3445 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
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| Job Information | Description | Date Added | |
| 1 | Idexx Worthington, OH Medical Lab Technician - Parasitology - temporary HS diploma/AS/BS Exp: 1+ year(s) |
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: Parasitology: Examining samples to identify parasites, utilizing fecal flotation and various microscopic techniques. etc. | 3/9/2020 |
| 2 | ThermoFisher St. Louis, MO Biopharmaceutical Technician II- Nights HS Diploma/GED, BS/BA preferred Exp: 1-2 years in GMP preferred |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 3/7/2020 |
| 3 | ThermoFisher Miami, FL Manufacturing Technician I HS Diploma/GED Exp: 0-1 years |
Commitment to Safety, by following site safety procedures and utilizing safety equipment as required for daily tasks. Ability to document Near Miss reports, safety opportunities, accident reports, etc. Uses batch record instructions, job aids, standard operating procedures, and product specifications to execute production activities. Maintains accurate documentation, records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization). | 3/7/2020 |
| 4 | Fluke Glenwood, IL Field Support Technician II unspecified Exp: 1-2 year(s) |
Performs calibration and repairs of assigned test and measurement products and equipment: Basic calibrations. Analyzes, troubleshoots, makes repairs, resolves technical problems and performs maintenance service on equipment returned to the service center by customers. Achieves a timely turn-around on all equipment and service. Enters data into Oracle and/or an asset tracking database. etc. | 3/4/2020 |
| 5 | Fluke Glenwood, IL Laboratory Technician II BS in a life science or comparable Exp: 1-2 year(s) |
We are seeking an individual to join our growing Laboratory operations team. Please read on if you are looking for a start to a long term career. Calibrates radiation detection equipment using ionizing radiation sources/techniques. Assures customer satisfaction and on time delivery of calibrated devices. Able to meet production rates. Reviews generated analytical data before assignment of official calibration certificate. etc. | 3/4/2020 |
| 6 | Fluke Everett, WA Production Assembler/Operator HS diploma or equivalent Exp: 1-2 year(s) |
Product Assembler/Operators perform wet, dry, mechanical and/or electromechanical processes to produce quality saleable product (components, instruments and/or systems). Position may require extended periods of stationary work in assembly and/or light fabrication. Primary Responsibilities: Prepare, process, wind, clean, install, assemble, rework, calibrate, test, solder and/or inspect product at various stages of assembly from component to final. etc. | 3/4/2020 |
| 7 | Takeda Social Circle, GA Manufacturing Technician I AA or equivalent, or BS/BA Exp: BS/BA: 0 years, AS/AA: 1 year |
Executing processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Clean, Set up, operate, and teardown of equipment such as tanks, filtration systems, and production lines. Operate general production equipment (such as pH and conductivity meters, autoclave, portable mixers, etc.). | 2/29/2020 |
| 8 | Teligent Buena, NJ Clean Room Services Operator – 3rd Shift HS Diploma/GED Exp: 1 year in topical/steril filling/manufacturing |
Cleaning and sanitization of controlled cleanroom environments such as Equipment Preparation rooms, , and all ancillary areas. Additional responsibilities may include cleaning and sanitization of process tanks, mixers, compounding and filling equipment, product formulation processes, terminal product sterilization, finished product inspection, etc. Proactively identify equipment issues and perform root cause analysis, make recommendations and aid in implementation for more complex and non-reoccurring issues. | 3/1/2020 |
| 9 | Stryker Portage, MI Design Engineer - Mechanical BS/BA in mechanical engineering Exp: 0-3 years |
As a Design Engineer- Mechanical, you will work to develop innovative new products for the Surgical technologies group. A passion for innovation and creativity is desired for this role. Plan and conduct engineering research, design, development projects as assigned. Monitor and control progress of projects to ensure sound application of engineering principles are used and design intent is being followed/achieved | 2/22/2020 |
| 10 | Stryker San Jose, CA Quality Engineer BS/BA in engineering Exp: 0+ years in regulated manufacturing environment |
As a Quality Engineer you will provide support in quality assurance, control, and preventative activities with a focus on continuous improvement of internal products and processes. You will own identified internal and supplier driven non-conformances and manage the timely closure of NC's within Trackwise. You will communicate with suppliers regarding non-conformances, escalating supplier corrective action, changes and process qualifications requests as required. You will engage in the development, improvement and sustaining of the internal manufacturing processes for existing and new products. | 2/22/2020 |
| 11 | Stryker Davie, FL Assembly Technician I HS Diploma/GED Exp: 1 year experience |
"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. | 2/22/2020 |
| 12 | Stryker Leesburg, VA Entry Level Fulfillment Clerk HS Diploma/GED Exp: 1 year related experience/training |
Ensures complete fulfillment of all replenishment orders. Unloads daily shipment of incoming surgical sets and does the precautionary cleaning of incoming sets. Verifies kind and count of replenishments prior to shipping. Processes and stages outgoing replenishments. Performs the last check of replenishments and surgical sets prior to final boxing for shipment | 2/22/2020 |
| 13 | Surrozen South San Francisco, CA Research Associate, Protein Sciences -Protein Expression/Purification BS or MS in protein biochemistry or related Exp: 1-4 years lab experience (class, internship, academic) |
The Research Associate position for Protein Expression/Purification within the Protein Sciences Group is a great opportunity for experienced associates as well as recent graduates to expand their skills in state-of-the-art biochemical techniques while accelerating therapeutic discovery and development in regenerative medicine. Characterize and purify protein samples using SDS-PAGE, chromatography, and related techniques. Perform mammalian cell transfections for recombinant protein expression | 2/23/2020 |
| 14 | Surrozen South San Francisco, CA Research Associate, Protein Sciences - Molecular Biology/Protein Expression BS or MS in protein biochemistry or related Exp: 1-4 years lab experience (class, internship, academic) |
Produce recombinant DNA clones and plasmids using standard molecular biology protocols. Perform small scale transfection in mammalian cells for recombinant protein expression. Characterize purified protein samples by SDS-PAGE and related techniquques. Preparation of presentations, technical reports, summaries and detailed protocols, and contribute to company reports as requested | 2/23/2020 |
| 15 | Surrozen South San Francisco, CA Research Associate - Senior Research Associate, In vivo Pharmacology BS or MS in molecular/cell biology, biochemistry, genomics, etc. Exp: 1+ years research experience |
Help develop and implement disease and injury models for characterization of lead molecules. Conduct independent in vivo studies and contribute to collaborative activities. Perform tissue necropsy. Perform tissue sample analysis, such as clinical biochemistry, ELISA, qPCR and immunohistochemistry. Maintain mammalian cell culture, perform gene expression studies and in vitro functional assays (e.g., RT-qPCR, reporter assays, FACS analysis). | 2/23/2020 |
| 16 | Sutro Biopharma San Carlos, CA Quality Control Associate MS in chemistry, biochemistry, bioanalytical chemistry or scientific related Exp: 1-3 years |
Perform analytical assays on daily basis. The assays include wet-lab chemistry, HPLC, CE, icIEF, ELISA, Electrophoresis, UV spectroscopic based methods, and compendial methods required for the release and stability testing of water, raw material, in-process, and final products. Perform data review and analysis. Support method transfer and validation activities | 2/23/2020 |
| 17 | Editas Medicine Boulder, CO Research Associate II/Senior Research Associate, Analytical Chemistry MS in a life science Exp: 1-2 year(s) |
This new role on the Analytical Chemistry team in Boulder provides a unique opportunity to contribute to Editas’ efforts through the development of the analytical characterization of guide RNAs (identity, purity, stability), mainly in support of Process Development Team in Boulder. Key Responsibilities: Work closely with the Process Development group at the Boulder Colorado site to develop analytical methods and solve technical problems. Develop, execute, and qualify/validate methods for analytical characterization of oligonucleotides (identity, purity, impurity characterization, stability). etc. | 2/25/2020 |
| 18 | Endologix Irvine, CA Quality Assurance Technician HS diploma or equivalent Exp: Entry level |
Performs audits, inspections, configuration checks, and functional testing of in-process materials, parts and subassemblies used in the manufacture of partially assembled or finished medical devices. Responsible for assuring that the company’s products have been manufactured, inspected and tested using company approved procedures documents and equipment. Work with R&D, Manufacturing, and Quality to implement solutions to quality related problems. Coordinates, initiates, and implements Document Change Orders. Reviews quality records to ensure completeness and compliance to applicable quality procedures. etc. | 2/25/2020 |
| 19 | Semma Therapeutics Cambridge, MA Quality Control Associate MS in pharma/biotechnology Exp: 1 year |
This position will perform QC tests for pre-clinical and clinical material from specific manufacturing steps associated with ES derived pancreatic islet production, from cell bank thaw through fil/finish. QC testing will include stability test 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 | 2/16/2020 |
| 20 | Semma Therapeutics Cambridge, MA GMP Manufacturing Associate, Clinical Materials BS/BA in biological/bioengineering/chemical engineering Exp: 6 months in process development/manufacturing |
Perform product manufacturing for clinical materials according to cGMP standards. Includes assembling raw materials, following specific standard operating procedures (SOP), aseptic technique, completing batch records, reporting deviations. Participates and facilitates technology transfer and final process development from the Research to the Manufacturing group. Assists in the development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with Research and Quality Systems groups | 2/16/2020 |
| 21 | LabCorp Overland Park, KS Data Entry Operator/Lab Data Entry HS Diploma/GED Exp: 1-3 years |
Operates various data entry terminals and automated data systems to record and verify billing/accounts receivable information, customer demographic data and laboratory data identification and results, for computer processing. Resolves suspend and billing problems and manually process OE batches. Follows standard sequences and coding in entering and/or keying in data in correcting, editing, and verifying all data entered into automated systems. | 2/16/2020 |
| 22 | LabCorp RTP, NC Molecular Oncology Tech Trainee/Technologist (1st Shift) BS/BA in biology/chemistry Exp: 1 year in clinical OR research lab |
Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. | 2/16/2020 |
| 23 | LabCorp Dublin, OH Medical Technologist - Virology BS/BA in biology/chemistry/med tech/etc. Exp: 1 year in clinical lab experience |
This position will work within the Virology section of the microbiology department.Testing performed will include Virology testing, IFOBT, H.Pylori breath bag testing and cepheid testing. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. | 2/16/2020 |
| 24 | LabCorp Shelton, CT Laboratory Technologist Trainee - Histology BS/BA in biology or chemistry Exp: 1 year in research lab |
Perform all technical grossing procedures required to process and submit specimens for microscopic review as per standard operating procedures under the indirect and direct supervision of pathologists. Operate and maintain automated tissue processors, perform tissue embedding, Cryostat sectioning, operate and maintain tissue embedding units. Operate and maintain H&E stainers, IHC stainers, special stains stainers and coverslipping units, perform manual coverslipping | 2/16/2020 |
| 25 | LabCorp Burington, NC Specimen Processing Specialist (1st Shift) HS Diploma/GED Exp: 1-3 years in clinical lab |
This position will have first shift hours with the following schedule: 9:00am-5:30am Tuesday to Saturday. This is a multi-discipline role 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. Assigns specific computer generated identification numbers, checks for accuracy and records all items processed. Performs all paperwork, technical and non-technical procedures required to process and submit specimens. | 2/16/2020 |
| 26 | Signant Health Blue Bell, PA Application Specialist BS/BA in comp sciences Exp: 1-3 years in SQL knowledge |
Perform requirements gathering and business analyst tasks for eCOA collection, reporting and data transfer. Provide guidance to the client on the most suitable solution, ensuring that all recommendations are achievable within the scope of the product. Develop eCOA solutions using proprietary TrialMax platform (Web, Slate, Touch) according to the requirements gathered and interpretation of the client clinical protocol. Present eCOA solutions at client design review and testing (UAT) meetings at customer sites (as required) | 2/16/2020 |
| 27 | SonoSite Bothell, WA Manufacturing Associate (2nd shift Transducers, Temporary 12 months) HS Diploma/GED Exp: 0-1 years in high tech manufactruing |
Follow all required procedures such as Assembly Instruction, Personal Protective Equipment, and Device History Record while performing the job responsibilities. Weighing and mixing epoxy-based materials. Cleaning and assembling high precision molds. Light mechanical assembly of small components using hand tools and torque drivers. Work with hands under a microscope performing hand soldering of fine pitch cables and flexible circuits. | 2/17/2020 |
| 28 | Sprint Cleveland, OH Sales and Customer Support Associate BS/BA Exp: 0-2 years in sales/customer support role |
Accurate, efficient and timely data management within CRM (Customer Relationship Management) Tool. Order processing and shipment. Provide phone support and coaching to patients, physicians and other internal and external resources. Assists sales team in lead creation and account management. Supports sales team by recording patient procedure and follow-up data | 2/17/2020 |
| 29 | Colopast Coral Springs, FL Inside Sales Representative (Physician Relationship Manager) HS diploma or equivalent Exp: 1+ year(s) |
Comfort Medical, a wholly owned subsidiary of Coloplast, is seeking an Inside Sales Representative to join our team in our Coral Springs office. You will build your own sales relationships/accounts, resolve customer questions, and offer solutions to drive company revenue. Your primary call points will include Physicians' and healthcare providers' offices. Comfort Medical preferred manufacturers, and customers. This role is heavily phone-based. Responsibilities: Present and sell company services to new and existing customers. Prospect and contact potential customers. Achieve agreed upon sales targets by the deadline. etc. | 2/17/2020 |
| 30 | Corvus Pharmaceuticals Bulingame, CA Animal Technician/Lab Assistant AS/BS in biology or related Exp: 0-2 years |
Role and Responsibilities: Performs the general husbandry of research animals for experimental purposes. Performs animal welfare checks. Performs cell inoculations via multiple routes (SC, tail vein, RO). Performs dosing via multiple routes (IV, PO, SC, IM). Performs necropsy/tissue sample collection for evaluating PD endpoints. Performs bleeding via multiple techniques (RO, cardiac punch, cheek) for evaluating drug PK. Performs various vivarium cleaning duties. etc. | 2/17/2020 |
| 31 | Covance Madison, WI Research Assistant (I) - Immunotoxicology BS/BA in a related scientific field Exp: 1-2 year(s) |
We have a great opportunity for a Research Assistant (I) - Immunotoxicology in our Immunology and Immunotoxicology (InI) Group in Madison, WI. Covance’s work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients' lives while growing your career. In this role, you will set up and prepare equipment for sample processing, data acquisition/analysis according to study protocol, Policies/SOPs, Methods, and regulatory guidelines. You will also be responsible for performing assays, maintenance, and general laboratory support duties. Organizes and conducts routine and non-routine processing in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. Documents work and maintains study documentation and laboratory records. etc. | 2/17/2020 |
| 32 | Covance Greenfield, IN Sampling Handling I Assistant HS diploma or equivalent Exp: Entry level |
In this role it’s a unique combination of sample management and archive tasks, including labeling, receipt, transferring, tracking, inventory, archival, shipping, and disposal of samples and/or materials. Samples include paper data, wet tissues, slides, blocks and frozen biological samples. Excellent keyboarding skills required as this position will have a high degree of data input into tracking and archive database, may involve repeated lifting of up to 50 lbs. Excellent customer service skills are required as position interfaces with internal and external customers in retrieving and storage of samples all while maintaining strict business confidentially. etc. | 2/17/2020 |
| 33 | Covance Salt Lake City, UT Sample Handling Assistant HS diploma or equivalent Exp: Not required |
Job Overview: Performs any combination of sample management and/or archive tasks, including labeling, receipt, transferring, tracking, inventory, archival, shipping, and disposal of samples and/or materials. Sample accession core tasks, including box opening, inventory/labeling, receipt/store, and pulls/returns. Uses tracking systems as appropriate to maintain sample and study integrity. Accurate protocol and relevant documentation interpretation (i.e., Sample Analysis Outline, client paperwork). Document and communicate discrepancies to appropriate personnel, and assists with problem solving. etc. | 2/17/2020 |
| 34 | CTK Biotech Poway, CA Production Assistant AS/BS Exp: 0-3 years |
The Production Assistant is mainly responsible for manufacturing biological products following SOP and maintaining production related records. Essential Duties and Responsibilities: Production of Recombinant proteins, monoclonal antibodies, and other biologics per work instruction. Conducting general lab maintenance, including glass washing, buffer/reagent preparation, proper disposal of waste, and inventory organization. etc. | 2/17/2020 |
| 35 | CTK Biotech Poway, CA Production Associate MS Exp: 1+ year(s) |
The Production Associate is mainly responsible for manufacturing biological products following SOP, maintaining production records and generating production document. Essential Duties and Responsibilities: Produce qualified antigens, antibodies, and other biologics per work instruction. Conducting general lab maintenance, including glass washing, buffer/reagent preparation, proper disposal of waste, and inventory organization. Communicating constantly with team members and related departments. etc. | 2/17/2020 |
| 36 | Biotronik Lake Oswego, OR Master Data Analyst BS/BA Exp: 1-3 year(s) |
BIOTRONIK is looking to add a Master Data Analyst to our Finance and Sales Operations team. The Master Data Analyst will be the gatekeeper to all master data and is critical to the overall success of the organization. This position is responsible for overseeing key processes and projects associated with the accuracy, integrity and timeliness of critical master data domains. The analyst will take an active role in fulfilling the additional demand generated by the organization changing into to a data-driven company and help develop the tools to educate and empower stakeholders. Analysts in this position are also responsible for analyzing large amounts of data to develop data management recommendations, effectively communicating related results and implications of the various options across multiple integrated teams. etc. | 2/11/2020 |
| 37 | Bioventus Union County, NJ Associate Sales Representative - New Brunswick, New Jersey BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 38 | Bioventus Worcester, MA Associate Sales Representative - Worcester, MA BS/BA Exp: 0-2 year(s) |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. etc. | 2/11/2020 |
| 39 | Bioventus Bozeman, MT Sales Rep - Montana BS/BA in sports medicine or life sciences Exp: 1-3 year(s) |
The Sales Representative plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. They also educate patients on the proper use of our products. The Sales Representative is fully responsible for managing their own territory – a role that’s perfectly suited to highly motivated self-starters with an entrepreneurial spirit! Ideal candidates have strong interpersonal skills and determination to provide the best possible experience to our customers and coworkers. They strive for excellent performance, driven by the willingness to both teach and learn. They are good team players, dynamic, optimistic, accurate, well-organized, and ambitious about developing as a sales professional. etc. | 2/11/2020 |
| 40 | BlueRock Therapeutics Toronto, ON Research Associate, Immunology MS in immunology, cell biology, or molecular biology Exp: 1 year |
We are seeking a Research Associate for our Translational Immunology Team. This position will report to the Scientist of Translational Immunology and will have various responsibilities for hands-on lab work, developing T cell, NK cell and myeloid cell assays. This is an outstanding opportunity for a talented associate to contribute to bringing a new class of cellular therapies to patients and gain valuable career experience in Translational Immunology in the life sciences industry. We are seeking a Research Associate for our Translational Immunology Team. This position will report to the Scientist of Translational Immunology and will have various responsibilities for hands-on lab work, developing T cell, NK cell and myeloid cell assays. etc. | 2/11/2020 |
| 41 | Boston Analytical Cambridge, NH Microbiologist BS/BA in microbiology or related Exp: 0-2 year(s) |
The QC Microbiologist I 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 through compendial methods and client specific test protocols. Primary Duties and Responsibilities: Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). Performs genetic analysis of microbial growth to determine Genus/Species of unknown isolates. Collects Environmental Monitoring Samples onsite and offsite at client manufacturing sites. Documents work in a clear and organized manner. etc. | 2/11/2020 |
| 42 | Brooks South Plainfield, NJ Bioinformatics Scientist MS in bioinformatics Exp: 1-3 year(s) |
Responsibilities: Work collaboratively with bench scientists, comprehend project objectives, evaluate and provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows. Integrate statistical analysis to project design and data interpretations. Work closely with IT specialists to build robust infrastructure. Support company intellectual property management. Support NGS with data analysis and delivery, pipeline development and automation. Provide customer support for NGS data analysis results. Support Sales and Marketing departments and related business development efforts. | 2/11/2020 |
| 43 | Brooks South Plainfield, NJ Associate Scientist, Clinical Development BS in a biological science Exp: 1+ year(s) |
The Associate Scientist position in our Clinical Services department is a great entry-level role with room for growth and advancement. If you have the desire to work in a casual yet results-driven environment that embraces innovation- then you’re just what we’re looking for! Responsibilities: Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies. etc. | 2/11/2020 |
| 44 | Brooks South Plainfield, NJ Sales Associate I BS in a life science Exp: 1+ year(s) |
Responsibilities (maximum 8 key tasks and responsibilities of this position): Conduct marketing and sales independently in academic and small biotech accounts including hall walking, planned meetings, vendor shows, lunch and learns, and cart shows. Conduct sales strategy, account management, partnership negotiations, and phone/email prospecting under the direction of the manager/team lead. Achieve defined metrics for sales activity revenue growth in assigned accounts. Update price lists, create new price lists, and write quotes. Execute CDA's, service agreements, and other documents. etc. | 2/11/2020 |
| 45 | Brooks South Plainfield, NJ Inside Sales Associate BS in a life science Exp: 1+ year(s) |
The Sales Associate is expected to grow the revenue and expand the GENEWIZ brand in the assigned territory/accounts with strong support, direction and mentoring by the Assistant Manager, Inside Sales Team. Key work interactions (main interfaces with who the jobholder will have regular contact): Co-workers, Managers, Customers. Responsibilities (maximum 8 key tasks and responsibilities of this position): Achieve annual sales goals within defined territory/ accounts. Develop and implement an effective territory business growth plan. Conduct sales and marketing activities independently in academic and biotech accounts. Conduct sales strategy, account management, partnership negotiations, and phone/email prospecting under the direction of the manager. etc. | 2/11/2020 |
| 46 | Brooks Cambridge, MA Laboratory Technician I HS diploma/AS/AA Exp: 1+ year(s) |
Our Lab Techs are: 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. etc.Our Lab Techs are: 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. etc. | 2/11/2020 |
| 47 | Renaissance Lakewood, NJ Associate Microbiologist I BS/BA in natural sciences Exp: 0 years |
The Associate Microbiologist performs various types of microbiological testing under supervision. Evaluates, and records data. Assists lab management and microbiologists as directed. Schedule flexibility is required. This is a salaried position and exempt from overtime pay. | 2/8/2020 |
| 48 | Repligen Rancho Dominguez, CA Assembler I HS Diploma/GED Exp: 0-1 years in production/manufactruing |
This assembly position performs a wide variety of fiber assembly, filtration product assembly or sub-assemblies. Determines and/or follows methods and sequence of operations in performing fiber bundling, filter potting, filter welding, fitting on assembly units and packaging. The employee also works as a team member in whatever capacity and job function is required to deliver a quality product to our customer in a timely fashion. | 2/8/2020 |
| 49 | Repligen Waltham, MA Manufacturing Associate II- Biomanufacturing 2nd Shift BS in biological sciences or related Exp: 0-2 years in biotech manufacturing |
This position is for the 2nd shift in the Biomanufacture group, however; cross training into other departments may be required. The successful candidate will play a key role in ensuring that the department’s production and quality goals are met. Applicants must have strong technical knowledge and problem-solving skills. Must be able to follow oral and written instructions accurately, learn complex tasks quickly, and complete tasks in a timely manner. Experience working in a GMP/document-controlled environment would be beneficial. Attention to detail, and the ability to work in a team environment are essential. | 2/8/2020 |
| 50 | Repligen Marlborough, MA Manufacturing Technician HS Diploma/GED Exp: 1+ years in membrane related processes |
. The successful candidate will play a key role in ensuring that the department's safety, Quality, and Production goals are met. Experience working in a classified cleanroom, and knowledge of GMP/ISO/document controlled processes and GDP would be beneficial. Attention to detail, and the ability to work in a team environment are essential. Ability to read and understand standard operating procedures is required. | 2/8/2020 |
| 51 | ReShape Life Sciences San Clement, CA Administrative Assistant HS Diploma/GED Exp: 1+ years in administrative support |
The Administrative Assistant will assist management and all visitors to the company by handling office tasks, providing polite and professional assistance via phone, mail and e-mail, making reservations or travel arrangements and generally being a helpful and positive presence in the workplace. The Administrative Assistant should be professional, polite and attentive while also maintaining accuracy and willing to meet challenges directly. | 2/8/2020 |
| 52 | Philips Monroeville, PA Usability Validation Engineer BS/BA in engineering Exp: 1+ years in engineering on med devices |
The selected candidate will work under direct supervision of the Engineering Lead to produce clear and concise validation documents for medical devices. Focus will be designing and conducting usability test programs in accordance with IEC 62366-1 and FDA Guidance “Applying Human Factors and Usability Engineering to Medical Devices” in conjunction with ISO14971. | 2/8/2020 |
| 53 | Philips Gainesville, FL Assembly Technician 1, Second Shift HS Diploma/GED Exp: 1 year in manufacturing |
Set and operate production equipment for the purpose of assembling our MRI coils during our second shift, 3:30pm to 12:00am. Performing various repetitive electronic assembly operations on components or subassemblies (under supervision). Using schematics or blueprints, wiring lists, and verbal and written instructions to assemble, modify, rework, or reassemble units. Properly executing the established process and the process parameters | 2/8/2020 |
| 54 | Rockland Limerick, PA Associate Scientist (Quality Control) BS/BA in biological/chemical sciences Exp: Entry Level |
We are seeking a talented and highly motivated team player as an addition to our Quality Control (QC) Department. The applicant should be highly motivated, demonstrate broad scientific knowledge, problem solving and troubleshooting skills, show attention to details, high level of independence and display a fundamental understanding of immunoassays. | 2/8/2020 |
| 55 | RS Medical Shreveport, LA Field Support Representative HS Diploma/GED Exp: 6 months in clinical/hospital/med office setting |
The Field Support Representative works with a Sales Account Manager within a defined sales account base to assist and support in clinical and administrative duties. Support the daily order flow within established sales accounts. Schedule patient education sessions in a timely manner. Control and account for all product inventory. Conduct patient education sessions within a clinical setting on the use of the prescribed RS Medical product. | 2/8/2020 |
| 56 | Sanofi Ridgefield, NJ Aseptic Technician Associate HS Diploma/GED Exp: 1-3 years in cGMP environment |
Aseptic Technician Associate will Independently perform the tasks of the production operation specific to aseptic manufacturing, filling, and packaging. Maintains batch record documentation and logs as required by corporation and regulatory agencies. Performs cleaning and sanitizing of production equipment and classified production space. Prepares, according to procedures, various stock solutions and buffers as required by the production process. | 2/8/2020 |
| 57 | Sanofi Swiftwater, PA Maintenance Technician 2 year trade certificate in HVAC or general mecahnics Exp: 0-1 years |
The Maintenance Technician is responsible for supporting the design, installation, maintenance, troubleshooting and repair of all site-wide equipment in order to maintain a Quality Class A environment in GMP facilities. This position will have interactions with HSE, Engineering, Outside Contractors/Consultants, Industrial Operations and Research & Development departments. | 2/8/2020 |
| 58 | SCA Pharma Little Rock, AR Aseptic Sanitization Specialist (3) HS Diploma/GED Exp: 1 year in pharma |
The Aseptic Sanitization Specialist will be responsible for sanitizing products prior to them entering the cleanroom. The position will also ensure that the detail, scheduling, and methods of cleaning are sufficient according to the standard operating procedures to protect the raw materials, products, clean room (material transfer, formulation, bag fabrication and fill rooms) and non-clean room (cart loading, sterilization and pack-out areas) environments from the introduction of microbial contamination or infestation. | 2/9/2020 |
| 59 | SCIEX Framingham, MA Regulatory Affairs Specialist BS in sciences Exp: 1-4 years in regulatory affairs |
Support the regulatory submission activities to obtain and maintain approvals for commercially distributing in vitro diagnostics products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements. Key Responsibilities:- Supports Design History File development, reviewing documentation for regulatory requirements and current standards. | 2/9/2020 |
| 60 | Purigen Biosystems Pleasanton, CA Research Associate I/II BS in biological/life sciences Exp: 1-3 years in biotech |
The Research Associate will be responsible for growing and maintaining various cell lines for quality control and product validation testing and performing a variety of tests on our unique Sample Preparation Instrument. Execute new and standard protocols for performance testing of Purigen’s custom Sample Preparation platform, including instrumentation and microfluidic chip prototypes. Set-up and execute bioanalytical QC assays, including qPCR, RT-qPCR, fragment sizing (e.g. Bioanalyzer assays) and nucleic acid quantitation assays (e.g. Nanodrop, Qubit) | 2/1/2020 |
| 61 | QuVa Sugar Land, TX Production Technician - Post Compounding HS Diploma/GED Exp: 1 year in pharma manufacturing preferred |
This position supports daily manufacturing activities for non-sterile and sterile bulk/CSP operations. Perform line clearances, assure equipment is operating correctly, and assure Post Compounding checks are performed according to current SOPs and Batch Record Instructions. Maintains records of every movement of Controlled and Non-Controlled Substances from the point they are received from compounding. Monitors the daily use of Controlled and Non-Controlled Substances throughout the process to assure people and processes are in a continuous state of compliance with DEA regulations, company policies and procedures and safety requirements | 2/2/2020 |
| 62 | QuVa Sugar Land, TX Quality Assurance Technician HS Diploma/GED Exp: 1-2 years in FDA regulated operations |
The Quality Assurance Technician performs basic QA functions related to verification of incoming and/or outgoing materials. Quality review / verification of critical information related to the receipt of incoming goods or the distribution of finished goods for customer orders. Ensures compliance of incoming materials prior to use in Manufacturing Operations. Supports packaging of finished goods for customer shipments and verifies accuracy of the order | 2/2/2020 |
| 63 | QuVa Sugar Land, TX Supply Chain Technician HS Diploma/GED Exp: 1-2 years in distribution/warehousing/shipping/etc |
QuVa Pharma is seeking a motivated and organized Supply Chain Technician to complete inventory replenishment process utilizing manual or automated technology. You will be integral in ensuring that inventory is correctly stocked and labeled, protecting the integrity of sterile supplies. Our ideal candidate is highly organized, a master of prioritization and able to shift gears at a moments notice. | 2/2/2020 |
| 64 | Regeneron Rensselaer, NY Associate Process Engineer (Filling) BS or MS in engineering Exp: 0 years |
Provides engineering support for the design and development of robust drug product processes that enable the delivery of life transforming medications to patients globally. The individual will support drug product unit operations from primary container development through drug product filling and inspection, with specialization in the development, industrialization, and technical oversight of primary container components. | 2/2/2020 |
| 65 | Regeneron Rensselaer, NY Process Engineer (Filling) BS or MS in engineering Exp: 0 years |
Provides technical support for the development of robust drug product processes that enable the delivery of life transforming medications to patients globally. The individual will characterize and support drug product unit operations from freeze/thaw through filling and inspection and will be part of a team responsible for development, industrialization, troubleshooting, and validation of drug product processes at our new fill/finish manufacturing site. | 2/2/2020 |
| 66 | Regeneron Rensselaer, NY QC Stability Technician BS/BA in life sciences Exp: 0-2 years |
Performs a variety of activities to maintain stability chambers and stability inventory in support of the company’s quality program. Ensures that equipment operates in a compliant state; qualified, calibrated and properly maintained. Monitors Environmental Chamber conditions, ensuring continuous documentation. Collaborates with Stability Coordinators and other departments to receive material to be put on stability. | 2/2/2020 |
| 67 | AMETEK Wallingford, CT Industrial Maintenance Technician I HS Diploma/GED Exp: 1-3 years |
Maintenance Technician is a multi-disciplined technician responsible for the repair and maintenance of production, support and facility equipment to ensure safe, reliable operation. They also contribute to support activities, continuous improvement efforts and special equipment projects as directed. | 2/3/2020 |
| 68 | Renaissance Lakewood, NJ Associate Microbiologist I BS/BA in natural sciences Exp: 0 years |
The Associate Microbiologist performs various types of microbiological testing under supervision. Evaluates, and records data. Assists lab management and microbiologists as directed. Schedule flexibility is required. This is a salaried position and exempt from overtime pay. | 2/3/2020 |
| 69 | BillionToOne West Menlo Park, CA Laboratory Technician BS in biology or a clinical science Exp: 6+ months |
BillionToOne (Y Combinator S17) is looking for a Laboratory Technician - Clinical Laboratory Associate (CLA) I to perform UNITY, the only non-invasive prenatal test that can detect inherited disorders such as sickle cell disease, spinal muscular atrophy, and cystic fibrosis in the baby directly from maternal blood. You will join our growing CLIA team responsible for processing of pregnancy blood samples in a high complexity CLIA setting. This is a full-time 12-month contract position with an hourly rate of $25/hr. Hours and days may vary depending upon operational needs. The CLA I is responsible for assisting with the day-to-day operations and equipment maintenance in the Clinical Laboratory. etc. | 2/3/2020 |
| 70 | BioFire Diagnostics Salt Lake City, UT BioReagents Formulator - Day Shift AS Exp: 1+ year(s) |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including Film Array. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, RT-PCR real-time PCR, and use of fluorescence based nucleic acid detection techniques. Assists in complex functional testing and troubleshooting product, process material or formulation processes. Applicant must be mathematically competent, detail orientated, and able to follow written directions well. etc. | 2/4/2020 |
| 71 | BioFire Diagnostics Salt Lake City, UT BioReagents Formulator - Swing Shift AS Exp: 1+ year(s) |
This is a full-time non-exempt position. Responsible for manufacturing and formulation of all BioReagents products and sub-assemblies including Film Array. Operates production equipment and performs duties under compliance of cGMP manufacturing. Weighs, measures, and checks raw materials to assure that manufactured batches, lots, buffers and sub-assemblies contain the proper reagents and qualities. Has knowledge of commonly used concepts, practices, and procedures including PCR, RT-PCR real-time PCR, and use of fluorescence based nucleic acid detection techniques. Assists in complex functional testing and troubleshooting product, process material or formulation processes. Applicant must be mathematically competent, detail orientated, and able to follow written directions well. etc. | 2/4/2020 |
| 72 | Biomarin Novato, CA Specialist, QC I (Temporary) BS/BA in the life sciences Exp: 0-3 years |
Coordinate the calibration, maintenance and repair of analytical laboratory instruments and support equipment using the BioMarin’s Enterprise Computerized Maintenance Management System (CMMS). Responsible for the completion of QC equipment related documentations. Perform change request using the BioMarin’s Enterprise Quality Management System (Trackwise). Maintain vendor service contracts using BioMarin’s SpringCM system. Maintain good working relationships with vendors to ensure vendor meets BioMarin’s current and future needs. Work with vendors to troubleshoot equipment. Maintain the laboratory equipment inventory for tracking equipment assets and vendor contacts. etc. | 2/4/2020 |
| 73 | Biomarin San Rafael, CA Research Associate I (Temporary) MS Exp: 0-2 years |
Duties: Performing Immunohisotchemical and In Situ Hybridization Assays. Performing basic histologic techniques (including but not limited to): Fixation, Embedding, Sectioning, and Staining. Epifluorescence and Confocal Microscopy. Image Analysis. Assay development and trouble-shooting. Performing mammalian cell line maintenance and cell based assays. Execute and document laboratory procedures and experiments with great attention to detail. | 2/4/2020 |
| 74 | Biomarin Novato, CA Associate , Manufacturing (Temporary) BS in a related science or engineering Exp: Not necessary for BS candidates |
PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, protein purification and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Demonstrated proficiency Gain experience with automation systems (LIMS, MES, PI, etc.). etc. | 2/4/2020 |
| 75 | Biomarin Novato, CA Analyst, QC I (Temporary) BS/BA in a biological or biochemical science Exp: 0-2 years |
The Quality Control Microbiology, Environmental Monitoring, Analyst I under direct supervision, is responsible for performing microbiological, biochemical, and chemical evaluations of the manufacturing facilities, utilities, and equipment. With experience they would perform as a back-up for QC In-process and QC Microbial ID testing. Under direct supervision, the incumbent will be primarily responsible for performing environmental monitoring sampling and testing of the facilities, equipment, and utilities under cGMP guidelines. In addition they will be responsible for performing biochemical and microbiological assays of samples under cGMP and GLP guidelines. Work assignments will encompass activities from routine to semi-routine in nature with the ability to recognize deviations from accepted limits and practices. etc. | 2/4/2020 |
| 76 | Biomerics Athens, TX Engineering Technician HS diploma/BS/BA Exp: 1 year |
Engineering Technician will provide technical support in the design and development of processes needed to manufacture products that are safe and cost effective. RESPONSIBILITIES: Assist Engineering in the design of product and processes that have the capability to be robust and produce parts and assemblies so that the normal distribution is well within specification and yet cost effective. etc. | 2/4/2020 |
| 77 | Bio-Rad Hercules, CA Field Service Engineer I AS/AA in electronics Exp: 0-1 year(s) |
Bio-Rad is seeking a Field Service Engineer. This position requires up to 75% travel throughout the San Francisco Bay Area. Responsibilities: Provide customer site service on all CDG/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. | 2/4/2020 |
| 78 | Bio-Rad Seattle, WA Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers in the Greater Seattle Area. Responsibilities: Provide customer site service on all CDG/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. etc. | 2/4/2020 |
| 79 | Bio-Rad Pleasanton, CA Research Associate II MS in molecular biology, biochemistry, cell biology, or a related life science Exp: 0-2 years |
Bio-Rad’s Digital Biology Center is a multidisciplinary team developing products using our Droplet DigitalTM technology that are having a large impact in both research and healthcare. Every day, scientists and clinicians around the world use our ddPCRTM and ddSEQTM NGS sample prep systems to make new discoveries, and are revolutionizing clinical decision making with break-through liquid biopsy applications. We’re looking for an energetic and talented Research Associate II (IVD Development) to join our team. Responsibilities: You will work in an assay research and development team on new in vitro diagnostic (IVD) oncology tests using state-of-the-art droplet digital PCR (ddPCR) technology, in a multi-disciplinary department that includes assay research and development scientists, hardware engineers and software engineers. etc. | 2/4/2020 |
| 80 | Bio-Rad Nashville, TN Field Service Engineer BS/BA Exp: 1 year |
Bio-Rad is seeking a Field Service Engineer who will perform repairs, upgrades, and preventive maintenance on our instruments for clinical diagnostics, life science, and biopharma customers based in Nashville, TN traveling 50 – 75%. Responsibilities: Provide customer site service on all CDG/LSG products including emergency service. Maximizes system uptime through proactive preventive maintenance. etc. | 2/4/2020 |
| 81 | Astellas Marlborough, MA Research Associate I BS/BA Exp: 0-3 years |
We are seeking a highly motivated Research Associate, who will work on multiple stem cell and exosome related projects at AIRM. The research associate will be supporting cell culture and differentiation needs for the ocular team. They will also provide technical support for cell characterization through qPCR, ICC etc. They will also be supporting the extracellular vesicle (EV) team for multiple projects for EV isolation, characterization, in vivo studies etc. | 1/28/2020 |
| 82 | AstraZeneca Gaithersburg, MD R&D Associate I/II - Upstream & Downstream - BPD BS/MS in a scientific or engineering discipline Exp: 0-2 years |
As a Research Associate, you would enter a 2-year program that would give you experience creating our new next generation manufacturing process in three areas: upstream process development, downstream process development, and either pilot-scale equipment design, debugging, and automation, or analytical sciences. You would join a team developing AstraZeneca’s Next Generation Manufacturing Platform. You and the team would develop the continuous and integrated purification platform for biological therapeutics, including antibodies, bispecific antibodies, and Fc-fusions. You would apply the Next Generation Manufacturing methods to drug candidates in Phase I, II, and those entering Phase III. etc. | 1/28/2020 |
| 83 | AstraZeneca Gaithersburg, MD Research Associate II - Lab Support MS in a biological or chemical science Exp: 0-2 years |
As a Research Associate II, you will function as the point person for the procurement and management of laboratory reagents and supplies. Coordinate maintenance of non-computer-based equipment and prepare associated documentation in accordance with GXP; supporting operations of a regulated laboratory that performs PK and ADA bioanalyses in compliance with GLP / GCP guidelines. Specific Responsibilities include: Responsible for the ordering and stocking of laboratory reagents and supplies to meet development, validation and sample testing needs of regulated bioanalytical lab (HBS and GXP compliance). Coordinates across departments, vendors and systems to schedule preventative maintenance, calibration and validation activities of laboratory non-computer-based equipment to ensure GLP compliance. etc. | 1/28/2020 |
| 84 | AstraZeneca West Chester, OH Aseptic Control Technician - Operations HS diploma or equivalent Exp: 1-2 year(s) |
The Aseptic Control Technician Autonomously performs tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Class 100 aseptic environment and in a laboratory setting. Essential Job Functions: Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts from technical documentation. Maintain accurate and complete records (for example: laboratory notebooks, quality records, sample receipts). Complete required training. etc. | 1/28/2020 |
| 85 | Athenex Clarence, NY Manufacturing Process Operator I (2nd Shift - 2pm to 10:30pm) HS diploma or equivalent Exp: 1-3 year(s) |
Our Manufacturing Process Operator I is responsible for ensuring the accurate production and documentation of pharmaceutical products and maintain a safe manufacturing environment. Essential Job Functions/Responsibilities: Participate in the manufacturing process by performing visual inspection of compounded drug product per procedure. Participate in the manufacturing process by performing labeling and final packaging of drug product. etc. | 1/28/2020 |
| 86 | Athenex Clarence, NY Manufacturing Process Operator I (1st Shift 7am to 3:30pm) HS diploma or equivalent Exp: 1-3 year(s) |
Our Manufacturing Process Operator I is responsible for ensuring the accurate production and documentation of pharmaceutical products and maintain a safe manufacturing environment. Essential Job Functions/Responsibilities: Participate in the manufacturing process by performing visual inspection of compounded drug product per procedure. Participate in the manufacturing process by performing labeling and final packaging of drug product. etc. | 1/28/2020 |
| 87 | Avion Pharmaceuticals Boston, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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’ & Rheumatology 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. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 88 | Avion Pharmaceuticals Brooklyn, NY Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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’ & Rheumatology 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. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 89 | Avion Pharmaceuticals Charleston, SC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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’ & Rheumatology 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. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 90 | Avion Pharmaceuticals Charlotte, NC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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’ & Rheumatology 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. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 91 | Avion Pharmaceuticals Chicago, IL Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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’ & Rheumatology 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. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 92 | Avion Pharmaceuticals Fayetteville, NC Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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’ & Rheumatology 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. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 93 | Avion Pharmaceuticals Flint, MI Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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’ & Rheumatology 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. Develop and maintain an in-depth knowledge of our products that enables the Pharmaceutical Sales Representative to engage in meaningful dialogue when calling on healthcare providers. etc. | 1/28/2020 |
| 94 | Avrobio Cambridge, MA Research Associate (Process Development Group) BS/MS in biology, biochemistry or related discipline Exp: 1+ year(s) |
We are seeking a Research Associate to join an exciting and fast-growing company to develop gene therapies for rare diseases. The successful candidate will join the process development group at Avrobio, focusing on development of analytical methods for ex vivo genetically modified cells to support the development of gene therapy programs. The individual will develop quantitative assays measuring gene modification in target cells, cell-based assays measuring the expression and the biological functions of specific genes. The successful candidate will, perform, and analyze experiments for multiple preclinical and clinical programs and will work independently to support process development, product characterization, and technical transfer to CMOs and GMP test labs. etc. | 1/28/2020 |
| 95 | Bausch Health Clearwater , FL Manufacturing Associate II HS diploma or equivalent Exp: 1+ year(s) |
Perform various operations in the fabrication of intraocular lenses according to production specifications and standards. Responsibilities: Performs various lens fabrication and inspections duties to include operating lathe and milling machines, lens polishing, finished production inspections and primary packaging. Ensure product meets all acceptable criteria per SOP's. Follow all regulatory guidelines and regulations regarding traceability, and safety procedures. Support, encourage and participate in team related activities; report ideas or suggestions to supervisor. Assist in training manufacturing associates using prescribed training methods and tools as assigned by supervisor/management. Report unusual conditions and problems to supervisor and manufacturing lead; practice good housekeeping. etc. | 1/28/2020 |
| 96 | Bayer Kansas City, KS Bayer Crop Science OIT Chemical Operator Rotating Shift HS diploma or equivalent Exp: 1 year |
The primary responsibilities of this role, Bayer Crop Science OIT Chemical Operator are: Prepares packaging materials; Read and understand SOP's; Stages raw and finished materials; Takes required samples during production process; contaminates equipment and piping for maintenance or disposal; Utilizes Personal Protective Equipment Matrix; Maintains inventories of disposable, production, and safety related materials; Recognizes material compatibilities; etc. | 1/28/2020 |
| 97 | Bayer New Orleans, LA Lab Tech AS/BS in chemistry or related Exp: 1-3 year(s) |
The primary responsibilities of this role, Laboratory Technician, are to: Determine conformance to accepted specifications for a particular chemical or physical property; Monitor and verify quality in accordance with statistical process or other control procedures; Perform troubleshooting and calibration of instruments; Prepare reagents, solutions, and standards; Maintain instruments and apparatus according to established procedures to support testing activities of the unit; etc. | 1/28/2020 |
| 98 | Bayer Myerstown, PA Associate Technician-3rd Shift HS diploma or equivalent Exp: 6+ months |
The primary responsibilities of this role, Associate Technician, are to: Comply with all workplace standards and safety procedures, including lockout tagout, current good manufacturing practices (CGMPS), occupational safety and health administration requirements (OSHA), standard operating procedures (SOPS), and company guidelines; Take ownership of training and learning to develop high performance competencies such as technical skills, communication skills, and skills to build a team-oriented culture; Demonstrate willingness to learn, maintaining qualifications/skills, training team members, motivating and supporting team members, sharing knowledge to continuously improve the process, etc.; etc. | 1/28/2020 |
| 99 | Bayer St. Louis, MO Agronomic Research Specialist MS in agronomy, engineering, life sciences, or computer sciences Exp: 0+ years |
The primary responsibilities of this role, Agronomic Research Specialist, are to: Collaborate with project team members to deliver detailed experimental protocols that enable advancement decisions by our scientists and placement decisions to our customers; Handle the operation of research equipment, note taking, data management with internal IT systems, comply with regulated seed stewardship standards, complete and/or participate in safety inspections/training and comply with all policies and standard operating procedures; etc. | 1/28/2020 |
| 100 | Bayer Lubbock, TX Agronomic Research Specialist MS in agronomy, engineering, life sciences, or computer sciences Exp: 1 year |
The primary responsibilities of this role, Agronomic Research Specialist, are to: Responsible for Delivering the highest quality field data as part of North America’s Plant Breeding R&D pipeline by providing optimal trial management, at times working on an internal R&D effort that spans across crops, sites, and a region; Independently Responsible for the implementation of unique and innovative technology solutions designed to improve research design and operations success through the use of new tools and methodologies to improve overall plant breeding phenotyping such as the pilot and use of geospatial systems, agronomic planting and harvesting tools, harvesting shelling systems, and data capture applications; etc. | 1/28/2020 |
| 101 | Penumbra Roseville, CA Quality Engineer BS/BA in engineering or sceicnes Exp: 1-5 years in biomedical/chemical/material engineering |
As a Quality Engineer at Penumbra, you will participate in all aspects of product manufacturing in order to ensure the highest level of quality in new and existing products, and their compliance to applicable regulations and standards. You will apply your passion for detailed analysis to identifying problems and determining the appropriate course of action. You will be looked to for ensuring compliance and building a culture of quality within your project teams. Represent Quality Engineering on process improvement projects, interfacing among multiple departments and teams such as Manufacturing, QC, R&D, Regulatory Affairs, Operations/Planning, and Marketing. | 1/25/2020 |
| 102 | Perkin Elmber Waltham, MA Entry Level Consolidations Accountant BS/BA accounting or finance Exp: 0-2 years |
The Entry Level Consolidations Accountant will be an integral part of the Corporate Accounting team. The key areas of focus will be supporting the monthly close process, reviewing worldwide results and working with sites to make corrections, resolving accounting issues, and preparing global internal financial statements and financial data to support the consolidated external financials. This position also supports cross-functional finance teams across the organization through maintaining reliable financial reporting which requires an understanding of finance and accounting concepts as well as an aptitude for working with financial systems. | 1/25/2020 |
| 103 | Pharm-Olam Houston, TX Clinical Trial Associate BS/BA Exp: 1 year as CTA II |
Acts as the primary administrative support to local Pharm-Olam clinical study teams, as required by Project Managers and Sponsors, thus ensuring that the clinical trial is conducted in accordance with international and local regulatory and ethic laws, ICH Guidelines for Good Clinical Practice and Standard Operating Procedures. Assists the local study team with the day-to-day conduct of international clinical studies. | 1/25/2020 |
| 104 | Poseida Therapeutics San Diego, CA Research Technician or Associate Nanoparticle Formulation BS or MS in pharma sciences, bioengineering, chemistry Exp: 1+ years in industry |
his position offers an exciting opportunity to develop non-viral delivery tools for gene editing and gene therapy applications. This person will be engaged in execution of formulation discovery experiments directed toward discovering and developing novel nanoparticle systems for delivering nucleic acids and proteins. Work at the direction of senior Formulation scientists to formulate multi-component nanoparticles encapsulating nucleic acids | 1/26/2020 |
| 105 | PRA Health Sciences Salt Lake City, UT Medical Research Associate HS Diploma/GED Exp: 1+ year in medical/clinical field |
Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability | 1/26/2020 |
| 106 | Promega Madison, WI Custom Product Finishing Technician 1 HS Diploma/GED Exp: 2 year in product environment |
Work in a team environment to finish products to quality standards in order to meet custom production goals and productivity guidelines set by Promega. Fulfill customer requirements, meet and exceed customer expectations, to produce high quality, safe and effective products. This position will have a basic understanding of product finishing including process order execution, labeling, dispensing, and kitting. | 1/26/2020 |
| 107 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician (Consumable--WES) 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 robotic and manufacturing equipment. Ability to use hand tools such as small wrenches, pliers, tweezers, etc. | 1/26/2020 |
| 108 | AMRI Grafton, WI Quality Assurance Associate BS in chemistry or related Exp: 1-3 year(s) |
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. etc. | 1/20/2020 |
| 109 | ARL Bio Pharma Oklahoma City, OK Sample Administrator I / Receiving HS diploma or some college experience Exp: 0-2 years |
Occupations that fit well with this position are pharmacy technician and medical office administrative assistant. The job is performed in an office environment. This position is to perform all data entry processes needed or required to facilitate the accurate reporting of all samples submitted for testing. The Accessioner maintains sample integrity to ensure accurate and timely testing and reporting by the appropriate lab. Additionally, the Accessioner may perform additional duties requested by the Accessioning Supervisor. Minimal to moderate supervision is required. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. Marijuana is one of the substances included in the drug panel screening. etc. | 1/20/2020 |
| 110 | ARL Bio Pharma Oklahoma City, OK Data Review Chemist I BS in chemistry or related Exp: 0-2 years |
