts and practices. Performs standard engineering assignments under the direction of others. | 1/8/2019 |
| 1308 | BD Columbus, NE Process Engineer BS Exp: 0 years |
This position is responsible for supporting the manufacturing operation. This individual will develop and implement improved methods of manufacturing, procedures and processes that result in improved efficiencies; yields, machine operations, and quality. Provides technical support to the development group for the implementation of new products or processes. | 1/8/2019 |
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| 1310 | Berg Framingham, MA Lab Operations Specialist I – Precision Medicine AS or BS in Project management or life sciences Exp: 0-2 years |
Reporting to the Chief Precision Medicine Officer, the entry level Laboratory Operations Specialist will process laboratory specimens (aliquoting and accessioning) along with maintain operational activities within the precision group. Process laboratory specimens, including transporting specimens within the lab, centrifugation and aliquoting and labeling specimens. Identify problems with specimen types, missing information, etc. | 1/12/2019 |
| 1311 | Berg Framingham, MA Research Associate I – Functional Lipidomics BS in chemistry, biochemistry or related Exp: 0-2 years |
BERG is seeking a highly motivated individual to join our “Omics” group, reporting to the Chief Precision Medicine Officer. The candidate will join a team responsible for biomarker discovery/validation in multiple disease areas, including neurodegenerative diseases, diabetes, obesity, and cancer, using state-of-the-art quantitative lipidomics platforms. The successful candidate is a highly motivated individual with experience in lipid analysis, lipidomics, or small molecule analysis using LC-MS/MS platforms. | 1/12/2019 |
| 1312 | BioAgilytix Durham, NC Laboratory Technician 2-year technical degree Exp: None |
Responsible for the routine maintenance of laboratory equipment including performance checks, preventative maintenance, and logbook completion and maintenance, ensuring calibrations are performed as scheduled and documented in logbooks and electronic systems. May assist with developing and reviewing equipment SOPs and to ensure adherence to GLP, GMP, GCP | 1/12/2019 |
| 1313 | BioAssay Systems Hayward, CA Scientist- Manufacturing College degree in chemistry, biochemistry or biology Exp: 0-2 years |
We are currently looking for an enthusiastic scientist 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. | 1/12/2019 |
| 1314 | BioAssay Systems Hayward, CA SCIENTIST - ASSAY DEVELOPMENT College degree in chemistry, biochemistry or biology Exp: 0-2 years |
We are currently looking for an enthusiastic scientist 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. | 1/12/2019 |
| 1315 | Biocare Medical Columbus, OH Lab Services Laboratory Assistant BS in relevant biological science Exp: 1-2 years |
Work as part of Lab Services team to provide support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers. | 1/12/2019 |
| 1316 | Biocytogen Wakefield, MA PK/PD Research Associate BS or MS in biological sciences Exp: 1-2 years |
Major responsibilities of the PK/PD Research Associate include performing prelinical pharmacology studies, understand in vivo efficacy/toxicity studies and PK/PD data, and prepare experimental result summaries and reports. | 1/12/2019 |
| 1317 | Biodesix Inc Boulder, CO Laboratory Technician BS in chemical, physical, or biological sciences Exp: 0 years |
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. The position also works closely with the Development and Operations management team, the Laboratory Directors, as well as cross-functional team members in Customer Service, Quality and other departments as needed. Ongoing training will be provided to supplement key skills required to perform the functions of this position as applicable. | 1/12/2019 |
| 1318 | Bioduro San Diego, CA Oncology Research Associate S in scientific field Exp: 0-3 years lab experience |
The Research Associate is responsible for implementation of in vivo, pharmacology or toxicology studies through animal handling in a vivarium or laboratory environment; including compound administration by multiple routes – dosing, tumor implanting and harvesting tissue and blood samples. Surgical and necropsy techniques are preferred for senior level candidates. | 1/12/2019 |
| 1319 | Biogen Cambridge, MA Associate Sci II/Engineer I, Protein Formulation and Process Development BS or MS Exp: BS: 2-4 years, MS: 0-2 years |
As a member of Biogen’s Drug Product development team, the candidate will be responsible for providing formulation and process development support for injectable protein drug product development programs. Planning, executing, and communicating results from laboratory studies is a requirement of the position. Laboratory support of department innovation initiatives is also an expectation of the position. | 1/12/2019 |
| 1320 | Biogen Cambridge, MA Engineer I, Process Biochemistry BS or MS in biochemistry, chemistry, chemical engineering or related Exp: BS: 0-4 years, MS: 0-2 years |
The candidate’s primary responsibilities will be to design and execute lab-scale chromatographic process development studies, analyze process and product quality data, participate in viral clearance studies, author development reports, and evaluate innovative new technologies. Critical thinking, problem solving, and collaborating with other functional groups within Protein Development are keys to success for this role. | 1/12/2019 |