With moderate guidance, the Data Review Chemist I is responsible for utilizing the Quality Management System (QMS) standard operating procedures (SOP) and work instructions (WI) to perform quality review and approval of test results and data for compliance. The Data Review Chemist I will independently apply technical aptitude and experience to troubleshoot non-compliant data and work supportively with other Chemists to ensure generation of compliant data. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. etc. | 1/20/2020 |
| 111 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Microbiology Lab AS/BS in chemistry or related Exp: Not necessary for AS/BS candidates |
Under the supervision of the laboratory supervisor the Microbiology Lab Technician provides support tasks in a fast-paced laboratory setting. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. Marijuana is one of the substances included in the drug panel screening. Possession of a medical marijuana license will not excuse you from the testing process, or the consequences of testing positive for marijuana. etc. | 1/20/2020 |
| 112 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - Analytical Lab AS/BS in microbiology or related Exp: Not necessary for AS/BS candidates |
Under general supervision, the Laboratory Technician is responsible for working collaboratively with Chemists and performing integral support tasks to ensure overall efficient testing of samples. Essential Functions: Adhere to Quality Management System (QMS). Follow prescribed safety rules and regulations in performing all assigned duties. Follow written and oral instruction. Prepare reagents, solutions, and mobile phases required for testing. Perform timely peer review of laboratory notebooks. Sample management including retrieval, storage, and disposal. Work and think independently, yet share ideas and work towards team goals. etc. | 1/20/2020 |
| 113 | ANGLE Toronto, ON Laboratory Manufacturing Associate HS diploma or equivalent Exp: 1-2 years |
The Manufacturing Associate works in a laboratory and clean room environment maintaining and operating standard laboratory equipment and executing routine manufacturing procedures following prescribed SOPs. Essential Duties and Responsibilities: Assembly of consumables in a clean room environment. Maintenance and operation of standard laboratory equipment such as centrifuges, pipettes, balances and pH meters. Receipt of incoming materials. Labelling and packaging manufactured products. Recording all data and results with accuracy and responsibility. etc. | 1/20/2020 |
| 114 | Arcus Biosciences Hayward, CA Research Associate BS/MS in immunology, cell biology, biochemistry or related Exp: 1-2 year(s) |
Our Pharmacodynamics (PD) group is focused on the development and execution of assays to evaluate engagement of our drugs and their biological effects in patient samples. Our role within the Quantitative Biology (QB) department is a central, critical element of our translational research engine. We are looking to expand the size and scope of this team, with positions available immediately. The ideal candidate will have a working knowledge of immune-based in vitro assays, flow cytometry, ELISA, common molecular biology techniques, and data analysis/visualization software. Direct experience with isolation and culture of primary cells is strongly preferred. etc. | 1/21/2020 |
| 115 | Argonaut Manufacturing Services Carlsbad, CA Drug Product Manufacturing Assistant HS diploma or equivalent Exp: 0-2 years |
The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing. General Responsibilities: Performs various routine manufacturing tasks under the direction of internal SOP’s and cGMP guidelines. Prepares material components for manufacturing operations. Documents steps clearly and completely in production batch records, log books and other controlled forms. Participates in inspection readiness activities. Performs basic arithmetic and algebraic computation. Maintain cleanliness of areas and equipment. etc. | 1/21/2020 |
| 116 | Johnson & Johnson Eugene, OR Junior Sales Consultant (Trauma) – Eugene, OR BS/BA Exp: 0-3 years relevant experience |
Assist team in retaining and supporting further penetration with existing customers, while supporting product conversions with new customers. Assist in the attainment of established sales goals including market share objectives in prescribed territory. Apply knowledge of sales process, product portfolio and customer knowledge to improve sales outcomes. | 1/18/2020 |
| 117 | Johnson & Johnson Malvern, PA Associate Scientist, Drug Product Development Engineer MS in related sciences Exp: 1 year lab experience |
The Associate Scientist, Drug Product Development Engineer in the Parenterals and Liquids (P & L) group will be responsible for performing experimental studies related to process improvement and quality compliance efforts as it relates to formulation/process development and testing of therapeutic proteins or other biologics including monoclonal antibodies (mAbs). This includes the mathematical modelling; and development and optimization of the technical operations associated with liquid and lyophilized biologics formulations/processes, as well as execution of pharmacy manual and stability studies. | 1/18/2020 |
| 118 | Johnson & Johnson Malvern, PA Assistant Scientist BS or MS in biological sciences Exp: BS: 1-2 years, MS: 0 year |
The Assistant Scientist in the Parenterals and Liquids (P & L) group in Drug Product Development will be responsible for performing experimental studies as it relates to process development and testing of therapeutic proteins or other biologics including monoclonal antibodies (mAbs), virus like substances, cell-based therapeutics (CAR-T) and gene therapy related molecules. This includes the development and optimization of the technical operations associated with liquid and lyophilized biologics processes, as well as execution of stability studies. Additional responsibilities include but are not limited to development and optimization of liquid and lyophilized biologics formulations, as well as execution of characterization plans and stability studies | 1/18/2020 |
| 119 | Bausch Health Lynchburg, VA Distribution Associate I (579) HS Diploma/GED Exp: 6 months distribution/warehouse experience |
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, returns processing, 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. | 1/18/2020 |
| 120 | Bausch Health Greenville, SC Distribution Associate (306) HS Diploma/GED Exp: 1 year distribution/warehouse experience |
Receiving operation is responsible for accurately receiving product from the B&L Manufacturing Operation along with other third party vendors, putting product into assigned storage locations, and retrieving product and delivering it to the pick area and/or shipping lanes. Also, perform shipping duties including preparing orders for shipment consisting of pallet stacking, labeling and wrapping. All order transaction controlled via RF computer. Shipping operation is responsible for accurately retrieving product from the pick area. Also, perform shipping duties including pallet stacking, labeling and wrapping. Other responsibilities include truck loading and general warehouse housekeeping. All order transaction controlled via RF computer. | 1/18/2020 |
| 121 | Pace Analytical Golden Valley, MN Food Sample Handling HS Diploma/GED Exp: 0-3 years relevant experience |
The Sample Handling Lab Technician will work as part of a fast-paced sample prep team that organizes and processes materials for further analytical testing. Responsibilities include knowledge or use of various grinding mills and procedures for the preparation of samples for Analytical testing. Other responsibilities include filing, data entry, customer service and general lab upkeep (e.g. ordering and stocking supplies, cleaning, equipment maintenance) | 1/18/2020 |
| 122 | Pace Analytical Maplewood, MN Complaint Analyst - Health Care BS/BA in biomedical sciences or pre-med Exp: 1+ years |
This candidate will manage and support complaint handling workflow for one or more client products. Assure appropriate prioritization and timely closure of complaints. Assure compliance with all FDA regulations and internal procedures related to complaint handling. Manage complaint handling workflow. Meet daily team and individual complaint handling output goals. Perform complaint investigation to either close the complaint or determine need for more in-depth analysis | 1/18/2020 |
| 123 | Pace Analytical Maplewood, MN Lab Analyst - Mechanical Engineer BS in sciences/engineering Exp: 0-1 years in mechanical engineering |
This Lab Analyst will work in a product development lab to design and build hardware related to food safety equipment. Perform reliability testing and analysis related to hardware usage. Design and develop high level prototypes. Analyze data and create summary reports . | 1/18/2020 |
| 124 | Pace Analytical Naperville, IL Lab Analyst - Chemical and Physical Testing AS/AA in applied sciences, BS in chemistry/biology preferred Exp: 0-2 years |
The main function of a laboratory technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. Set up and conduct chemical experiments, tests, and analyses using techniques such as chromatography, spectroscopy, physical and chemical separation techniques, and microscopy. Conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials | 1/18/2020 |
| 125 | Pace Analytical Minneapolis, MN Quality Engineer Assistant BS in chemistry or related Exp: 1+ years in QA |
Candidate will work with Quality Assurance as a Quality Engineer Assistant to ensure compliance of manufacturing processes in a GMP environment. This person will serve as reviewer and/or approver for required documentation in a pilot plant/manufacturing setting. This position is very project orientated, so the QE Assistant can expect every day to be different with changing responsibilities and priorities. | 1/18/2020 |
| 126 | Pall Houston, TX Material Handler I HS Diploma/GED Exp: 1 year in distribution/warehouse |
Incumbents must possess basic material handling skills and must be willing to learn and continuously expand knowledge, skills and abilities required to support this large distribution center. Collaboration and assisting/training others in completing daily work is an expectation and is critical for the role. Read and understand Standard Operating Procedures. Learn and follow standard work for all areas within a Value Stream. | 1/19/2020 |
| 127 | Par Pharmaceutical Rochester, MI Chemist I BS in chemistry/chemical engineering Exp: 0-1 years |
The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. | 1/19/2020 |
| 128 | Par Pharmaceutical Chestnut Ridge, NY Manufacturing Operator l HS Diploma/GED Exp: 0-2 years |
The Manufacturing Operator I performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs). Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. Learns to apply skills and knowledge to recognize issues and to increase efficiency, throughput and quality. Learns, understands and runs processes to meet the assigned standards/routers and fulfills the assigned schedule; when these are not achieved, may participate in the debrief to understand the reasons why and what needs to be corrected moving forward. | 1/19/2020 |
| 129 | Parexel Billerica, MA Software Engineer BS in computer science, information systems, or related Exp: 0-3 years relevant experience |
Provide programming skills and expertise in the design and development of Enterprise Architecture projects: System Integrations, Analytical and Metrics Clinical Data Warehouse, Management of Production Release processes. Independently implement solutions following provided design blueprints, using established frameworks and design patterns, adhering to requirements, standards, and functional specifications. Responsible for unit testing of all code produced using preferred unit test frameworks and technologies | 1/20/2020 |
| 130 | NuVasive West Carrolton, OH Production Associate - 2nd shift HS Diploma/GED Exp: 0-1 years |
The Associate Post Processing Technician is responsible for the finishing/assembly operations to ensure quality products are produced. The Post Processing Technician helps in driving best practices and creates open communication across all teams to foster a collaborative, high functioning culture. Follow standard applications in order to achieve dimensional integrity and required finish characteristics. Follow the router protocol to ensure the product moves through channels efficiently and GDP is correct prior to moving the product to the next area. | 1/11/2020 |
| 131 | NxStage Medical Lawrence, MA Quality Analyst - NxStage BS/BA Exp: 0-3 years in related |
The incumbent will be responsible for receiving and processing customer product complaints in Fresenius/NxStage’s postmarket surveillance department with a primary focus on performing functions in support of the quality engineering and clinical teams. Process incoming customer complaints and adverse events as assigned for device and drug-related incidents. Interface with distributor contacts and customer clinical staff to obtain detailed information regarding reported incidents as required, ensuring patient confidentiality throughout | 1/11/2020 |
| 132 | ThermoFisher Scientific West Hills, CA Scientist I, Manufacturing Sciences BS in biological sciences or related Exp: 1-2 years biological lab experience |
The Scientist I, Manufacturing Sciences is responsible for understanding, performing daily testing, and analysis for development and, improvement of DNA-based diagnostic reagents. Simultaneously manage and prioritize multiple projects and products across multiple functional groups while meeting target due dates with guidance of supervisor/lead. Design, create experimental task, run tests and be able to look at data and complete analysis using Fusion, Orchid, or equivalent software. Can provide experimental task(s) to designated Scientist with Supervisor approval. | 1/11/2020 |
| 133 | ThermoFisher Scientific Cambridge, MA Specialist I, Quality Assurance BS/BA in sciences Exp: 0-2 years in quality |
The Quality Assurance Specialist will be the primary point of contact for the customer on all matters related Quality Assurance Operations. Perform activities in support of dispositioning product and/or raw materials while ensuring compliance with directives and procedures, customer requirements, and regulatory standards. | 1/11/2020 |
| 134 | ThermoFisher Scientific Suwanee, GA Lab Tech II BS/BA Exp: 1-3 years |
The Lab Technician II performs sample handling, receipt, storage, and shipment for a biorepository as well as entering inventory information into a laboratory information management system. Additionally, he/she performs specialized services including sample manipulation, aliquoting, and other sample handling functions that may require aseptic technique. | 1/11/2020 |
| 135 | ThermoFisher Scientific Alachua, FL QA Specialist, GMP Plant Quality BS/BA in life or chemical sciences Exp: 1+ years in GMP environment |
Ensures the quality of all GMP manufacturing activities, executing manufacturing record reviews in accordance with specified timelines. Performs robust master and executed batch review and disposition activities to meet specified timelines. Performs robust document review and approval activities to meet specified timelines and ensure the adherence to Quality Agreements. Documentation may include batch records, SOPs, investigations, corrective actions, change controls, technical documents, | 1/11/2020 |
| 136 | ThermoFisher Scientific Allentown, PA Associate Project Engineer BS in mechanical/industrial engineering Exp: 0-3 years in related |
The individual will establish a solid focus on long-term continuous improvement activities through interaction with the entire Engineering and Operations Staff.Recommend methods for improving worker efficiency, reducing waste, and utilities such as restructuring job duties, reorganizing workflow, relocating workstations, equipment, and justify and oversee purchase of new equipment / technology.Recommend and lead cost saving initiatives as it relates to business objectives, current projects, future investments in technology and Production / Manufacturing processes.Will lead and manage multiple project engineering driven assignments from start to finish with sound project management methodologies | 1/11/2020 |
| 137 | ThermoFisher Scientific Lenexa, KS Customer Service Representative I HS Diploma/GED Exp: 1+ years in call center/customer service |
Employee is responsible for entering order into the MBD-Lenexa ERP system and assisting our internal and external customers with resolution of customer service issues and complaints. Enter orders as they are received via fax, email and/or phone as assigned by management; perform quality verification of customer shipping information, order details, and pricing. | 1/11/2020 |
| 138 | AGC Biologics Bothell, WA QC Associate I/II BS/BA Exp: 1-3 year(s) |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. PRINICIPAL RESPONSIBILITIES: Supports projects / initiatives / team goals by delivering on all assigned tasks. Analyzes issues and makes decisions based on standardized processes and procedures under direct supervision. Seeks opportunities for continual learning. Receives close and regular instruction, guidance and direction from others in the form of steps and tasks. Perform general QC testing such as pH, Osmolality, Protein Concentration. etc. | 1/12/2020 |
| 139 | Agilent Boulder, CO Manufacturing Quality Engineer - Entry BS/BA Exp: 1+ year(s) |
Ensures that high-quality products are designed, engineered and manufactured by Agilent, in conformance with required standards and regulations. This is a Quality position with direct support of manufacturing floor responsibilities. Provides guidance, expertise and services to ensure process, data and product quality. Participates in process improvement opportunities and provides quality-related services to quality control, R&D, manufacturing engineering, production, procurement, and others. etc. | 1/12/2020 |
| 140 | Agilent Boulder, CO Manufacturing Tech (2nd Shift) unspecified Exp: None required |
Responsible for performing a variety of technical support duties in one or more manufacturing areas. Duties may be related to installation, maintenance, repair and support of manufacturing equipment, technical support of one or more production processes, product test and troubleshooting, and technical analyses and problem-solving. Conducts tests, experiments and/or problem resolution associated with components, parts, products or processes/systems. May design and/or build tools. etc. | 1/12/2020 |
| 141 | Agilent Wilmington, DE Analytical Instruments Technical Support BS in chemistry, biology, or related Exp: None required |
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. etc. | 1/12/2020 |
| 142 | Agilent Wilmington, DE R&D Electrical Engineer BS/MS in electrical engineering Exp: None required |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Most projects require mechanical, electrical and firmware engineers, as well as chemists and software engineers, to create a complete system. As part of those projects, you will also work with our marketing, manufacturing, purchasing and service organizations to transform your designs into shipping products. etc. | 1/12/2020 |
| 143 | Ajinomoto Bio-Pharma Services San Diego, CA Aseptic Cleaning Technician HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Part Time Aseptic Cleaning Technician (3rd shift) responsible for formulating cleaning solutions and sanitizing manufacturing core, operation equipment, and monitoring production processes and operations as necessary. The Aseptic Cleaning Technician will record information in documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), and review documentation as appropriate. This role frequently works in a professional manufacturing environment with computer equipment, machinery, tools, and loud noise and activity. etc. | 1/12/2020 |
| 144 | Ajinomoto Bio-Pharma Services San Diego, CA Document Control Assistant HS diploma or equivalent Exp: 0-2 years |
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: Coordinates document changes within an electronic document management system. Issues batch records, laboratory notebooks, and logbooks for use in GMP production and testing activities. Collaborates with document authors and reviewers to process document changes within project timelines and in accordance with established procedures. Facilitates client review and approval of documents. Esures proper maintenance of document master copies and original production records. | 1/12/2020 |
| 145 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Inspection Technician - 1st and 2nd Shift HS diploma or equivalent Exp: 0-2 years |
We are looking for multiple Drug Product Inspection Technicians for 1st and 2nd shifts. 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. Please Note: 1st shift hours are 6:30 - 3:00 pm and 2nd shift hours are 3:00 - 11:30 pm. Responsibilities: Performs various manufacturing tasks under the guidelines of established SOP and cGMP regulations. Performs visual inspection. Labels and boxes filled goods. etc. | 1/12/2020 |
| 146 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant HS diploma or equivalent Exp: 0-2 years |
We are looking for multiple Drug Product Manufacturing Assistants for 1st Shift! The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Implements production and manufacturing procedures. Performs visual inspection. Prepares components, media, buffers, and other solutions as needed. Accurately documents data and completes batch records as needed. May cross train and/or focus in various manufacturing tasks including fill/finish, formulation, fermentation, preparation. etc. | 1/12/2020 |
| 147 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Packaging Assistant HS diploma or equivalent Exp: 1-2 year(s) |
Ajinomoto Bio-Pharma Services is currently seeking a Drug Product Packaging Assistant. This position is responsible for performing a wide variety of packaging and labeling tasks in a GMP environment. In this role you will utilize automated equipment as well as perform manual packaging activities to support commercial drug product operations. Typical hours for this role are 7:00 to 3:30 pm Monday through Friday. Responsibilities: Performs various routine manufacturing tasks under the guidelines of established SOP and cGMP regulations. Performs final product assembly, packaging, and labeling and has completed required qualifications where applicable. Accurately documents data under cGMP guidelines. etc. | 1/12/2020 |
| 148 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Substance Manufacturing Assistant - Support Services HS diploma or equivalent Exp: 0-2 years |
Ajinomoto Bio-Pharma Services is currently seeking a Drug Substance Manufacturing Assistant - Support Services responsible for performing solution formulation and/or sterilization of in-process manufacturing materials in support of cGMP manufacturing under the guidelines of established SOP's and cGMP regulations. Responsibilities: Transfers raw materials from warehouse staging area to production suite, labels materials for applicable client use. Conducts inventory and storage of raw materials in production area. Prepares components, buffers and other solutions and/or operates autoclave, washer, or depyrogenation oven. Completes in-process analytical testing as needed to confirm suitability of solutions and submits samples to QC for release testing via LIMS system. etc. | 1/12/2020 |
| 149 | Ajinomoto Bio-Pharma Services San Diego, CA Environmental Monitoring Assistant HS diploma/BS in a life science Exp: 0-2 years |
We are looking for an Environmental Monitoring Assistant to support Ajinomoto Bio-Pharma Services’ manufacturing. This 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 an Environmental Monitoring Assistant you will acquire an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. Responsibilities: Performs environmental monitoring within the microbiology laboratory, manufacturing suites, clean rooms, and drug product operations. Performs enumeration and gram staining of bacterial colonies. Sampling and analysis of the utilities including water, steam, and compressed gasses. etc. | 1/12/2020 |
| 150 | Alcon Huntington, WV Production Technician HS diploma or equivalent Exp: None required |
The role of the Production Technician is to perform a number of different tasks and operations typically within a full-scale environment production manufacturing operation while maintaining compliance with Standard Operating Procedures, Good Documentation Practices and regulatory requirements. | 1/13/2020 |
| 151 | Alcon Fort Worth, TX Scientist I BS/BA Exp: None required |
Job Description: Assist with in-vivo testing of raw materials, finished goods, products, investigations per schedule and per standards/SOPs. Collect, calculate, and interpret test results. Enter and report test results. Take ownership and execute revisions for SOPs related to testing programs, laboratory operations and/or equipment operation. Assist with investigative testing to support laboratory investigations. Conduct peer review of data collected by co-workers. Coordinate equipment calibration & maintenance. etc. | 1/13/2020 |
| 152 | AliveCor Mountain View, CA Hardware Test Engineer BS in electrical engineering Exp: 1-5 year(s) |
AliveCor, the creator of the Kardia Mobile ECG app, seeks a Hardware Test Engineer to join an exciting start-up that is changing the face of mobile health. As the Hardware Test Engineer, you will be a crucial member of hardware R&D team responsible for ensuring that AliveCor products perform as intended and meet/exceed customer expectations. You will work closely with our Quality, Regulatory, Software Engineering, Product Management, and Creative teams to ensure new products perform as intended while fully documenting the verification process. You will also work with our manufacturing team to implement and support manufacturing test fixtures. If you have what it takes to drive change in the medical marketplace, then this is the opportunity for you. etc. | 1/13/2020 |
| 153 | APi North Augusta, SC MFG - Laboratory Technician HS diploma or equivalent Exp: Entry level |
The Laboratory Technician position is an entry level position. The person in this position will be trained and responsible for following instructions and procedures in support of manufacturing processes in a controlled GMP environment, as well as performing related activities. SPECIFIC DUTIES AND RESPONSIBILITIES: Must manage and organize the glass cleaning operation according to approved standard operating procedures. Works closely with Warehouse technician and Quality Assurance to perform and complete all Final Product packaging’s. Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. Follow approved GMP manufacturing directions such as standard operating procedures and other instructions in support of production. etc. | 1/13/2020 |
| 154 | APi North Augusta, SC Purification Chemist BS in chemistry or related Exp: Entry level |
The Purification Chemist I position is an entry level chemist position. The person in this position will be trained and responsible for following the peptide manufacturing process in a controlled cGMP environment, as well as performing related activities. PRIMARY RESPONSIBILITIES: Work in a cGMP environment to perform the peptide purification processes through chromatography as well as other various purification techniques. Use analytical skills to prevent and solve possible process complications and problems. Work as part of a team to complete specific projects in a timely manner. Follow approved cGMP manufacturing directions such as production batch records, standard operation procedures and standard test procedures. Help the team to install, test, operate and maintain equipment for manufacturing and in-process testing. etc. | 1/13/2020 |
| 155 | APi North Augusta, SC MFG - Laboratory Technician II HS diploma or equivalent Exp: 1-2 year(s) |
The Laboratory Technician II position is an experienced lab position. The person in this position will be trained and responsible for following instructions and procedures in support of manufacturing processes in a controlled GMP environment, as well as performing related activities. SPECIFIC DUTIES AND RESPONSIBILITIES: 1) Must manage and organize the glass cleaning operation according to approved standard operating procedures. 2) Works closely with Warehouse technician and Quality Assurance to perform and complete all Final Product packaging’s. 3) Must manage time well. Must be able to perform daily tasks in a timely manner – improving productivity while minimizing idle time. etc. | 1/13/2020 |
| 156 | American Regent New Albany, OH Metrology Technician I - 2nd Shift HS diploma/AS in electronics Exp: 1-5 year(s) |
NATURE AND SCOPE: A technical position involving instrument calibrations and operation intended to keep the facility instrumentation and equipment (i.e. process, utility, and general equipment) within compliance of cGMPs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Perform Calibrations. Follow written calibration procedures. etc. | 1/13/2020 |
| 157 | American Regent New Albany, OH Equipment & Process Technician I - 1st Shift HS diploma or equivalent Exp: 1+ year(s) |
The Equipment and Process Technician I works with the Inspection and Packaging Supervisor in the activities associated with the inspection and packaging of sterile pharmaceuticals in accordance with company procedures and cGMPs. The incumbent meets inspection and packaging schedules while maintaining accurate records and professional behavior within the inspection/packaging areas. The Technician will perform manual inspection and train in the automatic inspection/packaging area for setup, of automated equipment and manual inspection processes, labeling and packaging equipment duties, line clearances and assist with inspection/packaging schedule. In conjunction with the Supervisor, the Technician plays a critical role in assuring safe, effective and compliant activities are performed in the manual inspection process while maintaining production schedules. The Equipment and Process Technician I will be proficient in all activities associated with the inspection process and be able to work with minimal supervision. etc. | 1/13/2020 |
| 158 | AMRI Grafton, WI Quality Control Analyst I BS in chemistry or other natural science Exp: 1-3 year(s) |
The Quality Control Analyst is an integral part of the AMRI team, contributing to our success by ensuring that our products meet all specifications before being released to the customer through raw material testing, method development, validation, equipment calibrations, environmental monitoring, stability testing and final product testing. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture. etc. | 1/13/2020 |
| 159 | Xeris Pharmaceuticals Chicago, IL Legal & HR Associate BS/BA Exp: 0-2 years |
The Legal & HR Associate is a key role responsible for supporting the Legal and Human Resources teams in an administrative capacity, working with employees across multiple states in the USA. The Legal & HR Associate is the face of Legal and Human Resources, interacting with and supporting all employees. The ideal candidate is ambitious, high energy and excited to get their foot in the door of an innovative company. This is a fantastic opportunity for someone interested in the legal or human resources functions within a company. etc. | 1/6/2020 |
| 160 | 10X Genomics Pleasanton, CA QC Associate 1 BS in chemical or biological engineering, molecular biology, or analytical chemistry Exp: 0-2 years |
10x Genomics is looking for an outstanding individual to join its Quality Control team. This person will be responsible for the qualification of consumable products associated with Next Generation Sequencing chemistries. As well as ensuring a reliable supply of quality consumables, this person will be a key contributor to the development of manufacturing infrastructure required to support a commercial product in the life science field. etc. | 1/6/2020 |
| 161 | Abcam Branford, CT Senior Research Associate BS/MS in molecular biology or related Exp: 1-3 years |
The successful candidate will play a hands-on role in the company’s use of a variety of molecular biology, assay development, and protein purification techniques in support of various commercial and academic customer projects to deliver high-quality and on-time customized recombinant antibodies. He or she will partner closely with other team members within the group and be required to make observations, analyze data, and interpret results with supervision. etc. | 1/6/2020 |
| 162 | Abcam Eugene, OR Research Associate (temporary) BS in biology, immunology, or related Exp: 1+ year(s) |
We are seeking a Research Associate to assist in the development of novel immunoassays in our Eugene, OR facility. The core responsibility will be to provide support to the immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis. etc. | 1/6/2020 |
| 163 | AbSci Vancouver, WA Research Associate - Fermentation BS in chemical or biochemical engineering, microbiology, or related Exp: 1-2 years |
The Fermentation Research Associate will play a significant role in our upstream process development. Core responsibilities include executing bench-scale fermentations with the goal of achieving high cell densities and maximizing yields of recombinantly expressed proteins. This position will be responsible for independently operating bioreactors at small scale (1L or less), preparing media, processing samples, and analyzing results. Candidate is enthusiastic about laboratory bench work, exhibits meticulous attention to detail, and an eagerness to learn new techniques. etc. | 1/6/2020 |
| 164 | Absorption Systems Exton, PA Associate Scientist – Cell & Molecular Biologist BS/MS in biochemistry, molecular biology or related Exp: 0-2 years |
Absorption Systems provides analytical support for gene and cell therapy products through every stage of development and non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. Absorption Systems is headquartered in Exton, PA. Currently we are seeking a talented and highly motivated Associate Scientist – cell and molecular biologist in Exton, PA to contribute to multiple bioassay development projects. etc. | 1/6/2020 |
| 165 | Absorption Systems Exton, PA Associate Scientist / Scientist – GMP Molecular Biology & Gene Expression BS/MS Exp: 1-3 years |
Primary Responsibilities: Conduct GMP study projects: Preparation for protocol of assay, planning and conducting experiments under the direction of a senior scientist. Conduct studies on molecular biology assays, such as qPCR assays. Prepare and maintain cell cultures and reagents. Document all results in GMP laboratory notebooks and present research data in group and other meetings. Write report for the study project under the direction of management. | 1/6/2020 |
| 166 | Absorption Systems Exton, PA Associate Scientist / Scientist – Drug Transport & Metabolism BS/MS Exp: 1-3 years |
Absorption Systems provides analytical support for gene and cell therapy products through every stage of development. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. 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. etc. | 1/6/2020 |
| 167 | Acella Pharmaceuticals Indianapolis, IN Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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 & Rheumatology 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. etc. | 1/7/2020 |
| 168 | Acella Pharmaceuticals Portland, OR Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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 & Rheumatology 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. etc. | 1/7/2020 |
| 169 | Acella Pharmaceuticals Seattle, WA Pharmaceutical Sales Representative BS/BA Exp: 1 year |
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 & Rheumatology 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. etc. | 1/7/2020 |
| 170 | ACIST Medical Systems Eden Prairie, MN Quality Engineer BS in engineering or related Exp: 0-5 years |
Provide hands-on quality engineering technical support for to the development of new medical devices, as well as changes to existing commercialized devices. This will include development of quality requirements/plans for new products, design/process validation requirements, test method validation and ongoing change management for finished device manufacturing. The Product Quality Engineer plays an active role in the processes to ensure product changes meet quality standards consistent with ACIST Medical Systems policies, while meeting all applicable regulatory requirements. The role works upstream and downstream ensuring the total product lifecycle is maintained and that our products continue to perform as designed. etc. | 1/7/2020 |
| 171 | Acumed Nashville, TN Associate Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Associate Sales Representative (ASR) exceeds sales quota within an assigned territory by delivering Acumed product on time and providing high quality technical assistance in the OR. The ASR assists in the assessment of the customer base to identify new business opportunities and executes a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 172 | Acumed Hillsboro, OR Regulatory Associate BS in a science, health, or technical discipline Exp: 0-2 years |
The Regulatory Associate supports the overall regulatory function by helping to maintain regulatory processes and systems. S/he utilizes computer and software proficiencies to create, coordinate, procure and/or maintain data and documentation to support US and OUS medical device registration. The Regulatory Associate also employs an attention to detail and developing familiarity with products and processes to ensure databases, dashboards and documents are current and correct. etc. | 1/7/2020 |
| 173 | Acumed Danville, PA Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 174 | Acumed New York, NY Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 175 | Acumed Boston, MA Sales Associate BS/BA in a business or medical discipline Exp: 0-3 years |
The Sales Associate (SA) exceeds sales quota within an assigned territory by driving the market acceptance and adoption of Acumed products. S/he converts key surgeons to Acumed's products by utilizing a high level of technical and surgical knowledge. S/he focuses on developing relationships, listens to customer needs, and provides product solutions and services that exceed customer expectations. The SA provides technical advice to customers to ensure optimum use of our products to maximize surgeon satisfaction and patient outcomes. etc. | 1/7/2020 |
| 176 | Acumed Wichita, KS Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Sales Representative (SR) exceeds sales quota within an assigned territory by delivering Acumed product on time providing high quality technical assistance in the OR and assists in driving market acceptance and adoption of Acumed Products utilizing technical and surgical knowledge. The SR assists continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 177 | Acumed Nashville, TN Sales Representative BS/BA in a business or medical discipline Exp: 0-2 years |
The Sales Representative (SR) exceeds sales quota within an assigned territory by delivering Acumed product on time providing high quality technical assistance in the OR and assists in driving market acceptance and adoption of Acumed Products utilizing technical and surgical knowledge. The SR assists continuously assesses the customer base to identify new business opportunities and develops a targeted sales strategy for each identified opportunity proactively ensuring all leads are followed up on appropriately. etc. | 1/7/2020 |
| 178 | Aesculap Allentown, PA General Manufacturing Associate (Detailed Assembler) 3rd Shift - Pain Control HS diploma or equivalent Exp: 0-1 years |
This position is to assemble, package and inspect medical devices in accordance with the quality and production standards established by our organization. This includes working with chemicals, machines and measurement equipment. This position must follow procedures, policies and applicable regulatory policies to meet the requirements of our Quality Policy. Responsibilities: Essential Duties: Follows established procedures and guidelines to manufacture the organizations products according to specifications and schedules; volume, cost and waste targets; quality standards. etc. | 1/7/2020 |
| 179 | NantKwest La Jolla, CA Research Associate BS Exp: 1 year in lab |
The individual will be responsible for laboratory maintenance, group-support activities to further our NK & T cell initiative from primary tissue sources. This is a great opportunity for a recent college graduate or individual willing to diligently take care of laboratory maintenance and pick up cutting edge scientific skills at the same time to support different projects. Laboratory maintenance that includes ordering, stocking of laboratory and accessory facilities with necessary reagents and supplies. | 12/30/2019 |
| 180 | NantKwest La Jolla, CA Research Associate BS or MS in biochemistry, biological sciences Exp: 1-3 years as research technician |
Daily tasks associated with the construction and purification of vaccine vectors. Demonstrated proficiency and understanding of concepts of chromatography: HPLC and/or FPLC. Operation and maintenance of laboratory instruments such as centrifuges, incubators, electrophoresis instruments, TFF, imagers, and other measuring instruments and devices. Preparation of laboratory reagents, stocks, cultures, and cell lines | 12/30/2019 |
| 181 | Natera Austin, TX Production Engineer - Statistics/Data Analysis BS/BA in engineering, bioinformatics, math or related Exp: 0-2 years |
Production Engineer - Statistics performs basic data analysis to manage daily operations for the product and its algorithms. Manage daily operations for the product algorithms. Track ongoing product performance metrics and investigate any variations, in cooperation with lab operations. Investigate data quality concerns using Python/R. Drive informed and timely solutions for unexpected scenarios. Track issues, coordinate new feature releases, and provide data analysis support to laboratory operations. | 12/30/2019 |
| 182 | Natera San Carlos, CA Quality Assurance Specialist BS/BA in life sciences, engineering or software Exp: 1+ years in biotech |
This is an entry-level position to assist the Quality Department in continuous compliance and improvement. Assist with collecting and trending quality metrics. Assist with assigning IDs for CAPAs, Deviations, SCAR, Complaints, and NCRs and filing completed records. Stays current on applicable regulation and guidance from FDA, ISO13485, CLIA, CAP, etc. Assist with review and approval of qualification records | 12/30/2019 |
| 183 | Natera San Carlos, CA IQC Associate HS Diploma/GED Exp: 1-2 years in medical device manufacturing |
The IQC Associate conducts incoming material inspections required to assure product safety and compliance to specifications, GMP’s, and ISO requirements. Works with other Quality Inspectors and Laboratory personnel to complete testing, special projects and other projects as required. Ensures compliance with quality systems, policies, procedures and practices and all local, state, federal and safety regulations, policies and procedures. | 12/30/2019 |
| 184 | Natera Austin, TX QC Equipment Specialist 1 BS/BA in biological sciences Exp: 0-2 years |
The Quality Control Equipment Specialist 1 is responsible to ensure superior performance of all equipment and instrumentation utilized in the Operations laboratory. The QC Equipment Specialist will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications | 12/30/2019 |
| 185 | Natera Austin, TX Clinical Laboratory Operator I BS/BA in biological sciences Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. Assist in testing of patient samples according to standard operating procedure. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures. Follows GLP (good laboratory practice): maintain clean and organized workspace | 12/30/2019 |
| 186 | Natera San Carlos, CA Clinical Lab Scientist II BS/BA in med tech/biological sciences, or related Exp: 1-2 years as medical technologist |
Analyzes specimens and maintains equipment in good operating condition. Verify the proper specimen being analyzed and perform tests that need to be completed. Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab | 12/30/2019 |
| 187 | Natera Austin, TX Clinical Data Operator 1 HS Diploma/GED Exp: 0-1 years |
Clinical Data Operator 1 accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. | 12/30/2019 |
| 188 | Natus Medical Madison, WI Repair Technician (I or II) AA in relevant field Exp: 0-6 months |
Test and calibrate assemblies to meet quality standards as well as perform electronic calibration and verify fixtures. Trouble shoot assemblies independently with exceptional computer skills. Maintain a strong commitment to high quality work with less than 2% failure rate on repairs. Maintain a 10 business day repair turnaround time on customer owned properties. Maintain minimum stock with refurbished parts to assure same day order fulfillment to assure best in class customer satisfaction | 12/30/2019 |
| 189 | Natus Medical Boston, MA Field Service Technician AA or equivalent Exp: 6-12 months experience/training |
The Field Service Technician provides industry-best technical support on computer-based medical instrumentation and establishes strong relationships with customers, managers and the national service team. This position will be based remotely and responsible for multi-state service coverage (Region:CT, ME,MA, NH, RI and VT). | 12/30/2019 |
| 190 | Navitas Life Sciences Rockville, MD Research Specialist - KAI Research BS/BA in biological/health sciences Exp: 0-1 years |
Demonstrate a thorough understanding of the application of basic clinical research methodologies to meet protocol and regulatory requirements. Develop client materials according to project requirements, including but not limited to, project-specific documentation, operating procedures, standards, and work flows. Monitor project changes to ensure documentation and systems/software conforms to new requirements. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensures appropriate distribution of materials to internal and external research personnel and sites. | 12/30/2019 |
| 191 | Navitas Life Sciences Rockville, MD Research Assistant - KAI Research BS/BA in biological/health sciences Exp: 0-1 years |
Apply basic clinical research methodologies to meet protocol and regulatory requirements. Assist in the development of client deliverables according to project requirements, including but not limited to, project-specific documentation, operating procedures, and work flows with direction of more experienced staff. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensure appropriate distribution of materials to internal and external research personnel and sites. | 12/30/2019 |
| 192 | Nelson Lab Itasca, IL Lab Analyst - Chemistry - M-F, Days HS Diploma/GED to BS Exp: 0-1 years |
The 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. | 12/30/2019 |
| 193 | Nelson Lab Salt Lake City, UT Lab Analyst HS Diploma/GED to BS Exp: 0-1 years |
The 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. | 12/30/2019 |
| 194 | Nelson Lab Salt Lake City, UT Development Chemist BS/BA in chemistry or related Exp: 1-3 years |
This position involves decision making in the areas of analytical chemistry, equipment maintenance, data quality, and workflow. Duties include analysis of a wide variety of samples following establish methods or standards, and supporting the development and implementation of laboratory policies and procedures. Experience with instrumentation/equipment and software, such as gas chromatography/mass spectroscopy (GC/MS), high performance liquid chromatography/mass spectroscopy (HPLC/MS), and Inductively coupled plasma/mass spectrometry (ICP/MS). (Ideal candidate needs to have experience with least one of these instruments.) | 12/30/2019 |
| 195 | Neocis Miami, FL Control Software Engineer BS in computer science/electrical engineering Exp: 0-2 years |
Neocis is looking for a robot control software engineer to contribute significantly to the core design. You will be responsible for software design and development of a real-time robot controller, verification and validation testing for safety and reliability and support and contribute to intellectual property development. You will work with cross-functional teams including software and electrical engineers and marketing as well as clinicians and clinical staff. | 12/30/2019 |
| 196 | Nephron Pharma West Columbia, SC Quality Assurance OnlineEvening 12 hour Shift ONLY HS Diploma/GED Exp: 1-2 years in QA/Production |
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. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 12/30/2019 |
| 197 | Nephron Pharma West Columbia, SC Microbiology Analyst I BS in biological/life sciences Exp: 1 year in pharma preferred |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. 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. | 12/30/2019 |
| 198 | NeuMoDx Ann Arbor , MI Manufacturing Specialist, Reagent BS/BA in science or chemistry Exp: 1+ year in lab/reagent production |
Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks | 12/31/2019 |
| 199 | Neurocrine Bioscience San Diego, CA Associate Scientist, In Vivo BS/BA in biology or related Exp: 1 year or more related experience |
The primary tasks for this position will include transgenic animal colony maintenance and breeding, compound formulation and dosing, behavioral assessments, stereotaxic surgery and tissue collection. This position requires a high level of organization and attention to detail as well as the willingness and ability to work both independently and as part of a team. Previous experience with stereotaxic surgery, AAV administration and mouse colony maintenance preferred. | 12/31/2019 |
| 200 | Nevro Redwood City, CA Quality Engineer I - Temp BS in technical sciences Exp: 0-2 years in quality/regulatory |
The Quality Engineer I is responsible for Quality Assurance activities related to the life cycle of the product. Trave to and manage manufacturing assembly process at Suppliers. Perform data analysis for root cause investigations | 12/31/2019 |
| 201 | Nevro Redwood City, CA Firmware Engineer BS in computer engineering or related Exp: 1-2 years, familiarity with C, C++, C# or other |
The Firmware Engineer shall participate in research and product development activities ranging from product concept through transfer to manufacturing. This position will apply knowledge of engineering principles and practices for software development of implantable medical devices and accessories. | 12/31/2019 |
| 202 | Nevro Redwood City, CA Technial Support Specialist - Temp BS in scientific, technical, or medical field Exp: 1+ year in customer service |
Great Customer Experience is one of the keys to Nevro’s success. The Quality Compliance Specialist is one of the few roles in Nevro that has a direct customer touchpoint to resolve product and therapy questions or issues. This role is critical to ensure that the customer is served as best as we can to ensure that our product and therapy continues to deliver much needed relief to our customers. | 12/31/2019 |
| 203 | New England Biolabs Bethesda, MD Associate Field Representative - Mid-Atlantic BS in core life sdciences Exp: 1 year in lab preferred |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the Mid-Atlantic Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Bethesda, MD area. | 12/31/2019 |
| 204 | New England Biolabs New York, NY Associate Field Representative - Tri-State BS in core life sdciences Exp: 1 year in lab preferred |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the Tri-State Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Manhattan, NY area. | 12/31/2019 |
| 205 | New England Peptide Gardner, MA Lab Technician BS/BA in biology or chemistry Exp: 1 year preferred |
Duties include: Operations and maintenance of peptide synthesis instrumentation, liquid chromatography instrumentation, etc. Peptide cleavage data analysis and characterization of peptides using HPLC and Mass Spec. | 12/31/2019 |
| 206 | New England Peptide Gardner, MA Facility Maintenance AS/AA in industrial/electrical/mechanical engineering Exp: 1-2 years in related |
This role will be responsible for assisting in the completion of the day-to-day activities involving the maintenance of the facility, equipment and machinery and the overall facility appearance. Participate and assist in the maintenance of all company property, including but not limited to, manufacturing equipment, buildings, grounds, HVAC, electrical, plumbing, safety and others as necessary. | 12/31/2019 |
| 207 | New England Peptide Gardner, MA Lab Assistant HS Diploma or higher Exp: 1 year preferred |
NEP is seeking a highly motivated individual interested in a career in the Biotech/Pharmaceutical industry. Local candidates only. No experience necessary, we will train! Working alongside other Peptide Scientists and Technicians, the Lab Assistant will help support the production process. | 12/31/2019 |
| 208 | New England Peptide Gardner, MA Lab Technician BS/BA in biology or chemistry Exp: 1 year preferred |
Duties include: Operations and maintenance of peptide synthesis instrumentation, liquid chromatography instrumentation, etc. Peptide cleavage data analysis and characterization of peptides using HPLC and Mass Spec. | 12/31/2019 |
| 209 | Avecia Pharma Services Irvine, CA Chemist I - QC BS/BA in chemistry or related Exp: 1-2 years in pharma |
Perform routine laboratory analysis of raw material and container closure system samples according to established specifications and procedures using basic analytical chemistry techniques in accordance with Customer, Company and cGMP requirements. | 1/5/2020 |
| 210 | Nkarta Therapeutics South San Francisco, CA Research Associate MS in molecular/cell biology, immunology Exp: MS: 0-3 years |
The ideal candidate will interact closely with group leaders, scientists and research associate to drive discovery and development of new therapeutics in pre-clinical development. Duties include: Mammalian tissue culture, including isolation and culture of primary human cells from whole blood. Perform studies utilizing cellular immunology to develop and analyze in vitro cell-based assay to support early discovery efforts and pipeline. Perform studies utilizing cellular immunology to develop and analyze in vitro cell-based assay to support early discovery efforts and pipeline. | 1/5/2020 |
| 211 | Nkarta Therapeutics South San Francisco, CA Research Associate (in vivo) MS in biological sciences Exp: 1 year in pharma/biotech |
Conducts pharmacological evaluation of test agents (cell products or small molecule) in subcutaneous, systemic and orthotopic in vivo oncology models. Assists in sample processing, homogenization, or generation of single cell suspensions for ex vivo flow cytometry analysis or PCR analysis | 1/5/2020 |
| 212 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS in biological sciences Exp: 0-3 years in lab |
Execute a broad range of cell based functional and phenotypic assays for characterization of engineered NK and T-cells to accelerate projects in pre-clinical development. Conduct in vitro mechanism of action studies using primary human or mouse immune cells and cell lines to evaluate activity of candidate therapies. | 1/5/2020 |
| 213 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS in cell biology or related Exp: 0-3 years in lab |
Generate stable cell lines and master cell banks for both in vitro assays and in vivo pharmacology studies. Oversee and perform daily activities related to the maintenance and scale up of in-house cell lines and primary human immune cells | 1/5/2020 |
| 214 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior/Process Engineer MS in biological sciences Exp: 1-6 years |
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 | 1/5/2020 |
| 215 | Nobel Life Sciences Woodbine , MD Study Coordinator BS/BA in sciences Exp: 1 year related work |
Assist Study Director in determining staffing requirements, scheduling and documenting all critical events. Assist Study Director with protocols and reports preparation. | 1/6/2020 |
| 216 | Nobel Life Sciences Woodbine , MD Quality Control Associate BS/BA in sciences Exp: 1 year in QC position |
Responsibilities include: Supervise day to day quality control operations and documentation. Assist in writing and reviewing SOPs, study protocols and reports. Coordinate in-house and external routine maintenance including calibration and certification and maintenance of lab equipment. etc. | 1/6/2020 |
| 217 | Nobel Life Sciences Woodbine , MD Animal Lab Tech BS/BA in sciences Exp: 1 year in GLP, preferred |
Follow and perform standard operating procedures (SOP) & Protocols on study and stock animals, including, but not limited to: clinical observations, food consumptions, body weights, urine collection, administering anesthesia, mating procedures, blood draws dose administration, restraint, euthanasia, catheter placement, feeding, food removal, on laboratory animals. | 1/6/2020 |
| 218 | Nobel Life Sciences Woodbine , MD Animal Care Tech BS/BA in sciences Exp: 1 year in GLP, preferred |
Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol. Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate log. | 1/6/2020 |
| 219 | Nordson Minneapolis, MN NPI Engineer I BS in mechanical/biomedical/manufacturing engineering Exp: 0-3 years in medical device product development |
The desired individual will possess a broad range of medical device design and development skills and experience, as well as depth of knowledge of process development, process validation, lean manufacturing methodology, and statistical process control. Develop and document manufacturing processes for medical devices (disposable and reusable), catheters, implants, and/or packaging, from concept through market introduction. | 1/6/2020 |
| 220 | Nordson Elk Grove Village, IL Field Service Technician AS/AA Exp: 0-2 year |
Responsible for performing on-site installation, servicing and repair of complex equipment and systems. Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. | 1/6/2020 |
| 221 | Nordson Salem, NH Production Associate 1 (Balloons) Third Shift Temp to Hire HS Diploma/GED Exp: 0 years required |
Position consists of manufacturing of medical components in a clean room environment while under general supervision in accordance with specifications and written procedures. This position may include machine operation, manual production using hand tools, visual inspection, physical measurements, and packaging of finished product. This position requires the ability to work with small and delicate components using a high degree of dexterity and accuracy. | 1/6/2020 |
| 222 | Norwich Pharma Norwich, NY Validation Engineer I BS/BA or work experience Exp: 0-4 years |
The Validation Engineer I - Cleaning conducts validation assessments of equipment, facilities and process systems. Compile and analyze validation data, prepare protocols, reports and make recommendations for changes and/or improvements and maintains appropriate validation documentation and files. | 1/6/2020 |
| 223 | Norwich Pharma Norwich, NY Technician I Pilot Manufacturing HS Diploma/GED Exp: 1-3 years in manufacturing enviornment |
Primary Responsibilities include: support pilot plant functions. Accurately execute all GMP documentation including batch records, cleaning records, logbooks, etc. Escalates documentation and process errors, events, and deviations immediately to PDTS Manager/Group Leader and PDTS QA. | 1/6/2020 |
| 224 | Nostrum Laboratories Kansas City, MO Packaging Technician HS Diploma/GED Exp: 1 year in pharma/food/manufacturing |
The Packaging Technician performs routine packaging operations for the production of pharmaceutical products; operates packaging line equipment according to established SOPs and department procedures. Prepares and cleans room, equipment, facility and documents for manufacturing and packaging process | 1/6/2020 |
| 225 | Notable Foster City, CA Research Associate - High Throughput Screening BS/MS in biological sciences/engineering Exp: 6 months in lab experience |
You will be supporting our numerous projects and be an integral part in scaling up for future upcoming projects. Will be responsible for processing primary samples and preparing them for our automated high-throughput screens. | 1/6/2020 |
| 226 | Nova Biomedical Waltham, MA Repenishment Associate HS Diploma Exp: 1+ year in distribution/ordering |
Essential Responsibilities are to ensure the accurate movement (stocking, replenishing, consolidating, blocking, fulfilling) of materials and products within the Distribution Department and report any /all batch number or quantity discrepancies related to Distribution materials. Perform cycle counting of assigned materials / products, assist in reconciling variances, identify materials/ products with assigned placards (short-dated, Quality holds, etc.) | 1/6/2020 |
| 227 | Nova Biomedical Waltham, MA Reagent Packager I - First Shift HS Diploma/GED Exp: 1+ year in related |
The Packager, under general supervision, will follow established procedures in packaging reagent kits. This individual is responsible for working on an assembly line to assemble the various kits within the established quality and time standards. The individual will work with various packaging equipment such as: automated/manual tape machines, manual pallet trucks, conveyors, flow racks and other packaging devices | 1/6/2020 |
| 228 | Nova Biomedical Waltham, MA Jr Electornic Technician HS Diploma/GED Exp: 1+ year as test technician |
The Jr. Electronic Technician at Nova Biomedical is responsible for operating test and measurement equipment, such as Oscilloscopes and multimeters, to test instruments and assemblies. Essential Responsibilities include: ability to troubleshoot with limited supervision to the component level on low complex boards (thru-hole). Ability to use small hand tools for soldering. Basic knowledge of computers and electronic components. Basic understanding of menu driven computer programs. | 1/6/2020 |
| 229 | Vicarious Surgical Charlestown, MA Artificial Intelligence Engineer MS in computer science Exp: 1-3 years |
Joining the Research & Development team as an Artificial Intelligence engineer, you will lay the groundwork for a brand new team at Vicarious Surgical giving intelligence to the next generation of surgical robotics. We are looking for dynamic, collaborative individuals with a passion for AI who thrive in a fast-paced, creative, and strategic environment. You will enjoy working with a highly talented and diverse team of engineers to develop Artificial Intelligence, Perception, Computer Vision, and Robotic Controls features for our robots. This job entails: Research and develop technologies for conventional AI, Computer Vision, Machine Learning, multi-sensory perception, sensor fusion, scene understanding etc. for robotics applications. etc. | 12/17/2019 |
| 230 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 1:00 AM to 9:30 AM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. 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. etc. | 12/17/2019 |
| 231 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 8:00 AM to 4:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. 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. etc. | 12/17/2019 |
| 232 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Monday - Friday, 8:00 AM to 4:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. 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. etc. | 12/17/2019 |
| 233 | Viracor Lee's Summit, MO Clinical Laboratory Scientist I BS/BA in a laboratory science Exp: 1 year |
This is a Full Time position. Schedule is Tuesday - Saturday, 12:00 PM to 8:30 PM (opportunity for 10-hour shift with rotating day off following training), with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. 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. etc. | 12/17/2019 |
| 234 | Viracor Lee's Summit, MO IT Business Analyst I AS/BS in laboratory science Exp: 1-2 years |
This is a Full Time position. Schedule is Monday - Friday, 8:00AM – 5:00PM, with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. The IT Business Analyst supports the organization by assessing the impact of requested changes, capturing and documenting requirements, and ensuring that those requirements are delivered by IT. In addition, the Business Analyst is responsible for the documentation and execution of test plans for the delivered functionality while supporting the business through the implementation process. Business Analysis is part of the Software Development Life Cycle (SDLC) and the Business Analyst will be involved from initial concept through final implementation, including requirements gathering, design, testing and implementation. Employee Responsibilities: Consult with different areas of the organization to identify and document the requirements for new systems and enhancements to existing systems. Document business functions and processes using a best practice standard developed by the Business Analysis team. etc. | 12/17/2019 |
| 235 | Viracor Lee's Summit, MO Research Scientist I BS/BA in a laboratory science Exp: 0-3 years |
This is a Full Time position. Schedule is Monday – Friday, 1:00pm- 9:30pm with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. 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. Employee Responsibilities: 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. etc. | 12/17/2019 |
| 236 | Viracor Lee's Summit, MO Research Scientist I BS/BA in a laboratory science Exp: 0-3 years |
This is a Full Time position. Schedule is Monday – Friday, 8:30pm- 5:00pm with overtime as needed. Candidates currently living within a commutable distance of Lee’s Summit, Missouri are encouraged to apply. 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. Employee Responsibilities: 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. etc. | 12/17/2019 |
| 237 | Visterra Waltham, MA Research Associate BS in biochemistry or related Exp: 1 year |
Visterra, Inc., is looking to hire a highly motivated Research Associate with research experience in biochemistry, protein sciences and/or molecular biology applied in the context of antibody-based therapeutic drug discovery. This individual will play a key technical role in advancing Visterra’s early research programs in autoimmunity, immunology and other related areas of therapeutic interest through the design and implementation of library-based screening methods, recombinant protein production, protein engineering, and biochemical, biophysical, and biological characterization of early and late stage leads to support the discovery andvalidation of therapeutic antibody candidates. etc. | 12/17/2019 |
| 238 | Voyager Therapeutics Cambridge, MA Clinical Trial Associate (Contract) BS in a life science Exp: 0-2 years |
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. The CTA will also assist the CTM for assigned studies in the operational and logistical aspects of clinical trials according to ICH-GCP and Voyager standard operating procedures. This position reports in directly to the Associate Director of Clinical Operations. Responsibilities: Support project meeting logistics such as: calendar management, room & equipment set up, attendance tracking, agenda preparation, drafting of meeting minutes, and collation of materials. Set up, maintain and periodically audit Trial Master Files and ensure all relevant study documents are filed and archived based on the appropriate guidelines/processes. Execute assigned study tasks, awareness of priorities and timelines, assist in tracking study metrics, maintenance and distribution of trackers, support preparation of study newsletters, communicate with and oversee CRO for assigned start-up activities. etc. | 12/17/2019 |
| 239 | Voyager Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Molecular Biology BA/BS Exp: 1-3 years |
Voyager Therapeutics seeks a highly motivated and experienced molecular biologist to contribute to its research team at its facility in Cambridge, Massachusetts. The candidate will be involved in novel AAV capsid discovery, screening AAV variant libraries in small and large animals and engineering capsids for desired properties. This is an ideal position for an individual with extensive hands-on cellular and molecular expertise, who has a can-do attitude and strong work ethic, and thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment. Requirements: Molecular cloning and prepare rAAV constructs or AAV capsid libraries. Perform plasmid purification by miniprep and maxiprep. Maintain and culture mammalian cell lines, perform transient transfection for gene expression or AAV vector production at a small or medium scale. etc. | 12/17/2019 |
| 240 | WAVE Life Sciences Cambridge, MA Research Associate – Biology BS/MS in biology or related Exp: 0-3 years |
WAVE Life Sciences USA seeks a highly motivated biologist to join its research team in Boston, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and crossdisciplinary biotech environment. The candidate will be responsible for designing, executing and analyzing experiments as a member of teams focused on advancing therapeutic programs and discovery research platforms. This candidate will contribute to all levels of in vitro and in vivo discovery research to support development of optimized nucleic acid therapies in multiple disease areas. Prior experience in animal handling and tissue processing are preferred, but not required. Position Responsibilities: Experience in cell and molecular biology, including primary cell culture, transfections, mRNA quantitation by qPCR, and protein quantification by ELISA or western blot. etc. | 12/17/2019 |
| 241 | WCCT Global Cypress, CA Laboratory Accessioner HS diploma or equivalent Exp: 3-6 months |
The Laboratory Accessioner is responsible for entering all patient information, demographics, and ordered tests in the laboratory information system. The Accessioner will QC daily data entry and work under the direct supervision of the Research Laboratory Supervisor. Daily tasks include organizing requisition forms, data entry, filling out send out requisitions for outside testing, cleaning up work area, and performing waived testing. Essential Job Functions: Enter all pertinent information from the requisition into the computer correctly. Enters "special handling" and/or frozen requisitions. When handling frozen samples, will set up work areas by retrieving dry ice, ice chests, racks, and stickers. Accessioners will also be responsible for signing for the integrity of frozen specimens, received from the couriers. At the end of each night, the accessioners will deliver the specimens to the appropriate departments. Take complete inventory of contents of envelope. etc. | 12/17/2019 |
| 242 | WCCT Global Cypress, CA Laboratory Assistant HS diploma or equivalent Exp: 3-6 months |
The Laboratory Assistant is responsible for conducting the biological sampling activities related to each clinical trial. This position assists with the preparation, collection, documentation, processing, inventory and shipment of biological specimens for each study and reports to the Laboratory Supervisor. ESSENTIAL JOB FUNCTIONS: Conducts all operational activities within the laboratory related to the preparation of sample collection containers, processing biological specimens, performing testing, documenting procedures, and preparing specimen shipments. Ensures that all lab procedures are done correctly with minimal error. Follows the policies and procedures for laboratory facilities and equipment maintenance. etc. | 12/17/2019 |
| 243 | WCCT Global Cypress, CA Phlebotomist/Medical Assistant - On Call HS diploma or equivalent Exp: 3-6 months |
The On Call Research Assistant is an entry level position assisting in a variety of duties involved in the collection, compilation, and documentation of clinical research data in various departments as assigned. All data collected is quality control reviewed and is compliant with study and non-study regulations including, but not limited to the study protocol, HIPAA, OSHA, GCP, GDP, CFR, ICH Guidelines and site SOPs and Work Instructions. ESSENTIAL JOB FUNCTIONS: Follow all study and non-study regulations including, but not limited to: Patient/Volunteer Privacy (HIPAA), OSHA, Good Clinical Practice (GCP), Good Documentation Practice (GDP), Standard Operating Procedures (SOP), and department specific Work Instructions (WI). Follow proper safety and emergency policies and procedures as set forth by WCCTG. etc. | 12/17/2019 |
| 244 | Westat Rockville, MD Research Assistant BA/BS in social sciences or education Exp: 1 year |
Westat has an immediate opening for a research assistant who will work with a project team to train and support staff in state education agencies to implement a national assessment of students and to develop data analyses and reports. Provide analytical and operational support to the project and to staff in state education agencies; Develop and manage training materials; conduct web-based and in-person trainings; Provide secondary support to project Support Desk and project intranet website on an as-needed basis; Develop and maintain project schedule of web-based trainings; Review and manage data for quality control purposes and project evaluation, maintain and enhance databases of project information; Monitor the productivity and quality of the data collection effort; Work with IT and project staff on system requirements. | 12/17/2019 |
| 245 | Westat Rockville, MD Research Assistant MS/MA in a quantitative social science Exp: Not necessary for MS/MA candidates |
Westat is seeking a research assistant to work on survey research projects, assisting expert data managers in defining and processing survey data and metadata from collection through delivery to Westat’s clients. Data review and documentation writing are both part of the role. Write technical specifications for programming survey instruments and analytic variables. Define data dictionaries for complex files, test survey instruments to ensure accurate data capture, and review collected data at the detailed level. Create data descriptions and harmonize data from multiple sources; the data are collected in a variety of technologies and formats with a wide breadth of subject areas. etc. | 12/17/2019 |
| 246 | Westat Rockville, MD Research Assistant BS/BA Exp: 1 year |
We have an immediate opening for a research assistant with experience in data collection procedures and materials along with a background in quantitative research and data analysis. The successful candidate will work closely with a multidisciplinary research team working on an innovative longitudinal health and aging study and a caregiving study. Job Responsibilities: Develop specifications for computer-assisted survey data collection instruments. Draft instrument testing scripts and related materials. Working with project and IT staff on technical specifications for survey management systems. Assist in developing data collection procedures, respondent materials, and field memos. etc. | 12/17/2019 |
| 247 | Wolfe Laboratories Woburn, MA Research Associate BS/MS in chemistry, biochemistry, or related Exp: Recent graduates |
We are seeking a talented and passionate scientist who is eager to be part of our success, and who embraces our core values: Integrity, Excellence, and Teamwork. This role requires a highly driven and proactive scientist with a passion for drug development, the curiosity and flexibility to work on diverse projects, and the tenacity to tackle complex questions by developing/applying new methods to solve previously intractable problems in drug development in a dynamic, fast-paced, team-oriented and collaborative environment. etc. | 12/17/2019 |
| 248 | Worldwide Clinical Trials Austin , TX Bioanalysis Support BS Exp: 0-2 years |
The Scientific Associate, Bioanalysis Support works under the guidance of the Senior Manager, Leader of Bioanalysis and is responsible for providing support and performing analyses ranging from routine to complex using accurate and efficient analytical techniques. Understand and apply GLP guidelines in all aspects of work. Perform chemical assays ranging from routine to complex with consistent accuracy and precision. Accurately prepare stocks, reagents, standards and quality controls as needed. Work with a variety of scientists/technicians. Perform basic mathematical calculations. Document promptly and clearly all procedural processes. etc. | 12/17/2019 |
| 249 | WuXi AppTec San Diego, CA Research Associate I AS/BS in biology or related Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate I to join the team. Responsibilities: Assist with in vivo pharmacology experiments for preclinical contract research. Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models with supervision. Monitor mouse groups enrolled in drug efficacy, mechanism of action, PKPD and proof-of-concept studies. Perform drug dosing by various routes of administration. Perform in-life blood sampling through various routes. Perform necropsy and tumor/organ sampling and processing. Monitor in-life study measurements: tumor volume, body weight, tracking overall health condition and survival of mice. etc. | 12/17/2019 |
| 250 | WuXi AppTec Cranbury, NJ Associate Scientist I BS in animal science, biology, or related Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. Operates lab equipment including oxidizers, centrifuges, LS counters, and cage/tunnel washers. Essential Job Functions: Under regular close supervision, performs routine in vivo experimental functions in rodents, which may include: in life observations, dose administrations, sample collections, sample analysis, necropsy, and euthanasia procedures. Trains on various techniques to become proficient in in vivo. Performs husbandry tasks including observations, cage change outs, daily cleaning, and operating the cage washer. Assists with routine vivarium facility environmental monitoring (RODAC, pest control, lighting checks, etc.). etc. | 12/17/2019 |
| 251 | WuXi AppTec King of Prussia, PA Scientist Downstream Process Development BS/MS Exp: 0-5 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine Downstream cell culture processes. Responsibilities: Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. Design and execute lab-scale experiment in supporting downstream process development, verification, characterization. Perform purification experiments in BSL-2 labs and document experiments in lab notebooks. Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers. | 12/17/2019 |
| 252 | WuXi AppTec King of Prussia, PA Scientist Upstream Process Development BS/MS Exp: 1-2 years |
The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Responsibilities: Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. Perform data analysis and interpretation, and develop strategies for optimization and troubleshooting. Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. etc. | 12/17/2019 |
| 253 | WuXi AppTec Austin , TX Clinical Project Associate HS diploma/AA/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. 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. Under direct supervision designated Clinical Trial Management System (CTMS) to track and process clinical trial information, (e.g., site lists/personnel, regulatory documents, Institutional Review Board re-approvals) in order to provide analysis of information to PM. Prepares and provides status reports to customers with oversight from assigned PM. Under direct supervision assures the maintenance of the TMF. etc. | 12/17/2019 |
| 254 | WuXi AppTec Philadelphia, PA Research Associate, Analytical Development - Virology BS in a biological science Exp: 1+ year(s) |
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. Responsibilities: Executes R&D studies planned by supervisor or technical lead. Works under close supervision from supervisor or senior personnel. Executes QP and VPs, and other GMP methods under supervision by supervisor or technical lead. Drafts test methods/RPs/SOPs under guidance of supervisor or technical lead. etc. | 12/17/2019 |
| 255 | Micr Indianapolis, IN Medical Research Coordinator Associate: BS/BA Exp: 1-3 years clinical research experience preferred |
We are seeking an experienced individual who has been involved in clinical research. 1-3 years of clinical research experience is preferred for this full-time position. | 12/8/2019 |
| 256 | MRIGlobal Kansas City, MO Electrical Engineer MS in eletrical/electronics engineering Exp: 0-3 years |
MRIGlobal has an exciting full-time opportunity for an Associate Electrical Engineer in our Intelligence, Surveillance, and Reconnaissance Division located in Kansas City, MO. In this unique opportunity, the selected candidate will work with other engineering and technical disciplines in the design, prototyping, and testing of custom systems to meet customer requirements. Furthermore, the selected candidate will: Design a broad range of analog and digital circuits, Design and layout custom circuit boards to meet challenging packaging and performance requirements, etc. | 12/9/2019 |
| 257 | Merck KGaA Verona, WI Associate Production Scientist BS in Chemistry, Biochemistry, Chemical Engineering, or equivalent Exp: <1 year |
Position primarily involves the safe and efficient manufacturing of API’s according to cGMP requirements. Kilo Lab and Pilot Plant manufacturing of APIs and intermediates. Demonstrate proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines. Maintain the safety and cleanliness of production areas and all related equipment during each shift, specifically potent compound handling techniques | 12/9/2019 |
| 258 | Merck KGaA Billerica, MA Research Associate - Protein Expression Bachelor’s degree in Biology, Microbiology or other related Science Exp: <1 year |
We are seeking a motivated researcher to join our recombinant protein expression team at EMD Serono. The Operations group, as part of the Protein and Cell Sciences (PCS) department, generates micrograms to grams of purified protein. The successful candidate will primarily be responsible for small and large scale expression of therapeutic and reagent proteins primarily by transient transfection of mammalian cells lines or from stable cell lines to support preclinical research. The incumbent would also be responsible for maintaining expression cell lines, cell passaging, generating stable mammalian cell lines, selection of high expressing cell lines, creation of research cell banks, optimizing cell growth and protein expression. | 12/9/2019 |
| 259 | Merck KGaA Oakland, CA Field Service Engineer - Northern CA HS Diploma/GED Exp: 1+ year in field service/mechanics |
In the role of Field Service Engineer (FSE), you will be responsible for the installation, repair, preventative maintenance and qualification of water purification systems throughout Northern CA (Oakland/North Bay/Richmond/Walnut Creek) area. You will also be responsible to provide backup support to nieghboring territoriess as required. | 12/9/2019 |
| 260 | Merck KGaA St. Louis, MO Packaging Operator I HS Diploma/GED Exp: 3+ months in ISO/GMP environment |
To stage, fill (manually or semi-automatically), cap, label, and over pack liquid, powder, and lyophilized products per approved packaging specifications. Clean laboratory glassware and batch tanks. Complete appropriate packaging documentation per FDA, ISO, and GMP procedures and deliver products to inventory. Assemble and package chemical kits. Fill, cap, and label chemical products. Manually fill liquids or powders. Utilize semi-automated equipment to fill liquids or powders. Fill products utilizing aseptic techniques. Perform fills in environmentally controlled areas. Fill hazardous products. Transfer bulk utilizing peristaltic pumps. Filter bulk materials using pumps and in-line filters or vacuum filters. Operator automated and semi-automated cappers. Manually torque caps with wrenches | 12/9/2019 |
| 261 | Merck KGaA Rockville, MD Flexible Resource Associate Scientist BS or MS in sciences Exp: BS: 1+ years, MS: 0 years |
The Flexible Resource Associate Scientist is a dynamic contributor with an opportunity to work in many different laboratories. You will conduct important assays by making scientific observations, maintaining detailed workbooks, and documenting to GLP/GMP standards. Deployment duration and the specific laboratory and will be coordinated via the Sales and Operations Planning (S&OP) process. | 12/9/2019 |
| 262 | Merck KGaA Springfield, MA Research Engineer, Life Sciences BS or MS in Mechanical, Electrical, Bioprocessing, Biochemical or Biomedical engineering Exp: <1 year |
You will be working in the life sciences group focusing on the development of the acoustic affinity cell selection platform. You will work on all aspects of the early stages of new product development, i.e., brainstorming, concept selection, engineering design and analysis, prototype assembly, testing and documentation. You will perform acousto-fluidic affinity cell selection experiments participate in design of experiments. You will take on SOP writing and lab management duties as needed to enable the team to maintain a fast and steady flow of experiments. You will develop into an independent thinker, innovator and contributor to the development of the cell selection platform. | 12/9/2019 |
| 263 | Merck KGaA St. Louis, MO cGMP Associate Production Scientist BS/BA in chemistry, biochemistry, biology, chemical engineering or related Exp: <1 year |
The cGMP Associate Production Scientist is responsible for the manufacturing of active pharmaceutical ingredients (APIs) Chemicals and bulk pharmaceuticals regulated by the Food and Drug Administration (FDA). They are responsible for following manufacturing protocols, consistent with and established according to current Good Manufacturing Practices (cGMP), and ensuring the accuracy of documentation. | 12/9/2019 |
| 264 | Miltenyi Biotec Gaithersburg, MD Manufacturing Associate - Upstream and Downstream BS/BA Exp: 0-2 years in GMP setting |
The qualified candidate will be responsible for adhering to GMP’s by following Standard Operating Procedures and executing Batch Production records using good documentation practices. Your exceptional ability to perform aseptic processes in a GMP cleanroom environment will contribute to the manufacture of lentiviral vectors used in human clinical trials, and propel Lentigen Technology’s continued growth and success. | 12/9/2019 |
| 265 | Miltenyi Biotec Auburn, CA Accounting Associate AS/AA Exp: 1-3 years in business/accounting |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. You will use your collaborative nature to effectively coordinate intercompany communications and transactions with various departments, with management, and the parent company to enable the continuous success of Miltenyi Biotec as a whole. | 12/15/2019 |
| 266 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in clinical processing/cell culture |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. Overall, your keen ability to carry out key cell processing and manufacturing procedures will champion the continued development of Miltenyi Biotec products and growing success. | 12/15/2019 |
| 267 | Miltenyi Biotec Sunnyvale, CA Process Development Associate BS/BA in life sciences Exp: 0-2 years |
As a member of Miltenyi Biotec’s Process Development team, you will have the exciting opportunity to support the development of new processes that will generate cellular therapeutic products. You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. In addition to your primary responsibilities, you will document activities for reproducibility, clean and maintain laboratory equipment and support team members as needed. Your superb organizational and documentation skills will be instrumental in the tracking and communication of data and will ensure efficient progress towards achieving team objectives. Overall, your attention to detail and keen ability to reliably produce cell cultures in a cross-functional team will champion the continued development of Miltenyi Biotec’s new products and growing success. | 12/15/2019 |
| 268 | Miltenyi Biotec Gaithersburg, MD Research and Development Scientist, RCL/HIV MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to perform duties within the area of development of new tests, including the development of a standard RCL test and in a second instance of an automatized RCL test. This includes the set-up of a standard test based on the use of C8166 cells, the characterization of the C8166 cells with respect to susceptibility and propagation of HIV over many cell passages, etc. A very issue related to this development is that the test has to comply with FDA requirements with at the end the transfer of the test to the QC department for routine use. Furthermore, you will be involved in the automatization of this specific test and eventually of other tests in the future. In this context, you will be directly involved in the conceptualization of such a test, responsible for designing specific experiments and analyzing the data using appropriate statistical methods. The particular duties of this position will allow you to work as part of a collaborative team environment | 12/15/2019 |
| 269 | Miltenyi Biotec Gaithersburg, MD PD Associate I BS/BA Exp: 0-2 years |
As a member of the Lentigen Technology Process Development team, you will have the exciting opportunity to support the development and tech transfer of processes to manufacture purified Lentiviral vectors used for pre-clinical and clinical products. You will apply your knowledge and prior laboratory experience to support the pre-clinical and clinical manufacturing of Lentiviral vector products. Familiarity with cell culture and/or purification technologies and analytical methods will enable you to assist in the development and tech transfer of processes compliant with GMP manufacturing requirements. | 12/15/2019 |
| 270 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS/BA in biological sciences Exp: 1-3 years in clinical processing/cell culture |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. | 12/15/2019 |
| 271 | Miltenyi Biotec San Diego, CA Executive Assistant AS/AA in business or related Exp: 0-2 years |
As a key member of the Miltenyi Biotec team, you will have the opportunity to provide administrative support to the President as well as other department heads in assigned activities. The unique duties of this position will allow you to oversee schedules, track activities, and serve as key contact between executives and internal/external clients. Additionally, you will assist in preparing agendas and presentation materials for associated events, meetings, and seminars. Overall, your particular skillset and efforts will drive Miltenyi Biotec’s continuing business success. | 12/15/2019 |
| 272 | Miltenyi Biotec Gaithersburg, MD R&D Scientist, Purification & Characterization MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to develop methods for the separation of different particle types and their characterization. Also, you will develop, evaluate and implement novel analytical methods for the fine characterization of viral vectors and exosomes, in view of the distinction of viral vectors from exosomes. You will design specific experiments to test LV function, perform statistical analysis of results, and communicate results internally, for use in publications, and in scientific meetings. Your responsibility will also include the development of chromatography-based separation steps in-view of the optimization of an existing purification protocol and their standard characterization. | 12/15/2019 |
| 273 | Mirus Madison , WI Shipping and Product Finishing Assistant HS Diploma/GED Exp: 1-2 years |
This position is required to provide department coverage 11am-3pm Monday-Friday. The position is offered at 32-40 hours per week. Prepare and execute domestic and international shipping of Mirus products using FedEx, UPS, DHL and freight forwarders. Receipt of incoming deliveries (e.g. supply orders, freight and parcel deliveries) | 12/15/2019 |
| 274 | Mission Pharma Boerne, TX Particle Technician HS Diploma/GED Exp: 1 year related experience |
Produces bulk pharmaceuticals, operates machinery and equipment, handles raw materials with and without handling equipment, completes documentation, and cleans and sanitizes equipment and rooms per SOP’s. Performs duties such as weighing, labeling, storing, moving, raw materials. Operates a mixer, forklift, powered pallet jacks, scales, dust collectors, hand tools, Fitzmill and sifter, NOL-TEC system and moisture removal controller. Weighs out and sample finished product. Processes the finished product for transport. Performs mixing duties such as introducing materials into the mixer, watching for overflow, dumping materials, scraping the inside of mixers and transfer s materials to drying racks and/or bins. | 12/15/2019 |
| 275 | Qiagen Frederick, MD QC Associate Scientist II MS in biological sciences Exp: 0-2 years |
Perform routine testing on manufactured products including incoming raw materials, in-process products, and finished goods. Testing covers reagents of multiple product groups with a focus on NGS-related panels, chemistry, and indices using NGS platforms and various PCR platforms. Support tech transfer and QC workflow implementation during new product transfer and launch. These include performing validation tests, help to writing of instruction and protocol/SOP. Support continuous quality improvement by conducting tests for root cause analysis, or for revised QC process validation, or for new QC instrument verification and validation. | 12/15/2019 |
| 276 | Qiagen Beverly, MA QA Associate BS/BA Exp: 1-3 years in QA |
The QA Associate role assists with all QA compliance activities; including reviews of CAPAs, deviations, NCMRs, customer complaints and recalls. Position responsibilities also include participation at internal and external regulatory audits, document reviews and support of companywide QA initiatives. | 12/15/2019 |
| 277 | Qiagen Germantown, MD Technical Associate - Kit Assembly Operations HS Diploma/GED 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. Assist in the setup and preparation of required production related materials. | 12/15/2019 |
| 278 | Qiagen Germantown, MD Technical Associate - Automated Assembly Operations HS Diploma/GED Exp: 1-3 years |
The 2nd shift Technical Associate in Production and Assembly comprehends and performs assigned automated and manual production tasks according to established standard operating procedures. Responsible for Automated and/or 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 automated assembly equipment, as well as other production related equipment within the assembly area. | 12/15/2019 |
| 279 | Qiagen Mobile, AL Field Service Specialist (Mobile, AL area) BS/BA in sciences, med technology, or engineering Exp: 0-3 years |
On site Field support of QIAGEN, Peak Service and Excalibur supported instrumentation. Position based in Mobile, AL area. Install, maintain, troubleshoot, repair, and support instruments on all levels (Hardware and Software). Maintain and develop positive relationships with customers and references. Assist in meeting/exceeding sales targets and related KPI's in relation to maintaining high customer satisfaction. Ensure all paperwork is completed accurately, in a timely fashion and in lines with any regulatory requirements. Utilize relevant databases to input and provide information to the organization. | 12/15/2019 |
| 280 | Moderna Cambridge, MA Candidate Experience Associate HS Diploma/GED Exp: 1 year in HR environment |
This role is the steward of Moderna’s candidate experience at every step of our recruitment process. The ideal hire for this role is curious about people, is completely ‘customer focused’ and has a desire to grow their career in Talent Acquisition or Human Resources. Partner with our Talent Acquisition Team and Hiring Leaders to provide a streamlined and efficient interview scheduling process. Create and communicate interview schedules, travel and hotel details to talent and third party executive search partners. Help define and reinforce a consistent interview scheduling process at Moderna that results in a superior candidate and hiring manager experience. This includes pushing back, where needed, and educating others on SLA’s (service level agreements). | 12/15/2019 |
| 281 | Moderna Cambridge, MA (Contract) Sr. / Research Associate, Cell-based Assay Development MS in biological sciences Exp: 0-2 years |
The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development The individual will participate in the development and performance of cellular and biochemical assays to support advancement of Moderna’s mRNA clinical development candidates. Standard mammalian cell culture support including maintaining and plating of cell lines. Development of in vitro assays (e.g. immunoassay, ELISA, PCR, Western blot, luminescence, bDNA, functional activity) using cultured mammalian cells to support product development. Optimize assay performance (precision, accuracy, robustness) and implement high throughput sample testing to support product development | 12/15/2019 |
| 282 | Moderna Cambridge, MA (Contract) Research Associate, Analytical Operations BS or MS Exp: BS: 1-3 years, MS: 0-2 years |
The primary responsibilities of this role will be to support development and performance of analytical methods for messenger RNA therapeutic drug substance and drug products. The incumbent will be expected to undertake laboratory work to support testing and data collation. Additional responsibilities include developing high throughput methods using liquid handling and end-to-end sample tracking for drug substance/product components and impurities. This position will support cross-functional teams in Research and Development, Production and Quality. Additionally it is expected that the role will require the individual to generate technology transfer documents and enable the physical transfer of methods to receiving groups as part of a broader functional responsibility. The anticipated time frame for this assignment is six months. | 12/15/2019 |
| 283 | Moderna Cambridge, MA (Contract) Document Associate BS in related Exp: 1-2 years in regulatory operations |
This role is an exciting opportunity to be an integral part of the talent engine fueling a high growth organization that is radically changing the biotech industry. Reporting to the Senior Director, Regulatory Operations, the Document Associate, Regulatory Operations will be responsible for assisting with document formatting, publishing, quality control, and interactions with third party vendor(s) to ensure compilation of high-quality electronic submissions. | 12/15/2019 |
| 284 | Danaher Fremont, CA Customer Success Representative HS Diploma/GED Exp: 1-3 years in customer service |
In this role you will have an impact on the customer experience, helping to create and sustain customer loyalty through enablement of their success. A successful candidate will have a positive attitude with the ability to readily adapt to change and solve problems. Additionally, the candidate should be able to demonstrate empathy for both internal and external customers, and will be expected to work closely with sales, product support, repair teams, and customer support to create value and enable an exceptional customer experience. | 12/15/2019 |
| 285 | Molecular Templates Austin, TX Research Associate BS/BA in life sciences Exp: 1 year in lab setting |
This position will perform functions related to production of pre-clinical drug product and early-stage process development for protein sciences, including routine protein purification, equipment maintenance checks and calibration, data management, and assist in review and development methods and procedures to control or modify the process. This position will also aid in identifying continuous process improvement areas. This will require excellent technical, analytical and organizational skills, along with adherence to written and verbal instructions and accurate and timely completion of manufacturing batch records. | 12/15/2019 |
| 286 | Molecular Templates Austin, TX downstream process development AS/AA in biotechnology preferred Exp: 1-2 years previous experience preferred |
This position will be responsible for working with fellow team members to develop robust, efficient and scalable methods for protein purification/manufacture. This position will perform functions related to downstream process development of recombinant biologics, including experimentation involving protein purification, cell lysis, clarification, chromatography, ultrafiltration, diafiltration and filling. Additional activities will include solution preparation, equipment maintenance and calibration, data management, report authoring, and review of manufacturing processes. | 12/15/2019 |
| 287 | Molecular Templates Austin, TX Associate Scientist BS/BA in life sciences Exp: 1 year in lab setting |
The Associate Scientist will be responsible for working with fellow team members to develop robust, efficient and scalable methods for protein purification/manufacture. This position will perform functions related to downstream process development of recombinant biologics, including experimentation involving protein purification, cell lysis, clarification, chromatography, ultrafiltration, diafiltration and filling. Additional activities will include solution preparation, equipment maintenance and calibration, data management, report authoring, and review of manufacturing processes. | 12/15/2019 |
| 288 | Molecular Templates Austin, TX Manufacturing Associate AS/AA in life sciences, engineering or related Exp: 1 year or more in GMP manufacturing |
This position will perform functions related to production and GMP manufacturing operations, including execution of protein fermentation steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. | 12/15/2019 |
| 289 | Molecular Templates Austin, TX Manufacturing Associate AS/AA in life sciences, engineering or related Exp: 1 year or more in GMP manufacturing |
This position will perform functions related to production and GMP manufacturing operations, including execution of protein purification steps. Equipment, facility, process and people will be prepared to deliver quality ETBs, the next generation of immunotoxins, to patients in clinical trials. The Manufacturing Associate will provide on-the-floor execution to bioprocessing unit operations requiring attention to detail, working in a team environment and interest in learning about bioprocessing operations. The Manufacturing Associate will be responsible for adhering to Standard Operating Procedure (SOP) guidelines, Good Manufacturing Practices and all safety requirements in a state-of-the-art biologics manufacturing facility. | 12/15/2019 |
| 290 | Mylan Sugar Land, TX Quality Assurance Specialist MS in pharma/med devices Exp: 0-2 years |
Perform quality assurance documentation record review and batch disposition. Determines the disposition (i.e. release or rejection statuses) for packaging components (container/closures), raw materials, bulk products and finished packaged products. Assists in compiling data for Annual Product Reviews. Assists in QA product complaint activities which include: Daily electronic reviews - Logging – Investigating- Trending. | 12/15/2019 |
| 291 | Mylan Greensboro, NC Quality Technician, Inspections- 2nd Shift BS/BA Exp: 0-2 years |
Coordinate release documents, perform product releases in SAP, and perform product inspections. Write specifications and SOP’s, perform warehouse investigations, review rejections, place products on quality hold, process sample requests, returned goods and donations, ship studies, and review temperature data. Process sample requests as requested. Process and/or review returned goods and assign disposition. Process shipping studies when received. | 12/15/2019 |
| 292 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS or MS in sciences Exp: 0-2 years |
The Laboratory Technician is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 12/15/2019 |
| 293 | Myriad Genetics South San Francisco, CA Intake Associate BS/BA Exp: 0-2 years |
At Myriad Women's Health, the Intake team is responsible for the timely and accurate data entry and management of patient orders. You will be a significant contributor to our high-throughput workflow and an integral part of our busy CLIA lab. Input and manage patient data from a variety of sources, and ensure that orders are fully processed at the highest level of accuracy. Identify issues and trends and collaborate with your team and leadership to develop best practices to ensure we are providing the best service and experience to all customers | 12/15/2019 |
| 294 | Myriad Genetics Salt Lake City, UT Laboratory Technician III MS in clinical lab science, chemical/physical/biological science Exp: 6 months |
The Laboratory Technician III is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 12/15/2019 |
| 295 | Myriad Genetics Salt Lake City, UT Clinical Laboratory Assistant HS Diploma/GED Exp: 1-3 months |
Myriad Autoimmune is seeking a Clinical Laboratory Assistant to assist in the preparation of sample aliquots; retrieving samples for testing as directed by work schedule; performing inventories and orders for laboratory and office supplies; performing clerical duties that do not involve interpretation or judgment; receiving and accessioning samples into the CLIMS; and assisting CLS' with various lab duties (temperature monitoring, CLIMS sample batching, preparation of buffers), reporting issues to management. | 12/15/2019 |
| 296 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS in chemical, physical, biological or clinical laboratory/medical technology science Exp: 0-2 years |
The Laboratory Technician in the LegacyX Lab is responsible for preparing high-performance liquid handling robots for specimen processing. The technician must maintain patient sample integrity through demonstrating competency and repeatability in performing specimen processing as defined by the department’s standard operating procedures. This is a production environment, not a research environment. Pay starts around $18/hour depending on experience. | 12/15/2019 |
| 297 | Myriad Genetics Austin, TX RBM Laboratory Technician - Testing BS/BA in engineering/sciences 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. | 12/15/2019 |
| 298 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 12/15/2019 |
| 299 | NAMSA Northwood, CA Lab Technologist - In Vivo BS in sciences Exp: 0-3 years |
May prepare all testing/test article and animals according to written instructions and protocols. May execute routine testing per NAMSA SOPs, with appropriate data analysis. May communicate test schedule updates to NAMSA management as needed. May prepare and maintain reagents and/or test articles as required for testing.May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. | 12/15/2019 |
| 300 | NAMSA Irvine, CA Microbiology Technologist BS/BA Exp: 0 years |
May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitor. May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. May be required to perform personal gowning environmental testing, and submit organisms from gowning, environmental and sterility test positives for identification and inclusion in monthly trending data, as required for specific testing as applicable. | 12/15/2019 |
| 301 | Nanostring Seattle, WA Manufacturing Research Associate I/II BS/BA in sciences Exp: 0-2 years in lab |
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. | 12/15/2019 |
| 302 | Nanostring Bothell, WA Manufacturing Research Associate I BS/BA in sciences 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. | 12/15/2019 |
| 303 | Nanosyn Santa Clara, CA Research Associate / Screening and Compound Profiling BS in biology/chemistry Exp: 0-2 years in biotech/pharma |
The candidate will play a key role in the organization by being responsible for the planning and timely execution of in vitro biochemical and cell-based assays for Nanosyn’s screening and profiling services. He/She will be responsible for consistently generating high quality data and meeting agreed upon timelines. Applicants must have a strong focus on quality and attention to detail, have the ability to work on multiple projects simultaneously, and be productive both independently and as part of a team. | 12/15/2019 |
| 304 | Upsher-Smith Maple Grove, MN Network Systems Analyst I BS in computer science or related Exp: 0-2 years |
The Network Systems Analyst will be primarily responsible for managing and configuring security information and event monitoring (SIEM) tool. Research security enhancements and identifies solutions to enhance IT security. Evaluates and recommends security products, services, and/or procedures to enhance productivity and effectiveness. Provides technical support of IT infrastructure at all Upsher-Smith locations. Support will include assisting with installation, configuration, recovery, administration and security of infrastructure components. Incumbent will work on implementation projects as well as have responsibility for daily monitoring and support activities. etc. | 12/10/2019 |
| 305 | Upsher-Smith Maple Grove, MN Corporate Sales Representative BS/BA in business, science, communication or related Exp: 1-3 years |
The Corporate Sales Representative is responsible for the development and management of a designated territory with the goal of maximizing sales while improving patient lives. Patients are central to all USL strategies, and the CSR will be responsible for developing business relationships with targeted neurologists, epileptologists, seizure specialists and other healthcare practitioners and members of the health care community. The CSR may work in a team with a Corporate Sales Specialist (CSS), Regional Trainer, Managed Care - Regional and National Account Manager to increase sales, market share and profitability of USL products. Time allocation of 75% inside sales and 25% field sales is expected; however, this may vary as business needs arise. | 12/10/2019 |
| 306 | United States Biological Salem, MA Information Technology and Marketing Associate BS/BA in computer science Exp: 1+ year(s) |
United States Biological is a local, growing manufacturing company seeking enthusiastic individuals to be part of our team. We specialize in thousands of antibodies, ultra pure molecular biology reagents, cell culture media and enzymes. Troubleshoot and provide hands-on support to all personnel. Work with company president on all areas of website, graphics and IT. Set up and format new workstations as needed. Design and create newsletters. Maintain systems, databases and website, as needed. | 12/10/2019 |
| 307 | Veeva Toronto, ON Associate Software Engineer BS in computer science, engineering, mathematics, or related Exp: Recent graduates |
As part of our Network development team, working on our master data management product (MDM), or as part of our Vault team, working on our Enterprise Content Management (ECM) product, you will be part of a team building scalable solutions that complement our existing solutions. In these exciting roles, you would have the opportunity to work with technologies like Java, Spring, Hibernate, Mule, Maven, Git, Tomcat, Solr, MySQL, and more. We work in a fast-paced, agile environment that releases features every four weeks. What You'll Do: Responsibility for all aspects of the software cycle: design, implementation, tuning, testing, and monitoring of the functional areas that you will own. etc. | 12/10/2019 |
| 308 | Veeva Toronto, ON Associate Performance Engineer BS in computer science or related Exp: Recent graduates |
The Vault Performance Engineering Team works within the Vault Development Team and participates in all phases of the software development life cycle. What You'll Do: Test new features pre-production to make sure they will scale and perform. Collaborate with Vault team members in Product Management, Engineering Management and Quality Assurance to help design and develop performance tests. Implement and execute load tests in JMeter. Use and update Python scripts for managing test systems. Work with Senior Performance Engineers to profile code and identify bottlenecks. | 12/10/2019 |
| 309 | Veeva Philadelphia, PA Associate Consultant (Remote) BA/BS in a business, computer, engineering, or life science field Exp: Recent graduates |
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. What You'll Do: Collaborate with experienced Senior Consultants and Solution Architects. Learn technical consulting, application design, industry knowledge and project management skills. Conduct solution design, application configuration, and documentation of system requirements to help deliver successful implementations. Passion to use technology to make business processes more efficient. etc. | 12/10/2019 |
| 310 | Veeva Pleasanton, CA QA Engineer BS in mathematics or computer science 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. We are a fast-paced team who takes pride in building great software and making customers happy. What You'll Do: Design and implement test strategies. Develop deep expertise in the product. Build effective test cases that are used for manual and automation testing. etc. | 12/10/2019 |
| 311 | Veracyte South San Francisco, CA Clinical Lab Scientist BS/MS in a biological science or medical technology Exp: 1 year |
The Veracyte Clinical Laboratory continues to grow! We are seeking a new Clinical Laboratory Scientist (CLS) to perform cutting-edge diagnostic testing on patient specimens in our collaborative, high-energy work environment. S/he will accurately perform molecular genetic testing, using a variety of molecular biological techniques including expression microarray analysis. Other key aspects of the role include: Conduct daily quantitative and qualitative assessment of molecular data generated during the course of testing. Carry out QC/QA activities as part of the company’s Quality program and commitment to patient safety. etc. | 12/10/2019 |
| 312 | Vericel Cambridge, MA Engineer, Validation I MS Exp: 1+ year(s) |
Responsible for performing validation in a GMP biotech manufacturing facility. Core Responsibilities: Perform validation activities in the media preparation, cell culture, utilities and QC areas of a cGMP biotech manufacturing facility. Perform hands on execution of Installation, Operational and Performance Qualifications for equipment, facilities, utilities, as well as cleaning, sterilization, and manufacturing processes in accordance with predefined test protocols. Analyze validation results and compile data into reports for initial qualifications and re-qualifications. Coordinate testing schedule with impacted area managers and quality control based on project needs. Provide input to technical composition of standard operating procedures. etc. | 12/10/2019 |
| 313 | Vericel Cambridge, MA Sales Operations Associate BS/BA in business administration, marketing, or related Exp: 1+ years |
Essential Functions: Coordinate on-boarding of all new sales personnel with internal departments. Administer all sales training content through company’s Learning Management System. Primary administrative resource for two sales teams (first point of contact). Provide logistical support for all sales training meetings and events. Work with marketing to provide regular updates to brand websites. Work with marketing to provide logistical support for tradeshows, surgeon training programs and other commercial programs/events. etc. | 12/10/2019 |
| 314 | Verge Genomics South San Francisco, CA Molecular Biology Research Associate / Senior Research Associate MS in molecular biology, neuroscience, or equivalent Exp: 0+ years |
What you'll do: Perform and enable high-throughput sample processing and RNA extraction for transcriptomic analysis, which impacts all drug discovery and development efforts. Successfully conduct library prep of samples for RNAseq. Have the opportunity to learn across function and discipline, by contributing to ongoing studies and by utilizing techniques such as cell culture, high-throughput screening, plasmid preparation, virus preparation, IF, qPCR, or WB. Be responsible for evaluating and presenting your work at team and company level meetings. | 12/10/2019 |
| 315 | Vero Biotech Atlanta, GA Manufacturing Technician Technical degree Exp: Not needed |
Routine Manufacturing operations for the production of clinical and/or commercial products, operation of production equipment according to SOPs and other daily activities on the manufacturing floor. Essential Duties and Responsibilities: Performs manufacturing activities including but not limited to work functions in electromechanical assembly and disposable assemblies (cassettes, cartridges) in a correct and timely manner. Maintains records and controlled-room environment to comply with regulatory requirements, GMPs, and SOPs. Provide in process testing to assure batches meet specifications. Will train personnel in new and revised procedures. etc. | 12/10/2019 |
| 316 | Verve Therapeutics Cambridge, MA Associate Scientist, In Vivo Pharmacology MS in biology, biochemistry, pharmacy, or related Exp: 1-2 years |
Verve is seeking an Associate Scientist with experience in in vivo pharmacology to execute pivotal studies in rodents. You will be responsible for planning gene editing studies in mice and rats, dosing of animals (IV or IP), collecting blood samples (serial and terminal bleeds), necropsy and tissue harvesting. In addition, you will be analyzing the collected samples using a series of ex vivo and in vitro assays. The role requires hands-on experience in rodent handling, dosing and sampling as well as the ability to develop and run assays such as ELISA, qPCR or FACS. The scientist in this position will be part of an integrated R&D project team. | 12/10/2019 |
| 317 | LabCorp Monrovia, CA Histotechnician - (3rd Shift) AS/AA in related Exp: 1-3 years in Histology |
The Monrovia lab is seeking a 3rd shift Histotechnician for the Histology department. This position will perform all technical duties related to the production of histo-pathological slides including but not limited to the following: Examines and prepares histologic slides from tissue sections for microscopic examination and patient diagnosis. Uses rapid tissue processing and frozen section technique to freeze, cut, mount, and stain tissue specimen received from surgery, biopsy, and anatomical tissues upon preparation of sections of human or animal tissue for immediate examination. Operates computerized laboratory equipment to fix, dehydrate, and infiltrate with wax, tissue specimens to be preserved for study by Pathologist. | 12/8/2019 |
| 318 | LabCorp Utica, NY Specimen Processing Specialist (Laboratory Associate) HS Diploma/GED Exp: 1 year in lab |
Prepare laboratory specimens for analysis and testing, Spin samples, pour urine tubes, and create frozen samples, Pick up and deliver samples to, clients/hospitals, Unpack and route specimen to their respective staging areas, Accurately identify and label specimens, Pack and ship specimen to proper testing facilities, Properly prepare and store excess specimen samples | 12/8/2019 |
| 319 | LabCorp Raritan, NJ Lab Assistant - 3rd Shift HS Diploma/GED Exp: 1 year in health-related work or college level courses in lab sciences |
The Forensic Accessioning (Processing) Lab Assistant works in fast paced, production type environment performing a vital component of medical laboratory science. Receive on the job training for the pre-analytical processing of medical samples. Complete all documents accurately and neatly. Monitor chain of custody, and custody and control forms for completeness and acceptability. Perform all duties accordingly to standard operating procedures and/or supervisory instructions | 12/8/2019 |
| 320 | LabCorp Richmond, VA Specimen Accessioner HS Diploma/GED Exp: 0-2 years related experience |
Prepare laboratory specimens for analysis and testing, Spin samples, pour urine tubes, and create frozen samples, Pick up and deliver samples to, clients/hospitals, Unpack and route specimen to their respective staging areas, Accurately identify and label specimens, Pack and ship specimen to proper testing facilities, Properly prepare and store excess specimen samples | 12/8/2019 |
| 321 | LabCorp Huntsville, AL Technologist BS/BA in biology, chemistry, med tech, or related Exp: 1 year clinical lab experience |
Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation. Demonstrate the ability to make technical decisions regarding testing and problem solving. | 12/8/2019 |
| 322 | LabCorp Oklahoma City, OK Laboratory Data Entry/Specimen Accessioner HS Diploma/GED Exp: 1-2 years in data entry |
Our LabCorp office in Oklahoma is expanding its team and looking for dynamic individuals to be Specimen Accessioner (s) who will perform specimen preparation duties. Their work involves receiving and unpacking specimens, preparing them for lab tests and ensuring that they are correctly preserved before they are sent off. | 12/8/2019 |
| 323 | LabCorp McLeansville, NC Customer Service HS Diploma/GED Exp: 1-3 years in call center/customer service |
Customer Service- FT 10-7pm OR 11-8pm- Work from Home Opp-Onsite needed first! Answer 70+ inbound calls per day from patients, doctor's office and/or private insurance carriers. Initiate payment plans for patients for outstanding balances. Maintain telephone statistics and quality goals | 12/8/2019 |
| 324 | Medtronic Danvers, MA Associate Regulatory Affairs Specialist - Coronary and Structural Heart BS/BA in biology, chemistry, med tech, or related Exp: 0 years in medical device |
The Associate Regulatory Affairs Specialist (ARAS) is responsible for planning and executing global regulatory activities necessary to obtain and maintain regulatory approvals within the US and International Regions. The Regulatory Affairs Specialist will provide support for regulatory activities including: technical writing to support regulatory submissions, product labeling and instructions for use creation. | 12/8/2019 |
| 325 | Medtronic North Haven, CT Manufacturing Engineer I BS/BA Exp: 0 years |
The Associate Manufacturing Engineer is a key operations representative within the Advanced Stapling Technology Manufacturing Engineering team. The Associate ME will be responsible for completing tasks which support the completion of operations deliverables for AST Focused Factory. General responsibilities include manufacturing process evaluation, mechanical product troubleshooting and support of in-house manufacturing processes. They will assist with engineering studies to support process validation and contribute to maximizing production performance. The Associate ME will work under the direction of Principal/Senior level Engineer in a fast paced collaborative environment supportive of program initiatives and compliant with company best practices. | 12/8/2019 |
| 326 | Medtronic Memphis, TN R&D Engineer II MS in engineering Exp: 0 years |
This position has the responsibility and authority to apply education and learned knowledge toward developing world class medical products for Spinal surgery. Designs, develops, analyzes, troubleshoots and provides technical skills during research and/or product development. Uses multidisciplinary engineering knowledge to design and develop medical devices or components / subsystems in support of strategic plans. | 12/8/2019 |
| 327 | Medtronic Tempe, AZ IC Test Engineer I BS/BA in electrical/computer engineering Exp: 1-2 years in circuit testing/design/verification |