| 1321 | Biogen Research Triangle Park, NC Engineer I / Associate Scientist II, Cell Culture Development (Small Scale) BS or MS in Bio/Chemical Engineering Exp: 0-5 years |
This position will focus on development of high productivity and robust cell culture processes through classically and statistically designed experiments. The candidate’s goals will be to increase process robustness and productivity through comprehensive understanding of levers important to mammalian cell culture. A major component of the role will involve conducting and documenting laboratory bioreactor experiments with a focus on process definition and understanding, experimental design and troubleshooting, and data analysis. The ideal candidate will be able to work collaboratively with pilot scale and tech transfer teams for execution of development projects. In addition, the ideal candidate will contribute to improving laboratory process workflows, making laboratory work more efficient and with greater impact. The right candidate may also contribute to novel laboratory technology or continuous improvement projects. Candidates must be strong team players and have an ability to collaborate effectively on complex projects. A strong affinity for the laboratory with demonstrated success using those techniques is expected. | 1/12/2019 |
| 1322 | Biogen Research Triangle Park, NC Engineer I / Associate Scientist II, Cell Culture Development (Small Scale) BS or MS in Bio/Chemical Engineering Exp: 0-5 years |
This position will focus on development of high productivity and robust cell culture processes through classically and statistically designed experiments. The candidate’s goals will be to increase process robustness and productivity through comprehensive understanding of levers important to mammalian cell culture. A major component of the role will involve conducting and documenting laboratory bioreactor experiments with a focus on process definition and understanding, experimental design and troubleshooting, and data analysis. The ideal candidate will be able to work collaboratively with pilot scale and tech transfer teams for execution of development projects. In addition, the ideal candidate will contribute to improving laboratory process workflows, making laboratory work more efficient and with greater impact. The right candidate may also contribute to novel laboratory technology or continuous improvement projects. Candidates must be strong team players and have an ability to collaborate effectively on complex projects. A strong affinity for the laboratory with demonstrated success using those techniques is expected. | 1/12/2019 |
| 1323 | Biogen Research Triangle Park, NC Associate II , Inventory Control Except BS Exp: 0 with some inventory control knowledge |
Performs PM revisions, & other CMMS inventory management tasks. The incumbent maintains knowledge of planned preventive maintenance techniques and procedures; maintains good working knowledge of mechanical equipment to provide support to Maintenance, Manufacturing, I&C and Engineering staffs, and functions as the primary contact for all inventory related issues for MRO purchases and stock. | 1/12/2019 |
| 1324 | BioLegend San Diego, CA Quality Control Associate I - Cell Biology BS in life science Exp: 6+ months of lab experience |
In this role, you will be responsible for Western blot (WB), Immunoprecipitation (IP) and Immunocytochemistry (ICC) testing of BioLegend products such as antibodies and reagents for cell biology and related research fields. You will also assist with preparation of cell lysates and culturing of various cell lines, performing experiments (e.g. lysate preparation, cell culture, WB/IP/ICC testing), production and analysis of reliable, reportable data, maintaining accurate documentation, utilization of internal company databases for product filing and retrieval, following company SOPs and ISO requirements. | 1/12/2019 |
| 1325 | BioLegend San Diego, CA Quality Control Associate - Flow Cytometry BS in life science Exp: 1+ years of lab experience |
he employee will perform surface, intracellular, and multicolor testing and analysis, and will assist with preparation of primary cells and culture of various cell lines, as well as the set-up of cell stimulations needed for testing. Primary responsibilities include performing experiments (e.g. cell culture, cell preparation and flow cytometry testing); production and analysis of reliable, reportable data; maintaining accurate documentation; utilization of internal company databases for product filing and retrieval; following company SOPs and ISO requirements. | 1/12/2019 |
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| 1327 | BioLegend San Diego, CA Immunoassay Manufacturing Associate BS in biology, chemistry Exp: 1+ years |
The Manufacturing Associate will be working closely with the manufacturing lead and others on the team to ensure the timely production of high quality multiplex bead-based immunoassay products. The primary responsibilities for this position are performing antibody beads conjugation, antibody biotinylation and immunoassay testing, planning and production of immunoassay components and kits following Standard Operating Procedures (SOPS), investigating issues associated with production and identifying root causes, maintaining production batch records and ensuring accuracy and completeness, organizing and updating document files for manufacturing activities under ISO13485:2003 standards, maintaining accurate inventory of supplies and finished products, an documenting work details and helping others when needed. | 1/12/2019 |