As a member of this Test Engineering Team, you will be involved in all phases of product development, including definition, design for testability, test hardware and software design, hands-on debug, characterization, manufacturing release under a heavily regulated quality and regulatory standard operating procedures. You will be an important part of an experienced test development team whose goal is to deliver the highest quality test application to test ICs for use in live saving medical devices | 12/8/2019 |
| 328 | Medtronic Memphis, TN Assoc Supplier Qual Engineer BS in engineering/sciences Exp: 0 year of work |
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. 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. | 12/8/2019 |
| 329 | Medtronic Irvine, CA Design Quality Engineer I BS in engineering/sciences Exp: 0 years in quality/engineering |
Applies knowledge of Design Control principles and quality engineering techniques positively influence new product development efforts, including those for design verification, validation, specification development, and risk management. Hands on participant in early stages of product development including but not limited to physician interaction, product engineering, competitive product testing, and prototype testing. Identifies and manages risk throughout the development process with the use of FMECA and/or other risk management tools. | 12/8/2019 |
| 330 | Medtronic Jacksonville, FL Supplier Qual Engineer I BS/BA Exp: 0 years |
The Restorative Therapies Group (RTG) develops life-restoring therapies and healthcare solutions that span the care continuum; integrating technologies and applying clinical and economic evidence to increase patient access, improve efficiency of procedures and deliver successful patient outcomes. Within RTG the Supplier Quality department focuses on developing Supplier Owned Quality (SOQ). This is a process allowing suppliers to use portal system in which supplier data is electronically transmitted to Medtronic via an Internet or secure FTP port. The portal system provides real-time material acceptance confirmation, shipment authorization and feedback to supplier prior to release of the product and identifies opportunities to reduce variation in the process. It also reduces the burden on Incoming Quality Assurance. | 12/8/2019 |
| 331 | Merck West Point, PA Associate Scientist, Vaccine Process Development BS in engineering or biological sciences Exp: 2020 graduate |
The successful candidate will perform lab-scale process development/scale-up studies, develop robust, efficient, scalable cell culture processes for vaccine production, participate in the manufacture of Current Good Manufacturing Practices (CGMP) clinical bulks, and transfer processes to clinical or commercial manufacturing facilities for vaccine candidates. Duties may include: lab scale fermentation, cell culture, and/or bioconjugation process development, in-process assay support, process scale-up and engineering, CGMP document preparation and modifications, maintaining/coordinating raw material, and equipment inventories, technology transfer to manufacturing, and functioning as a key member of a process development team. | 12/8/2019 |
| 332 | Merck West Point, PA Associate Shift Engineer BS in engineering or sciences Exp: 1 year |
The function of this position is to provide technical support for ourfacility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (3rd shift Monday through Friday). Specifically, the position will be required to: 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 | 12/8/2019 |
| 333 | Merck Elkhorn, NB Technician, Operations HS Diploma/GED Exp: 1-2 years in production lab |
The Operations Technician is responsible for critical laboratory procedures and duties in the production of veterinary products. Technicians work with a variety of technical equipment while completing duties involved in blending, filling vials or packaging finished products for distribution. At all times technicians must follow Good Manufacturing Practices and Standard Operating Procedures (SOP) and adhere to all safety and company policies while performing assigned duties. | 12/8/2019 |
| 334 | Merck West Point, PA Shift Engineer BS in engineering Exp: 1 year |
The function of this position is to provide technical support for our facility while actively supporting, participating in, and embracing an empowered culture. This role is for Off-Shift Engineering Support (2nd Shift Monday through Friday). Specifically, the position will be required to: 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 | 12/8/2019 |
| 335 | Merck Ames, IA Technician, Operations AS/AA in biology, microbiology, or related Exp: |
The primary purpose of this position is to perform entry-level laboratory procedures and assist others in more advanced procedures for the production of veterinary biologicals according to strict government and company imposed guidelines. Assist in all areas of the production of RNA (RP) Particle Vaccine products manufactured in a USDA licensed facility. | 12/8/2019 |
| 336 | Merck North Wales, PA Entry Level Field Sales - Chronic Care - (Forest Hills, NY) BS/BA Exp: Entry level, some sales experience |
The entry level Chronic Care Representative (CCR) is the primary point of contact for a variety of customers within their assigned geography. The Chronic Care Representative is a key member of the local Customer Team that works collaboratively with other Company field-based employees such as the Account Executives, Integration Delivery Systems leaders as well as other members of the extended team. Professionals to align customer needs and Company products in accordance with product labeling. | 12/8/2019 |
| 337 | Merck West Point, PA Entry Level Field Sales - Vaccines -Chico, CA BS/BA Exp: Entry level, some sales experience |
He/she is responsible for engaging with customers in a way that supports the local market focus on population health and centers on the highest potential business opportunities that will improve our impact on public health. He/she will work with the local market team to understand and identify customer needs, proactively align products and services, support pull-through activities relative to integrated strategies, and ensure that MV is viewed as demonstrating value and better health outcomes to healthcare professionals and their patients. Responsible for ensuring all activities adhere to the spirit and letter of all Company Policies and US Laws and Regulations. | 12/8/2019 |
| 338 | Meridian North Billerica, MA Clinical Research Associate - MAG BA/BS in biological/health sceinces Exp: 1 year as CRA |
The Clinical Research Associate assists in the administrative of clinical research projects including development of key study documents, over-site of the clinical trial, and ensuring the quality and integrity of the data according to GCP, ICH and SOPs. Interact with data management and study sites with generation and reconciliation of queries in order to meet business timelines. Provide answers to common protocol study related questions under the supervision of the Clinical Director or Associate Trial Manager | 12/8/2019 |
| 339 | Meridian Cincinnati, OH Quality Systems Software Engineer BS/BA in Communications, Computer Systems, or equivalent Exp: 0-2 years related experience |
The Quality Systems Software Engineer position at Meridian Bioscience within the 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 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. | 12/8/2019 |
| 340 | Merieux NutriSciences Madison, WI Entry-Level Laboratory Sample Receiving Technician HS Diploma/GED Exp: Entry Level |
We are looking for an Entry-Level Laboratory Sample Receiving Technician to sit in our Madison, WI location. Receive and log in sample in preparation for analysis. Review sample and any attached documentation to assign an identification number and enter information into Laboratory Information Management System (LIMS). Prepare documentation as necessary. Contact client, when necessary, to obtain and clarify missing or unclear information to ensure that identification of client code, test code, and sample contents are accurate. Store sample in appropriate manner until analysis is completed and appropriately dispose of extra sample. Ensure sample integrity is maintained. | 12/8/2019 |
| 341 | Merieux NutriSciences Crete, IL RESEARCH MICROBIOLOGIST AS/AA or BS/BA in chemistry/biology Exp: 1-2 years |
This position is responsible for working in a cooperatively team environment where scientists collaborate on contract research designed to promote the safety, quality and nutrition of the global food supply. The incumbent is responsible for the testing of samples supporting research studies using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. The incumbent contributes to defined contract research projects by performing lab tests, data interpretation and maintaining documentation in accordance with required specifications, established procedures, and customer service standards. | 12/8/2019 |
| 342 | Merieux NutriSciences Crete, IL CHEMIST I BS/BA in chemistry Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. This position reports to the Supervisor of Chemistry. Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. | 12/8/2019 |
| 343 | Merieux NutriSciences Allentown, PA Lab Assistant HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 344 | Merieux NutriSciences Columbus, OH Micro Tech HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 345 | Merieux NutriSciences Grand Prairie, TX Microbiology Technician BS/BA Exp: 1 year of PCR/ELISA experience |
The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 12/8/2019 |
| 346 | Merieux NutriSciences Salida, CO Micro Tech HS Diploma/GED minimum Exp: No experience needed |
Work as a member of a team to prepare food samples for testing. Carry out a number of procedures including reading test labels and preparing samples for analysis by recording, weighing and blending. Pipette sample solution into tubes or plates according to the analysis process being performed. Set up and sterilizing equipment needed for analysis of food samples. | 12/8/2019 |
| 347 | MeritMedical South Jordan, UT Process Operator Wafer I HS Diploma/GED Exp: 6 months in silicon wafer fab. Preferred |
This position is for a Process Operator Wafer I at Merit Sensor Systems. Merit Sensor Systems is a manufacturer of piezoresistive pressure sensors (learn more at www.merit-sensor.com). This Process Operator Wafer I could be working in the wafer fabrication, wafer dicing, and/or electronic assembly areas. | 12/8/2019 |
| 348 | MeritMedical South Jordan, UT Material Handler I / with a $500 Hiring Bonus HS Diploma/GED Exp: 3 months work 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. | 12/8/2019 |
| 349 | MeritMedical South Jordan, UT Molding Technician I - Day Shift HS Diploma/GED Exp: 6 months molding experience |
This position provides entry level mold set-up services under the direction and supervision of a Technician and/or Supervisor. Assists in mold changes and EOAT setup/verification. Assists in set up of all auxiliary equipment related to the process. Ensures that correct materials are utilized, safety checks are performed, and that room organization and cleanliness is maintained. | 12/8/2019 |
| 350 | MeritMedical South Jordan, UT Technician II (Injection Molding) AS/AA Exp: 1 year |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts in an injection molding environment, and may service or repair simple instruments or equipment. 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. | 12/8/2019 |
| 351 | MeritMedical South Jordan, UT Accounts Payable Clerk I HS Diploma/GED Exp: 1 year |
This position provides accounting support for processing employee expense reports, maintaining the filing system, processing the daily customer checks and maintaining the Construction Work in Progress (CWIP) filing system. | 12/8/2019 |
| 352 | MeritMedical South Jordan, UT Production Operator II - Part Time HS Diploma/GED Exp: 6 months experience preferred |
Performs a variety of medical assembly and processing tasks as a production team member. Assembles medical products on an assembly operation, performing a variety of tasks on a rotating basis. Performs on-line and in-process visual inspection of products to ensure specifications per work order and procedure are followed. Assists Team Leader and Technicians with product and/or machine change-overs | 12/8/2019 |
| 353 | MeritMedical South Jordan, UT Material Handler I HS Diploma/GED Exp: 3 months work 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. | 12/8/2019 |
| 354 | Merz Franksville, WI Supply Chain Associate BS/BA Exp: 1-3 years work or intern experience in supply, manufacturing, or quality |
The individual will be involved with people and processes associated with various aspects of Supplier Management and Procurement at Merz. The successful candidate will implement the supplier selection and approval process; manage existing suppliers; place purchase orders (PO’s); evaluating supplier performance; resolve delivery issues; assess and reduce supply chain risk; save money by reducing TCO (total cost of ownership). | 12/8/2019 |
| 355 | Merz Franksville, WI Tech Ops Development Associate BS/BA in engineering, sciences, business or communications Exp: Entry |
As a member of Merz’s Technical Operations Development Program, you will have three assignments over the course of three years. The roles are crafted to help you develop exceptional functional and leadership traits by working on a wide range of projects while providing exposure to different leaders in the company. These Operational experiences will develop you and put you on the fast track to future operations leadership opportunities at Merz. | 12/8/2019 |
| 356 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 357 | MSD Rockville, MD Production Control Tech I BS in life sciences, chemical sciences, MS preferred Exp: 1 year in biotech lab/manufacturing |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. The position will help standardize and improve documentation, manufacturing procedures and processes to increase production efficiency and ensure best practices are followed. The position will also help implement new products, projects and processes within Manufacturing Operations. Some degree of professional latitude, creativity and self-management is expected. | 12/8/2019 |
| 358 | MSD Rockville, MD Customer Service Rep I BS/BA Exp: 1 year in customer support |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. | 12/8/2019 |
| 359 | MSD Rockville, MD Customer Service Rep I BS/BA Exp: 1 year in customer support |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. | 12/8/2019 |
| 360 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 361 | MSD Gaithersburg, MD Research Associate I, Immunoassay Development BS in life sciences, chemical sciences, MS preferred Exp: 1 year in assay development |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. | 12/8/2019 |
| 362 | Analytical Lab Group Concord, CA QA Assistant BS in sciences Exp: 0-2 years in pharma/biotech |
The main duties of the Quality Assurance (QA) Assistant are to ensure timeliness of testing, meeting client requirements and providing a safe work environment for employees. The QA Assistant must provide services that are compliant to the ALG-West Quality Manual, client requirements and regulatory requirements as applicable, including ISO/IEC 17025:2017, USP, EU, GLP, GMP, FDA and ICH guidelines. | 12/8/2019 |
| 363 | Analytical Lab Group Concord, CA EM Technician AS/AA Exp: 0-2 years in cleanrooms |
Analytical Lab Group is looking for laboratory technicians to perform environmental monitoring at client facilities and microbiology testing in the microbiology lab. This is a full-time position at our West Coast location. The schedule will be Monday-Friday, 7 a.m. to 3:30 p.m., but you must be able to work flexible hours, including different shifts and weekends. At this time, the starting hour is 5 a.m. and will require OT. | 12/8/2019 |
| 364 | Micropoint Santa Clara, CA Quality Control Associates MS in chemistry, biology or related Exp: 0-2 years |
We are looking for highly motivated QC Associates (two openings) to join our quality team. These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. | 12/8/2019 |
| 365 | Micropoint Santa Clara, CA Manufacturing Operators HS Diploma/GED Exp: 0-2 years in pharma/food/med manufacturing |
There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging. Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection. Prepare materials used in the cartridge production process | 12/8/2019 |
| 366 | Micr Indianapolis, IN Medical Research Study Coordinator: BS/BA Exp: 1-3 years clinical research experience preferred |
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. | 12/8/2019 |
| 367 | LGC Manchester, NH Junior Staff Accountant BS/BA in accounting or finance Exp: 1-3 years in accounts |
The Junior Staff Accountant will be responsible for supporting a fast growing company at two locations (Manchester, NH & Charleston, SC) by providing transactional and reconciliatory assistance to the local Finance and Accounting team which supports both sites. The candidate will contribute across multiple key accounting areas including Fixed Assets, Accounts Receivable, and Accounts Payable. The position is located in Manchester, NH. | 11/28/2019 |
| 368 | LGC Novato, CA EH&S Technician AS/AA or BS/BA in sciences Exp: 0-2 years |
This role is responsible for all EH&S and Material Management functions at the Novato facility. This includes but is not limited to managing raw materials coming in to the facility, movement throughout the facility, waste management, and emergency equipment inspection. Responds to all EH&S requests at the Novato facility. Organizes all hazardous waste and interfaces with hazardous waste contractor for waste disposal. Performs all safety inspections throughout the Novato facility. Documents all inspection finding and informs functional manager of pertinent findings. Acts as the Facility Operations liaison when necessary. | 11/28/2019 |
| 369 | LGC Manchester, NH Sales Representitive BS in chemistry or life sciences Exp: 1 year in sales |
The person in this position will function primarily as a sales representative and develop and profitably grow the North American (US & Canada) revenue of the Standards business, primarily in the Food, Beverage and Cannabis sectors. The successful candidate will sell into both private and public organizations associated with Food, Beverage and Cannabis Industries and will possess ability to develop strong customer relationships. | 11/28/2019 |
| 370 | American Regent Hilliard, OH Process Equipment Technician I - 1st Shift HS Diploma/GED Exp: Entry Level |
This entry-level position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensure aseptic and sanitary conditions are maintained where required, that appropriate manufacturing area and equipment records are neat and accurate and that safe, effective and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company goals. The Team Member will be able to participate in all aspects of the Equipment Process. The Equipment Process includes cleaning, assembling, and sterilizing small and large pieces of equipment in accordance with established production records in a concerted effort to manufacture sterile liquid pharmaceuticals. | 11/28/2019 |
| 371 | American Regent New Albany, OH R&D Technical Services Chemist I MS in chemical engineering/pharma chemistry Exp: 0-1 years |
Conduct the experiments under the supervision of Scientists for Tech Transfer, Process R&D/Scale up/Validation, and other activities needed for introduction of a new product into cGMP manufacturing site or to support process improvements of existing products. Execute laboratory experiments as per the protocols or under supervision to study material compatibility studies and/or cleaning validation activities. Ensure all work is performed and documented in accordance with existing company policies, procedures, current Good Manufacturing Practices, and health and safety requirements. | 11/28/2019 |
| 372 | American Regent Shirley, NY Compounder I HS Diploma/GED Exp: Entry Level |
This entry level position is a member of the Formulation Team, who comprise a portion of the Manufacturing Team. This position will be expected to execute the required responsibilities and tasks necessary to perform as a Compounder I using current Good Manufacturing Practices (cGMP) according to approved SOPs in order to support the overall mission of the Manufacturing Team. | 11/28/2019 |
| 373 | American Regent Shirley, NY QC Microbiologist I, EM Lab BS/BA in sciences Exp: 0-2 years in pharma lab |
The QC Microbiologist I will perform microbial testing according to current guidance and established procedures for analysis of samples in the Environmental Monitoring laboratory. Perform support work such as Quality control testing of in-house prepared and commercially purchased media, stock culture maintenance, data trending, etc. | 11/28/2019 |
| 374 | Lumen Bioscience Seattle , WA Lab Technician BS/BA in biological sciences Exp: 1-2 years lab experience |
The full-time Lab Technician will join an essential team involved in our development of oral antibody-based therapeutics. The team member will be expected to execute leading edge molecular biology protocols, support the construction of novel cyanobacteria strains, and aid in the continued development of protocols that have made Lumen Bioscience the worldwide leader in Spirulina genetic engineering. The position requires strong organizational skills to meet quality and productivity goals. Effective communication skills are also crucial in coordinating with other members of the team, providing status updates, and raising quality or trouble shooting issues as they may arise. | 11/28/2019 |
| 375 | Lumenis Salt Lake City, UT Test Technician AS in Laser/Electro Optics is highly desired Exp: 1-2 years in laser/optics preferred |
Responsible for performing the set-up, calibration, testing, troubleshooting of circuits, components, instruments, optical and mechanical assemblies. Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams. Tests and troubleshoots assemblies and Laser systems. May complete rework on assemblies and or systems as a result of testing. As required, prepares technical reports summarizing findings and recommending solutions to technical problems. May assist in the selection and set-up of specialized test equipment. Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making recommendations. | 11/28/2019 |
| 376 | Luuminex Austin, TX LOGISTICS COORDINATOR I - Limited Assignment -SHIPPING HS Diploma/GED Exp: 1 year in logistics/supply chain |
The Logistics Coordinator I performs a variety of shipping, stockroom, and receiving tasks. This coordinator prepares items for shipment ensuring cost effective courier services and compliance to global trade, OSHA, DOT and other regulations. Must have a high regard for compliance, attention to detail, and inventory accuracy. Responsible for material transactions within ERP System. Compares information on packing slip with purchase order to verify accuracy; Also includes reverse logistics support. | 11/28/2019 |
| 377 | Luuminex Northbrook, IL LOGISTICS COORDINATOR I - US HS Diploma/GED Exp: 1 year in logistics/supply chain |
Performing administrative and physical duties to successfully execute shipments. This position coordinates with transportation companies, handles routine questions and problems, and communicates with other departments and customers throughout the delivery cycle to ensure a high rate of customer satisfaction. Completing documentation that is in compliance with international, hazmat, or FDA standards. | 11/28/2019 |
| 378 | Lundbeck San Diego, CA Research Associate BS or MS biological sciences Exp: 1-3 years lab/bench experience |
The Research Associate In Vitro Screening and Biochemistry will contribute to the identification and development of novel small-molecule drugs and support Lundbeck’s CNS discovery programs. The successful candidate will work in multidisciplinary teams to discover new therapeutics, collaborating with biologists and medicinal chemists to select molecules for further in vitro characterization and to identify trends in structure-activity relationships. | 11/28/2019 |
| 379 | United Therapeutics Corporation Silver Spring, MD Clinical Trial Administrator I BS/BA Exp: 0-1 years related experience |
The Clinical Trials Administrator I provides administrative and operational support with the set-up, execution and close-out of clinical studies as well as infrastructure development projects. Supports the department’s requirements to adhere to GCP and oversight of clinical trials. Assist the Clinical Operations team in completion of all required tasks to meet departmental and project/study goals. Develop and maintain knowledge of relevant Lung Biotechnology Inc. SOPs and Lung Biotechnology internal tracking systems. | 11/28/2019 |
| 380 | United Therapeutics Corporation RTP, NC Research Associate I/II - Tissue Engineering, Bioprocess Development BS or MS in biological sciences/engineering Exp: BS: 1-3 years, MS: 0-2 years |
Evaluate the function of native and engineered lung tissues and assist with implementation of new analytical regimes to characterize the function of the engineered lung tissues. Assist with data collection and analysis in support of these objectives. Contribute to preparation of human and non-human organs and tissues for experimentation. Prepare specific supplies and materials for designated testing, including design and construction of tubing circuits, preparation of perfusate, and maintenance of equipment used for functional assessment experiments. | 11/28/2019 |
| 381 | United Therapeutics Corporation RTP, NC Bioprocess Technician - Cell Biology AAS/BA/BS in biological sciences Exp: 1+ year in industry/lab |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays). Generate data for process development studies to improve yield, purity, and quality of primary lung cell types | 11/28/2019 |
| 382 | Lygos Berkeley, CA Analytical Chemistry Research Associate I BS in chemistry or related Exp: 0-3 years analytical experience |
Lygos is seeking an analytical chemistry research associate candidate to set up, run, clean, and maintain HPLC instruments. The successful candidate will have experience with general lab procedures, data interpretation, and reporting in a fast-paced and dynamic work environment. Execute analytical methods including: sample, standard, and mobile phase preparation, HPLC operation, HPLC calibration, data analysis, and data entry. Collaborate with the metabolic engineering team, fermentation team, and downstream processing team to ensure that results and conclusions are communicated clearly. | 12/2/2019 |
| 383 | Lygos Berkeley, CA Software Engineer BS or higher in computer sceinces Exp: 1+ years |
The successful applicant will serve as a software engineer developing systems for that improve and automate data handling and analysis related to R&D processes at Lygos. Investigating users’ workflows and needs, creating specification documents, writing applications, and supporting both deployment and end users of applications will be necessary elements of the successful applicant’s duties. The successful applicant will be expected to advance critical aspects of Lygos’ software development efforts through both effective individual and team efforts. | 12/2/2019 |
| 384 | LSNE Bedford, NH QC Microbiology Technician (A shift - Sun - Wed 6:00 - 4:30 pm) BS Exp: 0-1 years in cGMP environment |
Conducts sampling of incoming raw materials, product 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. | 12/2/2019 |
| 385 | LSNE Bedford, NH QC Chemist I (Mon - Fri 1st shift) BS in analytical chemistry or related chemistry Exp: 0-3 years in analytical chemistry/QC |
This position will have responsibility for supporting all activities in the Quality Control Laboratory. This includes the testing of in-process samples, finished product and stability samples and raw materials. This may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 12/2/2019 |
| 386 | LSNE Bedford, NH QA Associate I - Ops (Wed - Sat 3:30 pm - 2:00 am) BS in sciences Exp: 0-2 years |
This position provides QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. QA Associates maintain the quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner. | 12/2/2019 |
| 387 | LSNE Bedford, NH QA Associate I - Ops (Sun - Wed 6:30 am - 5:00 pm) BS in sciences Exp: 0-2 years |
This position provides QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. QA Associates maintain the quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner. | 12/2/2019 |
| 388 | LSNE Bedford, NH Manufacturing Technician I/III (Wed - Sat 3:30 pm - 2:00 am) HS Diploma/GED Exp: 0-2 years in GMP manufacturing, pharma/medical devices preferred |
This position is responsible for performing a variety of tasks in support of all manufacturing activities in accordance with current GMPs. Executes basic manufacturing procedures (cleaning, solution prep, equipment prep) under direct supervision. Accurately follows and completes required documentation (batch records, forms, Quality system documentation) under direct supervision. Expected to adhere to all procedures, including gowning and safety requirements, at all times. Supports manufacturing activities outside of core hours under direct supervision. | 12/2/2019 |
| 389 | Mallinckrodt Pharmaceuticals St. Louis , MO Quality Tech II AAS/AA or BS/BA in chemistry/biology Exp: 1-3 years in cGMP |
Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods. Follow good documentation practices for the accurate and timely documentation of all activities. Perform wet chemistry testing using GMP documentation in notebooks and also ELN. Assist with establishing and maintaining safe work standards in the lab | 12/2/2019 |
| 390 | Mallinckrodt Pharmaceuticals Hobart, NY Maintenance Tech I HS Diploma/GED Exp: 1-2 years in mechanical/electrical trades |
Performs basic preventative maintenance activities and repairs to buildings and facilities including; office areas, pharmaceutical manufacturing and processing areas, laboratories, warehouse areas, loading docks, and parking lots and driveways. May perform maintenance or simple repairs to selected types of plant equipment or systems for which mechanic has received training on. Works with various types of construction materials used for construction and finishing of walls, ceilings, and floors. Works under the supervision of the Facilities Maintenance Supervisor or, a more highly-skilled mechanic. | 12/2/2019 |
| 391 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - A Shift 4on/4off 6am-6pm HS Diploma/GED Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities. | 12/2/2019 |
| 392 | Mallinckrodt Pharmaceuticals St. Louis , MO Quality Assurance Technician II HS Diploma, AS/AA or BS/BA preferred Exp: 1-3 years in document review in cGMP environment |
The Quality Assurance Technician II performs a variety of review processes with the intent to correct record errors in manufacturing process documentation that includes batch record review and documentation issue resolution. This role is also responsible for return good inspections, cGMP area inspections and product inspections. This role ensures QA compliance and that cGMP principles are adhered to. | 12/2/2019 |
| 393 | Mallinckrodt Pharmaceuticals St. Louis , MO Chemical Process Engineer BS in chemical engineering Exp: 1-3 years related experience |
The Chemical Process Engineer is the recognized technical leader for chemical manufacturing processes and for the improvement of existing chemical processes. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies. Serve as main point of contact for chemical manufacturing processes in their area in regards to safety, quality, and continuous improvement activities. | 12/2/2019 |
| 394 | Mallinckrodt Pharmaceuticals Hobart, NY Packaging Maintenance Technician - 2nd Shift HS Diploma/GED Exp: 1-2 years in mechanical/electrical trades |
Performs preventative maintenance activities on specific pharmaceutical manufacturing and/or packaging equipment and systems. Provides maintenance support to manufacturing personnel during the operation of manufacturing and packaging equipment and systems. Diagnoses problems and performs repairs on manufacturing and packaging equipment. | 12/2/2019 |
| 395 | Mallinckrodt Pharmaceuticals Hobart, NY Project Engineer BS in engineeering Exp: 1-3 years |
Works as a key technical resource in supporting company objectives with respect to engineering design and project management in the implementation of capital projects and non-capital process improvements. Responsibilities include working with and/or leading the team to help identify, develop and execute projects to meet or exceed all company goals with respect to quality, schedule and spending. This could include: developing design concepts with the users; providing detailed design documents for some projects (e.g. P&IDs, construction drawings) ; equipment and instrument specification and installation; engineering calculations, developing request for proposals to bid projects; coordination with customers, contractors and consultants; reviewing documents, preparing capital appropriation requests, creating purchase orders, reviewing and paying invoices;; monitoring progress; assisting with training; executing commissioning activities; and ensuring proper project closure. | 12/2/2019 |
| 396 | Mammoth Biosciences San Francisco, CA Research Associate BS/BA or MS in biology or chemistry Exp: 1-3 years in molecular biology/genetics |
Mammoth is seeking a Research Associate experienced in nucleic acid and protein biochemistry techniques to support our product development team. The ideal candidate will have experience with assay development and product commercialization related to molecular tests and reagent kits. The candidate will be comfortable working as part of a team, be highly motivated, and display excellent time management skills. The Research Associate will report directly to Director of Assay Development. | 12/2/2019 |
| 397 | Masimo Irvine, CA [CLINICAL] Clinical Research Associate BS/BA in sciences Exp: 0-4 years |
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. This position must ensure that all activities will be conducted in accordance with Government Regulations (FDA, MDD and International), Good Clinical Practices (GCP) and Department Operating Procedures (DOP). Plan, implement and conclude clinical studies in support of project timelines/market release goals with minimal supervision; An advanced individual may conduct more complicated studies, as well as contribute to study proposals and protocols, applying principles of clinical study design and research methodology to assigned research projects; | 12/2/2019 |
| 398 | Master Control Salt Lake City, UT Enterprise Support Engineer II 4-year technical degree Exp: 0-4 years |
The Enterprise Support Engineer (TSE) provides in depth, high-level technical support to MasterControl customers. The ESE II maintains systems-level expertise and root cause-level troubleshooting while resolving advanced technical issues for customers. ESE II's work with fellow team members, service consultants, sales operations and other company resources to increase customer satisfaction and loyalty. TSE's are responsible for special projects, and will maintain one or more team projects that track team analytics and team success. TSE's will be subject matter experts (SME) in one or more subjects pertaining to the support of MasterControl Customers. | 12/2/2019 |
| 399 | Masy Bioservices Pepperell, MA Quality Associate I HS Diploma/GED Exp: 1+ year in related |
This position provides day to day support assisting in areas such as GMP, ISO 9001 and ISO 17025 compliance and the company’s quality system. Duties include quality assurance and control activities in technical, systems, operations and service areas. This position may require frequent interaction with multiple departments. Works under general supervision of management or team lead. | 12/2/2019 |
| 400 | MDxHealth Irvine, CA Specimen Accessioner I HS Diploma, degree preferred Exp: 1-2 years |
The Specimen Accessioner I performs all paperwork and non-technical procedures required to prepare, process, and submit specimens to the laboratory for testing. Responsibilities will include but not limited to: receiving, triaging and accessioning patient samples, distribution of patient reports and specimens to clients, performing quality control of accessions and labeling. | 12/2/2019 |
| 401 | MED Institute West Lafayette, IN Mechanical/Biomedical Engineer BS or MS in biomed/mechanical engineer Exp: 1-3 years |
This position requires a technically sound engineer capable of driving a project to completion with minimal supervision. A qualified candidate should be able to demonstrate a solid understanding of first principles, build a design from the ground up, perform independent research utilizing all available tools and resources, communicate well with customers, maintain good documentation practices, and develop and validate new test methods. Examples of commonly performed tests include accelerated fatigue, corrosion, electrosurgical, simulative use, and others that are used to evaluate material properties and/or functionality of a finished medical device. In addition, this person will be responsible for the maintenance of well-controlled documentation, including written protocols and reports, data forms, and laboratory notebooks. | 12/2/2019 |
| 402 | Medicomp Melborne, FL Amazing Cardiac Monitoring Technician HS Diploma Exp: Certified Cardiovascular Technician |
Review data from Cardiac monitors to provide physicians with results to help determine treatment for patients. This position requires a strong ability to read and interpret EKG strips as well as communicate with Doctors, patients, and other departments throughout the organization. This is a 24/7 facility and shifts are scheduled with differential available for 2nd, 3rd and weekend shifts. | 12/2/2019 |
| 403 | Medicomp Melborne, FL Technical Services Associate AS/AA degree Exp: 0-1 year |
We are seeking a Technical Services Associate that under minimal supervision and using average manual dexterity, performs varied skilled assembly tasks and soldering tasks necessary to produce a product by performing the following duties. In addition, this position requires basic computer skills to make transactions, transfer yield rates and data into Excel. | 12/2/2019 |
| 404 | Medidata Metropark, NJ B2B Marketing Associate BS/BA Exp: 1-3 years in marketing/sales |
This marketer will drive direct targeted marketing for our platform and solutions by developing programs that leverage outbound marketing efforts - across online/digital and tele-prospecting tactics - to drive overall preference, satisfaction, technology adoption of our platform/portfolio and amplify market impact of our technology innovation stories. Assist and lead in the development of outbound marketing programs across a variety of product offerings, industries, segments, and personas (e.g., Clinical Ops, Data Management, Finance, IT). | 12/2/2019 |
| 405 | Medidata New York, NY Software Engineer (C# / .Net) BS/BA Exp: 1-3 years in various coding languages |
Coder is a mature, single-instance, multi-tenant web service supporting hundreds of clinical trials. Our application is built with C#, leverages Microsoft’s SQL server database and is hosted in AWS. Our front end uses Asp.NET, HTML/CSS, Bootstrap and AngularJS. As an engineer on Coder, you'll be challenged both to develop new features in response to market demand and improve the performance and scalability of the application to meet the rapidly growing user base. | 12/2/2019 |
| 406 | AstraZeneca Wilmington, DE Contract Operations Analyst BS/BA Exp: 0-4 years |
The Sr. Contract Operations Analyst is responsible for working with internal/external customers on all aspects of Market Access; Master Data, Contracting, Membership, Chargebacks and Rebates. They are responsible for the receipt, analysis, impact, resolution and posting/reporting of all contractual payments across multiple customer segments including Health Plans, GPOs, Specialty Pharmacies, Physicians and Wholesalers as well as maintaining all related documentation for those payments. The Sr. Contract Operations Analyst is responsible for developing Market Access contracts including: template development, strategy interpretation, language negotiation, approval, and execution In this role, they will manage and meet deliverables of business operations to monitor, evaluate and administer claims to be paid and ensure payments are accurate, timely, formulary compliant and entered in contract systems consistent with agreement terms, following corporate controls/approved guidelines and SOX regulations. | 12/2/2019 |
| 407 | AstraZeneca Frederik, MD Quality Control Analyst BS in sciences/biotech/pharma Exp: 0-5 years |
Performs selected quality control testing activities, dependent upon assigned area, including the following: Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. Identifies and troubleshoots equipment problems. Enters data evaluated for compliance to specifications and reports abnormalities. Reads, understands, and follows SOP’s and complies with cGMP’s | 12/2/2019 |
| 408 | AstraZeneca Gaithersburg, MD Research Animal Technician I BS/BA in biological sciences Exp: 0-1 years |
At AstraZeneca as the Research Animal Technician I, you will support oncology using basic technical skills such as performing daily health/mortality checks, evaluating health status of animals and performing basic technical procedures such as SC, and IP injections, cardiac blood collection, and oral gavage. Observe appropriate safety and study requirements by reading, understanding and following Standard Operating Procedures (LAR Guidelines), applicable regulations and study protocols. Observe appropriate safety and health practices including personal protective equipment and barrier requirements. | 12/2/2019 |
| 409 | AstraZeneca Wilmington, DE Patient Safety Associate (Quality Excellence) BS/BA in biosciences, healthcare, IS/IT Exp: 1 year in pharma |
The BioPharmaceuticals Business Unit (BBU) creates and executes meaningful therapeutic area and product strategies that are focused on addressing the unmet needs of patients around the world. Conducts activities and interactions consistent with company values and in compliance with the Code of Conduct and supporting policies and standards relevant to the role. Completes all required training on AstraZeneca’s Code of Conduct and supporting policies and standards on time. Reports potential issues of non-compliance. Demonstrates a working knowledge and compliance with organizational global and local procedural documents and local implementation of objectives, policies, processes and procedures and regulatory requirements, guidelines and obligations relevant to pharmacovigilance activities and adverse event reporting, including periodic safety reporting. | 12/2/2019 |
| 410 | AstraZeneca Frederik, MD Quality Control Technician - Laboratory Management Services (LMS) - Operations HS Diploma/GED Exp: 0-2 years work experience |
Sampling of the Utilities Systems (for example WFI, Specialty Gases, Compressed Air, Steam). Sample management activities including receipt, visual inspection for integrity, storage, distribution and disposal. Parts and glassware washing and autoclaving, including proper documentation of these activities. Detailed supervision and detailed instructions given for routine work as well as any new activities or special assignments. | 12/2/2019 |
| 411 | Kimball Electronics Jasper, TX Manufacturing Engineer BS/BA in eletrical/mechanical engineering Exp: 0-3 years |
Leads manufacturing efforts with respect to direct customer product launches and sustaining activities. Guides, mentors and manages engineering support teams. Development of processes and DFx activities to meet customer requirements. Selection, specification and implementation of manufacturing equipment. Work directly with program management and quality engineering to ensure profitability. | 12/2/2019 |
| 412 | Cantel Medical Pomezia, IT R&D Microbiology Associate MS in biology or related Exp: 1 year in R&D projects |
The junior microbiologist will assure to support the “in vitro” test according to EN/ISO Standards requirements. Respecting the deadlines; Check the expiration date of the reagents and the microbial strains; Fill laboratory notebooks and record the results. Ability of preparation of culture media and microbial strains suspension. They will report to local manager. | 12/2/2019 |
| 413 | MedPace Home based, na Home-Based Clinical Research Associate - Clinical Research Coordinator Experience BS/BA in health/sciences Exp: 1 year minimum |
This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Perform qualification, initiation, monitoring, and closeout visits; Establish an open line of communication with site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Evaluate the quality and integrity of site practices – escalating quality issues as appropriate; | 12/2/2019 |
| 414 | MedPace Cincinnati, OH Clinical Research Associate-Cincinnati Entry Level BS/BA in health/sciences Exp: 1 year work experience preferred |
Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence: PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA. | 12/2/2019 |
| 415 | Viant Collegeville, PA Process Engineer - Metals BS/BA in material science/metallurgy or mechanical engineering Exp: 1 year |
The Process Engineer must be able to recognize, communicate, and measure technical risk for a variety of metals for use in medical, aerospace, and industrial products along with the processes and equipment used to manufacture these products. The process engineer is a central leader for addressing concerns of a technical nature. Provide diversified range of technical services to both internal and external customers supporting the attainment of company goals. Areas of support include mechanical testing, cold drawing, heat treating, nondestructive testing, and failure analysis of metal tubes | 12/2/2019 |
| 416 | MedSpark San Luis Obispo, CA Product Development Engineer BS/BA in mechanical engineering Exp: 1 year |
You will be part of a small and nimble team that conceptualizes, develops, and proves-out designs that make an impact on the world of medicine. Your primary role is driving conceptualization, development, and prototyping of new product concepts, focused on inventive uses of new and existing technologies that open up entirely new product concepts. Work hours and days are extremely flexible, based on need and your availability. | 12/2/2019 |
| 417 | T2Biosystems Lexington, MA Research Associate, Molecular Assay Development BS in biology, biochemistry, or related Exp: 0-2 years |
As a motivated, curious and goal-oriented research associate, you will join a dynamic R&D team and contribute towards the development of novel molecular methodologies and assays for diagnostic applications. You will execute studies, conduct data analysis, and document results. As a contributor you will interact with other individuals and groups across our research and product development teams. You must have strong communication, analytical and quantitative skills and thrive working with highly skilled teams on multiple, simultaneous projects in a fast-paced technical setting. etc. | 12/4/2019 |
| 418 | T2Biosystems Lexington, MA Research Associate - Process Development BS/MS in biology, biochemistry, biotechnology, or related Exp: 1-2 years |
We are seeking a talented and highly motivated individual to join our multi-disciplinary team as a Research Associate. This individual will be a key contributor to executing reagent formulation activities including technology transfer, process development, analytical method development, verification and validation. The position will be located in Lexington, MA. Responsibilities: Development, optimization, scale up, and validation of reagent processes and measurement systems; including DOE and capability analysis. Experimental planning, execution, and data analysis. etc. | 12/4/2019 |
| 419 | T2Biosystems Lexington, MA Research Associate /Research Associate II - Microbiology (Contract to Perm) BS/MS in molecular biology or related Exp: 0-3 years |
This position is to fill a need within our Microbiology group working in our Lexington, MA location. The RA will provide aid in the development of laboratory protocols for the cultivation and characterization of pathogenic organisms. The individual will work with the T2 Microbiology staff to expand on our established protocols and methods to enable the accurate production of test samples for development of novel assays in conjunction with the Assay Development group. This role consists of hands-on execution in the laboratory and data analysis within the Microbiology group. etc. | 12/4/2019 |
| 420 | Talis Biomedical Menlo Park, CA Research Associate MS in biology, microbiology, molecular biology, biochemistry 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. Position Responsibilities: Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Participate in design of molecular assays. etc. | 12/4/2019 |
| 421 | Talis Biomedical Menlo Park, CA Test Engineer - Embedded Software & Firmware BS in an engineering field Exp: 0-4 years |
Position: Learn and develop expertise on our firmware and embedded software requirements, in order to create automatable test scripts. Author basic functionality, stress, and reliability tests using state-of-the art tools, and novel in-house test fixtures. Document and perform root cause analysis on testing failures. Collaborate closely and clearly communicate test plans and results to cross-functional team members. Other duties as assigned. | 12/4/2019 |
| 422 | Tango Therapeutics Cambridge, MA Associate Scientist, Immunology BS/MS in immunology or related Exp: 0-8 years |
We are seeking an innovative, collaborative and enthusiastic immunologist to work on building our immunology and Immuno-Oncology Programs. This individual will work primarily at the bench to help drive target identification, validation, and patient selection strategies. Job Responsibilities: Culture and engineer primary human T cells and murine T cells using genetic tools. Culture and engineer primary human tumor cell lines and murine cell lines using genetic tools. etc. | 12/4/2019 |
| 423 | TCR2 Therapeutics Cambridge, MA Research Associate/Senior Research Associate, Analytical Process Development BS in biochemistry, cell biology, immunology or related Exp: 1-2 years |
Responsibilities: Learn and execute on all assays used by the analytical team (qPCR, ELISA, T-cell based assays). Assist in the analysis and characterization of lentiviral vectors for use by multiple internal research groups. Work with process development teams to investigate, improve, and implement advanced vector production processes. Analyze results, solve problems, and troubleshoot assays. Participate in assay development of established analytical tools and help develop new assays. Develop and maintain various cell lines used in cell-based analytical assays. etc. | 12/4/2019 |
| 424 | TCR2 Therapeutics Cambridge, MA Research Associate, Vector Production BS/MS in molecular biology, biochemistry, protein chemistry, or related Exp: 1-2 years |
Responsibilities: Generation and maintenance of various cell lines and used by internal research groups. Production of retroviral vector stocks using various transfection methodologies. Assist analytics team in evaluation of in-process and endpoint samples. Thorough documentation of procedures and experiments. Coordinate with various internal groups for the generation and evaluation of emerging vector products. Assist in drafting of SOPs, technical documents, batch records, etc, for transfer to external CMOs. Participation in internal and external meetings detailing ongoing work. etc. | 12/4/2019 |
| 425 | TE Connectivity Manfield, OH Electrical Engineer BS in physics or electrical or mechanical engineering Exp: 0-1 years |
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. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. etc. | 12/4/2019 |
| 426 | TechLab Blacksburg, VA Research Technician BS in a life science Exp: 1 year |
TechLab, Inc. develops, manufactures and distributes medical diagnostic tests. Our company places emphasis on science and collaboration with Universities. We are hiringa Research TechnicianforourScientific Affairs teams.The Research Technicianwill aidthe team with experiments and research. The Research Technician can be expected to perform protein purification using chromatography, write Standard Operating Procedures and Master Batch Records, and assist with assay development and optimization. etc. | 12/4/2019 |
| 427 | Tecomet Warsaw, IN Material Associate HS diploma or equivalent Exp: 1-3 months |
The Material Associate will receive, unpack, verify, and store raw materials. Issue raw material to job routers and deliver to appropriate work areas. Maintain movement of subcontract production parts returning from vendors. This is accomplished by maintaining Tecomet principles of Safety, Quality, Customer Satisfaction and Innovation. Essential Duties and Responsibilities: Receive raw material and out-vend production parts and enter receipt into computer. Receive delivery of UPS, Fed-Ex and other transportation carriers and document receipt in computer. Issue raw material to specific job routers and deliver to specific production unit.Document receipt in computer. Perform weekly cycle-counting to ensure material counts are correct. etc. | 12/4/2019 |
| 428 | Tempus , MI Account Associate BS in a life science, business, or marketing Exp: 0-2 years |
Responsibilities: Building and maintaining relationships with physicians and office staff to drive clinical orders in the community. Building and maintaining relationships with pathology departments to ensure smooth specimen sendouts - tissue procurement. Maintain a regular cadence of touch points (in person, emailing value adds) with certain targeted accounts (ie 3 x month per physician). Coordinating Medical Affairs report review with physicians after clinical orders. Order Kit and literature replenishment at accounts. Identifying and attending approved local conferences. Working with accounts to obtain necessary clinical data / progress notes for Tempus-tested patients. etc. | 12/4/2019 |
| 429 | Tempus Chicago, IL Clinical Molecular Technologist MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: 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. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 430 | Tempus Chicago, IL Clinical Molecular Technologist (Shift Diff - Tuesday to Saturday) MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: 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. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 431 | Tempus Chicago, IL Clinical Molecular Technologist (Sunday-Wednesday with Shift Diff.) MS in medical technology, clinical laboratory science, or related science Exp: Not necessary for MS candidates |
What you’ll do: 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. Work our daytime shift Monday - Friday. | 12/4/2019 |
| 432 | TeVido BioDevices Austin, TX Biotech Manufacturing Technician AS/BS in biological sciences or engineering Exp: 0-1 years |
TeVido BioDevices is seeking a highly motivated individual to join our team as a Biotech Manufacturing Technician. We are a small Austin, TX-based biotech company that is addressing unmet needs in reconstructive and cosmetic surgery. The company has launched the manufacturing of our first product, cellular grafts, to treat patients with skin pigmentation disorders such as vitiligo. The person in this role will be responsible for performing daily production operations, including processing, quality control tests, and production facility cleaning; documenting work; and aiding improvement projects. This individual should be detail-oriented and self-motivated. An Associate’s degree in biological sciences or bioengineering and experience with aseptic technique in a laboratory or cleanroom is required. This is a challenging and exciting opportunity to contribute to an innovative, fast-paced startup in Austin, TX whose mission is to enhance patients’ quality of life using their own tissue. etc. | 12/4/2019 |
| 433 | Thermalin Cleveland, OH Research Associate-Protein Formulation MS in biochemistry or related Exp: 1 year |
Thermalin is looking for a Research Associate – Protein Formulation to join our team. In this role, you will formulate insulin analogs for preclinical development. Research Associate Responsibilities: Formulate novel insulin analogs using established protocols. Quantify insulin analogs using reverse-phase (RP) analytical chromatography. Characterize insulin formulations with novel excipients using various biochemical methods. Develop new formulation schemes for insulin analogs. Optimize procedures and protocols to improve throughput. Perform laboratory tasks safely, rapidly, and efficiently. Report results in written and verbal format. Record results accurately and meticulously. | 12/4/2019 |
| 434 | ThermoFisher Scientific Greenville, NC Formulation Technician II HS diploma/AS Exp: 1 year |
How will you make an impact? Sets-up, operates, and maintains the classified environments and manufacturing equipment for pharmaceutical products. Ensures operations are performed in a safe and responsible manner striving to create an injury-free and incident free workplace. What will you do? Operation of aseptic filling, freeze drying and capping equipment. Ensures pharmaceutical products in manufacturing are in accordance to SOPs and current GMP and other batch related activities. Verifies and documents production activities in batch records, logbooks, etc. Assists in troubleshooting operational and production problems in order to identify appropriate corrective actions. Performs the disassembly, assembly, cleaning, and operation of area manufacturing equipment. etc. | 12/4/2019 |
| 435 | ThermoFisher Scientific , IL Field Service Technician BS in engineering, biology, chemistry, or related Exp: 1+ years |
The Field Service Technician (FST) performs planned maintenance, repairs and other verification/qualification services on a variety of laboratory instruments in assigned territory. The FST engages with customers and provides basic instrument services in a professional and timely manner. Essential Functions: Provides planned maintenance (PM), basic repair services and temperature verifications. Displays professionalism, understanding, tact, fairness and technical knowledge in all customer interactions. Follows all reporting responsibilities of Remote Service Dispatch (RSD), Escalation, Field Problem Report (FPR) and Field Service Report (FSR) submissions. etc. | 12/4/2019 |
| 436 | ThermoFisher Scientific Gainesville, FL Associate, Quality Assurance HS diploma Exp: 1 year |
The QA Associate will participate in the day to day operations related to release functions in the Quality Assurance Department. The incumbent is responsible for the timely review and disposition of controlled materials needed to support manufacturing. These materials include, but are not limited to, sterile supplies, cell banks, viral banks, and reagents used by manufacturing or for testing processes. The associate identifies areas for improvement and ensures materials, products, and equipment within the warehouse remain in a state of control. etc. | 12/4/2019 |
| 437 | ThermoFisher Scientific Los Angeles, CA Sales Representative BS Exp: 0+ years |
Our Sales Representative is responsible for the sales of research products and services within a defined territory, serving customers engaged in pharmaceutical, biomedical, chemical, and other fields of research and development, as well as quality assurance labs such as in food and environmental testing. The Sales Representative maintains effective customer relations, develops opportunities for growth within an existing customer base, and assures market penetration and profitability while achieving sales and profit forecasts. etc. | 12/4/2019 |
| 438 | ThermoFisher Scientific Cincinnati, OH QC Lab Technician AS in chemistry or related Exp: 1-2 years |
Responsibilities: Testing of raw materials, finished product, and stability samples while meeting deadlines and following an assigned schedule. Accurately documenting all tests/test materials/equipment used and all results obtained. Work in accordance with approved methods, SOPs, and cGMPs/GLPs, while performing tests. Responsible for safety and to protect themselves and fellow employees from harm. | 12/4/2019 |
| 439 | ThermoFisher Scientific High Point, NC Continuous Process Verification (CPV) Engineer BS in pharmaceutical science, chemistry, statistics, or related Exp: 1+ years |
The CPV Engineer will apply Project Management and technical expertise within the pharmaceutical industry to successfully deliver CPV program goals and outcomes while interacting with customers and meeting their expectations. CPV is a global regulatory compliance requirement which focuses on ensuring product and process stability, control, and operation within the intended design space. What will you do? Demonstrate highly effective oral and written communication skills and possess project management skills including the ability to engage the organization at multiple levels and organize CPV efforts. Work with Business Managers and the business team with Technical Transfers, new business, or other situations as related to CPV. etc. | 12/4/2019 |
| 440 | ThermoFisher Scientific Lenexa, KS Quality Control Technologist I BS in a biological science Exp: 1-2 years |
Responsible for all quality control aspects of finished product testing. Ensure that performance of finished product is in compliance with testing standards per IFU and SOP's in addition to customer requirements and regulating agencies' guidelines. Documentation control duties per Quality assurance compliance requirements. Key Responsibilities: Review and maintain product compliance specifications, documentation control. Gain proficiency on all performance benches. Documentation of testing results and determining disposition. Maintain consistency in training in Master Control. Establish and maintain SOP criteria for inspection/testing. Responsible for maintaining department equipment and requesting consumables as needed. etc. | 12/4/2019 |
| 441 | Invenra Madison, WI Research Associate - Antibody Display BS in biological sciences Exp: 1 or more year in research |
This individual will support the development of the Invenra antibody discovery platform. Aspects of the job entail cloning, antibody library panning and protein target preparation. The successful candidate will work with other scientists within the team and will become proficient in antibody display technologies. The position requires excellent scientific and problem-solving skills, with a strong focus on creative solutions to technical problems. | 11/20/2019 |
| 442 | Invenra Madison, WI Laboratory Support Technician HS Diploma/GED and enrolled in college Exp: 0 years |
Invenra is seeking a highly motivated laboratory support technician. This individual will maintain the laboratory and laboratory supplies in a clean, ready and working order. The position will work collaboratively with others to implement process improvements that increase efficiency and quality in the laboratory. This is a part-time position. | 11/20/2019 |
| 443 | Invicro Boston, MA Associate Scientist, Chemistry MS Exp: 1-3 years in academic/pharma labs |
We seek individual who is an accomplished scientist with some experience in radiochemistry of small and large molecule imaging tracers for preclinical nuclear medicine imaging studies, including both PET and SPECT. Though the radiochemistry experience is not mandatory, the ideal candidate needs to have experience in organic synthesis and analytical chemistry. The candidate should have strong desire to learn radiochemistry and be able to operate and troubleshoot automated synthesis systems and analytical equipment. Most of the radiochemistry training will be provided but hands-on experience with handling radioactive materials, labeling with radioactive isotopes, purification, and formulation for in vivo imaging and biodistribution studies will be an advantage. | 11/20/2019 |
| 444 | Invicro Boston, MA Histology Technician BS or histotech certification Exp: 0-2 years in histology/autoradiography |
The Histology Technician works in the laboratory to perform and support ex vivo studies including, but not limited to, histology, autoradiography, 3D fluorescence imaging, and cell culture. The ideal candidate will have hands-on experience in a pharmaceutical histology laboratory performing standard histology studies – embedding, sectioning and chromagen/fluorescent antibody staining. In addition, the ideal candidate will have a proven track record and competence in histology or autoradiography method development. The individual in this role will be expected to understand and carry out analysis to inform his/her own development efforts and assist in-house analysts. | 11/20/2019 |
| 445 | Invitae San Francisco, CA Lab Accessioning BS in sciences/clinical lab studies Exp: 0-2 years |
Our Laboratory Accessioning Associates are responsible for preparing laboratory specimens prior to laboratory analysis and testing. This individual should have excellent attention to detail, effective communication skills and the ability to work independently and in a team environment. This role requires being on-site at our SF office location, with either a Monday - Friday or Tuesday - Saturday schedule. | 11/20/2019 |
| 446 | Thermo Fisher Scientific Fair Lawn, NJ Distillation Tech. - Liquids HS Diploma/GED or AA/AS Exp: 1-2 years in admin |
The Distillation technician supports the Operations Manager and Production Supervisor in achieving daily production targets prioritized by Safety, Quality, Delivery and Cost. Following the priorities set by the Manager and Supervisor ensures that distillation columns are operating safely per procedures and to meet daily production goals laid out by supply chain. | 11/20/2019 |
| 447 | Thermo Fisher Scientific Cambridge, MA Lab Technician BS in life sciences Exp: 1-3 years industry experience |
The Sr. Associate is an associate with a moderate level of technical expertise and experience. May perform complex activities outside of routine manufacturing operations commensurate with their experience and training. Will participate in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls under limited supervision. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. | 11/20/2019 |
| 448 | Thermo Fisher Scientific Foster City, CA Labware Technician I HS Diploma/GED Exp: 0-2 years in cGMP environment |
This position is focused on service delivery excellence for UnityTM Lab Services. Specific activities relative to the job function could include: laboratory glassware and inventory management. This position will utilize the basic functionality of systems and equipment relevant to the job function, such as: industrial glasswasher, sterilizers, and ovens. Strong communication skills are also required | 11/20/2019 |
| 449 | Thermo Fisher Scientific Foster City, CA Labware Technician II HS Diploma/GED Exp: 0-2 years in cGMP environment |
This position is focused on service delivery excellence for UnityTM Lab Services. Specific activities relative to the job function could include laboratory glassware and inventory management. This position will utilize the basic functionality of systems and equipment relevant to the job function, such as: industrial glasswasher, sterilizers, and ovens, Microsoft Office suite. Strong communication skills are also required. | 11/20/2019 |
| 450 | Thermo Fisher Scientific Cincinnati, OH QC Scientist I BS/BA in physical sciences, chemistry or biology preferred Exp: 0 years required |
Conducts routine chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. Executes validated test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, and dissolution by HPLC, GC, dissolution, spectroscopy, and traditional quantitative analysis, utilizing HPLC, GC, LC/MS, dissolution, spectroscopy, and/or traditional wet chemical testing. Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems. Performs daily instrument calibrations / verifications as required. | 11/20/2019 |
| 451 | Thermo Fisher Scientific Eugene, OR Manufacturing Operator I HS Diploma/GED or AS/AA preferred Exp: 0 years required, lab experience a plus |
Operate processing and packaging equipment. Equipment includes: balances, labelers, band sealers, pumps, filtration systems, and other packaging equipment. Weigh, measure and check raw materials with assistance of computer interface to assure batches manufactured contain proper materials and quantities. Calibrate/operate semi-automated and automated manufacturing equipment. Complete and maintain Quality Records in compliance with regulatory requirements, GMP’s and standard operating procedures. | 11/20/2019 |
| 452 | Thermo Fisher Scientific Eugene, OR Manufacturing Operator I HS Diploma/GED or AS/AA preferred Exp: 0 years required, lab experience a plus |
Operate processing and packaging equipment. Equipment includes: balances, labelers, band sealers, pumps, filtration systems, and other packaging equipment. Weigh, measure and check raw materials with assistance of computer interface to assure batches manufactured contain proper materials and quantities. Calibrate/operate semi-automated and automated manufacturing equipment. Complete and maintain Quality Records in compliance with regulatory requirements, GMP’s and standard operating procedures. | 11/20/2019 |
| 453 | Invivoscribe San Diego, CA Manufacturing Associate I/II BS in sciences Exp: 1+ years in GMP lab |
As a Manufacturing Associate I/II for Invivoscribe you will assist with all aspects of production, including the production of master mixes, controls and assay kits. You will contribute to the drafting and review of new documents, including SOPs, Batch Records and Purchasing Specifications. Details include: Oversee, perform, plan and schedule production. Work with suppliers of core raw materials to ensure quality, quantity, price and availability. Create, review and revise production documents. Implement and train on the use of those documents. Participate in the production of master mixes and ASR, reconstitution of oligonucleotides, controls, reference standards and general purpose reagents by following manufacturing batch records, work instructions, standard operating procedures, forms and validated Excel spreadsheets. | 11/20/2019 |
| 454 | Invivoscribe San Diego, CA Research & Development Associate I/II BS in technical/science field Exp: 1+ years in lab |
As a Development Associate I/II at Invivoscribe you are responsible for generating and documenting laboratory data with direct supervision. Your performance will contribute to a quality data generation in a regulated environment following good laboratory practices. More specifically: Support development projects that can include generating analytical data for an FDA submission. Use laboratory techniques such as PCR, gel and capillary electrophoresis, aseptic technique for mammalian cell culture, magnetic beads purification, DNA quantification and NGS. Execute and document experiments that support the development of diagnostic reagents and assays. Experimental design will include all of the appropriate controls. | 11/20/2019 |
| 455 | Invivoscribe San Diego, CA Quality Control Laboratory Associate I/II BS in sciences Exp: 1+ years in GMP lab |
As a for a Quality Control Laboratory Associate I/II at Invivoscribe you will be responsible for receiving samples and performing data entry for specimens received as well as performing all aspects of clinical laboratory patient testing. More specifically: Test raw materials in process and final product and generate testing data. Releases products to QA for final approval. Ensure that all customer complaints and inquiries are resolved. Conduct and maintain the real time stability study testing. | 11/20/2019 |
| 456 | Medical Diagnostic Laboratories, LLC Broken Arrow, OK Entry Level Sales Executive BS/BA Exp: 0-2 years |
As a Entry Level Sales Executive, you will be responsible for maintaining and growing a client base of both hospital and physician customers for MDL. Responsible for achieving annual sales and profit objectives for a defined territory. Obtain new business and exceed annual territory sales budget each year by presenting new test information, up selling and seeking out new sources of revenues from clients. Develop and present personalized sales presentations to professional audiences (physicians, laboratory staff, clinics and group practices); demonstrate how MDL's technical features and services could benefit the practice and help medical personnel provide quality patient care. | 11/20/2019 |
| 457 | Medical Diagnostic Laboratories, LLC Multiple Locations, na Entry Level Sales Executive BS/BA Exp: 0-2 years |
As a Entry Level Sales Executive, you will be responsible for maintaining and growing a client base of both hospital and physician customers for MDL. Responsible for achieving annual sales and profit objectives for a defined territory. Obtain new business and exceed annual territory sales budget each year by presenting new test information, up selling and seeking out new sources of revenues from clients. Develop and present personalized sales presentations to professional audiences (physicians, laboratory staff, clinics and group practices); demonstrate how MDL's technical features and services could benefit the practice and help medical personnel provide quality patient care. | 11/20/2019 |
| 458 | Invivotek Hamilton, NJ Research Associate - Animal Science/In-vivo BS in life sciences Exp: 1-2 years with rat/mouse handling |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 11/20/2019 |
| 459 | Invivotek Hamilton, NJ Vivarium Technician HS Diploma/GED Exp: 0-2 years |
We are seeking a motivated and talented Research Associate to perform laboratory assays for validation of potential drug development targets and characterization of pharmacological compounds. The Research Associate should have excellent laboratory skills to conduct in vitro bioassays on murine tissues and primary cells. Experience with tissue culture techniques and primary cell-based assays are required with a variety of readout technologies including flow cytometry, RT-PCR and ELISA. Excellent communication skills and motivation to learn are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 11/20/2019 |
| 460 | Iovance San Carlos, CA Contract Drug Safety Associate Healthcare professional degree w/BS or AA Exp: 0-2 years |
The Drug Safety Associate candidate works in a team-oriented, dynamic, and collaborative environment. This person would manage the drug safety mailbox, track case workflow, support the drug safety team, review serious/adverse event information, and review case narratives. | 11/24/2019 |
| 461 | Iqvia Atlanta, GA Vaccine Sales Representative BS/BA Exp: 1 year in healthcare/sciences |
Vaccine Sales RepresentativeThe Vaccine Sales Representative will be responsible for achieving stated business goals of product sales within assigned portfolio and geography through strategic territory and account management and building solid working relationships. Responsible for providing healthcare providers with all relevant information that promotes quality healthcare decisions. Maintains an expert product knowledge base including patient education, consumer education, and factors influencing the market environment. Understands and uses approved promotional materials to support marketing message. | 11/24/2019 |
| 462 | Iqvia San Juan Capistrano, CA Vaccine Study Specialist BS/BA in sciences Exp: 1 year in GCLP lab |
Provides internal oversight and conducts the day to day running of a project throughout its life at Q2 Solutions, including method development, method validation, and sample analysis while adhering to timelines, SOPs and performance metric standards. Serves as internal liaison between the production lab scientists and project management team. Provides daily direction and feedback to laboratory staff regarding Vaccines studies. Effectively and efficiently coordinates and communicates with relevant internal support groups as needed for the study. | 11/24/2019 |
| 463 | Iqvia New Brunwick, NJ QA Engineer 1 BS/BA in related field Exp: 1-2 years in software testing |
Work closely with Development, Functional/Business and QA teams in all the phases of SDLC. Review the requirements and provide the QA estimations and raise any concerns or issues as needed . Involved right from the requirements grooming and will prepare the logical test scenarios & test cases as needed. Prepare test scenarios & test cases and requirements traceability matrix (RTM) to ensure the complete coverage | 11/24/2019 |
| 464 | Ironwood Albany, NY Clinical Sales Specialist BS/BA Exp: 1 year in pharma sales |
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients. Representative must demonstrate a strong understanding of relevant disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. Drive sales performance in a compliant manner and work to meet or exceed territory sales goals through execution of regional and national marketing strategies | 11/24/2019 |
| 465 | Ironwood Tyler, TX Clinical Sales Specialist BS/BA Exp: 1 year in pharma sales |
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients. Representative must demonstrate a strong understanding of relevant disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. Drive sales performance in a compliant manner and work to meet or exceed territory sales goals through execution of regional and national marketing strategies | 11/24/2019 |
| 466 | FujiFilm Santa Ana, CA Powder Formulation Tech HS Diploma/GED Exp: 1-2 years hands on experience |
We are hiring for a Powder Formulation Tech. The Powder Formulation Tech is responsible for the formulation of our company’s powder cell culture media products. NOTE: The current opening is on our second shift (1:00 PM – 9:30 PM). Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. Uses Mettler-Toledo IND780 terminal system to ensure correct raw materials assigned in the batch record are used and at the specified quantity. Reviews lot folders for accuracy, completeness and availability of components necessary to complete job prior to the scheduled date of production | 11/24/2019 |
| 467 | Genetech San Francisco, CA QC Analyst BS/BA in sciences Exp: 0-5 years |
The Senior QC Analyst will perform analytical, biochemical, and/or biological testing; data review; and/or related activities that support QC operations. Perform a broad variety of basic and moderately complex tests with documentation according to GMP. Maintain accountability for deliverables affecting department and organizational objectives. Accountable for exhibiting behaviors as described by Genentech/Roche Core Competencies. | 11/24/2019 |
| 468 | Jubilant Spokane, WA Technician IV, Environmental Monitoring HS Diploma/GED Exp: 1 year in pharma/lab |
The Environmental Monitoring (EM) Technician IV is required to perform the basic functions associated with environmental monitoring. Incumbents are required to learn the laboratory functions, sanitization procedures, and donning scrubs for ISO 8 sampling requirements. Sampling, initiating tests and collecting test results related to defined quality parameters for surface, air, product and utility systems such as compressed gases and WFI. | 11/24/2019 |
| 469 | Just-Evotec Biologics Seattle, WA Associate Scientist, Drug Product BS in Chemistry, Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering or related Exp: 0-3 years |
Support scientific staff with various protein characterization methods including SE-HPLC, sub-visible particle analysis (HIAC and Flowcam), protein concentration (UV-Vis), pH, osmo, buffer exchange and viscosity. Execution of established high throughput biophysical methods. Perform lab maintenance tasks will include buffer preparation, tracking/ordering consumables, and shipping/receiving samples. | 11/24/2019 |
| 470 | Just-Evotec Biologics Seattle, WA Associate Scientist, Process Development BS in Chemistry, Biochemistry, Molecular and Cellular Biology, Chemical Engineering, Bioengineering or related Exp: 0-3 years |
The successful candidates will have some experience in one or more of the following areas including chromatography, filtration, electrophoresis, analytical chemistry, cell culture and/or bioreactor operations. Experience with high throughput, robotic techniques for analytical testing, chromatography, and/or protein expression, as well as statistical design of experiments and/or process modeling, is a plus. The ideal candidate has strong written and verbal communications skills and works well independently and in teams. This position may include the opportunity to rotate through different functional areas to gain experience in different techniques and disciplines. | 11/24/2019 |
| 471 | Just-Evotec Biologics Seattle, WA Process Engineer I/II – Purification BS in biological sciences/engineering Exp: 1-3 years |
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. | 11/24/2019 |
| 472 | Navitas Rockville, MD Research Assistant - KAI Research BS/BA Exp: Entry Level |
Assist in the development of client deliverables according to project requirements, including but not limited to, project-specific documentation, operating procedures, and work flows with direction of more experienced staff. Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensure appropriate distribution of materials to internal and external research personnel and sites. Prepare general correspondence, agendas and meeting minutes, reports, and other project-specific documentation. Ensure review, approval, and distribution to internal staff and external project participants. | 11/24/2019 |
| 473 | KBI Biopharma Durham, NC Research Associate I-Analytical Development (6 month temp to hire) BS Exp: 0-2 years |
Perform contract development services, including analytical development programs for monoclonal antibodies, recombinant proteins and peptides. Capable of performing bio-analytical techniques such as HPLC/UPLC, IEF, CE, Plate-based assays (ELISA, etc), qPCR, SDS- PAGE, Western Blot, with minimum training and under supervision. Prior hands-on experience or knowledge with chromatography, CE, IEF and plate-based assay is a plus. | 11/24/2019 |
| 474 | KBI Biopharma Durham, NC Manufacturing Associate I-Upstream (temp to hire) BS/BA or AA Exp: 0-1 years |
Responsible for a wide variety of cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Follow SOPs, perform daily tasks in a clean-room, retain records and write reports. May also be responsible for troubleshooting. Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities. | 11/24/2019 |
| 475 | KBI Biopharma Durham, NC Quality Systems Software Architect I/II BS/BA in pharma/biological sciences/ or chemistry Exp: 1-2 years in quality or validation |
Responsible for quality computer system administration, providing technical/end user support for quality computer system, and maintaining close communication with management to keep stakeholders apprised of quality computer system incidents/ resolutions, project validation status, and other relevant issues. The role requires leading and/or assisting in quality computer system validation efforts and ensuring all work is carried out in compliance with cGMPs, company policies and procedures, 21 CFR Part 11, EU Annex 11, ICH guidelines, and other applicable industry regulations. | 11/24/2019 |
| 476 | KBI Biopharma Boulder, CO Engineer I/II - Manufacturing Science and Technology BS/BA or MS in sciences or engineering Exp: BS/BA: 1-5 years, MS: 0-3 years |
The successful candidate will apply scientific and engineering principles to support new biopharmaceutical process enrollments into the cGMP manufacturing facility. The candidate will: Perform all aspects of facility fit activities to support program enrollment including generating process flow diagrams, bill of materials (BOM), new specifications, and Äkta chromatography methods. Collaborate with process development and manufacturing teams to perform technical transfer and facility fit activities for downstream processes. | 11/24/2019 |
| 477 | KBI Biopharma Durham, NC Research Associate/Sr. Research Associate BS or MS in chemistry/biochemistry Exp: 0 years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. 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. | 11/24/2019 |
| 478 | KBI Biopharma Boulder, CO Manufacturing Associate I/II HS/GED, or BS/BA Exp: HS: 0-3 years, BS: 0 years |
This position is for a 2-week cycle, day shift with every other weekend off. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality.Assist in execution of procedures for microbial manufacturing, purification, or support area of manufacturing using SOP's and batch record. Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. | 11/24/2019 |
| 479 | KBI Biopharma Boulder, CO Microbiology Environmental Services Associate BS in sciences Exp: 0 years |
Performs 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 within all classified manufacturing areas according to approved SOP’s and cGMP’s. Review EM data for completeness and accurate, and assist with data trending. Provide EM support for manufacturing during specified dynamic conditions. | 11/24/2019 |
| 480 | Keystone Nano State College, PA Research Chemist MS in biological sciences/chemistry/engineering Exp: 0-2 years lab experience |
Keystone Nano is looking for a Research Chemist able to play an important role in developing novel drug products for cancer applications. The successful candidate will join our laboratory in State College, PA to conduct chemical and physical experiments using our proprietary manufacturing techniques to develop and scale this technology for a variety of markets. Set up and conduct chemical experiments, tests, and analyses using techniques such as spectroscopy, chromatography, physical and chemical extractions, dynamic and quasi-electric light scattering and microscopy, Compile and interpret results of tests and analyses Prepare graphs and charts to document experimental results for presentation to management. | 11/24/2019 |
| 481 | KSQ Therapeutics Cambridge, MA Associate Scientist, ImmunoBiology Target Discovery/Validation BS or MS in biology/immunology Exp: 1-2 years research experience |
KSQ Therapeutics, Inc. is seeking an exceptional and highly motivated Associate Scientist, Target Discovery/Validation in the Immunobiology group to apply their experience in immunology towards the development of the next generation of impactful immunotherapies. This person will contribute to both target discovery and target validation efforts as well as in supporting our pre-clinical Immuno-Oncology small and large molecule portfolio. | 11/24/2019 |
| 482 | KVK Tech Newtown, PA Microbiologist MS in biological sciences Exp: 0-5 years |
Validate Bacterial Endotoxin test method and test of finished products with gel clot and kinetic method; Perform and validate anti-microbial effectiveness Testing; Perform Sterility testing and validation using Steritest equinox System for finished products, Aseptic process stimulation; Identify genus level microorganisms using Vitek-2 ID; Perform Environmental Monitoring in aseptic and other controlled areas in ISO-5/6/7/8; Recover Bio burden by Various Microbial enumeration methods; Endotoxin recovery studies, Qualification of Microbiological equipments like Steritest Equniox | 11/24/2019 |
| 483 | KVK Tech Newtown, PA Topical Formulation Associate MS in bio/chemistry/pharma sciences Exp: 1-3 years |
Person exhibits aptitude in assisting in the development of topical product pharmaceutical formulations, as well as meeting timelines for the department. Assist in the development of broad range of topical product pharmaceutical formulations including gels, creams, solutions and ointments. Develop pharmaceutical formulations utilizing Quality by Design (QbD) and risk assessment concepts. Contribute and support the analytical efforts and interpretation of data generated from experimental batches. | 11/24/2019 |
| 484 | KVK Tech Newtown, PA Quality Control Microbiologist BS in microbiology Exp: 0-1 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. | 11/24/2019 |
| 485 | LabCorp Lakewood, CO Specialty Lab Assistant HS Diploma/GED Exp: 1-2 years |
This position will work both in the processing of cytology samples for testing, as well as working in the accessioning department to receive samples. Processing of samples by loading them into instrumentation to make slides. Handling/Processing/Centrifugation of laboratory specimens, primarily blood and urine specimens. Running image guided slides through imager to prepare for testing | 11/24/2019 |
| 486 | LabCorp Houston, TX Medical Technologist/Medical Technician AA/AS or BS/BA in med lab technology Exp: 1-3 years |
Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. * Monitor, operate and troubleshoot instrumentation (can include specific dept instrumentation) * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Able to resolve technical, computer, and customer service problems within the specified department. * Deliver quality patient care while maintaining efficiency. * Perform preventive maintenance and quality control with appropriate documentation and communication. * Assist in processing of specimens when needed. | 11/24/2019 |
| 487 | LabCorp Humble, TX Medical Technologist/Medical Technician AA/AS or BS/BA in med lab technology Exp: 1-3 years |
Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. * Monitor, operate and troubleshoot instrumentation (can include specific dept instrumentation) * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Able to resolve technical, computer, and customer service problems within the specified department. * Deliver quality patient care while maintaining efficiency. * Perform preventive maintenance and quality control with appropriate documentation and communication. * Assist in processing of specimens when needed. | 11/24/2019 |
| 488 | LabCorp South Bend, IN Lab Assistant HS Diploma/GED Exp: 1-2 years |
The position will receive samples and prepare them for analysis via plating, centrifugation, gram stain preparation and maintenance of instrumentation.This position will include repetitive motion and extended time on feet, and also includes handling of biological samples (Urine, stool, bacterial swabs, sputum, body fluids). Prior experience handling samples preferred. | 11/24/2019 |
| 489 | Lake Pharma Worcester, MA Associate Scientist I, Cell Culture BS Exp: 0-5 years |
The successful candidate will be able to execute hands-on laboratory work in cell culture including planning and executing shake flask, bench scale bioreactor, bench scale purifications and large-scale bioreactor experiments. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. | 11/24/2019 |
| 490 | Lake Pharma Worcester, MA Associate Scientist I, Molecular Biology AS or BS in biology Exp: 0-3 years |
The employee will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. | 11/24/2019 |
| 491 | LifeMine Cambridge, MA RA, Microbiology BS or BA in biology Exp: 1 year of lab experience |
We are seeking a Research Associate level candidate to support media production and to handle and clean glassware and perform the appropriate cleaning services required for each piece of glassware. This individual will perform machine washing, handwashing, dry sterilizing, autoclaving, plugging and oven and air-drying of glassware. Plus prepare diverse media to support the discovery and scale-up fermentation teams. The incumbent will be enthusiastic about working in an exciting start up. | 11/24/2019 |
| 492 | LifeSensors Malvern, PA Entry Level Scientist BS or MS in biological sciences or related Exp: 0-2 years lab experience |
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. | 11/24/2019 |
| 493 | Lipocine Salt Lake City, UT Associate Scientist BS or MS in life sciences, chemical engineering or related Exp: 1-3 years in pharma/chemical lab |
Associate scientist needed in the area of pharmaceutical drug delivery research. Responsibilities include conducting laboratory experiments in support of formulation and process development. Qualified candidates will possess a BS/MS in life Science, chemical engineering or related field or 1-3 years experience in a pharmaceutical or chemistry laboratory. Knowledge of laboratory practices and demonstrated skills in analytical instrumental techniques (e.g. HPLC) are preferred. Excellent communication skills needed for preparing and following standard test methods and reporting experimental results. | 11/24/2019 |
| 494 | LoXo Oncology South San Francisco, CA Clinical Research Asscoiate BS in relevant Exp: 1-3 years in clinical trials |
The Clinical Research Associate in collaboration with the Clinical Trial Manager, contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities’ regulations/guidelines, and applicable SOPs/WPs. Responsibilities may include participation on one or more cross-functional study team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO) teams and vendors. | 11/24/2019 |
| 495 | Starkey Hearing Technologies Eden Prairie, MN Software Tester I BS/BA Exp: 1-2 years |
Software Tester: Conduct Software Testing on software applications. Perform system level testing on Starkey’s Software and Hardware systems working either in a team or independently. Follow standard Configuration Management practices and utilize a defect tracking tool. Tracking quality assurance metrics such as defect densities and open defect counts. Resolve and provide solutions to internal and external customer related issues. Participate in the development and implementation of structured testing concepts, methodologies and automated testing tools where applicable. etc. | 11/26/2019 |
| 496 | Starkey Hearing Technologies Eden Prairie, MN Mechanical Designer I - F&T AS/AA Exp: Not necessary for Associate candidates |
This position is responsible for designing new assembly tooling and assembly fixtures for product assembly. The position also requires designing tooling and solutions for specific tests and departments as requested. All tools/solutions must meet quality and manufacturing specifications provided by standards and the customer. Approach and Deployment: Design tools for production and specialty use. Utilize CREO to create accurate component, assembly and system models and drawings. Ensure designs meet performance, manufacturing, quality, cost and design requirements. Coordinate and lead design reviews as required. etc. | 11/26/2019 |
| 497 | Starkey Hearing Technologies Eden Prairie, MN Financial Analyst BS/BA in accounting, finance, or economics Exp: 1-2 years |
Starkey Hearing Technologies, a well-respected, mission focused and high-impact organization, is currently seeking a Financial Analyst. This position is responsible for analyzing and communicating the financial performance for assigned product lines and cost centers. The Financial Analyst will identify and implement lean work-processes and key reporting measurements. The Financial Analyst is responsible for the preparation and completion of annual operation and capital budgets – for assigned cost centers and product lines. etc. | 11/26/2019 |
| 498 | SDC Tempe, AZ Biostatistician MS in biostatistics, statistics, or related Exp: 1-3 years |
Supports lead biostatistician on clinical studies; may serve as lead biostatistician with oversight from a more senior biostatistician. Maintains the statistical integrity of clinical trials analyzed by SDC. Assists in preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, and writing statistical sections of clinical study reports. etc. | 11/26/2019 |
| 499 | Stealth Biotherapeutics Newton, MA Supply Chain Associate BS Exp: 1 year |
This position will report to our Director, Clinical & Commercial Supply Chain. This role is responsible for supporting continuous material supply in support of clinical and commercial demands. The individual will work with internal/external customers and suppliers in order to assist in developing processes for shipment of material and inventory reporting. Responsible for monitoring inventory levels and providing feedback regarding expiry and resupply. etc. | 11/26/2019 |
| 500 | Stellartech Milpitas, CA Quality Engineer I/II BS Exp: 0-2 years |
Stellartech is looking for a Quality Engineer to join our Team. Responsibilities: 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. etc. | 11/26/2019 |
| 501 | Stellartech Milpitas, CA Electrical Engineer BS in hardware or electrical engineering Exp: 0-2 years |
Stellartech is looking for a Electrical Engineer to join our Team. Responsibilities: Design, develop, and document electronic hardware for medical devices. Specify procedures and fixtures to test electronic medical devices. Assist manufacturing in prototype and pilot builds of electronic medical devices. Assist manufacturing in hardware problem analysis and solutions. Assist in training of technicians and manufacturing staff on new products and procedures. etc. | 11/26/2019 |
| 502 | Stereotaxis Saint Louis, MO Field Service Engineer AS/AA in electronics or equivalent Exp: 1-5 years |
Provide on site and remote service and support of Stereotaxis magnetic navigation systems including permanent magnets, and servo control systems. Interface with customers and vendors to ensure a quality service experience and that all expectations are met. ESSENTIAL JOB RESPONSIBILITIES: Interface with customers to obtain accurate details of the equipment service needs and provide updates regarding the progress of the service/installation. Diagnose and repair control servo control systems. etc. | 11/26/2019 |
| 503 | Stereotaxis New York City, NY Clinical Specialist BS in biomedical engineering, life sciences or related Exp: 1-3 years |
The Clinical Specialist (CS) provides customers and end users with product, clinical/ technical, educational, and sales support to maximize recurring revenue, utilization of company products, and customer service objectives. Must meet customer expectations by striving without reserve for the greatest possible reliability and quality in our products, processes, and systems by being accountable, having a voice, and taking action. Clinical Specialist will spend a high percentage of their time in procedures which requires a person to develop clinical knowledge within electrophysiology (EP), develop in-depth expertise of the Niobe remote navigation system, along with displaying outstanding sales abilities and the assertiveness needed to drive the Stereotaxis business. etc. | 11/26/2019 |
| 504 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 3rd Shift AS/BS Exp: 1+ year(s) |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 505 | Steripharma Syracuse, NY Production Maintenance Technician, 2nd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. etc. | 11/26/2019 |
| 506 | Steripharma Syracuse, NY Production, Clean Room Pharmaceutical Technician - 2nd Shift AS/BS Exp: 1+ year(s) |
This position operates production equipment, to include non-sterile filling machines, and packaging and labeling machines. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 507 | Steripharma Syracuse, NY Production, Pharmaceutical Production - 2nd Shift HS diploma or equivalent Exp: 1+ year(s) |
This position operates vial wash/packaging production equipment. Position is responsible to supply assigned positions with materials/items to complete work and according to standard operating procedures. Position is also responsible to clean equipment, production areas, and inspect parts/items following prescribed procedures. Provides troubleshooting on basic issues and may assist in providing training. etc. | 11/26/2019 |
| 508 | Steripharma Syracuse, NY Production Maintenance Technician, 3rd Shift, Pharma HS diploma or equivalent Exp: 0-2 years |
This position is responsible for the maintenance and efficient operation of production/manufacturing equipment for pharmaceutical operations. Position also responsible to perform both maintenance and preventative maintenance, and repair work to production equipment as needed. Provides troubleshooting on rudimentary issues and seeks guidance as part of an escalation process. How you make a difference . . . you will . . . Performs maintenance work, to include equipment repair and preventative maintenance work as required or assigned. Performs the repair and maintenance of APA area floors and walls. Completes work orders and projects as assigned, supporting each team member as directed. etc. | 11/26/2019 |
| 509 | Steris Scranton, PA Installation Technician AS/AA in electronics, mechanical, or similar Exp: 1+ year(s) |
STERIS’ Installation Technicians act as the face of STERIS by achieving One of a Kind Service for our Customers. The Installation Technician is a field-based, Customer-facing role that primarily travels to Customer sites (medical facilities) to install Operating Room and Sterile Processing Department equipment. They provide complete equipment installation in accordance with plans and specifications including scheduling, delivery, installation, check-out, and final inspection of equipment. Installation Technicians are also responsible for building positive relationships with Customers and peers, as well as completing necessary administrative tasks. | 11/26/2019 |
| 510 | Steris Sacramento, CA Field Service Representative I AS/BS in electronics, mechanical, or similar Exp: 1-2 years |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. Utilize advanced technology to complete administrative requirements, aid in troubleshooting issues and improve the overall Customer experience. Promote STERIS growth through identifying and recommending products and services to Customers. etc. | 11/26/2019 |
| 511 | Steris Martinez, CA Field Service Representative I AS/BS in electronics, mechanical, or similar Exp: 1-2 years |
Position acts as Trusted Advisor to STERIS Customers in maintenance and procurement of medical devices and consumable products as part of a high performing team. Drive an exceptional Customer experience by providing on-site preventative maintenance, troubleshooting, repair, equipment modification and installation support on complex mechanical, electro-mechanical and electronic units in a high stress healthcare environment. Provide superior Customer service by pro-actively interacting and communicating with Customers. Utilize advanced technology to complete administrative requirements, aid in troubleshooting issues and improve the overall Customer experience. Promote STERIS growth through identifying and recommending products and services to Customers. etc. | 11/26/2019 |
| 512 | Steris Chicago, IL Sterile Processing Technician HS diploma or equivalent Exp: 1+ year(s) |
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. Duties: Operates all mechanical machinery; cart washers, instrument washers, steam sterilizers, low temp sterilizers, ultrasonic and drying cabinets, within sterile processing. Uses established policies and procedures to complete work assignments. Learns and trains in all areas of sterile processing including decontamination, cleaning, assembly, wrapping, sterilization, and storage processes within all set professional standards and regulations. etc. | 11/26/2019 |
| 513 | Steris Birmingham, AL Customer Care Representative I BS/BA Exp: 0-2 years |
The primary focus of this position is to provide an outstanding Customer experience. Individuals in this role will be assigned to a manageable level of sales representatives and will serve as a liaison between the sales representative and the Customer. In this role, the Customer Care Specialist must have a thorough knowledge of all the Company’s products and services. Duties: Creates a personalized relationship with each assigned Account Mangers. Owns the service support experience for assigned Sales Representatives. Must be knowledgeable on where to send what repairs including responding to inquiries about IMS capabilities. Creates critical paperwork for the Customer and develops knowledge on how to make corrections, split orders and work multiple orders. etc. | 11/26/2019 |
| 514 | Steris Denver, CO Integration Technician AS/AA Exp: 1 year |
Install operating room integration equipment as directed by Integration Specialist (I and/or II) and/or Integration Project Manager. Perform preventative maintenance, troubleshooting, repair, equipment modifications, and installation on all integration equipment serviced by STERIS. Help drive STERIS initiatives for growth and development of business. Interact with customers in a professional and knowledgeable basis. Complete administrative requirements as required. Duties: Help install operating room integration systems. This includes physical placement of equipment, installation, termination and interconnection of all cables, downloading and configuration of software; and testing of all functions per test documentation as required. etc. | 11/26/2019 |
| 515 | Steris Bellevue, WA Field Service Technician AS/AA in electronics, mechanical, or similar Exp: 1 year |
The Field Service Technician provides preventive maintenance, troubleshooting, repair, calibration and installation support on various mechanical, electro-mechanical, and electronic units. The Technician Interacts with customers on a daily basis and completes associated administrative tasks as required. Think of this as an electrical-mechanical-plumber-Customer Service Technician all rolled into one! Every day, something special happens at STERIS. What will YOU help us do next? Duties: Perform preventive and corrective maintenance required on STERIS and related product lines. This includes: disassembling, replacing, or repairing defective parts; reassembling as required; troubleshooting, adjusting/calibrating ready for use by using standard and specialized tools by using technical manuals etc. etc. | 11/26/2019 |
| 516 | Surgical Specialties Tampa/Orlando, FL Sales Representative, Ophthalmic BS/BA in business or a medical field Exp: 1-3 years |
Caliber Ophthalmics is currently seeking a Surgical Sales Representative to be based in Florida. As a valued employee at Caliber, you will enjoy a total benefits package including competitive salary, medical/dental/vision/life insurance, short-and long-termdisability, 401k, and more. The Surgical Sales Representative is responsible for managing the Floridasales territory, working directly with surgeons for the sale and promotion of our Caliber Ophthalmic portfolio of surgical device products to include our disposable knives, suture, and other microsurgical products. Target call points are hospitals and ambulatory surgery centers. In this surgical sales role, you will be responsible for maintaining and growing annual sales volume in Florida. | 11/26/2019 |
| 517 | Saptalis Pharmaceuticals Hauppage, NY Analytical Scientist/Chemist BS in pharmacy, analytical chemistry, or related Exp: 0-3 years |
Develop analytical methods for actives, degradation and impurities, preservatives, and residual solvents in the new drug products.Perform analytical validation experiments per approved method validation protocols. Perform method verification and supplemental validation studies for active pharmaceutical ingredients and excipients. Perform release testing on actives, excipients, and packaging components to be used in GMP batch manufacturing. etc. | 11/19/2019 |
| 518 | Sciecure Pharma Monmouth Junction, NJ QC Data Review Specialist BS in chemistry or related Exp: 1-2 years |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. Responsibilities: Review of documentation generated during method validation, method verification, stability testing, routine testing and other analyses. Review documentation, results and reports from raw material and finished product analysis for accuracy and completeness. etc. | 11/19/2019 |
| 519 | Seattle Genetics Bothell, WA Research Associate I BioProcess Development BS in biology, chemical engineering, or related Exp: 1+ year(s) |
The BioProcess Development Department at Seattle Genetics is seeking a Research Associate to participate in the cell culture and purification efforts to support process development for our antibody and antibody-drug conjugate programs. Responsibilities: Generate monoclonal antibody (mAb) in support of Research and Process Sciences Program development. Responsible for all stages of mAb generation, from thaw of cryogenically stored vials through filling final formulated intermediate. etc. | 11/19/2019 |
| 520 | Seattle Genetics Bothell, WA Research Associate II/III Pharmaceutical Sciences MS in pharmaceutical sciences, chemistry, biology, or related Exp: 0-2 years |
The Pharmaceutical Sciences group at Seattle Genetics is seeking a highly motivated research associate to support development of therapeutic antibody-drug conjugates. This person will play a critical role in the formulation and drug product process development of a novel pre-clinical ADC. The ideal candidate will have working knowledge of biologics formulation development and experience in common analytical techniques, as well as strong critical thinking skills and the ability to design, execute, and draw conclusions from experimental studies with managerial guidance. The ideal candidate should have a background in formulation development or analytical biochemistry or a related discipline, good interpersonal skills, and an ability to work effectively in intra-departmental teams to achieve program goals. | 11/19/2019 |
| 521 | Sedia Biosciences Portland, OR QC Technician AS Exp: 1 year |
A Quality Control Technician works independently to provide quality control support of any area assigned where Sedia Biosciences is responsible for adhering to current Good Manufacturing Practices (cGMPs) for adherence to FDA regulations and applicable ISO standards including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review/disposition, and new product design review and transfer activities. Demonstrates a high level of independent judgment and discretion in the timely identification, investigation and resolution of events impacting the Quality of products and processes. etc. | 11/19/2019 |
| 522 | Sedia Biosciences Portland, OR Manufacturing Technican AS in biology, chemistry, or related Exp: 1 year |
The position will hold responsibility for assisting in the manufacturing of Sedia’s immunoassay product lines encompassing lateral flow and ELISA test. The holder of this position is expected to follow the guidance of their direct supervisor to assist in delivering company products in a timely and cost effective manner. The position will contribute in building product subassemblies or final assemblies. The Manufacturing Technician will adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance. etc. | 11/19/2019 |
| 523 | Sekisui Xenotech Kansas City, KS Research Assistant BS in a biological or chemical science Exp: 1+ year(s) |
Sekisui XenoTech, LLC is currently hiring for a Research Assistant for our Enzyme Incubations Team within the Program Execution department. 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. Essential duties and responsibilities include, but are not limited, to the following: Design and conduct routine and atypical experiments. Maintains laboratories and equipment and performs minor repairs on equipment, with supervision. etc. | 11/19/2019 |
| 524 | Seven Bridges San Francisco, CA Bioinformatics Support Engineer BS/MS in bioinformatics or related Exp: 1 year |
As a Bioinformatics Support Engineer you will be exposed to a wide range of translational applications and will work and learn from experts spanning numerous disciplines from informatics through cloud optimization and clinical data. You will work back to back with various members of our support and bioinformatics teams, helping our clients overcome obstacles they encounter. You will diagnose, resolve and explain issues and questions raised by our clients. Main responsibilities: Understand each client’s use case and their bioinformatics data processing pipelines. Debug, troubleshoot and resolve client issues associated with bioinformatics tools on the Seven Bridges platform. etc. | 11/19/2019 |
| 525 | Silicon Therapeutics Boston, MA Research Associate, Software Engineering BS in engineering or computer science Exp: 1-2 years |
Silicon Therapeutics is seeking a highly motivated Software Engineering Research Associate who wants to work in a multi-disciplinary organization with the aim of treating challenging diseases. Job Responsibilities: Build software infrastructure to support platform development. Implement and maintain software engineering best practices. Ensure scalability, extensibility, and portability of platform code. Integrate and maintain databases for storage and access of results. Scripting and workflow development for scientific applications. | 11/19/2019 |
| 526 | Silicon Therapeutics Boston, MA Research Associate, Machine Learning BS/MS in computer science, mathematics, engineering or related Exp: 1-6 years |
Silicon Therapeutics is seeking a highly motivated Research Associate, Machine Learning who wants to work in a multi-disciplinary organization with the aim of treating challenging diseases. Job Responsibilities: Work with a multi-disciplinary team (e.g. chemists, biologists, biophysicists) to discover novel medicines for challenging disease targets. Apply machine learning techniques to real-world drug discovery problems. Develop methods to improve the robustness of predictions from molecular dynamics simulations and quantify uncertainties associated with free energy simulations. Build state of the art machine learning infrastructure and workflows for molecular design. Work closely with bench scientists to understand critical project bottlenecks and how machine learning can help. | 11/19/2019 |
| 527 | Simbex Lebanon, NH Test Engineer AS/BS in engineering Exp: 1-3 years |
The Test Engineer will be responsible for component and system testing throughout the product life cycle from development through release for products in the consumer health and medical device markets. The Test Engineer will work closely with project and cross-functional teams to help develop and execute test plans. The ideal candidate is self-motivated, detail oriented, and quick learner who can work in a fast-paced environment and values quality and accountability. etc. | 11/19/2019 |
| 528 | Simbex Lebanon, NH Systems Engineer BS in mechanical or electrical engineering or related Exp: 0-3 years |
The Systems Engineer will be responsible for supporting every phase of the product development life cycle process in order to deliver high-quality products in the consumer and medical device markets. The Systems Engineer will work with the electrical, software, mechanical, product technical support, and quality teams to help develop, integrate, and test sub-assemblies into product. The ideal candidate has broad skills but deep knowledge/skills in one area, and is able to blend human-centric design with sound engineering principles across a wide range of engineering domains with a focus on quality and willingness to wear many hats. etc. | 11/19/2019 |
| 529 | Smith & Nephew Oklahoma City, OK Quality Engineer BS Engineering/Science Exp: Entry level |
This position will be responsible for ensuring the effective investigation of devices and information supplied through the complaint management process, as well as the facilitation of actions identified to improve device quality, reliability, customer experience and patient safety. This position will participate in the identification and implementation of complaint management system improvements, including updates to procedures and forms used in the investigative process. The role may support multiple business sites both remotely and through on-site visits as needed. etc. | 11/19/2019 |
| 530 | Smith & Nephew Memphis, TN Quality Assurance Inspector I HS diploma or related Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. Essential Responsibilities: Inspect raw materials, components, assembled product, semi-finished product & finished product per inspection procedures/drawings and to print specifications. Utilize attribute and variable measuring equipment/gauges as well as mating parts to determine as found/as left conditions of product. Support the qualification/validation processes for company product. etc. | 11/19/2019 |
| 531 | Smith & Nephew Oklahoma City, OK Bench Technician I HS diploma or related Exp: 0-3 years |
Performs routine assembly and/or rebuilding of electromechanical medical instruments and assemblies using released procedures, drawings, blueprints, etc.. to meet established quality and performance metrics. Performs functional testing of assemblies/instruments. etc. | 11/19/2019 |
| 532 | Smith & Nephew Andover, MA Quality Assurance Engineer I BS in engineering Exp: 1-3 years |
Support, and sustain elements of Smith & Nephew’s quality system through procedure generation, training, auditing, and technical support. Leading and supporting quality project initiatives. This position provides support and services in CAPA, complaints, validations, audits, quality holds, calibration and various other requirements of the medical device (US & International) regulations for R&D, Process Engineering, Manufacturing, Quality, and Regulatory plus any quality system support required. etc. | 11/19/2019 |
| 533 | Smiths Medical Southington, CT Team Technician 3rd Shift HS diploma/AS Exp: 1-2 years |
The Team Technician is responsible for ensuring the correct operation of automatic and semi-automatic assembly production equipment in accordance with governing documentation. This person will also initiate action to prevent the occurrence of nonconformances related to the product and equipment. Additionally, this role will identify and record problems relating to the product, process and or quality system. The Team Technician will also initiate recommendations, provide solutions, and verify the affectivity of continuous operational improvements. | 11/19/2019 |
| 534 | Solid Biosciences Cambridge, MA Contract QC Associate AS/BS Exp: 1-2 years |
Reporting to the Solid Quality Control (QC) Unit, the QC Associate is responsible for day to day operations related to sample submission and data management in support of QC GMP and cross-functional development. The candidate will maintain documentation in accordance with internal data entry, analysis and trending SOPs. In addition, coordinate domestic and international biologic sample shipments (at room temperature, on dry ice, or in liquid nitrogen) according to applicable guidelines. etc. | 11/19/2019 |
| 535 | Sorrento Therapeutics San Diego, CA Research Associate II BS/MS in immunology, molecular biology or related Exp: 0-2 years |
Sorrento Therapeutics’ is seeking an experienced Research Associate who will be responsible for the development and implementation of in vitro functional T cell assays to support pre-clinical validation of CAR-T cellular therapies against cancer. The individual must have knowledge and hands on experience in CAR-T, cell culture, Flow cytometry and T cell biology. WHAT YOU’LL DO: Design and execute experiments for development of preclinical CAR-T therapies. Isolate, expand, and manipulate T cells. Perform in vitro functional assays measing cellular activation, cytokine release, proliferation and killing. etc. | 11/19/2019 |
| 536 | Sorrento Therapeutics San Diego, CA Manufacturing Associate I BS/BA in a biological or chemica science. Exp: 0-1+ year(s) |
We are currently seeking a Downstream Manufacturing Associate I. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. This position will also be responsible for supporting the inventory control for the downstream group. etc. | 11/19/2019 |
| 537 | Sorrento Therapeutics San Diego, CA Manufacturing Associate II BS/MS in a biological or chemical science Exp: 1+ year(s) |
We are currently seeking a Downstream Manufacturing Associate II. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. An essential component of this position will be an understanding of cGMP methodologies: SOP’s, batch record preparation and execution, deviation control and general clean room maintenance. This position will also responsible for supporting the inventory control for the downstream group. etc. | 11/19/2019 |
| 538 | Spectrum Pharmaceuticals Irvine, CA Clinical Trials Assistant BS in a life science Exp: 1-2 year |
Responsibilities: Provide support to the Clinical Trial Managers and Clinical Research Associates in clinical trial conduct via preparation, distribution, and tracking of study supplies, mass mailings, copying, data entry, etc. Demonstrate superior communication and organizational skills in addition to the technical skills required for overseeing clinical studies. Recognize the urgency of meeting established schedules and be able to prioritize tasks and time to meet those schedules. Help manage and report on the conduct of clinical studies, as directed. Help identify and select trial sites. Conduct qualification, initiation, interim monitoring close-out visits, and perform drug accountability (approximately 25% travel required). etc. | 11/19/2019 |
| 539 | SQZ Biotech Watertown, MA Engineer/ Sr. Engineer BS/MS in bio, biomedical, or chemical engineering or related Exp: 0-2 years |
We are seeking a highly motivated Engineer/ Sr. Engineer to join our Process Development and Manufacturing team. The candidate will support process development efforts for novel cell therapy products. The candidate will perform hands-on laboratory work, data analysis, develop and maintain technical documentation, and collaborate with internal and external terms such as vendors to ensure successful execution of key development studies. The incumbent will also support manufacturing for technology transfers at CMOs and on-going cGMP production of clinical products. etc. | 11/19/2019 |
| 540 | Icon PLC North Wales, PA CTA BS/BA in life sciences Exp: Entry Level |
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint. ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research. | 11/11/2019 |
| 541 | Icon PLC Portland, OR Laboratory Assistant (Maintenance Tech) BS/BA Exp: 1 year in operations/sciences/equipment |
The Lab Assistant (Maintenance Technician) supports the activities of Production, Development, and the Clinical Laboratories. The Maintenance Technician performs equipment maintenance and cleaning, qualification, assists in the development of equipment specifications and other equipment or facility related activities to ensure proper qualification, function and reliability. | 11/11/2019 |
| 542 | ICON Boston, MA Laboratory Assistant - Full Time Days HS Diploma/GED Exp: 1 year lab experience |
As a Laboratory Assistant will assist and aid the technical staff with handling and accounting for biological lab specimens, reagent inventory, and any other relevant tasks. Assists with retrieval and set up of samples for analysis. Receives samples from Sample Management and segregate and distribute to the lab as per standard operating procedure. Monitor Sample Logistic Scan/pending list and search for lost samples. Troubleshoot issues with Sample Management when required. Member of the Lost sample Team. | 11/16/2019 |
| 543 | ICON North Wales, PA Clinical Research Associate HS Diploma/GED Exp: 18+ months as CRA |
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results. | 11/16/2019 |
| 544 | ICON Farmingdale, NY Laboratory Study Start-Up Specialist BS Exp: 1 year in clinical trails, lab, etc. |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/16/2019 |
| 545 | ICON Lexington, KY DPC Assistant HS Diploma/GED Exp: 1 year in medical office/admin |
The DPC Assistant will provide support services (logistical, technical and administrative) to the Direct to Patient Contact (DPC) project team all along the project, while complying with the deadlines, budgets, quality and regulatory requirements defined for each project. For each project, the Direct to Patient Contact Manager (DPCA) works under the technical and functional supervision of the dedicated Direct to Patient Contact Manager (DPCM). | 11/16/2019 |