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| 1329 | BioLegend San Diego, CA Research Associate Cell Analysis BS in life sciences Exp: 1+ year of lab experience |
BioLegend is seeking a highly motivated Research Associate to join our fast-growing, dynamic and collaborative Product Development team in San Diego. This position will actively participate in all stages of the development, optimization and validation of new products, including antibodies, proteins, and other probes for various research fields. The primary responsibilities include performing experiments (e.g. cell culture and flow cytometry), analyzing and reporting data, maintaining accurate documentations, etc. | 1/12/2019 |
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| 1331 | Biomarin San Rafael, CA Lab Operations Assistant (TEMPORARY) BA Exp: 0-2 years |
Lab Operations Associate - we are seeking an organized, detail-oriented, problem-solving individual. The successful candidate will have strong attention to detail, great communication skills, ability to prioritize a variety of tasks, and the ability to work independently. The Lab Operations Associate supports R&D scientists and research associates so they can keep developing our great products with speed, efficiency, and fun. This position reports to the Associate Director of Research Lab Operations. | 1/13/2019 |
| 1332 | Alan Lab San Diego , CA Chemistry Lab Technician AS or BS in chemistry or chemical engineering Exp: 2+ years required for AS, 0+ years for BS |
A Chemistry Lab Technician will be responsible for 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. 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. | 1/2/2019 |
| 1333 | Alcami Charleston, SC Assistant Scientist I Analytical BS in science Exp: 0-2+ years |
The Assistant Scientist I Analytical is accountable for performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Assistant Scientist I may also be required to work on method development/method validation projects. Typical types of testing includes: assays (potencies, related substances, residual solvents, metals, etc.), rate of release (dissolution), 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, AA and IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by the company). The role will work on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. | 1/2/2019 |
| 1334 | Alcon Sinking Spring, PA Quality Assurance BS in Engineering or Science Exp: 1-2+ years in Medical Devices/Pharma |
The Quality Engineer is responsible for working with the Quality and Manufacturing teams to support activities during the overall product life cycle of the assigned production area(s). The QE will support improvement projects, quality issue resolution, Non-conformances/CAPAs, process control, product transfers and validations. In some cases, the QE will be required to lead small to medium size projects. Responsibilities include data collection and analysis, implementation and revision of product conformance standards, continuous process improvement, reduction of reject levels and assigned projects and change control tasks, etc. Ensure there are adequate product and process controls in place for identified critical or major quality attributes/process parameters within assigned production area(s). Complete gap analysis against local, global, and industry standards, as needed, and support development/execution of actions to close gaps under minimal guidance. | 1/2/2019 |
| 1335 | Aldevron Fargo, ND Validation Engineer BS in Science/Engineering Exp: 0 years |
We are seeking a Validation Engineer to write and review validation documents, conduct performance testing, and oversee the validation of facilities, equipment, laboratories, and processes. Applicants should have a bachelor's degree in science or engineering. Participate in all phases of process validation, including process, cleaning, shipping and continued process verification activities. | 1/2/2019 |
| 1336 | Abbott Pomona, CA Research Associate I BS/BA in Chemistry, microbiology, biology, biochemistry or equivalent Exp: 1 year lab experience |
Key responsibilities for the Laboratory Technician are: Executing standard operating procedures for the supportof company products;maintaining documentation of signatures, dates,labels etc.,relating to laboratory supplies and operation of laboratory equipment | 1/2/2019 |
| 1337 | Abbott San Diego , CA Clinical Trial Assistant BS/BA in science or related field Exp: 0-2 years |
The Clinical Trial Assistant (CTA) is an integral member of the Clinical Affairs Department providing direct in-house support of clinical research investigations. Working under supervision, the CTA is responsible for the management and maintenance of the clinical central files (CCF), tracking and shipping of investigational product (IP) and other study related shipments, maintenance of study equipment, updating study related trackers and providing quality administrative support to our clinical research studies and the overall Clinical Affairs team. | 1/2/2019 |
| 1338 | Alkahest San Carlos, CA Research Assistant / Research Associate (in vivo) BS in field related to biomedical research/neuroscience/animal science 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. Responsibilities include design, planning, and performing rodent in vivo studies. | 1/2/2019 |
| 1339 | Alkahest San Carlos, CA Next Generation Sequencing Research Associate BS in Science/Engineering Exp: 1+ years working with biological samples for NGS |
The position necessitates Next-Gen Sequencing (NGS) experience to run bulk- and single cell RNAseq experiments, including library construction for Illumina sequencing. Resp |