| 546 | ICON North Wales, PA Configuration & QC Spec I BS Exp: 1 year in clinical trails, lab, etc. |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/16/2019 |
| 547 | ICON Portland, OR Laboratory Assistant (Maintenance Tech) HS Diploma/GED Exp: 1 year in operations/scientific equipment |
The Lab Assistant (Maintenance Technician) supports the activities of Production, Development, and the Clinical Laboratories. The Maintenance Technician performs equipment maintenance and cleaning, qualification, assists in the development of equipment specifications and other equipment or facility related activities to ensure proper qualification, function and reliability. | 11/16/2019 |
| 548 | ICU Medical Austin, TX Technician I, Biological Quality/Environmental Quality BS/BA in microbiology/biological sciences Exp: 1 year general micro course with lab, or 1 year working experience |
The BQ/EQ Scientific Technician I is responsible for performing routine and non-routine testing in support of all aspects of the manufacturing operations including but not limited to the utility systems, sterilizer systems, incoming raw materials, in-process product solutions and final product solutions while adhering to safety, standard operating procedures (SOPs), standard test methods (STMs) and specifications, current good manufacturing practices (cGMP), standard laboratory practices (SLP), current good documentation practices (cGDP) and plant policies/guidelines. | 11/16/2019 |
| 549 | IDEXX Memphis, TN Histology Laboratory Technician HS Diploma/GED, higher degree preferred Exp: 1-5 years |
You will be using microtomes, processors, embedding centers, automatic slide stainers and other diagnostic tools to perform tissue analyses that diagnose animal illnesses and diseases in support of veterinarian animal treatment. You will be responsible for transforming a tissue sample into a slide that will be read by a board-certified veterinary anatomic pathologist. It is expected you will follow SOPs (Standard Operating Procedures) and maintain a safe working environment. | 11/16/2019 |
| 550 | IDEXX Westminster, CO Sample Management Technician HS Diploma/GED, higher degree preferred Exp: 0-1 years |
The Sample Management Technician 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. May be cross-trained to perform basic Laboratory Technician duties, such as performing less complex tests. May be responsible for various support activities, including maintaining supply inventory, record-keeping, cleaning, clerical tasks, supply shipping and receiving, mail distribution and other related duties. Collects and prepares samples as requested/ required for R&D project teams. | 11/16/2019 |
| 551 | IDEXX Westminster, CO Medical Laboratory Technician - Parasitology HS Diploma/GED, higher degree preferred Exp: 0-1 years |
The Medical Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform variety of customer service activities for internal and external customers. Testing cell-related components of blood samples to enumerate and identify their cellular components, including the microscopic evaluation of blood smears and the use of automated and manual counting techniques. Processing blood and body fluids for microscopic examination by pathologists. Includes slide preparation and staining, utilizing manual and automated counting techniques. | 11/16/2019 |
| 552 | IDEXX West Sacramento, CA PCR Laboratory Technician Certified Vet Tech or Medical Lab Tech Exp: 0-1 years |
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: | 11/16/2019 |
| 553 | Imbed Biosciences Madison, WI Production Technician, Medical Device Manufacturing BS in sciences Exp: 1-4 years in chemistry/biological lab |
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. | 11/16/2019 |
| 554 | Immucor Norcross, GA Medical Laboratory Technologist I AS/AA or BS/BA Exp: 6-12 months related experience |
Immucor is seeking a Medical Laboratory Technologist to join our Quality Laboratory team. The Medical Laboratory Technologist is responsible for performing laboratory testing (including potency, specificity, reactivity and hemagglutination assays) and chemical evaluations (including protein, absorbance, chloride, osmolality, and pH) of Immucor products according to approved Standard Operating Procedures (SOP’s) within defined timeframes. | 11/16/2019 |
| 555 | Immucor Warren, NJ Manufacturing Associate AS/AA Exp: 1 year in cGMP manufacturing |
As the Manufacturing Associate, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Performing the following activities in a quality focused cGMP manufacturing environment: Formulating custom bulk reagents - involves working with pipettes and balances. Support BeadChip carrier assembly - involves both manual and automated equipment processes. Following detailed work instructions, forms, and SOPs | 11/16/2019 |
| 556 | Immucor Norcross, GA Medical Laboratory Technologist I AS/AA or BS/BA Exp: 6-12 months related experience |
Immucor is seeking a Medical Laboratory Technologist to join our Quality Laboratory team. The Medical Laboratory Technologist is responsible for performing laboratory testing (including potency, specificity, reactivity and hemagglutination assays) and chemical evaluations (including protein, absorbance, chloride, osmolality, and pH) of Immucor products according to approved Standard Operating Procedures (SOP’s) within defined timeframes. | 11/16/2019 |
| 557 | Immune Technology Corp New York , NY Sales Associate BS/BA in life sciences Exp: 1 year of sales/marketing experience |
Full/part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. Establishing and retaining customer relationships primarily through phone, e-mail and personal visit . Delivering requested documents, literature, and information to customers. Organizing and maintaining a database of customers and sales leads | 11/16/2019 |
| 558 | Immunomedics Morris Plains, NJ QC Sample Coordination Technician - (2nd shift) BS/BA in sciences Exp: 0-2 years |
The primary purpose of this second shift position is to provide support to the sample management group in a QC laboratory setting in support of commercial manufacturing. Responsibilities of the QC Sample Coordination Technician include collating receipt of samples and coordination of testing, preparation of samples using aseptic technique, organizing and tracking lot release data, submission of samples to contract testing laboratories and tracking sample custody. Activities include equipment maintenance, coordinating with Shipping and Receiving, and receipt of test results from contract laboratories. | 11/16/2019 |
| 559 | Immunomedics Morris Plains, NJ Manufacturing Specialist I AS/AA or BS/BA in engineering or sciences Exp: 0-2 years |
Responsible for pharmaceutical manufacturing in compliance with current Good Manufacturing Practice (cGMP). Ensures consistent completion of all the planned manufacturing activities assigned to him/herself. Organize workplace to maximize the throughput and minimize risks of errors. Follow well defined procedures closely, with attention to detail. Operate manufacturing equipment according to well defined procedures. Daily monitoring of the process. | 11/16/2019 |
| 560 | Imprimis RX Ledgewood, NJ Production Support Associate HS Diploma/GED Exp: 1 year in pharma, med devices or related |
The Production Support Associate is part of our production team. The Production Support Associate supports our production team by assisting in the main production area. Performs various routine production tasks under the guidelines of established SOP’s and CGMP regulations. Prepares components needed for production, such as washing vials, wiping of supplies needed for the clean room. Performs cleaning and disinfecting of manufacturing and clean rooms per established procedures. | 11/16/2019 |
| 561 | Indigo Biosciences State College, PA Associate Scientist MS in biological sciences Exp: 0-5 years |
The successful candidates will have formal training and demonstrated technical proficiencies / expertise in one or more of the following areas: mammalian cell biology, mammalian toxicology, receptor biology, assay development, molecular biology, and/or biochemistry methods. | 11/16/2019 |
| 562 | Indivior Austin, TX Specialty Pharmaceutical Sales Rep/Clinical Specialist (Austin) BS/BA Exp: 1+ year in pharma/medical/healthcare |
The Clinical Specialist is responsible for calling on practicing physicians, hospitals, clinics and other health-related organizations within an assigned territory. The Clinical Specialist must provide the healthcare professional with the most current information pertaining to Indivior products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Accomplishments of these goals must comply with the terms and conditions outlined in the Company Policy and Procedure Manual. | 11/16/2019 |
| 563 | Inova Diagnostics San Diego , CA Chemist I- Elisa Controls BS/BA in biological sciences Exp: 0-2 years in ELISA lab |
Participates in the activities associated with the manufacturing of ELISA reagents such as control, calibrator and HRP conjugate components in accordance with established procedures and schedules. Ensures supplies, testing components, raw materials and equipment required to meet manufacturing schedules are available. Alerts the supervisor of any material shortages, potential expiration date problems, equipment requirements and/or other circumstances, which may cause delays in the planned, manufacturing schedule. Maintains detailed Device History Records and/or any associated documentation for all manufacturing activities in accordance with current Quality Systems Regulations (QSRs). | 11/16/2019 |
| 564 | Inova Diagnostics San Diego , CA Lab Assistant I HS Diploma/GED Exp: 0-4 years lab work experience |
Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). Assists with the activities required to manufacture autoimmune diagnostic products by following established procedures. Major duties include the manufacturing of tissue sections and their placement onto glass microscope slides for use in Immunofluorescent Assay products. Participates in all activities associated with the manufacturing of the tissue sections and their placement onto glass microscope slides in accordance with written documentation and established procedures. Manufactures 8.5 eight-well ANA Plus Slides per hour after three months of training. 10 eight-well ANA Plus slides per hour within one year of employment. Thereafter, manufactures 10.5 slides per hour for eight-well slides and 21 slides per hour for four-well slides (all tissue types). | 11/16/2019 |
| 565 | Inovio San Diego , CA Research Associate I, Preclinical (2 positions available) BS in biological sciences Exp: 0-1 years research experience |
The Research Associate I (RA) is responsible for performing in vitro and in vivo experiments as part of a team to support development of DNA-based vaccines and therapeutics prior to clinical development. The RA performs a variety of techniques, including treatment and sample collection, immunoassays, cell-based assays, flow cytometry, and cell line maintenance. The RA troubleshoots problems, reviews and documents results, and presents findings at departmental or company meetings. The RA performs general lab duties as needed. | 11/16/2019 |
| 566 | Inovio Plymouth Meeting, PA Clinical Trial Associate BS in biological sciences Exp: 0-2 years in clinical trails monitoring/management |
The Assistant, Clinical Trials (CTA) is responsible for supporting, under the direct supervision of the supervisor/Clinical Project Lead (CPL), clinical trial execution, investigator 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. | 11/16/2019 |
| 567 | Omnipod Salt Lake City, UT Intake Associate AS/AA Exp: 0-1 years working experience |
The primary responsibility of this role is to review and process clinical documentation promptly and accurately to ensure proper reimbursement from contracted payors. The Intake Associate will utilize this clinical documentation to perform benefit investigations as well as prior authorizations with our contracted payors. This role will work with all department functions and must have a thorough understanding of the reimbursement process, clinical guidelines and medical policies. | 11/16/2019 |
| 568 | Omnipod Salt Lake City, UT Inside Sales OmniPod Associate AS/AA or BS/BA Exp: 0-1 years in medical devices/pharma/healthcare |
The Inside Sales - OmniPod Associate role is responsible for all patient communication during the sales process of starting patients on the OmniPod system. This role works closely and collaborates with the field sales and internal team members to provide the best patient experience possible. This role is responsible for communicating insurance benefit guidelines and cost share information with patients and assists them with their decisions regarding insulin pump therapy. | 11/16/2019 |
| 569 | Omnipod Billerica, MA Associate SQA Engineer BS in software engineering/computer sciences Exp: 0-2 years in software QA |
This position assists in the software quality assurance efforts related to new product development and product modifications for the Research and Development group. The position is responsible for ensuring that new products have been effectively and efficiently verified and validated prior to their release for shipment and that these designs effectively meet documented and implied user needs and requirements. Software quality assurance efforts are lifecycle oriented beginning during product requirements development and continuing throughout its lifetime. | 11/16/2019 |
| 570 | Omnipod Atlanta, GA Clinical Services Specialist BS/BA Exp: 0-2 years in clinical setting |
The Clinical Services Specialist (CSS) is primarily responsible for meeting 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 skilled at selling and using the OmniPod Insulin Management System. | 11/16/2019 |
| 571 | Omnipod Dallas, TX Clinical Services Specialist BS/BA Exp: 0-2 years in clinical setting |
The Clinical Services Specialist (CSS) is primarily responsible for meeting 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 skilled at selling and using the OmniPod Insulin Management System. | 11/16/2019 |
| 572 | Omnipod Acton, MA Business Analyst, Post Market Surveillance BS in sciences/engineering Exp: 1-3 years in data management/Quality systems |
This position is integral to supporting the department through complaint software enhancements, upgrades, report creation, data structure, and validation activities/documentation. The BA will be the primary connection to IT resources supporting the business unit. The BA will have a strong understanding of the business unit’s processes, context surrounding why the processes are in place, and what happens if processes are not functioning/followed. The BA will be an expert in the systems utilized by the business unit and understand the implications of system structure, how changes may impact systems, and how system data is utilized for reporting. | 11/16/2019 |
| 573 | Integer Trenton, GA Manufacturing Engineer I -1st shift BS Exp: 0-3 years related |
Manufacturing Engineer providing basic engineering support for existing or new products. Learning to use professional concepts. This position will provide hands-on engineering support for existing products and products transitioning from New Production Introduction (NPI) to manufacturing. | 11/17/2019 |
| 574 | Integer Plymouth, MN Design Engineer BS/BA in related field Exp: 0-3 years related |
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. | 11/17/2019 |
| 575 | Integra LifeSciences Mansfiled, MA Associate Product Development Engineer BS in engineering (electrical/computer) Exp: 0-3 years in product design/new product development |
The Engineer will participate in projects of varying scope and complexity across Integra with a focus on the Neuro Critical Care and will be responsible for the software and electrical design aspects of a project, interacting with external design and development partners, participating on cross-functional project team through all phases of the product development process, and assisting the technical team with planning, executing, documenting and communicating testing activities. The engineer will develop tools that will assist marketing and sales demonstrate Integra’s devices in an effective manner, and will develop test setups to automatize verification testing of different products. | 11/17/2019 |
| 576 | Integra LifeSciences Cincinnati, OH Finishing Technician HS Diploma/GED Exp: 0-2 years in manufacturing |
Performs deburr, finishing, and cleaning in a job shop or high volume applications. Processes components to meet print and or geometric tolerance requirements. Responsible for the setup, operation and maintenance of production equipment needed for deburr, finishing, and cleaning operations, maintenance of proper documentation, and support of the manufacturing engineering function. Under close supervision, completes tasks as directed by SOPs, routers, prints, work instructions, and manufacturing schedules. | 11/17/2019 |
| 577 | Integra LifeSciences Plainsboro, NJ Accoutant- Entry Level BA in accounting Exp: 0-3 years |
The accountant position is responsible for performing a combination of cost and general ledger accounting and financial close tasks, as assigned. Perform the monthly financial close process for the local ledger, including preparation of the monthly journal entries and balance sheet (cash, inventory, payables) and P&L account reconciliations, as assigned. Run various reports used to reconcile or analyze general ledger account balances. Assist in the preparation of the standard monthly management reports. Perform detailed monthly variance analysis on items in the P+L and balance sheet. | 11/17/2019 |
| 578 | Integra LifeSciences Plainsboro, NJ Accoutant- Entry Level BA in accounting Exp: 0-3 years |
The accountant position is responsible for performing a combination of cost and general ledger accounting and financial close tasks, as assigned. Perform the monthly financial close process for the local ledger, including preparation of the monthly journal entries and balance sheet (cash, inventory, payables) and P&L account reconciliations, as assigned. Run various reports used to reconcile or analyze general ledger account balances. Assist in the preparation of the standard monthly management reports. Perform detailed monthly variance analysis on items in the P+L and balance sheet. | 11/17/2019 |
| 579 | Integral Philadelphia, PA Biotechnology Marketing Associate BS/BA in sciences or marketing Exp: 1-2 years |
Plan and implement the creation of scientific and promotional materials in close collaboration with marketing, sales and scientific teams. Generate email blasts, website content, brochures, Google Adwords campaigns and slides. Create and update content to the company website using WordPress. Coordinate and organize team for appearances at industry conferences. Monitor and analyze effectiveness of marketing campaigns and website design | 11/17/2019 |
| 580 | Integral Philadelphia, PA Business Development Associate MS or MBA Exp: 0-2 years in tech transfer, consulting or product commercialization |
Our company is in an exciting growth phase where we are launching new products and reaching new markets. To support our growth, we seek a Business Development Associate to help launch new partnerships, businesses, and growth strategies. Successful candidates will also be involved with our marketing and sales teams to assist with strategic growth plans. | 11/17/2019 |
| 581 | Integral Philadelphia, PA Laboratory Instrumentation Engineer BS/BA Exp: 0-2 years in lab support/equipment |
We seek an associate to join us as our Laboratory Instrumentation Engineer. This is a specialized position that will be responsible for maintaining and using flow cytometers, robotic liquid handlers, and other equipment. You will be part of the team that supports lab operations, with opportunities for conducting experiments and leadership of the team. | 11/17/2019 |
| 582 | Integral Philadelphia, PA Research Associate I BS/BA in biology or bioengineering Exp: 1-2 years in lab/cell culture experience |
We seek a Research Associate I, who will work with a dedicated group of scientists on the development and commercialization of biomedical technologies. Conduct laboratory research and support general R&D efforts for customer-based biomedical research. Projects may involve cell culture, virology, DNA preparation, and liquid-handling automation. Perform cell-based assays (Western blot, ELISA, immunofluorescence, flow cytometry) | 11/17/2019 |
| 583 | IDT Morrisville, NC Future Lab Technician Roles Early 2020 BS/BA in sciences Exp: 0 years |
Synthesizes oligos on various synthesizer platforms. Cleaves and deprotects oligos utilizing appropriate methods. Quantifies and samples oligos for quality control tests. Attaches modifications utilizing various techniques. Adheres to safety regulations, lab SOPs, and contamination controls. | 11/17/2019 |
| 584 | IntegrityBio Camarillo, CA Research Associate BS in biochemistry, chemistry, or biological sciences Exp: 1-5 years |
To meet the growing demand on the part of our clientele regarding the outsourcing of projects and technologies, we are seeking candidates for the position of Research Associate I or II in Research and Development (R&D). Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. Analyzes, records, and reports the results and conclusions for laboratory experiments. Summarizes and interprets data. The candidate should also be open to learn new laboratory techniques and work under the guidance of experienced researchers. | 11/17/2019 |
| 585 | Intrexon Davis, CA Research Associate, Plant Traits BS or MS Exp: 1-3 years in molecular biology/plant biology |
Intrexon Corporation is seeking a highly motivated Research Associate, Plant Traits with molecular biology skills for our growing Agricultural Biotechnology Division (ABD) at Davis, California. The candidate will join a team to work on innovative technology to develop various traits in crops. The successful candidate will have hands-on experience with molecular techniques as well as supporting the senior scientist to develop other methodology to enable high-through-put, low-cost genotyping in multiple crops. Strong technical, organizational, and communication skills, as well as the ability to develop creative solutions to challenging problems in a fast-paced, milestone driven company, are essential. | 11/17/2019 |
| 586 | Intrexon South San Francisco, CA Research Associate I or II, Pilot Plant Ops BS in sciences, engineering or related Exp: 0-3 years industry experience |
We are seeking a talented Research Associate (level determined by candidate experience), Pilot Plant Operations for our Industrial Products Division (IPD) located in South San Francisco. The Research Associate will be responsible for operating pilot plant equipment, performing maintenance tasks, and have the skill set to thrive in a dynamic team environment. | 11/17/2019 |
| 587 | Intuitive Sunnyvale, CA Manufacturing Trainer 1 HS Diploma/GED Exp: 12 months in ISI product manufacturing |
Partner with Manufacturing to develop and sustain a well-trained and flexible workforce through hands-on training, mentoring, and formal certification. Maintain accurate manufacturing and training documentation to ensure the effectiveness of the training process. Develops and prioritizes quarterly training plans based on input from Production and Training Supervision. Conducts training, mentoring and formal certification of production technicians in accordance with S & V Training DOP’s and Manufacturing Process Instructions. | 11/17/2019 |
| 588 | Intuitive Sunnyvale, CA MRMA Repair Technician AA/AS Exp: 1-3 years related experience |
A Mechanical RMA Repair Technician II works under general direction, follows oral and/or written instructions, and performs repair and testing processes to produce tested electro-mechanical assemblies or associated sub-assemblies. Performs some-what complex tasks in preparation for repair and testing. Is able to verify assembly documentation accuracy, read engineering drawings etc. Sets up and operates machines/equipment /fixtures needed to perform repair and testing processes. | 11/17/2019 |
| 589 | Intuitive Los Angeles, CA da Vinci Clinical Territory Associate- North Los Angeles BS/BA in sales or related Exp: 1 year of sales or leadership experience |
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. | 11/17/2019 |
| 590 | Precision Biosciences Durham, NC Data Scientist - BioAnalytical Development MS in computer science, statistics, computional biology or related Exp: 0-2 years |
The Associate Scientist, Data Science works within the BioAnalytical Team at Precision Biosciences focused on the development of genome-edited allogeneic CAR-T therapeutics. The incumbent will play a lead role in the identification and implementation of existing and/or novel algorithms, analytical techniques and computational procedures to mine, clean, and interpret a wide variety of data derived from genomic, proteomic, metabolomic, and cellular phenotypic methods. This team member will be a part of our broader CMC organization which aims to drive technical excellence for the successful development of Precision Biosciences’ Cell and Gene Therapy Products, including allogeneic CAR-T cells, AAV viral vectors, and Lipid Nanoparticle-Encapsulated mRNA spanning a broad range of indications in immuno-oncology, infectious disease, and rare genetic disease. etc. | 11/12/2019 |
| 591 | Precision Medicine Group Frederick, MD Biorepository Technician - Entry Level BS in related field Exp: Entry level |
Play a critical role in helping patients gain access to the treatment they need. This position is responsible for specimens in our state of the art Specialty Labs facility that have been collected by our clients who are managing clinical trials to secure the required approval for potentially life-saving patient treatments. Clinical trials depend on biological specimen samples being withdrawn and deposited on a continual basis. etc. | 11/12/2019 |
| 592 | Precision Medicine Group Carlsbad, CA Biostatistician I – Clinical Trial Services MS in biostatistics/statistics Exp: Entry level |
What to expect day-to-day: Generating randomization schedules and providing sample size calculations. Providing input into development of case report forms (CRFs). Authoring and reviewing statistical analysis plans, including development of table and listing shells. Generating analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS. Providing programming support and quality control for SAS Programs and other study documents. etc. | 11/12/2019 |
| 593 | Precision Medicine Group Norton, MA Clinical Data Associate BS/MS Exp: Entry level |
How you will make a difference: Review, analyze, validate and maintain clinical trial data to ensure consistency, integrity and accuracy. Query data inconsistencies and update the databases by understanding standard operating procedures, client guidelines and regulatory agency guidelines. Perform User Acceptance Testing. Prepare Patient and Study Level Status/Metric reporting. Utilize dictionary coding such as MedDRA and WhoDrug. Generate data retrievals and summaries. | 11/12/2019 |
| 594 | Precision Medicine Group Oakland, CA Associate Research Statistician - HEOR MS in economics, health services, biostatistics or related Exp: 1+ year(s) |
As Research Statistician, you will perform a wide range of activities including: literature reviews; analysis; preparing reports, slide decks and meeting notes; and quality assurance/review. You will independently complete, evidence synthesis projects, including: client management; systematic literature review (SLR); (network) meta-analysis; economic modeling; and dissemination of results. etc. | 11/12/2019 |
| 595 | Precision Medicine Group Houston, TX Technologist – PBMC / IHC BS in medical technology, biology, or related Exp: 0-1 years |
As a Technologist, you will participate in simple and complex processing of tissue, PBMCs, blood and body fluids, both routine and non-routine procedures. You will work with scientists to carry out qualification of assays for new projects and be engaged in IF / IHC / Opal staining tasks. This position requires flexibility to work on different shifts as needed. etc. | 11/12/2019 |
| 596 | Promega Madison, WI Quality Technician HS diploma or equivalent Exp: 1-3 year(s) |
JOB OBJECTIVE: Perform Quality inspection and analysis activities including: Receiving inspection of purchased components and materials in accordance with written procedures, statistical sampling plans, inspection standards and engineering drawings and specifications, using measuring equipment. In-process and finished device inspection and release activities in accordance with the Device Master Record. etc. | 11/12/2019 |
| 597 | ProSciento San Diego, CA Clinical Data Associate BS in the life sciences Exp: Not necessary for BS candidates |
Under the supervision of the Associate Director, CRA Services, conducts site monitoring for clinical research studies according to ProSciento Standard Operating Procedures (SOPs) and ICH/GCP/GLP guidelines. Prepares monitoring reports and assists with query resolution. Performs duties in accordance with the company’s values, policies, and procedures. Essential Duties and Responsibilities include the following. Other duties may be assigned at the Company’s sole discretion. Responsible for all aspects of study site monitoring including site qualification visits, pre-study visits, site initiation visits, routine monitoring visits, and close-out visits of clinical sites. etc. | 11/12/2019 |
| 598 | PTC Therapeutics South Plainfield, NJ Research Associate - Neuroscience BA/BS Exp: 1-2 year(s) |
Reporting to a PhD Scientist in the Neuroscience Group at PTC, the Research Associate is involved in performing experiments using a variety of techniques, including analysis of RNA, protein, electrophysiology on brain tissue and imaging of cells and tissue sections. The successful candidate will: Work collaboratively with other PTC researchers to execute experiments in a highly matrixed environment. Analyze and interpret data generated. Assure that timelines are adhered to through efficient time management. Communicate effectively within the research team and across functional areas. Present data at internal meetings. etc. | 11/12/2019 |
| 599 | PTC Therapeutics Mountainview, CA Laboratory Technician/Research Assistant, Compound Management AS/BS in chemistry, biochemistry, or biology Exp: 0-2 years |
We are seeking a highly organized technician/research assistant to manage the proprietary compound collection at the PTC Mountain View Research Site. This individual will be a key member of the research group, providing samples to internal and external collaborators. Additionally, the compound management technician will perform routine chemical and biological assays to support various programs. The successful candidate will be almost pathologically detail-oriented and thrive performing high precision work. etc. | 11/12/2019 |
| 600 | Pyramid Laboratories Costa Mesa, CA Manufacturing Technician No degree required Exp: 1 year |
Under general supervision, perform various manufacturing related activities for a GMP compliant Fill/Finish operation applying standard practices, techniques and procedures. Able to assist in the preparation of reports, records, etc., for assigned tasks. PRINCIPAL DUTIES: Familiar with related GMP procedures and requirements, as directly related to the position. Ensure that appropriate procedures and processes are utilized without unauthorized modifications. Ability to set-up, maintain and perform various manufacturing related activities as required for a GMP compliant Fill/Finish operation. etc. | 11/12/2019 |
| 601 | Quick Biology Pasadena, CA Research Associate MS in biochemistry, molecular, or biological science Exp: 1-4 year(s) |
We are seeking a Research Associate I to perform sample preparation, RNA/DNA extraction, QC/QA, sequencing library construction and Illumina Hiseq sequencer operation in our sequencing team. The successful candidate should have knowledge of next-generation sequencing using the Illumina platform. The successful candidate should work somewhat independently to conduct laboratory experiments on NGS projects within well-defined guidelines; Ability to independently design and execute SOPs to meet project goals is essential. | 11/12/2019 |
| 602 | Regeneron Tarrytown, NY R&D Associate - Neurodegenerative Diseases MS in neuroscience, biochemistry, biology or related Exp: 1+ year(s) |
We are seeking a talented and motivated R&D Associate / Specialist to join our highly dynamic neuroscience team. The successful candidate will be responsible for the design and execution of experiments to understand the mechanisms of neurodegenerative diseases, discover new therapeutic targets and validate novel therapeutic strategies. We are looking to recruit a candidate with in vitro experience and strong in vivo expertise in neuroscience and models of neurodegenerative disease. etc. | 11/12/2019 |
| 603 | Repligen Waltham, MA Manufacturing Associate - ELISA AS/BS Exp: 1-2 year(s) |
This position is in Repligen’s ELISA group. The successful candidate will be responsible for the manufacture of ELISA kits and its components as well as in-process testing. The individual must be able to follow oral and written instructions accurately and complete tasks in a timely manner. Experience working in a GMP/ISO/document-controlled environment would be beneficial. Attention to detail and the ability to work in a team environment are essential. Candidates must be willing and able to learn new manufacturing processes as the company grows. | 11/12/2019 |
| 604 | RTI Surgical Alachua, FL Materials Tech 1 HS diploma or equivalent Exp: Entry level |
The Materials Tech 1 position at RTI represents an entry level function. Employees will develop technical skills in their assigned areas, an understanding of the rules and regulations that RTI administers, and the basic operating approach at RTI including: reading, understanding, and following work instructions; working in a team environment; and learning to work with minimal supervision. POSITION SUMMARY: Performs daily activities in accordance with applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). Unpacks, segregates, organizes, wraps, and packages various supplies and equipment. etc. | 11/12/2019 |
| 605 | RTI Surgical Alachua, FL BMS Technician HS diploma or equivalent Exp: 1 year |
POSITION SUMMARY: Maintains accurate records of all specimens received or sent out of the laboratory. Completes test request forms and enters the information into the Laboratory Information System. Performs specimen preparation for testing and archiving. Makes determinations as to acceptability of specimens, and files appropriate specimen rejection forms and revision request forms when necessary. Performs non-licensed testing, interprets non-licensed testing results, and prepares reports. Performs quality control and quality assurance in areas of the laboratory. etc. | 11/12/2019 |
| 606 | Samdi Tech Chicago, IL Research Assistant (Full-time) BS in biology, biochemistry, chemistry or related Exp: 0-3 years |
The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include supporting the preparation of reagents and materials for running biochemical assays, assisting in executing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, integrating automated liquid handling, and supporting fundamental laboratory functions. | 11/12/2019 |
| 607 | Samdi Tech Chicago, IL Research Associate- Biochemical Assay Specialist (Full-time) MS in biology, biochemistry, chemistry or related Exp: 1+ year(s) |
The Research Team leads target/enzyme-based projects for biotech and pharma clients to develop assays for high-throughput screening, and characterization of drug candidates and reaction mechanisms. The successful candidate will be organized and able to work under strict timelines in a fast paced environment. Primary responsibilities may include handling and processing of reagents and materials for running biochemical assays, designing and performing biochemical assays utilizing state of the art MALDI TOF mass spectrometry, take a project leadership role on multiple targets/enzymes, integrating automated liquid handling, and writing and maintaining Standard Operating Protocols (SOPs). | 11/12/2019 |
| 608 | GBT South San Francisco, CA CONTRACT - CLINICAL TRIALS ASSISTANT BS/BA or equivalent Exp: Experience preferred but not required |
The Clinical Trials Assistant (CTA) is responsible for providing support to the lead Clinical Trial Manager and the study execution team, clinical tracking and document maintenance as applicable to study vendors and clinical trial sites. The CTA will work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in compliance with GBT SOPs, ICH/GCP/regulatory guidelines, company goals, and budgets. | 11/9/2019 |
| 609 | Global Pharma Tek Edison , NJ Clinical Project Assitant BS in pharmacy, health care, or related Exp: 1-2 years |
Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines | 11/9/2019 |
| 610 | Global Pharma Tek Edison , NJ Equipment Validation Engineer BS in mechanical/industrial engineering Exp: 1-2 years |
Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Prepare protocols and reports for Validation Project Plan, Validation Master Plan, IQ, OQ, OQ, Traceability Matrix, Engineering test Plans, and Commissioning test strategies following the site Good Data and Documentation Practices (GDP) during protocol execution for qualifying the system or facility | 11/9/2019 |
| 611 | Global Pharma Tek Edison , NJ Regulatory Affairs II BS in pharma sciences or related Exp: 1-2 years |
Managing and delivering regulatory submissions to global health authorities required to support the maintenance, development and registration of products and performing the following required activities depending on the particular project and assigned submission(s). Establishing Dossier Plans for the assigned Global submission types as needed to support the lifecycle of one or more products in generating dossier plans that will reflect inputs from functional area representatives and key stakeholders; | 11/9/2019 |
| 612 | Global Pharma Tek Edison , NJ Lab Equipment Qualification Engineer BS/BA in pharmacy or chemistry Exp: 1-2 years |
Execute Validation and Qualification protocols which include installing, operating and maintaining of GMP Lab Equipment and Instruments (HPLC, UV-Vis Spectrometers, FTIR, GC, pH meters, Conductivity meters, Analyzers etc.) and manufacturing equipment like sterilizers and autoclaves to confirm if the instrument is compatible and compliant with Manufacturing, analysis, Company and FDA regulations. Perform validation and qualification documents include User requirement specifications, functional requirement specifications, Installation Qualifications (IQ), Operational Qualifications (OQ), Performance Qualifications (PQ), Validation summary reports, Change Control etc. for various lab instruments utilized by Quality control and Quality assurance teams; | 11/9/2019 |
| 613 | Global Pharma Tek Edison , NJ Associate Operations Specialist BS/BA in pharmacy or pharmacology Exp: 1-2 years |
Review, assess and process Lifecycle Safety data and information, across all service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Perform data entry for tracking and safety database, coding relevant medical terminology, writing, descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. | 11/9/2019 |
| 614 | Global Pharma Tek Edison , NJ Submission Specialist - Regulatory Affairs BS in regulatory affiars/health admin Exp: 1-2 years |
Performing hands-on daily submission compilation and publishing activities associated with preparation of various dossier types and safety reports, for both new product marketing applications and/or marketed product maintenance packages. Performing overall quality of the assigned documents and dossiers which must comply with all internal Bayer best practices, meet global regulatory requirements, and facilitate the review and timely approval by appropriate regulatory authorities. Supporting the compilation of global dossiers and to deliver technically compliant submission documents/reports, which contribute to the development of submissions that meet the technical requirements and standards set by relevant health authorities. | 11/9/2019 |
| 615 | Global Pharma Tek Edison , NJ Specialist Study Management BS in regulatory affiars/health admin Exp: 1-2 years |
Review and process start up documents, including Sub Investigator’s documents in compliance with ICH-GCP, and client’s Procedural Documents; Assist SATS with obtaining and maintaining essential documents in compliance with ICH-GCP, and client’s Procedural Documents; Attend weekly study team meetings and be prepared to provide a report on vendor spreadsheet status and sub I document status; Create and/or import clinical-regulatory documents into the A New Global Electronic Library (ANGEL) according to the Global Document List (GDL) ensuring compliance with the client’s Authoring Guide for Regulatory Documents to support publishing in ANGEL; | 11/9/2019 |
| 616 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Technician HS Diploma or AS in biological/physical sciences Exp: Entry Level |
Assists Upstream Manufacturing and Cell Culture Operations with Manufacturing in accordance with Master Batch Records and in compliance with GMP regulations and guidelines. Monitors Manufacturing Processes, Operates Analytical Laboratory Equipment and provides Operational Support for USP-MFG activities. Compiles electronic /laboratory notebooks, maintains laboratory equipment, and equipment logs and monitors supplies. | 11/9/2019 |
| 617 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Technician BS in biological/physical sciences Exp: 1-2 years in cell culture |
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. Assists 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. | 11/9/2019 |
| 618 | Gore Elkton, MD R&D Technician BS in chemical/sciences/engineering Exp: 1-3 years |
W.L. Gore & Associates Inc. is seeking an associate to join the R&D Technician Lab Team at one of the Fabrics Division’s facilities in Elkton, Maryland. The primary focus of this commitment is to support projects and hands on testing needs for our Durable Water Repellent coating on laminates. Performing lab functions accurately and efficiently, including but not be limited to: Hands on testing, sample preparation, and test method development. Writing and implementing procedures.Operating and maintaining analytical equipment | 11/9/2019 |
| 619 | Gore Flagstaff, AZ Electrical Automation Design Engineer BS in engineering Exp: 1 or more year (can be coop/internships) |
In this role, you will be involved in software design, electrical design, specification, installation, startup, validation, project management, and support for new and existing equipment and systems. Performing electrical design and hands-on support for process equipment (e.g., drives, programmable logic controller [PLC] logic programming, human-machine interfaces [HMIs], wiring schematics, power systems, instrumentation, and motor control systems). Being an integral member of a project team that specifies, constructs, commissions and validates new manufacturing equipment | 11/9/2019 |
| 620 | Gradalis Carrollton, TX Clinical Research Assistant BS in life/health sciences Exp: 1 or more years |
The Clinical Research Assistant coordinates the research and administrative activities of clinical trials for Gradalis. The Clinical Research Assistant works for the Clinical Operations Manager to provide support in compliance with the FDA Code of Federal Regulations (CFR), the ICH Good Clinical Practice (GCP) Guidelines, OHRP/DHHS guidelines and Gradalis Standard Operating Procedures. | 11/9/2019 |
| 621 | Grail Menlo Park, CA Research Associate 2 - R&D Technology Development MS in molecular biology, biochemistry, or related Exp: 1 year or more |
GRAIL is seeking a Research Associate for the R&D technology development team to contribute to the development and optimization of assays for early cancer detection. The successful candidate will be responsible for planning and execution of experiments and data analysis with the guidance of senior scientists. Develop experiment plans to support study objectives. Ensure laboratory activities are performed in compliance with best practices for assay and instrument operation, safety, and result documentation | 11/9/2019 |
| 622 | Grail Menlo Park, CA Equipment Engineering Technician BS/BA in engineering or sciences Exp: 0-2 years in lab |
As an Equipment Engineering Technician, you are responsible for supporting laboratory equipment management procedures, in alignment to our internal Quality Management System, to ensure better performance within Laboratory Operations. This will include global laboratory equipment support, sustainment, and operations activities across Production/Clinical, Product Development, Research and Development laboratories, in accordance with CLIA/CAP, FDA, cGMP and/or GLP guidelines. | 11/9/2019 |
| 623 | Grail Menlo Park, CA Clinical Lab Associate I BS/BA in Biomedical Laboratory Science, Clinical Science or related field preferred. Exp: 1-2 years |
The Clinical Laboratory Associate (CLA) is responsible for assisting the Clinical Laboratory Scientist and supporting the daily operations of the Clinical Laboratory. CLA may serve as a team lead to the CLA team to coordinate tasks, divide workload, manage projects and review documents as assigned. The work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask, be flexible with tasks and schedules and ability to work independently in a team environment. | 11/9/2019 |
| 624 | Grand River Grand Rapids, MI ASEPTIC MANUFACTURING ASSOCIATE - 3RD SHIFT HS Diploma/GED Exp: 0-1 years in manufacturing or lab work |
Responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. Follow production and manufacturing procedures. Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed. Train in various manufacturing tasks including, but not limited to: fill/finish, formulation, lyophilization, sanitization, component and equipment preparation, and finished product inspection and packaging activities. | 11/9/2019 |
| 625 | GreenLight Biosciences RTP, NC Research Technician Formulations BS in pharma sciences, or chemistry Exp: 0-2 years in lab |
GreenLight Biosciences is seeking for a Formulation Laboratory Technician to be part of the Formulation team to work on the design of new formulations under the guidance of a formulation scientist as well as the improvement of existing formulations and provide support to the manufacturing operations. The technician will be responsible for evaluating formulations, troubleshooting production when necessary and sample preparation. Strong technical, organizational and communication skills are essential. Applicant must be a team player able to function in a highly collaborative and fast-paced environment. | 11/9/2019 |
| 626 | Grifols San Diego, CA Research Associate 2 BS/BA or MS Exp: 1-3 years |
Research Associate 2 is responsible for designing and performing experiments while collaborating and communicating effectively. Performs moderately complex experiments with input from supervisor. Able to summarize related groups of experiments. Provides input to the experimental design. Is able to analyze experimental data with minimal input from supervisor. Interprets experimental results in context of overall experimental goal. | 11/9/2019 |
| 627 | Grifols Clayton, NC Associate Chemist-QC AS/AA or BS/BA Exp: 0-2 years with chemistry courses for degrees |
Performs chemical testing of moderate to advanced complexity within a Quality Operations Laboratory in a safe, accurate, and efficient manner following established written procedures while maintaining complete and accurate records of the work and results. This testing is required for the release of raw materials, in-process materials, and final containers. Conducts various routine and non-routine chemical testing (assays) according to procedure. Learns and follows the methods and the techniques of the chemical tests to be performed. This learning is a continuation of learning that occurred as Assistant Chemist. | 11/9/2019 |
| 628 | Grifols Savannah, GA Phlebotomist HS Diploma/GED Exp: 0-1 years |
You assist in determining the suitability of donors to undergo plasmapheresis prior to venipuncture. You establish rapport with donors to ensure overall customer happiness with the center to support long-term donation, all while ensuring donor confidentiality. Sets up, disconnects, and operates the automated plasmapheresis machines including response and evaluation of all autopheresis troubleshooting displays, documentation of exceptions, etc. Ensures the proper calibration and maintenance of autopheresis machines and associated equipment. May be trained to repair plasma equipment. Disconnects and disposes of all contaminated disposable equipment. Ensures proper cleaning of equipment and work area between donors. Maintains accurate and thorough documentation of production records. | 11/9/2019 |
| 629 | Grifols Ocala, FL Biomedical Technician HS Diploma/GED Exp: 6-12 months as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Responsible for preparing donors for plasmapheresis procedure. Review donor record files for accuracy and completeness. Collect plasma by setting up the autopheresis instrument, performing the venipuncture and utilizing an Automated Plasmapharesis machine. Evaluate vein performance by checking data with known norms to identify possible problems; make corrections in order to expedite donation time and ensure product quality. Conducts all phlebotomies in compliance with all federal, state, and Biotest regulations. | 11/9/2019 |
| 630 | Grifols Rock Hill, SC Biomedical Technician HS Diploma/GED Exp: 6-12 months as medical assistant or phlebotomy training |
Identify and screen donors by reviewing medical records and logs and evaluate the donor as to suitability. Screening includes asking health related questions and referring to medical staff when necessary; taking vital signs (blood pressure, pulse and temperature), performing fingerstick (HCT & Total Protein), and reviewing results using the applicable donor management system Maintain donor confidentiality at all times in all areas. Responsible for preparing donors for plasmapheresis procedure. Review donor record files for accuracy and completeness. Collect plasma by setting up the autopheresis instrument, performing the venipuncture and utilizing an Automated Plasmapharesis machine. Evaluate vein performance by checking data with known norms to identify possible problems; make corrections in order to expedite donation time and ensure product quality. Conducts all phlebotomies in compliance with all federal, state, and Biotest regulations. | 11/9/2019 |
| 631 | Grifols Clarkville, TN Quality Associate HS Diploma/GED Exp: 0 years |
Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual. Participate in the Quality Assurance meetings and be part of the Quality Assurance team. Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Perform weekly review of equipment incident logs. | 11/9/2019 |
| 632 | Grifols Moorhead, MN Phlebotomist HS Diploma/GED Exp: 0-1 years |
You assist in determining the suitability of donors to undergo plasmapheresis prior to venipuncture. You establish rapport with donors to ensure overall customer happiness with the center to support long-term donation, all while ensuring donor confidentiality. Sets up, disconnects, and operates the automated plasmapheresis machines including response and evaluation of all autopheresis troubleshooting displays, documentation of exceptions, etc. Ensures the proper calibration and maintenance of autopheresis machines and associated equipment. May be trained to repair plasma equipment. Disconnects and disposes of all contaminated disposable equipment. Ensures proper cleaning of equipment and work area between donors. Maintains accurate and thorough documentation of production records. | 11/9/2019 |
| 633 | Gritsone Pleasanton, CA MANUFACTURING ASSOCIATE I/II, DOWNSTREAM BS in biological/physical sciences Exp: 0-2 years in cGMP manufacturing |
The Manufacturing Associate will execute activities associated with purification manufacturing in a clean room environment. This role will also need to assist with cell culture, aseptic fill, and buffer prep processes as well as maintain material inventory in labs. Possess experience in purification activities including but not limited to tangential flow filtration, anion exchange chromatography, and diafiltration. Responsible for day to day manufacturing activities including stocking of materials, preparation of documentation, cleaning and sanitization of rooms and equipment, operation of process equipment. | 11/9/2019 |
| 634 | Guardant Redwood City, CA Clinical Trials Assistant BS/BA in biological sciences Exp: 1 year in clinical research |
The Clinical Trial Assistant (CTA) is primarily responsible for the coordination of activities associated with the setup and management of clinical studies under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. | 11/9/2019 |
| 635 | Guardant Redwood City, CA Reporting Assistant II AS/AA or BS/BA in lab/clinical sciences Exp: 1 year of lab experience |
The Reporting Assistant (RA)II is responsible for assisting the reporting Clinical Laboratory Scientists (CLS) and supporting the daily operations of the post-analytical reporting process.The RA IIis responsible for preparing all preliminary reports, labeling folders, documenting controls for CLS review and assisting sample status in the Clinical Laboratory. | 11/9/2019 |
| 636 | Guardant Redwood City, CA Client Services Associate BS/BA Exp: 1 year in client services |
We are looking for a full-time Client Services Associate (CSA). The CSA is responsible for providing exceptional support to Guardant Health customers, the Guardant Health Clinical Laboratory, Sales Representatives, and our billing partners. CSA is responsible for receiving and responding to all types of communication: phone, email and web inquiries from customers (physician offices, laboratories, and hospitals), sales representatives and patients. | 11/9/2019 |
| 637 | Harpoon Therapeutics South San Francisco, CA Clinical Research Associate BS/BA in science/health care Exp: 1-2 years in drug development |
The Clinical Research Associate is a key member of the team responsible for planning, successful implementation and management of one or multiple clinical trial(s). Responsibilities include assisting in the development of study protocols, case report forms, clinical reports, performing site monitoring visits, and interfacing with site coordinators, field clinical staff, CROs and other company representatives. High level relationships across all functional areas that interact with Clinical Operations (including Product Development, Research, Translational Medicine, etc.) will also be required. | 11/9/2019 |
| 638 | HealPros Atlanta, GA IT Support Technician HS Diploma or higher Exp: 6-24 months of electornics work |
We have an immediate opening for an IT Support Technician to be based out of our corporate office in Buckhead, GA. This is a full-time position and will be responsible for managing HealPros's equipment in our facility or at the location of our technologists. Under the supervision of the IT Administrator, the IT Support Technician will perform troubleshooting techniques to resolve equipment issues and maintain it in good working order. | 11/9/2019 |
| 639 | Health Decisions Durham, NC Business Development Associate (Inside Sales) BS/BA Exp: 1 year in sales |
We are seeking a Business Development Associate who will be responsible for lead generation by proactively prospecting and qualifying targeted leads by telephone and email. The ideal candidate will be highly skilled in fostering relationships with the goal of converting leads to new sales opportunities. Initate initial client engagement, including ensuring client-readiness of materials for client meetings including briefing documents and call presentation development; develops call agenda and hosts prep sessions with internal teams in advance of client engagement . | 11/9/2019 |
| 640 | Helmer Scientific Noblesville, IN Manufacturing Trainee HS Diploma/GED Exp: None |
Performs repetitive assembly/fabrication/materials tasks using basic hand tools to build either parts for or actual temperature-controlled storage units, refrigerators/freezers and thawing systems, Cleans and packs units, handles material for distribution. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. Ensure that device history records are completed according to FDA GMP requirements. Complete nonconformance records according to established procedures and GMP requirements. | 11/10/2019 |
| 641 | Helmer Scientific Noblesville, IN Assembler I* HS Diploma/GED Exp: 1-3 years in general assembly |
The Assembler I: Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customer. Performs repetitive assembly task using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems. May be assigned to clean and pack units. | 11/10/2019 |
| 642 | Helmer Scientific Noblesville, IN Assembler I - Clean & Pack* HS Diploma/GED Exp: 1-3 years in general assembly |
Performs repetitive assembly tasks using basic hand tools to build temperature controlled storage units, refrigerators/freezers and thawing systems or under counter temperature controlled storage units. May clean and pack units. | 11/10/2019 |
| 643 | High Point Clinical Trials Center High Point, NC Lab Supervisor CLS/MT Associates, BS, BA Exp: 1 year lab experience |
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. Completes all study procedures as per FDA regulations, GCP guidelines and protocol requirements. Assists with and performs laboratory procedures including sample check-in, preparation, centrifugation, storage and shipment. 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. | 11/10/2019 |
| 644 | High Point Clinical Trials Center High Point, NC Research Nurse NC nursing license Exp: 1 year practical nursing experience |
Assist in conduct of clinical studies. Provides licensed nursing coverage for studies and performs procedures as allowed by training and delegation. Assist in the conduct of clinical studies while providing licensed coverage. Performs all job responsibilities in accordance with standards of Good Clinical Practice (GCP), clinic standard operating procedures (SOP’s), and OSHA guidelines. Perform tasks such as EKG’s, vital signs, phlebotomy, insertion and maintenance of IV catheters. | 11/10/2019 |
| 645 | Hikma Cherry Hill, NJ Quality Lab Associate I, Env. Monitoring BS/BA Degree 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. 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. Audit personnel aseptic technique in controlled areas including during process simulations (media fills). Document test data clearly and accurately. Maintain data integrity and ensure compliance with company policies, procedures, cGMPs, and regulatory requirements. | 11/10/2019 |
| 646 | Hikma Columbus , OH Technician II, Chemstore 2nd Shift HS Diploma/GED Exp: Entry LEvel |
Performs the set of tasks referred to as “window work” within the Chemstore while collecting, washing, and redistributing laboratory glassware. Escalates any washer issues discovered to the GMP department and communicates shortages/inventory needs to their Manager. | 11/10/2019 |
| 647 | Hillrom Alexandria, LA Field Service Technician I HS Diploma/GED Exp: 0-2 years in FDA related industry/customer service |
The primary duties of a Medical Equipment Service Representative involve client facing customer service and minor medical equipment repairs. Responsible for the pick-up and delivery of medical equipment, using a company provided vehicle to customer facilities. Periodically work on an on-call rotation that involves a 24/7/365 operation. Responsible for direct customer contact | 11/10/2019 |
| 648 | Hillrom Albuquerque, NM Field Service Technician I HS Diploma/GED Exp: 0-2 years in FDA related industry/customer service |
The primary duties of a Medical Equipment Service Representative involve client facing customer service and minor medical equipment repairs. Responsible for the pick-up and delivery of medical equipment, using a company provided vehicle to customer facilities. Periodically work on an on-call rotation that involves a 24/7/365 operation. Responsible for direct customer contact | 11/10/2019 |
| 649 | Hillrom Batesville, IN Engineer I R&D - Embedded Software BS/BA in computer science/engineering Exp: 0-2 years in engineering/technical role |
As an Embedded Software Engineer, you will develop innovative medical software in a fast-paced environment. The ideal candidate will have a passion for bringing cool ideas to life and maximizing hardware and software performance. You will be responsible for writing firmware for device drivers, task manager, device manger, control algorithms, and various communication protocols which make our products exceptional. You develop tools which automate the software build process, system design and production testing. | 11/10/2019 |
| 650 | Homology Bedford, MA Research Associate, Analytical Development (6 Month Contract) BS/BA in biological sciences Exp: 0-2 years in biochemical/biological analyses |
The role of Analytical Development Research Associate is to aid in developing and refining analytical methods to characterize AAV vector products. The individual in this role will be a highly-skilled, talented and motivated researcher who will focus on the analysis of research/development-grade vector samples using multiple AAV-specific analytical methods. The candidate will participate in the comparison of AAV vector products produced internally with those produced externally as well as the optimization and qualification of molecular and bioanalytical assays such as HPLC and capillary electrophoresis. | 11/10/2019 |
| 651 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in engineering Exp: 1-2 years in chemical/pharma operations |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. | 11/10/2019 |
| 652 | Hovione East Windsor, NJ Process Engineer BS in chemistry/chemical engineering Exp: 1-3 years in chemical/pharma operations |
The Process Engineer will ensure that the use of the best process engineering knowledge will be applied in scaling up chemical and spray drying projects to maximize customer satisfaction and Hovione’s interests and in compliance with all Federal, State, Local and internal policies. Plan and design manufacturing processes based on chemical procedures to run safely and effectively in a pilot plant/kilo lab in accordance with the best known practices ensuring cGMP compliance. Contributes to the Process Hazard Analysis (PHA) of all processes under his/her responsibility and assures that all identified hazards are addressed prior to performing any activities within operations. | 11/10/2019 |
| 653 | iCAD San Jose, CA Mechanical Engineer - R&D BS in Mechanical Engineering, or closely related Exp: 1- 5 years |
Fundamental understanding of Mechanical Design and Engineering. Product design experience in plastics, ceramics and/or metals. Fixture design for assembly and inspection. Lead experimental builds related to the development of the product. Run validation protocols related to design and production. | 11/10/2019 |
| 654 | Icon PLC Farmingdale, NY Laboratory Study Start-Up Specialist BS Exp: 1 year in clinical trials |
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/10/2019 |
| 655 | Icon PLC Lexington, KY DPC Assistant HS Diploma/GED Exp: 1 year in medical office/admin |
The DPC Assistant will provide support services (logistical, technical and administrative) to the Direct to Patient Contact (DPC) project team all along the project, while complying with the deadlines, budgets, quality and regulatory requirements defined for each project. For each project, the Direct to Patient Contact Manager (DPCA) works under the technical and functional supervision of the dedicated Direct to Patient Contact Manager (DPCM). | 11/10/2019 |
| 656 | Icon PLC Brentwood, TN CTA BS/BA in life sciences Exp: Entry Level |
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint. ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research. | 11/10/2019 |
| 657 | Icon PLC Raleigh, NC Client Services Assoc II, PCS BS/BA Exp: 1-2 years in clinical research |
As a Client Services Associate II, you will be responsible for supporting efforts to maintain and expand upon client relationships for the assigned PCS service area(s) through costing and proposal development, single service project planning and support, and client communication management. Support clinical research projects in the areas of scale management, translations, printing and distribution, and technology implementation. | 11/10/2019 |
| 658 | Icon PLC North Wales, PA Configuration & QC Spec I BS Exp: 1 year in clinical research |
Our Configuration & QC Specialist plays a key role within ICON Laboratory Services (ILS). Support the Project Management Team (PM) in configuring and QC'ing new studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW) and create all supporting documents and site instructions to facilitate proper specimen collection, packaging and shipping, including visit requisitions, reference range tables and study specific Lab Manuals. | 11/10/2019 |
| 659 | Freudenberg Jerffersonville, IN Medical Device Assembly / Manufacturing Associate- 1st Shift HS Diploma/GED Exp: 0-2 years |
Hand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvementsHand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvementsHand assemble manufactured components. Complete required documentation for work performed. Quality inspect work performed. Follow defined work procedures. Provide suggestions of continuous line/process improvements | 11/2/2019 |
| 660 | Freudenberg Carpinteria, CA Tool Room Associate HS Diploma/GED Exp: 0-3 years |
Secondary operations and simple machining, including manual machining, grinding, honing, deburring, squaring of stock, and precision material removal to complex specifications with minimal instructions to the requirements of supplied Engineering Documentation. Maintenance of tool room equipment, and of production line molding, extrusion, and assembly equipment are vital functions of the role. Purchasing and stocking of hand tools, metalworking tools, and machining tools. Organization, cleaning, and maintenance of a 5S systematic program for workplace organization in the tool room. | 11/2/2019 |
| 661 | Frontage Exton, PA Associate Scientist, Bioanalytical Services BS or MS in sciences Exp: Entry level |
Associate Scientist / Bioanalytical Services Essential Functions Provide support for running sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Coordinate study activities with Responsible Scientist to ensure efficiency and quality. Maintain the proper level of regulatory compliance for each study, helping to address QA audit findings | 11/2/2019 |
| 662 | Frontage Secaucus, NJ Lab Technician Associates or bachelors in biomedical discipline Exp: 1-3 years in clinical research |
Develop a high level of familiarity and knowledge of the study protocol and flow chart of study procedures. Develop a strategy for implementing study procedures in compliance with study protocols. Performs laboratory procedures (g., preparation for admission testing, safety labs, and processing of biological specimen samples, shipment of samples and documentation of sample processing steps, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. | 11/2/2019 |
| 663 | Frontage Exton, PA Associate Scientist-Product Development- CMC MS in pharma sciences, chemistry or biology Exp: 0-4 years |
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. Assist in the equipment set up, operation, maintenance, cleaning as required for the project | 11/2/2019 |
| 664 | FujiFilm College Station, TX Information Technology – Technical Support I HS Diploma/GED or BS in computer sciences Exp: 1 year in technical support |
Deployment and relocation of desktop systems. Maintenance and repair of desktops, printers and associated peripherals. Supports other IT staff in installing, configuring, testing, maintaining and troubleshooting network, systems hardware and software. Administration of FDBT’s Building Information Management System (BIMS). | 11/2/2019 |
| 665 | FujiFilm RTP, NC Downstream Production Technician HS Diploma/GED or BS in computer sciences Exp: 1+ year in cGMP production |
Executing Development and Production processes as well as process documentation. Understanding processing principles and scientific theory behind operations steps. Demonstrating proficiency at the advanced skill level. Troubleshooting of equipment/processes. Authoring and routing SOP’s for approval. Assisting in the execution of validation protocols. | 11/2/2019 |
| 666 | FujiFilm College Station, TX Downstream Manufacturing Technician I AS/AA in biological sciences/engineering, or HS Diploma/GED Exp: HS: 1 year, AA: 0 years |
The Downstream Manufacturing Technician I will work directly with viral purification (either whole particle or split particle), continuous flow centrifuge operation, and sucrose gradient separation, techniques for filtration and chromatographic separation (i.e. column chromatography and HPLC) and viral inactivation. | 11/2/2019 |
| 667 | FujiFilm College Station, TX Cell Biology Technician BS/BA in biological sciences Exp: 0-2 years |
Writes and revises Standard Operating Procedures (SOPs) and other related Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP) documentation. Manages test samples, reagents and reference standards. Provides QC support for the Sample receipt for Manufacturing. Perform other duties as assigned. | 11/2/2019 |
| 668 | FujiFilm College Station, TX Calibration Technician II BS or MS in sciences/engineering Exp: 1-2 years in cGMP operations |
Perform calibrations of complex instrumentation on production, laboratory and facility systems ensuring all systems and devices are calibrated in accordance with manufacturer’s specifications and FBDT SOP’s. Assist in the development of investigations resulting from ‘out of tolerance’ conditions with respect to instrumentation. Assist in interfacing with calibration contractors ensuring work is compliant with FBDT SOP’s and cGMP’s to maintain state of the art technology within the facility. Assist in maintaining all calibration records, work orders, and investigations in an orderly and accurate manner in compliance with cGMP’s by the utilization of the site CMMS and Document Management Systems. | 11/2/2019 |
| 669 | FujiFilm RTP, NC Associate Scientist, Microbial MS or BS Exp: BS: 1+ years, MS: 0 years |
The Upstream Process Development group is seeking an Associate Scientist with experience in microbial technologies. An Associate Scientist assists in conducting experiments for programs. The individual monitors on going experiments and can identify unusual occurrences. An Associate Scientist understands and applies knowledge within area of expertise and can take an active role in non-routine process development activities. | 11/2/2019 |
| 670 | FujiFilm College Station, TX Associate Scientist – Downstream Process Development MS in chemistry, biology, or life sciences Exp: 1 year experience |
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). Maintaining detailed laboratory notebooks following FDBT procedures. Participate in developing and carrying out experimental protocols. | 11/2/2019 |
| 671 | Cosette South Plainfield, NJ ASSOCIATE SCIENTIST PRODUCT DEVELOPMENT MS in engineering, or life/pharma sciences Exp: 1-2 years |
he Product Development Scientist will assist the Manager of Product Development in all aspects of new drug product and process development including but limited to – prototype development, lab stability, document creation, process design and optimization, pilot scale-up, assist the process development group in supervising clinical trial manufacturing material, Registration/exhibit batch manufacturing, and process optimization to full scale commercial batch size. Collaborate with all of the Scientific Affair Department (including Process Development, Analytical R&D, Regulatory Affairs, Clinical and Project Management), commercial manufacturing and quality group. | 11/2/2019 |
| 672 | Cosette South Plainfield, NJ MANUFACTURING OPERATOR 1 - 3rd Shift HS Diploma/GED Exp: 1 or more year as machine operator |
Operate a number of machines used in the manufacturing of pharmaceutical products and have a good working knowledge of elements used in association with batch production, such as equipment cleaning, running filling machines, etc. The operator is responsible for producing acceptable product that meets G&W internal standards, and is also in conformance with GMP and safety standards. 3rd Shift Hours are 11:00 p.m. to 7:00 a.m. | 11/2/2019 |
| 673 | GenapSys Redwood City, CA Signal Processing Engineer/Data Analyst MS in electrical engineering, physics, math, stats, etc. Exp: 1-4 years in signal processing |
As a Signal Processing Engineer, you would be working in a cross functional R&D team to improve the performance of the core technology through close collaboration with lab scientists, genomic application scientists, and data scientists. You will develop DOE (design of experiments) for troubleshooting and failure mode analysis, extract information from biomedical sensors, develop DNA sequencing base calling algorithms, present written and oral reports and proposals to peers and management, and play an important role in shaping and productionizing new products and cutting-edge applications. | 11/2/2019 |
| 674 | GeneDx Gaithersburg, MD Microarray Lab Technician BS in medical tech/life sciences Exp: Entry Level |
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. | 11/2/2019 |
| 675 | GeneDx Gaithersburg, MD Quality Systems Specialis BS in related field Exp: 1-3 years in life science lab |
Implements Quality Systems programs that are consistent with company policies and regulatory standards. Audits and reviews quality data according to established procedures. Maintains tools for monitoring compliance training, corrective actions, audits, and document control. Supports corrective action task force initiatives | 11/2/2019 |
| 676 | GeneDx Gaithersburg, MD NGS Lab Tech BS in medical technology Exp: 0-1 years |
A GeneDx NGS Lab Technician performs a higher than 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. | 11/2/2019 |
| 677 | GeneDx Gaithersburg, MD DNA Extraction Technician BS in biology Exp: 0-1 years |
The Lab Technician performs all lab procedures in a prompt, accurate, and reliable manner according to established company and departmental policies and procedures. Prepares DNA dilutions and aliquots for use by downstream testing teams. Conducts diligent record-keeping and reporting. Prepares solutions. Performs equipment maintenance | 11/2/2019 |
| 678 | GenerationBio Cambrige, MA Associate Scientist, (Molecular Biology, Analytical Development) BS in biological sciences Exp: 0-2 years |
Generation Bio seeks a highly motivated Research Associate to support analytical molecular biology activities in a cross-platform function. The successful candidate will work part of an analytics team responsible for the development and testing of research drug substance, as well as performing experiments to better characterize and understand the composition of our drug. Perform bioanalytical assays, including purity, copy number, expression, and activity assays to support the Production, Pre-clinical, and Process Development groups | 11/2/2019 |
| 679 | Genewiz Cambridge, MA Laboratory Technician I, Genetic Analysis HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
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. | 11/2/2019 |
| 680 | Genewiz South San Francisco, CA Laboratory Technician I HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. 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. | 11/2/2019 |
| 681 | Genewiz South Plainfield, NJ Laboratory Technician I, Molecular Biology Prep HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
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. | 11/2/2019 |
| 682 | Genewiz South Plainfield, NJ Laboratory Technician I, Molecular Biology Prep HS Diploma/GED or AA/AS Exp: 1+ years in lab preferred |
Our Lab Techs strictly adhere to laboratory SOPs to ensure quality and safety and often communicate with our customers via email. 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. | 11/2/2019 |
| 683 | Genewiz South Plainfield, NJ Sales Executive Continuous Recruitment- NY/NJ BS/BA in life sciences/biological sciences Exp: 1 year |
GENEWIZ is seeking technical sales professionals to join our New Jersey/New York based Sales team. Achieve annual sales goals within defined territory/accounts through the development, maintenance, and enhancement of customer accounts. Develop and implement an effective territory business growth plan. Retain current business baseline revenue by managing relationships with customers and other account contacts by collaborating with business leaders and the customer interface teams | 11/2/2019 |
| 684 | Genewiz South Plainfield, NJ Bioinformatics Scientist MS in bioinformatics Exp: 1-3 years |
Work collaboratively with bench scientists, comprehend project objectives, evaluate and provide informatics solutions. Develop and implement bioinformatics analyses, applications, and workflows. Integrate statistical analysis to project design and data interpretations. Work closely with IT specialists to build robust infrastructure. | 11/2/2019 |
| 685 | Genewiz South Plainfield, NJ Associate Scientist I, NGS BS/BA in biological sciences Exp: 1+ year in lab |
Prepare amplified template libraries for high-throughput sequencing. Carry out DNA sequencing on next-generation DNA analyzers. Perform routine maintenance of DNA analyzers and related equipment. Check inventory and replenish consumable sequencing supplies . Communicate with customers by phone and e-mail in a friendly and professional manner | 11/2/2019 |
| 686 | GenMark Carlsbad, CA Research Associate II MS in biochemistry, molecular biology, or chemistry Exp: 0+ years |
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, including industry standard good laboratory practices. Identifies and solves problems in experiments or protocol designs, suggests improvements. Prepares documents meeting company standards, including data summaries, reports, SOPs and procedures | 11/2/2019 |
| 687 | GenMark Carlsbad, CA Quality Control Specialist I BS in life science or engineering Exp: 0-3 years in QC |
This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformance's, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 11/2/2019 |
| 688 | GenMark Carlsbad, CA Research Associate II, Technology Development MS in biochemistry, molecular biology, or chemistry Exp: 0 years in bio lab |
The Research Associate II will execute a range of molecular biology and bioanalytical procedures, reagent preparation, and laboratory duties under supervision for our technology development team. 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, including industry standard good laboratory practices | 11/2/2019 |
| 689 | Genomatica San Diego, CA Research Associate I/II MS Exp: 0-2 years |
Genomatica is seeking a highly motivated Research Associate I/II, Microbiology/Molecular Biology to join the Strain Engineering team. This team is responsible for construction, characterization, evolution and characterization of host strains. The successful candidate will utilize her/his knowledge of Microbiology/Molecular Biology for cloning genes, genetically engineering chromosomal DNA, sequencing and analyzing the genome, characterizing product titers, growth and by-products when grown with various feedstocks. | 11/2/2019 |
| 690 | Genomatica San Diego, CA Fermentation Associate I BS in Chemical/Biochemical Engineering, Bioengineering, Molecular Biology, Microbiology, or Biochemistry Exp: 1-4 years bio lab experience |
This position delivers high-quality fermentation data by applying optimal fermentor operating procedures, communicating observations clearly to Fermentation Science personnel, and works collaboratively to maximize experimental precision. This position will interface closely with the Fermentation engineers and scientists in the Fermentation Science Group to produce conclusive fermentation results that will guide process optimization and scale-up efforts | 11/2/2019 |
| 691 | NeoGenomics Aliso Viejo, CA Project Data Administrator I AS/AA or higher Exp: 1 or more years in data entry |
The Project Data Administrator I works under general supervision to support Pharma Services projects with a focus on study data entry, QC, and associated documentation. You will support internal teams, data entry and QC activities for many projects at a time. This is the Early role in the Project Data Administrator job category. In this position, you will handle data and perform related tasks from a full range of projects including Molecular, IHC, Flow Cytometry, MultiOmyx, FISH, and Cytogenetics. | 11/2/2019 |
| 692 | NeoGenomics Carlsbad, CA Clinical Laboratory Technologist I BS/BA in med technology, or chemical/biological/physical sciences Exp: 1+ year in clinical reference lab |
As a Clinical Laboratory Technologist I or II or III you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, 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. | 11/2/2019 |
| 693 | NeoGenomics Carlsbad, CA Client Advocate I HS Diploma/GED Exp: 1-3 years in customer service |
The Client Advocate I provides support and communications with NeoGenomics customers (physicians & medical staff) and couriers (FedEx and contracted couriers); as well as serves as the point of contact for internal customers such as territory business managers (sales), internal doctors, operational teams and senior leadership in relation to specialized diagnostic oncology testing via excellent telephone, written, and chat communication. This is the entry level in the Client Service organization and employees perform the full range of customer service activities; including inside sales functionality. | 11/2/2019 |
| 694 | NeoGenomics Ft. Myers, FL Order Entry Specialist I - Data Integrity AS/AA Exp: 1+ year in healthcare/med billing |
As an Order Entry Specialist I, you will enter patient demographic characteristics and insurance information into a proprietary database using company specific software and internal documents. Additionally, you will input diagnosis codes, charges and verify insurance in accordance with company policies. | 11/2/2019 |
| 695 | NeoGenomics Houston, TX Histotechnologist I AS/AA in histotechnology Exp: 1+ years related |
As a Histotechnologist I, II, III, you will work under general direction to precisely and accurately conduct a variety of routine and specialized histology procedures. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining and equipment maintenance. | 11/2/2019 |
| 696 | NeoGenomics Aliso Viejo, CA Laboratory Assistant I HS Diploma Exp: 1-2 years |
As a Laboratory Assistant you will assist the department technologist in performing various basic laboratory procedures laboratory instrumentation to facilitate production. This in an entry level position in the clinical laboratory job category and employees in this position may not manipulate samples. | 11/2/2019 |
| 697 | NeoGenomics Aliso Viejo, CA Accessioning Technician I AS/BS preferred, HS Diploma min Exp: 1+ year as acessioning technician |
As an Accessioning Technician I you will ensure proper handling of all specimens received and prepare specimens for laboratory testing. You will be performing functions such as matching patient information, data entry, and scanning documents. You will be responsible for reviewing all requisitions for missing information, working closely with Customer Care in order to obtain missing information in a timely fashion, and distributing new information to all departments involved. You will need to report problem holds and provide resolution in a timely fashion. | 11/2/2019 |
| 698 | GenScript Piscataway, NJ Lab Technician - Ligation BS/BA Exp: 0-3 years |
We are looking for a Laboratory technician to assist our daily production tasks. The successful candidate should have biology or related science background, excellent time management skills, strong problem solving ability. He or she will need to work directly with production team, fit with collaborative and competitive culture in GenScript. | 11/2/2019 |
| 699 | GenScript Piscataway, NJ Lab Technician - Plasmid Prep BS/BA Exp: 0-3 years |
We are looking for a Laboratory technician to assist our daily production tasks. The successful candidate should have biology or related science background, excellent time management skills, strong problem solving ability. He or she will need to work directly with production team, fit with collaborative and competitive culture in GenScript. | 11/2/2019 |
| 700 | GigaGen South San Francisco, CA Research Assistant BS/BA Exp: 1-3 years lab experience |
GigaGen seeks a talented, highly motivated Research Assistant to work alongside PhD-level scientists on research funded by a $50 million co-development deal with Grifols, plus Phase II SBIR grants from the NCI and NIAID. 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. | 11/2/2019 |
| 701 | Gilson Middleton, WI Verification and Validation Specialist I BS/BA in sciences Exp: 0-3 years |
The job holder is introduced to and performs a wide variety of laboratory tasks and procedures related to the verification and validation of hardware and software products. Operates and maintains laboratory equipment and computers to perform product verification. Performs lab maintenance tasks. Conducts accuracy and precision analysis on liquid handling instruments. Uses lab methods (HPLC, SPE, PCR, bio-assays, etc.) to verify product function and design | 11/2/2019 |
| 702 | Ginkgo Bioworks Boston, MA Research Associate - Protein Engineering BS/MS in biological sciences/engineering Exp: 1+ years in lab setting |
We are looking for someone who is excited about the field of synthetic biology and loves a challenge. 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. Responsibilities include: Enzyme purification and characterization, Data analysis, Automation of protocols | 11/2/2019 |
| 703 | Glaukos San Clement, CA Engineer, I BS in mechanical engineering Exp: 1-3 years |
Performs a variety of manufacturing engineering activities on ocular related products including manufacturing scale up, development, and sustaining activities. Responsibilities include developing creative solutions to manufacturing problems, development and execution of process, equipment, and product validations, ensuring the proper engineering deliverables are accurately generated, generation of 3D CAD models and 2D CAD drawings for assembly tools and fixtures, test procedures, project management and leadership, and maintaining schedule. May lead manufacturing related project teams with other engineers, technicians, and manufacturing staff with a focus on meeting manufacturing requirements with technically strong, high quality, cost effective approaches. | 11/2/2019 |
| 704 | Glaukos San Clement, CA Regional Clinical Research Associate I BS/BA in biological sciences, nursing or related Exp: 0-2 years as CRA |
Lead/manage assigned sites through regular contact with investigators and site staff to monitor progress, answer questions, and provide guidance during the course of the clinical study. Critically review and analyze site activities through frequent visits and contacts to monitor study sites and performance. Travel to investigative sites to conduct site qualification, initiation, interim monitoring, and close-out visits | 11/2/2019 |
| 705 | GSK Lincoln, NE Production Maintenance Technician AS/AA in lectromechanical Technology or Electronic Engineering Technology Exp: 1-3 years in industrial setting |
As Production Maintenance Technician you will be responsible for maintaining, troubleshooting, calibrating and modifying electrical and mechanical systems and equipment and document work on mechanical, electrical, hydraulic, and pneumatic equipment involved in the manufacture and packaging of pharmaceutical products. | 11/3/2019 |
| 706 | GSK Lincoln, NE Supply Chain – Future Leaders Program BS in business, supply chain, analytics, IT systems, or any sciences/enginnering Exp: 2020 Graduate |
Over three years, our Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You’ll have three stretching rotations within Pharmaceutical or Consumer Healthcare Supply, depending on your area. In both cases, you’ll take on business-critical roles that offer amazing insights into our end-to-end supply chain. You’ll learn about the synergies and challenges that come with delivering optimum value to the business and the customer. | 11/3/2019 |
| 707 | GSK Lincoln, NE Automation Engineer BS in engineering Exp: 1-3 years |
As an Automation Engineer, you will manage and execute projects related to industrial machine automation for both new and existing equipment. Lead the design and installation of instrumentation and control systems in some of the following areas: building automation systems, data systems, process control, DCS and utility PLC’s which are harmonized with GSK-standards. Provide technical support for existing instrumentation and automation systems. Analyze repairs and maintenance requirements in order to proactively address system weaknesses. | 11/3/2019 |
| 708 | GSK East Durham, NY Mechanical Engineering – Future Leaders Program, US – 2020 BS in mechanical/manufacturing/biomedical/etc. engineering Exp: 2020 Graduate |
Over three years, our Future Leaders Graduate Program will challenge and support you to grow professionally and personally. You’ll have three stretching rotations in business-critical roles within consumer healthcare supply. Your responsibilities will depend on your engineering discipline, but whatever your specialist area, you’ll get to meet senior leaders and network with other graduates. You’ll also improve your technical skills while gaining valuable leadership expertise. | 11/3/2019 |
| 709 | GSK Collegeville, PA Reagent Scientist BS ro MS in sciences Exp: 0-3 years |
Development and quality of critical reagents, including characterizing external antibody’s, building isotype-specific antibody reagents, purifying proteins, conducting protein conjugations (e.g. biotin, ruthenium and fluorescent labels), assessing their purity and affinity, and generating certificates of analysis (CofA). Monitor reagents life cycle and characterization to assist with reagent trouble shooting effort. | 11/3/2019 |
| 710 | GSK Carlisle, PA Packaging Operator- First Shift HS Diploma/GED Exp: 0-1 years in manufacturing |
As a Packaging Operator you will manually assemble, glue, tape and package boxes, cases and other material as needed. Activities also involve set-up, operation, and verification of printing, weighing and robotic equipment as well as staging packaging material, documenting, cleaning, and performing in-process quality checks. The work involves lifting up to 50 lb. containers on a regular basis and moving pallets, totes, and film using a hand truck or similar tools. A thorough understanding of each job function within the work center is essential. | 11/3/2019 |
| 711 | GSK Rockville, MD Calibration & Instrumentation HS Diploma/GED Exp: 0-1 years cGMP experience |
As Calibration and Instrumentation Staff you will be responsible for supporting the team to ensure manufacturing systems are current on calibration requirements. You will also assist the team with the calibration process system, laboratory equipment, and facilities related utilities. | 11/3/2019 |
| 712 | Global PharmaTek Edison, NJ Clinical Project Assitant BS in pharmascience,s pharma, health care, etc Exp: 1-2 years |
Responsible for strategic and operational activities of clinical research studies in blood cancer metabolism to ensure adherence to intended timelines and achievements of study goals, while ensuring quality by FDA, EMEA, ICH and GCP guidelines. Providing oversight in clinical research Organization (CRO), Central labs and other external vendors to ensure deliverables are met and methods of communication are developed to facilitate an efficient workflow. Facilitating interdisciplinary activities, participating in the clinical trial working group (CTWG), Site Management Team (SMT), and internal team meetings to meet the goals and established timelines | 11/3/2019 |
| 713 | Global PharmaTek Edison, NJ Equipment Validation Engineer BS in mechanical/industrial engineering Exp: 1-2 years |
Develop, Implement and Install filter integrity testing methods to available automated Filter Integrity Testers (FITs) available on site to verify the integral of the vent filters that will used in the process for WFI Tanks, Autoclaves, supply clean compressed air and as required. Provide technical support in developing, authoring, and executing the Commissioning, Installation and Qualification protocols for the chromatography skids and other supporting equipment that are used in the production of drug | 11/3/2019 |
| 714 | Global PharmaTek Irvine, CA Quality Engineer BS in mechanical engineering Exp: 0-2 years |
The Mechanical Engineer, Research & Development will support the Critical Care Mechanical team working on new product designs, technology development and sustaining of core product lines with an emphasis on hands on new product development. | 11/3/2019 |
| 715 | Pfizer St. Louis, MO Associate Scientist, Cell Line Development BS in cellular/molecular biology or related Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Cell Line Development (CLD) organization. The position will be primarily involved in mammalian CLD portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. The successful candidate will possess excellent aseptic technique and have experience with mammalian cell culture and recombinant protein expression. etc. | 11/5/2019 |
| 716 | Pfizer Andover, MA Associate Scientist, Cell Line Development BS in cellular/molecular biology or related Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Cell Line Development (CLD) organization. The position will be primarily involved in mammalian CLD portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. etc. | 11/5/2019 |
| 717 | Pfizer Groton, CT Technical Associate, Comparative Medicine HS diploma to BA/BS Exp: 1 year |
The Technical Associate’s primary responsibility is to provide basic husbandry, handling, restraint and health surveillance of laboratory animals in compliance with local regulatory requirements. This individual will also provide daily record keeping of common laboratory species, their environments, and provide basic technical assistance (i.e., restraint, injections, bleeds) to other technicians and researchers. Other more specialized functions, depending on interest and aptitude may be assigned in the areas of technical and research services. etc. | 11/5/2019 |
| 718 | Pfizer Sanford, NC Quality Control Associate Scientist BS/BA in related field Exp: No experience necessary for BS/BA candidates |
This position is an analyst role in the QC Bioanalytical laboratory. Experience with ELISA, PCR, and/or slot blot is preferred. Analyst will be responsible for ensuring the routine testing is scheduled and completed within appropriate timeframes as needed for manufacturing to maintain schedules (STAT testing) or the QA disposition group to disposition batches. Other responsibilities may include, SOP revisions, validation/qualification testing support, etc. etc. | 11/5/2019 |
| 719 | Pfizer Groton, CT Associate Scientist, Materials Science BS in pharmaceutical science, chemistry, engineering or other related science Exp: 0-2 years |
Pfizer’s Materials Science group is seeking team members with a desire to bring new, cutting edge medicines to patients around the world. The Associate Scientist, Materials Science position is a laboratory-based position with responsibility for investigating and understanding the solid-state chemistry and particle properties of Pfizer’s drug molecules. Responsibilities include generating and interpreting data using state-of-the-art instrumentation and computer models to allow new medicines to be brought to the market. etc. | 11/5/2019 |
| 720 | PMI Bio. Nashville, TN Chemist I, Analytical Development BS in chemistry, biology or related Exp: 1-2 years |
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. | 11/5/2019 |
| 721 | PMI Bio. Nashville, TN Microbiologist I, Analytical Development BS in biology or related Exp: 0-1 years |
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. | 11/5/2019 |
| 722 | PolarityTE Salt Lake City, UT Research Specialist I BS in biotechnology, engineering, computer science, or related science Exp: 0-2 years |
Under the general supervision of the Director of BME, the Research Specialist I, II or III will support R&D in conducting research projects by contributing to the following: develop protocols for and maintain laboratory equipment; troubleshoot and resolve problems; ensure compliance with lab protocols and safety standards, policies and procedures; performing complex data gathering and analysis. This role serves to assist with conducting pre-clinical research aimed at validating, testing products and discovering, developing innovative medical technologies. etc. | 11/5/2019 |
| 723 | Portola South San Francisco, CA Clinical Trial Associate unspecified Exp: 1+ year(s) |
The CTA will support the operational management and oversight of aspects of a clinical program. The CTA will participate in the activities associated with the evaluation, initiation, management, and close-out of clinical trials within the Clinical Operations Department. The CTA role provides an outstanding opportunity to work in a cross-functional environment and collaborate with colleagues in Clinical Research, Biometrics, Regulatory & QA, and Program Management. This individual will report into the Sr. Director of Clinical Operations. This is an in-house position. etc. | 11/5/2019 |
| 724 | Poseida Therapeutics San Diego, CA Research Associate, In Vivo Gene Therapy MS in immunology, molecular biology, or related Exp: 0+ year(s) |
The Research Associate will play a key role in advancing exploratory gene therapy programs that leverage our cutting-edge piggyBac® DNA Modification technology. Responsibilities: Actively participate in our proprietary gene therapy platform technologies to create new human therapeutic candidates. Develop and perform research involving various in vitro and animal laboratory techniques including ELISA, cell/tissue isolations, microscopy, in vivo procedures and animal imaging. Understand and analyze results, and communicate findings in team meetings. Maintain laboratory equipment and facilities, as required. | 11/5/2019 |
| 725 | Poseida Therapeutics San Diego, CA Temporary Research Technician, Immuno-Oncology BS in immunology, molecular biology or related Exp: 0-3 years |
The Research Technician will support the development of CAR-T cellular therapies against cancer and involve bench work, laboratory studies, and the coordination of research projects with the assistance of a senior lab member and/or the lab director. Please note that this is a temporary position. Responsibilities: Cloning and screening of CAR-T cellular therapies. Studies may include work with molecular biology and cloning techniques, tissue culture of human cell lines, isolation of cells from blood products, virus production, in vitro human cell based immunoassays, and cell separation techniques. | 11/5/2019 |
| 726 | PPD Richmond, VA Associate Scientist - PCR-Molecular Genomics BA/BS Exp: 1+ year(s) |
As an Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Problem solving with assistance pertaining to extraction and/or instrumentation problems. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines. etc. | 11/5/2019 |
| 727 | PPD Richmond, VA Assistant / Associate Scientist - Lab Robotics and Automation BS in biology, chemistry or related laboratory science Exp: 0-2 years |
As an Assistant / Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: 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. etc. | 11/5/2019 |
| 728 | PPD South San Francisco, CA Associate Scientist / Scientist - Small Molecules, Formulation, TGA, HPLC BS in pharmaceutical chemistry, pharmaceutics or related Exp: 1+ year(s) |
As an Associate Scientist/Scientist, you will work onsite at the client lab facility using state-of-the-art technologies involving preparation and dose analysis of formulations to support toxicology, pharmacokinetic, and other in-vivo studies. You will be responsible for laboratory equipment calibrations and verifications, ordering supplies, as well as designing and conducting Pre-formulation characterization of small molecules. etc. | 11/5/2019 |
| 729 | PPD Richmond, VA Assistant / Associate Scientist - Cell Culture - Vaccines Sciences BS in biology, chemistry or related laboratory science Exp: 0-2 years |
As an Assistant / Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: 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. etc. | 11/5/2019 |
| 730 | PPD Middleton, WI Assistant Scientist- HPLC BA/BS Exp: 0-2 years |
As an Assistant Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: 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. etc. | 11/5/2019 |
| 731 | PPD Richmond, VA Assistant / Associate Scientist - Immunochemistry BS in biology, chemistry or related laboratory science Exp: 0-2 years |
As an Assistant / Associate Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis skills are an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: Problem solving with assistance pertaining to extraction and/or instrumentation problems. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines. Manages QC/QA responsibilities without supervisor or QA input. etc. | 11/5/2019 |
| 732 | PPD Middleton, WI Assistant Scientist - Physical and Chemical Characterization BA/BS Exp: 0-2 years |
As an Assistant Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and sample analysis serves as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. Responsibilities: 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. etc. | 11/5/2019 |
| 733 | PRA Health Sciences Raleigh, NC Associate Clinical Data Coordinator BS/BA Exp: None required |
Supports and leads the clinical data review activities that contribute to delivery of an analyzable database. Responsibilities: Ensures trial deliverables are achieved in terms of timeliness and quality. Reviews clinical and external data for subjects enrolled in clinical research protocols based on edit specifications. Executes data validation programs and reports to facilitate data review. Issues clear, accurate, and concise queries to investigational sites. etc. | 11/5/2019 |
| 734 | Precision Biosciences Durham, NC Associate Process Engineer, Upstream MS in chemical engineering, biological engineering, or related Exp: 0-2 years |
The Associate Process Engineer, Upstream will work within the Process Development team and will participate in the development of upstream cell culture, delivering best-in-class process design for viral vector drug substances and drug products, for the development of in vivo and ex vivo gene therapies. The candidate will support the process development, process characterization and tech transfer of said processes for GMP manufacturing. The candidate will assist in the clinical progression of in vivo and ex vivo gene therapies by designing and executing process development experiments across a variety of process scales. etc. | 11/5/2019 |
| 735 | Precision Biosciences Durham, NC Associate Process Engineer, Downstream MS in chemical engineering, biological engineering, or related Exp: 0-2 years |
The Associate Process Engineer, Downstream will work within the Process Development team and will participate in the development of purification processes, delivering best-in-class process design for viral vector drug substances and drug products, for the development of in vivo and ex vivo gene therapies. The candidate will support the process development, process characterization, and tech transfer of said processes for GMP manufacturing. The candidate will assist in the clinical progression of in vivo and ex vivo gene therapies by designing and executing process development experiments across a variety of process scales. etc. | 11/5/2019 |
| 736 | Endo Pharmaceuticals Chicago, IL Sales Representative - Chicago BS/BA Exp: 1 year in business/biopharma/sales |
Accomplishes targeted sales and increases the market share of key (bio) pharmaceutical products. Calls on a select number of high value physicians in a specified geographic area and focuses on establishing durable relationships, effectively delivering product information, and aiding in training. Helps customers develop reliable processes for reimbursement and access. Is comfortable providing information to the entire office staff and has the ability to identify new sales opportunities and leads in their territory. | 10/26/2019 |
| 737 | Endo Pharmaceuticals Harsham, PA Manufacturing Associate l DSP BS/BA Exp: 0-3 years in biopharmacuetical manufacturing |
The Manufacturing Associate I – Fermentation works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture Collagenase Clostridium Histolyticum (CCH) bulk drug substance (BDS). This role is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. | 10/26/2019 |
| 738 | Envigo Cumberland, VA Study Technician II AS/AA or BS/BA in life sciences, animal technologies, etc. Exp: 6 months as animal technican |
To collect, document, and manage pertinent data including animal observations, test material administration, and clinical sample collection in compliance with appropriate SOPs and regulatory agency guidelines. To monitor animal health and welfare in compliance with the Animal Welfare Act and help maintain facilities for AAALAC compliance. Assess and document clinical observations, body weight data, food consumption data, environmental data, and other data on the appropriate data collection system (or by hand when necessary). | 10/26/2019 |
| 739 | Envigo Alice, TX Vet Tech 1 AS/AA or BS/BA in life sciences, animal technologies, etc. Exp: 6 months as animal technican |
Works closely with the veterinary staff in supporting the nonhuman primate (NHP) colonies in Alice, TX. Monitors animal health and welfare with the opportunity to work with different NHP species. Position includes assisting all departments onsite including the hospital, behavior, quarantine, shipping and outside colony teams. Performs technical medical procedures in the various departments and assists the veterinary team in all aspects of animal care. | 10/26/2019 |
| 740 | Envigo Madison, WI Machine Operator HS Diploma/GED Exp: 0-2 years |
Machine Operator to operate equipment to produce high quality diet in accordance with Envigo Teklad standards. Operate automated manufacturing process in accordance with established standard operating procedures. Follow production instructions of immediate supervisor to insure a safe work environment. To ensure a safe work environment; wear all PPE and all established safety procedures without exception. | 10/26/2019 |
| 741 | Envigo Cumberland, VA Animal Care Technician HS Diploma/GED Exp: 0-2 years |
Conduct routine husbandry and animal health procedures in accordance with departmental SOP’s and maintaining USDA and AAALAC compliance. Operate the power washer to clean and sanitize runs, feeders, walls, building and floors per SOPs. Ensure that all occupied runs have adequate feed available at all times. Perform general house cleaning throughout the support areas. Humane care and treatment of animals. | 10/26/2019 |
| 742 | Envigo Indianapolis, IN Animal Care Technician HS Diploma/GED Exp: 0-2 years |
To care for laboratory animals, their environment, and maintain records of their productivity and growth. To learn how and to maintain animals in inventory, to prepare animals for shipment, and to medicate or inject animals. Provide food, water, and clean housing to animals according to a rigid schedule. Maintain detailed records of animal production and inventory in precisely weighed and aged groups. | 10/26/2019 |
| 743 | Enzo Biochem Farmingdale, NY Medical Technologist- Generalist BS/BA in lab science, medical technology, etc. Exp: 1 year in medical lab |
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. | 10/26/2019 |
| 744 | Abcam Cambridge, MA Logistics Technician HS Diploma/GED or BS/BA Exp: Entry Level |
Process incoming shipments from suppliers, ensuring accuracy of all product data. Aliquot product into vials and assemble kits for customer orders and global stocking. Work with colleagues across the business to resolve discrepancies quickly. Maintain accurate inventory levels using both manual and automated systems. Fulfill customer orders using internal systems and processes, ensuring accuracy of all products in all orders. Work with teammates to improve the efficiency and accuracy of any processes implemented within the Logistics Department using creativity and resourcefulness. | 10/26/2019 |
| 745 | Abcam Burlingame, CA Research Associate - IVD BS in biological sciences Exp: 1-2 years in biological sciences |
Based in our Burlingame Office, this manufacturing position is a great opportunity to transition into the medical device Industry! This role will be responsible for carrying out GMP manufacturing of IVD IHC primary antibodies according to the requirements of SOP’s, batch production records, and approved protocols. Perform immunohistochemical (IHC) stain for development or manufacturing of IHC antibody, staining kits and ancillary reagents. | 10/26/2019 |
| 746 | Eurofins West Point, PA Biochemist BS/BA in biochemistry, biology, chemistry Exp: 1-3 years |
Perform assays on vaccine products, process intermediates, and related experimental samples using SDS-Page, Capillary Electrophoresis, ELISA, Biacor, nucleic acid quantification and other biochemical/analytical tests(e.g., spectrophotometric, electrophoretic, immunochemical methods). Maintain records and test results following good manufacturing practices (GMP). | 10/26/2019 |
| 747 | Eurofins Malvern, PA Bioassay Method Development Scientist BS or MS in sciences Exp: 0-2 years |
Perform method development, optimization, validation, and transfer of Bioassays. Immunoassays and PCR analysis. Troubleshoot method and instrumentation problems. Initiate and perform investigations. Carry out method transfers and feasibility studies. Validation protocols and reports | 10/26/2019 |
| 748 | Eurofins Columbia, MO Associate Scientist, Stability and Batch Release MS in biological sciences or engineering Exp: 0-2 years |
he Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. | 10/26/2019 |
| 749 | Eurofins Columbia, MO Associate Scientist, Biotech MS in biological sciences or engineering Exp: 0-2 years |
Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biotech team located in Columbia, Missouri. The Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. | 10/26/2019 |
| 750 | Eurofins Kalamazoo, MI Associate Scientist BS/BA in biolgical sciences, or chemistry Exp: 0-2 years |
Protein purification (mAbs, therapeutic proteins, reagent proteins) by affinity, ion-exchange, HIC, or other native methods. Use and troubleshoot the AKTA suite of purification instruments and automated high-throughput systems. Analytical characterization of proteins by SDS-PAGE, CGE, Western Blot, and analytical SEC. Quantitate proteins by UV and BCA assay. Maintain electronic laboratory notebooks and records in accord with scientific protocol | 10/26/2019 |
| 751 | Eurofins Dayton, NJ Analytical Chemist BS/BA in biolgical sciences, or chemistry Exp: 0-2 years |
Assist the Study Director with all phases of study design, scheduling and conduct. Act proactively to identify problems and potential problems. Assist in writing, reviewing and editing reports, protocols and SOP’s. Set-up and conduct experiments in accordance with Protocol and SOP's. Efficiently carry out procedures necessary to complete each project with minimal supervision. Meticulously maintain precise records of all experiments in accordance with good laboratory practices. | 10/26/2019 |
| 752 | Eurofins Phoenix, AZ 3rd Shift Aseptic Manufacturing Associate HS Diploma/GED Exp: 6 months in GMP manufacturing |
Manufacturing Associate performs a variety of environmental service duties to maintain and sterilize the manufacturing suite and equipment. Ensure all cleanroom areas and equipment are clean, disinfected and ready for production of sterile medical products. Operate Microsoft Applications (for charting, presentations, etc.) and other computer based systems utilized in the manufacturing department (i.e., MES, HMIs, etc.). Follow standard procedures and execute activities independently, as well as in a team environment | 10/26/2019 |
| 753 | Evonik Milton, WI Operations Technician HS Diploma/GED Exp: 0-2 years production experience |
Fill pails, drums, and totes with raw materials, intermediates, and finished products (including forklift operation). Run reactors/product blends per operating directions. Clean transfer lines within the plant and to the drumming station. Unload empty packages and stage for use, load box trailers with product for transfer. Maintain good housekeeping, perform housekeeping audits, run karl fisher analysis on titrators, and assist in filter change-outs, perform fork-lift inspections, etc. | 10/26/2019 |
| 754 | Evonik Janesville, WI Plant Process Engineer BS or MS in chemical engineering Exp: 1-2 years process engineering |
Support and execute plant productivity projects to drive continual improvements in the areas of growth, expansion, production capacity and cost reduction to meet business and OPTECH initiatives and targets. Generate detailed scope of work documents for CAPEX and plant expense based projects that include equipment and safety device sizing and specifications, piping design, materials of construction, control strategies and safety circuits and procedures. Provide day-to-day process engineering and technical support to plant operations including troubleshooting efforts. Support and execute plant productivity projects to drive continual improvements in the areas of growth, expansion, production capacity and cost reduction to meet business and OPTECH initiatives and targets. Generate detailed scope of work documents for CAPEX and plant expense based projects that include equipment and safety device sizing and specifications, piping design, materials of construction, control strategies and safety circuits and procedures. Provide day-to-day process engineering and technical support to plant operations including troubleshooting efforts. | 10/26/2019 |
| 755 | Evonik Lafayette, IN Process Engineer BS in chemical engineering 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. | 10/26/2019 |
| 756 | Exelixis Alameda, CA Outsourcing Operations Analyst I MS/MA Exp: 1 year related experience |
This role assists with financial operations and reporting in Global Strategic Outsourcing Department. Responsibilities include supporting the Associate Director with contract administration, budget estimates, payment processing and reporting to facilitate the outsourcing strategies and activities of the Research & Development Organization. This role also requires the ability to obtain appropriate information to administer contracts and payments for outsourced agreements and communicates regularly to internal and external stakeholders on status of contracts and payment requests. | 10/26/2019 |
| 757 | Exelixis Alameda, CA Outsourcing Operations Analyst I MS/MA Exp: 1 year related experience |
This role assists with financial operations and reporting in Global Strategic Outsourcing Department. Responsibilities include supporting the Associate Director with contract administration, budget estimates, payment processing and reporting to facilitate the outsourcing strategies and activities of the Research & Development Organization. This role also requires the ability to obtain appropriate information to administer contracts and payments for outsourced agreements and communicates regularly to internal and external stakeholders on status of contracts and payment requests. | 10/26/2019 |
| 758 | Biotechne San Jose, CA Manufacturing Technician I AA or HS Diploma/GED in biotech, chemistry, biology Exp: 1+ years in manufacturing |
Bio-Techne’s Protein Platform Division is looking for a Manufacturing Technician with a motivation to participate in the growth of a fast-paced company engaged in cutting edge biological research. The successful candidate will work with other members of the Reagent production team to make great products, performing tasks involving plate filling, labeling, vialing, and finishing materials. Operation of semi-automated liquid dispensing equipment is integral to the job. | 10/26/2019 |
| 759 | Biotechne Newark, CA Research Associate, Probe Design BS in biological sciences Exp: 0-2 years |
We are seeking a Research Associate Scientist to join the R&D probe design team. The candidate will be responsible for ordering probes for synthesis and updating probe databases as well as other supportive functions. Prepare and send probe sequences to vendors for oligo synthesis. Communicate with internal stakeholders (Sales, Operations, etc) promptly. Prepare various files and upload to internal databases | 10/26/2019 |
| 760 | Biotechne San Jose, CA QC Technician BS in biological sciences Exp: 1+ years in manufacturing |
This position’s responsibilities include QC testing in the Reagent and Consumables Manufacturing department at ProteinSimple. The primary responsibility will be working with QC and Production teams to schedule and test Maurice and Simple Western consumables in a timely manner.Precise and meticulous observation and recording of all details of the assay, which are not limited to but including: lot numbers, and physical observations of materials | 10/26/2019 |
| 761 | Biotechne San Jose, CA Manufacturing Laboratory Technician AA or HS Diploma/GED in biotech, chemistry, biology Exp: 1+ years in lab or manufacturing |
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. Document production batch records/travelers, and computer data entry | 10/26/2019 |
| 762 | Biotechne Minneapolis, MN Advanced Research Associate - Luminex Development MS in biological sciences or engineering Exp: 0-2 years |
The responsibilities of this position are to assist with feasibility, product development, verification, 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. | 10/26/2019 |
| 763 | Exsurco Medical Wakeman, OH Assembly Technician HS Diploma/GED Exp: 3 months in factory experience |
Primary role is to perform all forms assembly activities including equipment setup and tear down where required as well as in-process verifications. In addition, this position includes several cross-functional responsibilities comprising Shipping, Receiving, Job Picking, Warehousing and Plant Cleaning and some Maintenance activities. This position also has responsibilities associated with Servicing returned products (disassembly and reassembly, diagnosis and report writing). | 10/26/2019 |
| 764 | Facet Atlanta, GA QUALITY ENGINEER BS in engineering or sciences Exp: 1-3 years in quality engineering |
The Quality Engineer plans and directs activities concerned with development, application, and maintenance of quality processes, materials, and products. Additionally, responsible for investigation manufacturing and customer nonconformance’s, determining root causes and corrective actions, reviewing and approving protocols and final reports and developing product specifications and sampling plans. | 10/27/2019 |
| 765 | Fate Therapuetics San Diego, CA Research Associate, Cancer Immunotherapy BS in biological sciences Exp: 0-3 years in lab setting |
The candidate’s primary responsibility will be to generate lentivirus for editing and production of CAR-T cells in support of research efforts at Fate. Experience with current molecular biology techniques used for editing and engineering of hematopoietic cells is highly desired. The successful candidate will have excellent oral and written communication skills. | 10/27/2019 |
| 766 | Fate Therapuetics San Diego, CA Clinical Trial Associate BS/RN in relevant sciences Exp: 1 or more year hands on experience in clinical trial management |
Fate’s clinical operations group is seeking amotivated and talented individual to support development and management of an electronic trial master filesystem(Veeva)and assistour clinical trial managerswith administrative and project-specific support related to the conduct of clinical studies. The successful candidate will assure adherence to protocol(s) and GCP/ICH guidelines and applicable regulations. The ideal candidate will be familiar withphase I-IV protocols and have hands-on experience in developing and maintaining electronic clinical trial management systems. | 10/27/2019 |
| 767 | Ferring Parsippany, PA Technician, QC Micro (2nd Shift) BS/BA or MS in biology or related Exp: 1 year in QC microbiology |
To perform laboratory QC Microbiological testing for in-process and finished product, water sampling testing, and routine and batch processing environmental monitoring in aseptic classified cleanrooms. Perform Bioburden, Endotoxin, Total Plate Count, Coliform, Bacteriostasis &Fungistasis (B&F) and Biological Indicator testing. Perform clean utilities (compressed air, Nitrogen, WFI/DIW and Clean Steam) sampling and testing. Initiate and investigate microbiology related deviations (NCEs/NOE), OOS investigations, and implementing appropriate CAPAs as needed. | 10/27/2019 |
| 768 | Ferring Parsippany, PA Process Equipment Engineer BS/BA in sciences or engineering Exp: 0-2 years |
Responsible for process equipment engineering, overseeing, guidance, scheduling and coordination required to fully implement process equipment engineering projects in order to support manufacturing, QA, Tech services, IT, Procurement, other departments, external vendors and government agencies as required. The incumbent is considered a Subject Matter Expert (SME) responsible for all aspects of production equipment (complete sterile manufacturing train) and its interfaces including mechanical, electrical, process plumbing, and safety interfaces. The incumbent must have superior troubleshooting and problem solving ability to ensure minimal down time and interruption to production schedule. The incumbent interacts with Production, QA, Tech services, IT, and other departments as necessary obtain all applicable stake holder(s) information and decisions to collaborate high quality low risk results. | 10/27/2019 |
| 769 | Bfibrocell Exton, PA GMP Support Technician AS/AA Exp: 1 year |
The GMP Support Technicianwill perform a variety of tasks in support of the daily production of sterile cell therapy product. Operations are predominately performed within a cleanroom environment under Current Good Manufacturing Practices (CGMP) conditions. Provides operational support for manufacturing activities including media/reagent preparation, kitting, cell freezing and equipment/materials staging. Follow batch records, SOP’s and other cGMP documentation; complete all documentation in a clear and concise fashion | 10/27/2019 |
| 770 | Finch Somerville, MA Research Associate BS/BA in biological sciences Exp: 1-2 years industry experience |
Finch is looking to hire a detailed-oriented and driven Research Associate, Analytical Development, who will be responsible for developing and conducting analytical methods for drug products in Finch’s pipeline. This individual will ensure Finch microbial products meet standards by performing microbial analytical procedures to characterize in-process and commercial microbial samples. As an integral part of this team, the successful candidate will carry out laboratory work, establish protocols, and support cross-functional teams in Research and Development, Quality and Manufacturing. This position reports to the Senior Scientist. | 10/27/2019 |
| 771 | Finch Somerville, MA Process Development Engineer BS/BA in chemical/biomedical engineering, or related Exp: 1-3 years |
Assist with troubleshooting, root cause analysis and identification of corrective actions to support Pharmaceutical Development or GMP Manufacturing equipment and process issues. Support efforts to scale-up & undergo technical transfer of production processes to GMP Manufacturing. Lead planning, execution, and documentation of studies related to design of novel drug products. Work cross-functionally across Quality, Research, Clinical, and Manufacturing teams to achieve company goals. | 10/27/2019 |
| 772 | Flexion Multiple Locations, NA Flex Sales Representative BS/BA Exp: 1-3 years sales experience |
Promote Flexion's product(s) via the telephone (outbound and/or inbound calls) and in person (field visits) by engaging assigned HCP targets in in-depth program discussions to attain individual, territory and company goals for sales, market share, etc. In preparation for field activities when deployed to assigned territory or as part of vacancy management coverage. Coordinate and align a strategic field call plan with the Regional Sales Director prior to deployed into vacant territory. Verify and complete required data entry into the CRM systems, such as details of the target’s responses and any follow-through actions. | 10/27/2019 |
| 773 | Fluke Omaha, NE Sales Engineer BS/BA in engineering or technical field Exp: 0-3 years |
You will be working under the leadership of a Sr. Sales Engineer using your technical knowledge to support key sales efforts with our manufacturer representative agencies, distribution partners, and end-users and proactively set and meet stretch goals. Actively promote products and solutions and achieve sales quota by building rapport, providing training and support, and making end user calls with representative agencies and distribution account managers. Work under the direction of the Sr. Sales Engineer to drive the activities and performance of assigned representative agencies. | 10/27/2019 |
| 774 | Fluke Everette, WA Quality Engineer BS in engineering Exp: 1-3 years in quality improvement |
The Quality Engineer II will provide quality engineering and continuous improvement leadership to the operations, engineering, and quality organizations within Fluke at our headquarters in Everett, WA. They will be responsible for employing advanced quality engineering tools and the Fortive Business System tools in partnership with design and sustaining engineering, procurement, supplier quality, and operations to achieve continuous improvement in product safety, reliability and cost of quality. | 10/27/2019 |
| 775 | FORMA Therapeutics Watertown, MA Research Assoc/Sr Research Assoc, Biology BS or MS in biology Exp: 0-2 years |
The Biology Team at FORMA Therapeutics seeks a Research Associate/Senior Research Associate with a strong background in cancer biology to contribute to FORMA’s pre-clinical and clinical projects. The ideal candidate will be a highly motivated individual with a strong technical background in cancer biology. Develop, optimize and perform assays using molecular biology procedures and technologies including qPCR, quantitative western blots, ELISA. In vitro culture of cancer cell lines and primary cells as well as blood/tissue is required. | 10/27/2019 |
| 776 | Foundation Medicine Cambridge , MA Billing and Reimbursement Associate HS Diploma/GED Exp: 1+ years in customer service |
The Associate, Billing and Reimbursement contributes to the overall patient access to FMI products through support and education. The position supports the daily queues of incoming accessioned cases to review for complete and accurate billing information to determine the party responsible for payment, including benefits investigation and prior authorization processing. The incumbent acts to minimize reimbursement as a barrier to receiving physician orders and is responsible for answering questions by internal and external customers on billing inquiries, working with third party insurance companies and completing manual charge entries. | 10/27/2019 |
| 777 | Foundation Medicine Cambridge , MA Molecular Technologist I BS in biology or life sciences Exp: 1 year in CLIA/CAP lab |
We are currently looking to add to our Clinical Lab staff at various levels and shifts. Perform highly complex testing according to established SOPs (NGS library prep, hybridization, and sequencing). Operate automated 8-span and 96-head liquid handling platforms for sample processing. Complete projects fitting of level of expertise and is able to deliver results with minimum guidance. | 10/27/2019 |
| 778 | Foundation Medicine Cambridge , MA Laboratory Research Assistant BS in biological sciences Exp: 1+ year in science/technical work |
The Laboratory Research Assistant I is a core member of the Product Development team. This position supports all Product Development laboratory personnel who are developing the next generation of diagnostic assays. This position may include equipment maintenance, sample repository management, and reagent preparation in addition to other tasks in a highly complex laboratory environment. | 10/27/2019 |
| 779 | Foundation Medicine Cambridge , MA Client Services Representative I - Temp to Perm HS Diploma/GED Exp: 1 or more in service field |
The Client Services Representative is a vital position at FMI tasked with the responsibility of responding to and resolving a wide range of client inquiries and requests as well as acting as a liaison between departments within FMI, and between FMI and its partners, customers and the patient. The incumbent operates in a supportive function within the fast-paced Client Services department. | 10/27/2019 |
| 780 | Foundation Medicine Cambridge , MA Client Services Representative I - Mid Shift (Temp to Perm) HS Diploma/GED Exp: 1 or more in service field |
The Client Services Representative is a vital position at FMI tasked with the responsibility of responding to and resolving a wide range of client inquiries and requests as well as acting as a liaison between departments within FMI, and between FMI and its partners, customers and the patient. The incumbent operates in a supportive function within the fast-paced Client Services department. | 10/27/2019 |
| 781 | Fresenius Kabi Canton, MA CHEMIST, METHOD DEVELOPMENT MS in chemistry Exp: 1-3 years |
The Chemist, Method Development has broad expertise in routine as well as complex chemical methods of analysis. The incumbent conducts all aspects of Quality Control testing including method development, method validation, experimentation, routine and non-routine quality control testing, and record keeping. The incumbent must be able to develop, validate, and implement methods that meet project needs. The incumbent is typically assigned the more complex test methods due to their advanced training in specialized methods of analysis. The position is responsible for conducting studies with increasing complexity in nature and solving problems to ensure a robust method can be performed in the laboratory. | 10/27/2019 |
| 782 | Fresenius Kabi Grand Island , NY QC TECHNICIAN II Microbiology 2nd Shift AS/AA or BS/BA in life sciences, animal technologies, etc. Exp: AS/AA: 1-2 years, BS/BA: 0 years |
This position serves in the capacity of performing general laboratory tasks of testing finished products, stability, raw material, utilities, and monitoring for environmental control, as well as supporting validations of rooms, equipment and materials. This position reports to the supervisor for the functional area to which they are assigned and has no direct reports. The QC Technician II position works closely with other departments, such as validations, chemistry, Operations, Product Development, Quality Systems and Product Release to assure the support of the Microbiology department on various projects, studies and routine tasks. | 10/27/2019 |
| 783 | Fresenius Kabi Chicago, IL VALIDATION ENGINEER BS/BA in science or engineering Exp: 1-3 years in cGMP facility |
Responsible for providing technical support to operations in terms of equipment/system/process initial validation and equipment/system/process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 10/27/2019 |
| 784 | Fresenius Kabi Grand Island , NY ASSOCIATE INVESTIGATIVE WRITER BS/BA Exp: 1-2 years in pharma manufacturing or cGMP |
Works with Supervision and Investigative Writers to efficiently and thoroughly investigate deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the quality related deficiencies identified during the investigation process. Responsible to recommend proactive corrections, corrective actions and preventative actions based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of product discards, field actions, or recalls. The position requires working with moderate supervision to manage assigned investigations from initiation to completion. | 10/27/2019 |
| 785 | Fresenius Kabi Grand Island , NY ASEPTIC CONTROL OPERATOR I HS Diploma/GED Exp: 0-2 years |
Responsible for the operation and performance of high speed pharmaceutical equipment in a clean room (class 100) environment. Aseptic Control Operators are responsible for the cleaning, changeover, setup, startup, operation, and breakdown of filling lines. Additionally, they may be assigned tasks related to the general upkeep of the clean rooms, such as unloading ovens and sterilizers, performing routine cleaning, and performing minor maintenance. All of these activities are governed by strict procedures and regulations and require a high degree of training. Therefore, Aseptic Control Operators must complete all required training, and follow all applicable Standard Operating Procedures, Batch Records, and Protocols, and must be familiar with current Good Manufacturing Practices. | 10/27/2019 |
| 786 | Fresenius Kabi Bensenville, IL ASSOCIATE SUPPLY CHAIN ENGINEER BS in industrial engineering Exp: 1-3 years |
Assists in observation, data collection, and data analysis used in the improvement of all distribution center operational processes, including inbound, outbound, and inventory control functions for the US Fresenius Kabi finished goods distribution network. This role will report to the Senior Manager Supply Chain Solutions. | 10/27/2019 |
| 787 | Pace Analytical Maplewood, MN Lab Analyst - Optics BS in engineering, physics or related Exp: 0-1 years |
This candidate will perform routine lab experiments involving optics in a corporate research lab. The research project testing is completed as part of a process group in high throughput laboratory. RESPONSIBILITIES: Operate and maintain a variety of laser and optical testing instruments. Work with optical alignment on optical bench using light sources (white light, lasers, LEDs) and imaging systems (cameras, photodiodes). Sample collection, preparation, routine analysis, and interpretation results. etc. | 10/29/2019 |
| 788 | Pace Analytical Maplewood, MN Chemist - HPLC & GC Pharmaceutical BS in chemistry or related Exp: 0-3 years |
Candidate will perform analytical testing to support product development of pharmaceutical inhalation devices. RESPONSIBILITIES: Assist higher level analysts with product or method development work. Follow established methods to complete stability testing. Provide testing of customer products using HPLC, UPLC, and some GC. Comply with FDA guidelines and SOPs in a cGMP environment. etc. | 10/29/2019 |
| 789 | Pace Analytical Maplewood, MN Analytical Chemist BS in chemistry or related Exp: 1-2 years |
Seeking an analytical chemist to perform QC analysis of inhalation device components. RESPONSIBILITIES: Sample preparation and analysis using GC-MS and GC-FID. Testing methods using LC is also possible. Perform analysis on inhalation device components - performing extractable and QC testing on plastic, metal, and rubber components. Perform appropriate documentation of work in a GMP environment utilizing Electronic Lab Notebook (ELN), LIMS, and other software. etc. | 10/29/2019 |
| 790 | PacBio Menlo Park, CA Senior Technician, Manufacturing BS in mechanical, electrical, optical, or industrial engineering Exp: No expeience necessary for BS candidates |
Pacific Biosciences is seeking a talented Senior Manufacturing Technician to align, test, and calibrate complex opto-mechanical DNA sequencing systems. Responsibilities: The Manufacturing Technician is responsible for building and testing complex third generation DNA sequencing instruments. Manufacturing technicians are responsible for on-time completion of assigned instrument builds while following a tightly defined process for recording test results, documenting encountered issues, and troubleshooting issues to resolution. Some additional responsibility may include highlighting process improvements, redlining documents, and providing feedback to manufacturing engineers. etc. | 10/29/2019 |
| 791 | PACT Pharma South San Francisco, CA Senior Quality Control Associate MS Exp: 1+ year(s) |
We are currently recruiting for QC Associate, reporting to Manager of Quality Control. This position will be based in South San Francisco. | 10/29/2019 |
| 792 | PACT Pharma South San Francisco, CA Research Associate MS in immunology, immuno-oncology, or related Exp: 1+ year(s) |
We are currently recruiting for Research Associate in the Tumor Immunology group. The person in this role will be responsible for performing immunological assays to functionally characterize the patient private NeoE-specific T cells, as part of product selection for the manufacture of the adoptive cell therapy product (neoTCR-P1). This process is performed in a GMP-like laboratory setting. The candidate should enjoy operating in an exceptionally dynamic and cooperative environment and will communicate results to and coordinate efforts with a larger cross-disciplinary team of immunologists, biologists, engineers and bio-informaticians. | 10/29/2019 |
| 793 | PAR Pharmaceutical Rochester, MI Chemist II MS in chemistry, chemical engineering, or related Exp: 1+ year(s) |
The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Detects, participates and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. etc. | 10/29/2019 |
| 794 | PAR Pharmaceutical Rochester, MI Process Engineer I MS in engineering or chemical engineering Exp: 1+ year(s) |
The Process Engineer I, with guidance, performs various duties related to optimization and analysis of production processes, new products, processes and technology transfers. Prepare and execute engineering study protocols, manufacturing and packaging experimental / feasibility study / validation batch records and protocols and complete interim and / or final summary reports for marketed and new products. Perform or assist on-site and site-change technical transfer, scale-up or scale-down factor evaluation, manufacturing / packaging process and equipment troubleshooting, and SOP preparation and review. etc. | 10/29/2019 |
| 795 | Paragon Gene Therapy Harmans, MD Quality Assurance Associate I/II - Floor Support BS in an engineering or science field Exp: 1 year |
Quality Associate I or II (QA Floor Support) is responsible to provide Quality Assurance support real-time for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product to be used for human consumption. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. etc. | 10/29/2019 |
| 796 | Paragon Gene Therapy Harmans, MD Manufacturing Associate I - GMP Bioprocess AS/BS in a scientific or engineering discipline Exp: 0-1 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. Key Responsibilities: Performs Processing Steps and/or Manufacturing Support activities, monitoring process against the batch record. etc. | 10/29/2019 |
| 797 | Paramit Morgan Hill, CA Manufacturing Engineer 1 BS in mechanical, electrical, or industrial engineering Exp: 0-1 years |
Entry manufacturing engineering role in a dynamic and fast growing manufacturing company. Working with advanced products and processes in the revolutionary life sciences and medical instrumentation industry. Providing technical support to our manufacturing operations to overcome challenges and implement solutions. | 10/29/2019 |
| 798 | Paramit Morgan Hill, CA Test Development Engineer I BS in mechanical, electrical, or industrial engineering Exp: 1 year |
The Manufacturing Test Development Engineer I learn the inside details on the test development that includes creating test programs for AOI ( automated optical inspection ), AXI ( automated x-ray inspection ) and ICT ( in-circuit test ). The engineers get to use their analytical skills to create a suite of test scripts that can detect defects that human eye cannot catch and produce high quality PCBA products. | 10/29/2019 |
| 799 | PBL Assay Science Piscataway, NJ Assay Services Scientist I/II BS in a life science Exp: 1+ year(s) |
The Assay Services Scientist I / II works primarily with cell culture-based bioassays, executing antiviral bioassays, ELISAs and other highly sensitive immunoassays for characterizing proteins and reagents; analyzing data and drafting client reports; and developing new and custom assays to support the growth of the Assay Services Group. ESSENTIAL DUTIES AND RESPONSIBILITIES: Execute immunoassays on ELISA, and other highly sensitive platforms like Electrochemiluminescence (MSD), Single Molecule Array (Simoa), and Single Molecule Counting (Erenna). Execute antiviral and antiproliferative cell-based bioassays. etc. | 10/29/2019 |
| 800 | PBL Assay Science Piscataway, NJ Laboratory Technician BS in a biological science Exp: 0-3 years |
The Laboratory Technician is responsible for product manufacturing and ELISA kit optimization and stability testing following established guidelines and procedures and completing required documentation. The individual will routinely analyze raw data and generate summaries of work performed in compliance with Standard Operating Procedures (SOPs). The Laboratory Technician will make judgements based on knowledge and expertise as to the accuracy and reliability of analytical results; identify and report problems with results to supervisor; participate in investigations and data analyses; and troubleshoot instruments and methods. etc. | 10/29/2019 |
| 801 | PBL Assay Science Piscataway, NJ Quality Control Scientist I BS in a biological science Exp: 1-2 years |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability testing of interferons, antibodies, and manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays or immunoassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Product Development, Assay Services, or Manufacturing departments as needed: such additional duties may include designing and performing ELISA testing protocols, custom bioassays, and solution preparation. etc. | 10/29/2019 |
| 802 | PBL Assay Science Piscataway, NJ R&D Scientist I MS Exp: 0-2+ years |
The R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes design, development, and Manufacturing transfer of bioanalytical assays for product commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. etc. | 10/29/2019 |
| 803 | Penumbra Roseville, CA Quality Engineer BS in an engineering or science field Exp: 1-5 years |
As a Quality Engineer at Penumbra, you will participate in all aspects of product manufacturing in order to ensure the highest level of quality in new and existing products, and their compliance to applicable regulations and standards. You will apply your passion for detailed analysis to identifying problems and determining the appropriate course of action. You will be looked to for ensuring compliance and building a culture of quality within your project teams. etc. | 10/29/2019 |
| 804 | Performance Validation unspecified, Level 1 Staff Validation Specialist BS in the life sciences or related Exp: Entry level |
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. | 10/29/2019 |
| 805 | Performance Validation unspecified, Level 1 Staff Validation Engineer BS in mechanical, chemical, or biomedical engineering Exp: Entry level |
Performance Validation is seeking full-time Level 1 Validation Engineer/Specialists in the following locations: Indiana, Michigan, Illinois, and Kansas. The Level 1 Validation Engineer/Specialist is an entry level position and reports directly to the Division Director or Manager and is assigned to one or more project teams to perform work for Performance Validation’s customers. etc. | 10/29/2019 |
| 806 | Personalis Menlo Park, CA Laboratory Assistant (Temp to Perm) BS in molecular biology 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. Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. This position is 3 months temp to Perm. etc. | 10/29/2019 |
| 807 | Personalis Menlo Park, CA Research Associate - Operations (Temp to Perm) BA/BS in a biological discipline Exp: 0-2+ years |
Located in Menlo Park, CA, we are seeking a talented and highly motivated Research Associate to join our Operations Team. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization within budgetary constraints while adhering to quality technical standards. This is a 3 months temp to hire position. We have Multiple openings for swing and day shifts that include one weekend day (Tues - Sat or Sun - Thurs). etc. | 10/29/2019 |
| 808 | Nephron West Columbia, SC Microbiology Analyst I BS in biology, microbiology, or other life science Exp: 1+ years |
Position Summary: Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Demonstrate high proficiency level on tests performed. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. 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. etc. | 10/21/2019 |
| 809 | NGM Biopharmaceuticals South San Francisco, CA Research Associate - Nonclinical Safety (Temp to Perm) BS in a life science Exp: 1+ years |
NGM Biopharmaceuticals, Inc. is seeking a highly motivated Research Associate to join our Nonclinical Safety development group. This will be a temp to full time position. | 10/21/2019 |
| 810 | Nitto Milford, MA Operations Program Associate BS in industrial, chemical, or mechanical engineering Exp: 0-3 years |
Assist in managing a portfolio of strategic projects driven by the organization’s on-going continuous improvement efforts. Analyze and improve complex systems impacting the organization’s performance as it pertains to its customers and key stakeholders. Perform duties as required for major projects throughout the organization. Key Responsiblities: Help manage and interpret data analysis of CI stats. Report periodically to senior management on status and recommend modifications as necessary. Assist with strategic project analysis and modeling to determine the benefit to the organization and its stakeholders. Propose prioritization and resource requirements to management based on this analysis | 10/21/2019 |
| 811 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior Research Associate MS Exp: 0-3+ years |
We are currently offering a unique opportunity for a highly motivated researcher to join our team with experience in immune, in vitro, cellular and cancer biology. JOB DUTIES AND RESPONSIBILITIES: Execute a broad range of cell based functional and phenotypic assays for characterization of engineered NK and T-cells to accelerate projects in pre-clinical development. Conduct in vitro mechanism of action studies using primary human or mouse immune cells and cell lines to evaluate activity of candidate therapies. etc. | 10/21/2019 |
| 812 | Nkarta Therapeutics South San Francisco, CA Research Associate (In Vivo) MS in a pharmaceutical or biotechnological field Exp: 1 year |
We are currently offering a unique opportunity for a highly motivated researcher to join our team with experience in immune, in vitro, cellular and cancer biology. JOB DUTIES AND RESPONSIBILITIES: Conducts pharmacological evaluation of test agents (cell products or small molecule) in subcutaneous, systemic and orthotopic in vivo oncology models. Assists in sample processing, homogenization, or generation of single cell suspensions for ex vivo flow cytometry analysis or PCR analysis. Contributes to preclinical research through development or validation of new tumor models. etc. | 10/21/2019 |
| 813 | Nkarta Therapeutics South San Francisco, CA Research Associate/Senior/Process Engineer MS in a biology-related field Exp: 1-6+ years |
We are currently offering a unique opportunity for a highly motivated development associate to join our team with development experience in cell therapy. JOB DUTIES AND RESPONSIBILITIES: 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. etc. | 10/21/2019 |
| 814 | Noble Life Sciences Woodbine, MD Animal Care Tech BS Exp: 1 year |
The Animal Care Tech is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to the Vivarium Manager. Responsibilities include but are not limited to: Read, understand and follow all SOP’s, Quality Assurance Standards and perform duties in accordance with the study protocol. Monitor daily animal health and wellness checks and report any abnormal animal conditions to the supervisor and/or the Study Director and record observations in appropriate logs. etc. | 10/21/2019 |
| 815 | Noble Life Sciences Woodbine, MD Quality Control Associate BS Exp: 1 year |
The QC Associate is a key position within the organization with significant prospects for career growth as the company continues to increase the breadth and scope of its business. This position reports directly to Sr. Vice President and a Consulting Quality Assurance Unit. Responsibilities include butarenot limited to: Become and maintain intimatefamiliaritywith all applicable FDA and EPA GLPand other appropriate regulations and guidelinesas well as with the company SOPs and other QA systems. Supervise day to day quality control operations and documentation. etc. | 10/21/2019 |
| 816 | Nordson Minneapolis, MN Product Development Engineer I BS in engineering Exp: 0-3 years |
Applies broad knowledge of principles and practices in Design Engineering. Independently evaluates, selects, and adapts standard techniques, procedures, and criteria. Acquires general knowledge of principles and practices of related fields. Works on multiple projects with low level of oversight from project manager and/or technical lead. Essential Job Duties and Responsibilities: Provide engineering support to the project team to design and develop medical devices (disposable and reusable), catheters, implants, and/or packaging, from concept through market introduction. etc. | 10/21/2019 |
| 817 | NorthStar Medical Radioisotopes Beloit, WI Process Laboratory Technician BS in chemistry or a related physical science Exp: 1+ years |
Responsible for routine (chemistry) laboratory support in one of NorthStar’s research and development laboratories. This individual will be responsible for maintaining the laboratory space to cGMP standards, creating and documenting standard laboratory solutions, and assisting in the maintenance and calibration of analytical measurement equipment. etc. | 10/21/2019 |
| 818 | Norwich Pharma Norwich, NY Chemist I BS in chemistry, biology, or related Exp: 0-3 years |
The Quality Control Chemist I: 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. etc.The Quality Control Chemist I: 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. etc. | 10/21/2019 |
| 819 | Novo Nordisk West Lebanon, NH Manufacturing Technician Job BS Exp: No experience necessary for BS candidates |
Novo Nordisk in West Lebanon is looking for a Manufacturing Technician to join our team! This position has primary responsibility to support the manufacturing processes and requires strict adherence to established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 10/21/2019 |
| 820 | Novo Nordisk West Lebanon, NH QC Analyst - Analytical Job BS Exp: 1+ years |
We're looking for a detail oriented QC Analyst I. The ideal candidate will be proficient in method validation and equipment qualification with minimal supervision, as well as performing chemical testing for raw material, water and in-process samples supporting the manufacturing process. Demonstrates self-starter and independent worker with strong commitment in quality and compliance. Excellent analytical and wet chemical techniques. Strong team player with the ability to communicate effectively both verbally and in writing. The person will join our Analytical team to support routine testing such as SDS-PAGE, FTIR, HPLC/UHPLC, ELISA, UV-VIS and others. etc. | 10/21/2019 |
| 821 | Novozymes Research Triangle Park, NC Research Assoc/Assoc Scientist, Microbial Formulation Dev BS/MS in chemical engineering, biology, chemistry, or related Exp: 0-8 years |
Are you ready for a challenging role that lets you use both your scientific grounding and communication skills? If so, you could be our new colleague in our Formulation Development Group, a dynamic team of scientists and researchers located in RTP, NC. You’ll work within the internal research group, as well as with outside units, to develop advanced and scalable formulations and formulation processes for both existing and novel microbe-based products (i.e. bacteria, fungi and yeast). Alongside an in-depth understanding of the scientific principles of microbial formulation and process development, you demonstrate good stake-holder management and exceptional communication skills. In your daily work, you’ll use all of these talents to pioneer research and transform it into value-added products for a variety of industries, including agriculture, household care and biofuels. etc. | 10/21/2019 |
| 822 | Nurix San Francisco, CA Research Associate I-II, Cell Biology/Immunology BS/MS Exp: 0-4 years |
We are seeking a Research Associate with experience in cell biology and immunology to join our Nurix drug discovery team. Nurix is devoted to unlocking the therapeutic potential of the ubiquitin system to explore the possibility of modulating targets previously believed to be “undruggable”. Ubiquitin ligases play numerous roles in immune cell function, autoimmunity, inflammation and anti-tumor immunity. The successful candidate will support early drug discovery efforts in inflammation, oncology and immuno-oncology (IO). etc. | 10/21/2019 |
| 823 | Ora Andover, MA Clinical Trial Associate BS Exp: 1+ years |
Assists project managers in clinical conduct of ophthalmic clinical trials. Serves as point of contact for investigator sites and ensures compliance with protocol and overall clinical objectives. As a member of the clinical operations team, relies on instructions and pre-established SOPs to perform the functions of the job while working under supervision of a supervisor or manager. Performs day-to-day activities under the guidance of the clinical project managers. Placement at the CTA I, CTA II or Sr. CTA level will be determined based on the candidate’s qualifications. etc. | 10/22/2019 |
| 824 | Organogenesis Norwood, MA QC Analyst I - Microbiology BS in microbiology or related Exp: 6 months - 1 year |
The QC Analyst I/II performs quality activities in support of product production and releases. The position has interaction with other internal departments, including Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also has interactions with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, and reporting results. etc. | 10/22/2019 |
| 825 | OriGene Technologies Rockville, MD Research Associate – Immunology BS/MS in biology, biochemistry, or related Exp: 1-2 years |
Responsibilities: 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. Strong organizational skills and possess strong ability to identify, analyze and solve the problems independently. Records experiment procedure and results in notebooks and computer accurately. Prepares summary tables, reports, specification datasheets and presentation data on PPT-Maintains laboratory equipmentand a safe working environment. etc. | 10/22/2019 |
| 826 | OriGene Technologies Rockville, MD Research Associate – Molecular Biology BS in a life science Exp: 1+ years |
The qualified candidate will support company’smolecular biology operations,principally performing DNA cloning and molecular biology experiments following protocols. Job Requirements: Perform experimentsfollowing protocols for plasmid DNA purification, DNA digestion, gel electrophoresis,DNA fragment purification, ligation, transformation, DNA quantitation, DNA sequencing, PCRand cell culture. Responsible for assigned lab duties, maintaining lab stocks, solutions, reagents, and supplies. etc. | 10/22/2019 |
| 827 | Owl Biomedical Santa Barbara, CA Assembly & Test Technician AS/AA Exp: 1-3 years |
To support this effort, we are seeking an Assembly and Test Technician to support the assembly of designed parts for the company’s core medical instruments. Within this role, you will be responsible for supporting all tasks and functions in producing interposer to chip assemblies, while inspecting incoming raw materials and maintaining inventory for all production parts. Overall, your keen ability to work with a multi-disciplinary team to lead and advance product development efforts will champion the continued success of Owl biomedical. etc. | 10/22/2019 |
| 828 | Owl Biomedical Sunnyvale, CA Manufacturing Associate BS in a biological science or related Exp: 1-3 years |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. etc. | 10/22/2019 |
| 829 | Covance Greenfield, IN Study Technician - Dose Formulations BS/BA in life sciences Exp: 0-2 years |
The Study Technician is a true laboratory position where you collect and document study data step by step. You will perform study calculations and specific techniques for test material formulation. In addition you will: Prepare laboratory reagents, vehicles, diets, solution/suspensions, and capsules. Perform study calculations and specific techniques for test material formulation. | 10/16/2019 |
| 830 | Covance Dallas, TX Research Technician (On-call) BS, AS/AA or HS Diploma/GED Exp: AS/AA: 1 year clinical research experience, HS: 1-2 years |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Assist in the preparation of rooms and medical equipment. Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs. | 10/16/2019 |
| 831 | Covance Madison, WI Research Assistant I (Chemist) – Dose Analysis BS/BA in chemistry or related Exp: 1-2 years lab experience |
In this role, you will analyze biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. Organizes and conducts routine analyses in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. Sets up, operates and performs routine and non-routine maintenance on general equipment. | 10/16/2019 |
| 832 | Covance Somerset, NJ Animal Technician-Large Animal Toxicology BS/BA Exp: 0-4 years |
The Animal Technician provides primary care to the animals in the large animal toxicology department and performs routine invasive and non-invasive technical procedures on studies allocated to the team while ensuring that procedures are conducted according to protocol, SOP requirements, Good Laboratory Practice (GLP) and United States Department of Agriculture (USDA) regulations and the guidelines. | 10/16/2019 |
| 833 | Covance Madison, WI Research Nurse , Phase I Clinical Research Unit BSN/AND in WI Exp: 1+ years nursing experience |
Our Clinical Research Unit in Madison, Wisconsin is seeking Research Nurses to join our expanding team. As a Research Nurse at Covance you will be responsible for study unit activities in the conduct of clinical trials with emphasis on the safety and welfare of study participants. | 10/16/2019 |
| 834 | Covance Dallas, TX Research Technician (On-call) BS, AS/AA, or HS Diploma Exp: BS: 0 years, AS/AA: 1 year, HS: 1-2 years |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings. Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples. Assist in the preparation of rooms and medical equipment. Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs. | 10/16/2019 |
| 835 | CSBio Milpitas, CA Technician, R&D BS/BA in chemistry, biochemistry ,or related Exp: No experience required |
Perform peptide related lab operation under close supervision. Assist in setting up and operating peptide related lab equipment. Perform HPLC, mass spectrometry, and other analytical techniques. Follow standard operating procedures (SOP) to perform various laboratory tasks. Complete training and development on an ongoing basis | 10/16/2019 |
| 836 | CSL Lansing, MI Phlebotomist HS Diploma Exp: 12 montsh in medical/health care |
Responsible for the efficient and effective collection of plasma by performing venipuncture, monitoring the pheresis process and following Standard Operating Procedures (SOPs). In compliance with SOPs, performs all aspects of the pheresis procedure and plasma collection, including donor set-up, donor monitoring and donor disconnect. Evaluates vein performance of the donor to identify possible problems; makes necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments when necessary to make the process a positive experience for the donor. | 10/16/2019 |
| 837 | CSL South Portland, ME Quality Specialist Associate/Bachelors in business admin or biological sciences Exp: 1 year in leadership/regulated environment |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 10/16/2019 |
| 838 | CSL Smyrna, GA Quality Specialist Associate/Bachelors in business admin or biological sciences Exp: 1 year in leadership/regulated environment |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 10/16/2019 |
| 839 | CSL Holly Springs, NC Technician I/ II (Calibration) Day Shift HS Diploma or AS/AA Exp: HS: 1 year, AS/AA: 0 years |
Provides calibration and instrumentation support for processes, operations, and buildings on site. Responsible to execute scheduled calibrations, preventive maintenance and corrective maintenance on instrumentation and control devices in compliance with facility procedures and work instructions. Works within clearly defined standard operating procedures and/or scientific methods and adheres to quality guidelines | 10/16/2019 |
| 840 | CSL Palm Bay, FL Quality Specialist Associate/Bachelors in business admin or biological sciences Exp: 1 year in leadership/regulated environment |
This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. | 10/16/2019 |
| 841 | CSL Las Vegas, NV Customer Service - Donor Support Technician HS Diploma/GED Exp: 3 months |
Responsible for preparing the donor, donor area and equipment for the pheresis process. Monitors the donor and the pheresis process, responds to specific alarms or signals that may occur during the process. Maintains alertness and awareness to any reaction donor may have during or after the pheresis process and notifies appropriate staff.Uses Personal Digital Assistant (PDA) to record incidents that occur during the pheresis process, such as machine alerts and alarms, volume variances and donor adverse events. | 10/16/2019 |
| 842 | CSL Raleigh, NC Plasma Processing Technician HS Diploma/GED Exp: 3 months related |
Responsible for the accurate and timely sampling, testing, shipping and storage of plasma collected from donors. In compliance with Standard Operating Procedures (SOPs), responsible for collecting plasma samples and moving plasma units to freezer to ensure product quality. Utilizes sterile technique to draw samples and uses heat sealer to assure the sterility and quality of plasma unit samples per SOPs. | 10/16/2019 |
| 843 | CTI Covington, KY Clinical Safety Scientist I BS, or RN Exp: 1-2 years in GCP |
The Clinical Safety Scientist I is responsible for managing serious adverse events (SAEs) in clinical trials or post-marketing programs, focusing on all aspects of the collection, processing, evaluating and reporting of cases in accordance with CTI’s Global Drug Safety and Pharmacovigilance processes, International Council for Harmonisation (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and study procedures. This individual will track cases from receipt to closure, perform verification of safety data, and will utilize clinical / pharmacovigilance judgment in coding of serious events and synthesizing complex clinical information into accurate and complete narratives. | 10/16/2019 |
| 844 | CTI Covington, KY Clinical Safety Scientist I BS, or RN Exp: 1-2 years in GCP |
The Clinical Safety Scientist I is responsible for managing serious adverse events (SAEs) in clinical trials or post-marketing programs, focusing on all aspects of the collection, processing, evaluating and reporting of cases in accordance with CTI’s Global Drug Safety and Pharmacovigilance processes, International Council for Harmonisation (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and study procedures. This individual will track cases from receipt to closure, perform verification of safety data, and will utilize clinical / pharmacovigilance judgment in coding of serious events and synthesizing complex clinical information into accurate and complete narratives. | 10/16/2019 |
| 845 | Azurity Greenwood Village, CO Inside Sales Support 2 year college degree Exp: 1+ years in call center |
To increase product awareness through telemarketing and account support with pharmacies to help achieve company sales targets and improve profitability. To provide communication to key stakeholders for the field sales team to generate new business and maintain current business. Interact with pharmacies by use of appropriate questioning, clarification and language to build effective relationships to increase sales. To speak positively and enthusiastically about the company and its products to ensure that a professional company and brand image is provided at all times. | 10/16/2019 |
| 846 | Cytokinetics South San Francisco, CA Research Associate I, Pharmacology BS/MS in biology, physiology, pharmacology Exp: 1-3 years |
This individual will also be involved in managing transgenic mouse colonies, maintaining transgenic lines for experimental purposes and designing, optimizing, and implementing new assays to measure cardiovascular system function. As a member of a multidisciplinary team, you will work closely with team members to identify, characterize and advance compounds through research and preclinical development. | 10/19/2019 |
| 847 | Cytokinetics South San Francisco, CA Research Associate, Sample Management BS in chemistry Exp: 0-3 years lab experience |
This will be an entry level position that will provide a tremendous learning opportunity for the ideal candidate. The candidate will get to learn in-depth the functioning and nuances of a Sample Management group and also gain experience with the numerous assays that assess and characterize the properties of the compounds. The position demands an individual who is a quick learner and has a proactive attitude to pitch in to support research activities and help with dispensing compounds, trouble-shooting instrumentation, and running assays. | 10/19/2019 |
| 848 | CytomX Therapeutics South San Francisco, CA Research Associate I/II: Upstream Process Development BS or MS in biological sciences Exp: 0-3 years lab experience |
Operation, harvest, and cleaning of stirred-tank bioreactors (AMBR15, 2-20L glass vessels, 50 L SUB, fed-batch). Media and reagent preparation to support upstream activities. Execute and evaluate of fed-batch cell culture studies in shake flasks and micro-bioreactors. Execute and evaluate of fed-batch cell culture studies in shake flasks and micro-bioreactors. Support of GMP mfg; may include BPR review and PIP duties | 10/19/2019 |
| 849 | Cytovance Biologics Oklahoma City, OK DOWNSTREAM MANUFACTURING ASSOCIATE AS/AA in sciences or chemical engineering Exp: 0-2 years GMP production |
This position is accountable for the execution of procedures for purification manufacturing and support area of manufacturing using SOP’s and batch records. Operating production equipment for purification that may include process monitoring, purification and formulation. Interface with Quality Control department to submit in-process samples and coordinate environmental monitoring during key process steps. Demonstrate understanding in scientific concepts, technical operations, safety, and Good Manufacturing Practice. | 10/19/2019 |
| 850 | Cytovance Biologics Oklahoma City, OK UPSTREAM MANUFACTURING ASSOCIATE AS/AA in science or biotech Exp: 1-2 years in GMP |
Executes upstream manufacturing of clinical and commercial products. Executes pre and post processing activities such as: clean of production equipment, including the operation of automated bioreactor, harvest and media prep skids. This position is accountable for executing the manufacturing processes in Contract Manufacturing Facility and/or Master Cell Banking Facility. | 10/19/2019 |
| 851 | Cytovance Biologics Oklahoma City, OK SOLUTION PREP ASSOCIATE I AS/AA in science or biotech Exp: 1-2 years in GMP |
This position is accountable for producing and delivering large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. Batching and delivering both large and small-scale media and buffer batches. Assisting in the review & creation of operation documents by providing input to technical composition of documents. Following accurate oral & written procedures in operating production equipment & performing processing steps | 10/19/2019 |
| 852 | Dexcom Mesa, AZ Process Technician 1 BS/BA 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. | 10/19/2019 |
| 853 | Dexcom San Diego, CA Mechanical Engineer 1 BS in technical degree Exp: 0-2 years |
As a member of the R&D Mechanical Engineering team this engineer will understand and articulate the current and future needs of our customers and our business, explore and evaluate new technologies and concepts for meeting those needs, and rapidly demonstrate feasibility of such technologies through rigorous modeling, analysis, prototyping, experimentation, and other risk identification and mitigation activities. Design, develop, fabricate, assemble and implement fixtures and equipment to quantify prototype device performance | 10/19/2019 |
| 854 | Dexcom San Diego, CA Process Development Engineer 2 MS in technical discipline Exp: 0-2 years |
Develops new or modified process formulations, defines processing or handling equipment requirements and specifications, and reviews processing techniques and methods applied in the manufacture, fabrication, and evaluation of products. Involvement may begin at any step from pilot plant to full-scale manufacturing. Coordinates design requirement review with appropriate engineering/scientific personnel to ensure compatibility of processing methods. Compiles and evaluates test data to determine appropriate limits and variables for process or material specifications. May conceive and plan projects involving definition and selection of new concepts, equipment automation technology, and approaches in the processing or development of new or improved processes. | 10/19/2019 |
| 855 | Dexcom Mesa, AZ Manufacturing Clerk 1 HS Diploma Exp: 0-2 years related |
Provides administrative and clerical support specifically related to manufacturing department activities. May be assigned to various administrative tasks within manufacturing support. Basic understanding of general job aspects and limited understanding of the detailed aspects of the job. Acquires job skills and learns the policies and procedures required to complete routine tasks. | 10/19/2019 |
| 856 | Dexcom San Diego, CA Process Development Engineer 2 (Vision System) MS in technical discipline Exp: 0-2 years |
Supports development of new and modified sensor manufacturing processes. Assist lead engineers in defining processing or handling equipment requirements and specifications, and reviews processing techniques for manufacture of new products and to decrease cost, improve throughput, and improve overall quality for commercial product lines. Support transfer and work on process development/scale up or new products from R&D. Manufacturing support to identify and resolve technical issues. Involvement may begin from feasibility at vendors to full scale manufacturing. | 10/19/2019 |
| 857 | DNA Diagnostics Center Fairfiedl, OH Rep I, Client Services Representative HS Diploma Exp: 1-2 years in customer service |
The Rep !, Client Services Representative is a critical position in providing customer service satisfaction and representing DNA Diagnostics Center (DDC). Answer inbound telephone and email contacts. Able to explain and promote DDC's products and services professionally. Quickly understand and analyze customer needs, listen actively | 10/19/2019 |
| 858 | DSG San Diego, CA Business Development - San Diego, CA BS/BA in life sciences, business or computer sciences Exp: 1-3 years project management/internship experience |
The Business Development Manager is responsible for identifying new clients and for establishing and maintaining sales relationships. This candidate is also responsible for maintaining and strengthening relationships with existing clients. As a successful candidate, you will need to meet the following technical requirements and qualifications: Place outbound calls to market to qualify and build relationships with contacts, and secure meetings. Educate prospects on the eCaseLink suite of products and services. | 10/19/2019 |
| 859 | DSG Raliegh, NC Business Development - Raliegh BS/BA in life sciences, business or computer sciences Exp: 1-3 years project management/internship experience |
The Business Development Manager is responsible for identifying new clients and for establishing and maintaining sales relationships. This candidate is also responsible for maintaining and strengthening relationships with existing clients. As a successful candidate, you will need to meet the following technical requirements and qualifications: Place outbound calls to market to qualify and build relationships with contacts, and secure meetings. Educate prospects on the eCaseLink suite of products and services. | 10/19/2019 |
| 860 | Durect Cupertino, CA Operations Administrative Assistant HS Diploma Exp: 0-1 years in admin |
Provide operational support to multiple functional departments; Facility, Finance, IT, QA, BD, PSRD, and Legal to contribute to the development and implementation of organization goals. Coordinate department, project ,and, business development client meetings and webinars, related luncheons, prepare and distribute meeting documentation. Schedule and coordinate with external vendors, i.e. Facilities and Manufacturing, for service requests | 10/19/2019 |
| 861 | Dynosense San Jose, CA QA Engineer BS in computer science, engineering or related Exp: 0-2 years |
Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications. Estimate, plan, and coordinate testing activities. Perform ad hoc, functional, integration, and regression testing. Identify software defects and submit problem reports via bug-tracking system | 10/19/2019 |
| 862 | Nanolab Technologies Milpitas, CA Sample Prep Technician BS/BA in engineering/physical sciences Exp: 0-2 years in FIB/SEM operations |
Nanolab Technologies is looking for an enthusiastic TEM Sample Preparation Technician. Primary function is processing/imaging STEM/TEM samples using FEI 4xx/Helios Dual Bean FIB tools and TEM sample preparation of lamella. The work environment is fast-paced with firm deadlines. The successful candidate will work as a part of a team and be expected to rapidly gain a working knowledge of many analytical techniques. | 10/19/2019 |
| 863 | Editas Boulder , CO Research Associate, Medicinal Chemistry Group BS/BA in chemistry Exp: 1 year or more with synethtic organic chemistry |
This new role on the Medicinal Chemistry team in Boulder provides a unique opportunity to contribute to Editas’ efforts through the development of novel chemical compounds to improve CRISPR/Cas9 and CRISPR/Cpf1 performance. Design and synthesize compounds to improve the performance of ribonucleoproteins (CRISPR/Cas9 and CRISPR/Cpf1). Optimize synthetic methods for compounds of interest. | 10/20/2019 |
| 864 | Editas Cambridge, MA Research Associate I/II, In Vivo Pharmacology BS or MS in biological sciences Exp: 1-2 years lab experience |
The candidate will be responsible for conducting preclinical animal studies to support the development of gene-editing based therapies in multiple disease areas, including ophthalmology, oncology, and hematology. Perform basic molecular biology work such. Perform routine injections (sc, ip, iv) in mice, monitor animal health, collect tissue and blood samples, measure tumor volume, perform anesthesia and necropsies. | 10/20/2019 |
| 865 | Editas Cambridge, MA Research Associate I/II, Cell Biology BS or MS in biological sciences Exp: 1-3 years lab experience |
In this role you will contribute to the development of cell-based assays and ex vivo methods to evaluate gene editing. An ideal candidate should have a background in cell culture, ex vivo tissue dissection methods, and a strong interest in genome editing. Perform ex vivo tissue dissection and cell isolation. Perform routine DNA/RNA extraction and PCR, western blot, and ELISA. Development and optimization of cell-based assays | 10/20/2019 |
| 866 | Edwards Irvine, CA Engineer II, Automation & Process mS in Mechanical, Electronic, Mechanics, Mechatronics, Industrial Exp: 0-2 years in automation |
This is a great opportunity to lead and provide support in projects for the manufacturing area. This includes: automation projects for processes of new products, automation projects for cost reduction, quality, ergonomics and delivery improvements. In addition, validation and implementation of changes related to the projects. Develop moderately complex tests and experiments (including writing and execution of protocols) to qualify and validate manufacturing processes; follow up on protocol activities, train technicians; analyze results, make recommendations and develop reports. | 10/20/2019 |
| 867 | Edwards Irvine, CA Associate Analyst, Inventory BS/BA Exp: 1 year in finance/customer serivce/operation etc. |
Manage all consigned and customer owned inventories through a variety of processes and systems and provides insight to help improve and streamline current processes in collaboration with Commercial Contract, Finance, Sales, Supply Chain and Customer Operations. Perform basic analysis of field scan results (e.g., physical vs system of record inventory) for SOX Compliance through multiple systems, cross functional departments (e.g., Contracts, Sales, Finance, Quality, Implant Registry, Supply Chain, Customer Service, IT) and external partners to make recommendations to customer service for resolution. | 10/20/2019 |
| 868 | Edwards Irvine, CA Technician, R&D - Transcatheter Heart Valve HS Diploma Exp: 1+ years related experience |
Edwards Lifesciences is currently seeking a Research and Development Technician to perform a wide variety of tasks in support of Engineering activities for our Transcatheter Heart Valve Business Unit at our corporate headquarters in Irvine, CA. Perform set-up on textile and related machines involving mechanical components as well threading of fine textile yarns using mechanical tools . Support engineering activities such as test, check-out, modification, fabrication, and assembly under the close supervision of Engineers | 10/20/2019 |
| 869 | Edwards Irvine, CA CRA I, In House - Transcatheter Mitral and Tricuspid Therapies BS in related Exp: 1 year in documentation for clinical studies |
This is a unique opportunity to join an early-stage product development group, Transcatheter Mitral & Tricuspid Therapies (TMTT), focused on developing solutions for patients suffering from structural heart disease. The Clinical Research Associate I will ensure clinical trials are conducted and reported in accordance with all applicable regulatory requirements. Conduct reviews of documentation needed for internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations. | 10/20/2019 |
| 870 | Edwards Draper, UT Quality Engineer I, Quality BS or MS in engineering Exp: 0 years |
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Optimize Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk. | 10/20/2019 |
| 871 | Edwards Draper, UT Manufacturing Engineer II - Transcatheter Mitral and Tricuspid Therapies MS in engineering/sciences Exp: 0 years w/internships or senior projects |
Applies knowledge of technical principles and Edwards systems/procedures to optimize manufacturing processes. Improve manufacturing processes using engineering methods (e.g., LEAN methods, basic statistics) for continuous process improvement. Develop basic experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports. Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes. | 10/20/2019 |
| 872 | Edwards Draper, UT Supplier Quality Engineer I BS in engineering/sciences Exp: 1-2 years in medical devices |
Edwards Lifesciences has an exceptional opportunity for an Engineer I within the Supplier Quality group. This person will be responsible for supporting supplier quality vendor management, audits, and improvements while supporting continued Quality System improvements. In this position you will support activities sustaining quality engineering within Receiving Inspection, Manufacturing, and Product Verification as applied to supplier related issues. | 10/20/2019 |
| 873 | Elanco Greenfield, IN Associate-Advanced Analytics BS in finance/statistics or data Exp: 1 year in data analytics |
Creates, grows and maintains relationships with internal customer groups to facilitate data driven decisions on business critical projects. Key customer groups to consist of Marketing, Finance, Sales, Senior Leaders, Corporate Strategy and Supply. Responsibilities for providing ROI, efficiency and sales lift metrics to customer groups in a form that both drives decisions to spend and optimizes efficiency. Supports the creation of financial business cases and provides predicted outcomes that can be measures in subsequent ROI and efficiency reviews. | 10/20/2019 |
| 874 | Elanco Winslow, ME Biologist - QC MS in biological sciences Exp: 0-3 years lab experience |
The Biologist-QC will provide technical support including consultation/recommendation on various analytical topics to management where appropriate. He or she will support and sometimes manage laboratory related projects affecting QC. The Biologist will assist other laboratory personnel in the implementation of new technologies into the QC lab and improvement of existing processes. The Biologist will also coordinate non-routine analytic work and sample analysis to support relevant projects and initiatives when needed. The position will also include routine testing of in process and final product samples for the release of veterinary vaccines. | 10/20/2019 |
| 875 | Lilly Charlottetown, Pr Production Technician - Fermentation BS/BA in life sciences Exp: 1-2 years in GMP bio manufacturing |
To produce veterinary biologics according to a defined production schedule following cGMP guidelines and specific outlines of production to meet market demands for Aquaculture products. Comply with safety requirements, cGMP, SOP and manufacturing documentation. Produce antigens in a timely manner according to their approved Outline of Production/Product Dossiers and to cGMP guidelines. Support Antigen production and freeze dried vaccines production according to Standard Operating Procedures and Protocols. | 10/20/2019 |
| 876 | Lilly Indianapolis, IN Engineer-Automation-IDAP BS in engineering or computer science Exp: 0-3 years |
Develop, implement, and continuously improve process automation solutions within IDAP to ensure that business goals are achieved. Ensure that process automation solutions/systems are in-control, capable, and compliant. Stay tightly aligned and actively involved with internal customers. Understand their issues, priorities and objectives. Respond to and implement customer requests. Troubleshoot problems. Assure that all capital projects are aligned with the Automation Strategy and that all established standards are followed. | 10/20/2019 |
| 877 | Element Science San Francisco, CA Product Test Engineer BS in electrical engineering Exp: 0-2 years |
The Product Test Engineer is responsible for the co-development and maintenance of all production test equipment and software. Your role is critical as it takes a candidate that understands all the stages of test development to ensure our products are built correctly and ready as a Class III bio-medical device. You will work directly with product design engineers and use your production-level test knowledge to create effective test sequences, supporting hardware and software, and overall record keeping strategy. | 10/20/2019 |
| 878 | Lilly Columbus, OH Entry-Level Sales Representative-Ohio Valley Area Diabetes Primary Care (OH/MI/IN/KY) BS/BA Exp: license/certification for position |
Partner with health care professionals and those involved with patient care as a product expert to tailor solutions for patient therapy. Sell in a changing health care environment, utilizing critical thinking and a strategic mindset to understand the environment (payer, health systems, business) and gain access to the customers to make an impact on patients’ lives. Work in your own territory and also partner with team members and alliance partners for success in the territory | 10/20/2019 |
| 879 | Emerald Cloud Lab South San Francisco, CA Laboratory Operator II HS Diploma/BS/BA Exp: 1-3 years in life sciencesz |
As a Laboratory Operator II, you will be responsible for high fidelity execution of detailed protocols. Operators are relied on for the immediacy and reliability with which experiments are run on the ECL, so attention to detail is crucial. The Lab Ops team relentlessly clears the queue of customer experiments and keeps the robots in the labs running at all times, with a focus on exactness and increasing efficiency. The entire ECL facility is run in a systematic way, and the team purview encompasses all protocols that enable this, from maintenance and control of instruments to inventory intake. | 10/20/2019 |
| 880 | Emergent Biosolutions Camden, MD Packaging & Inspection Technician HS Diploma Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. Execute and document procedural steps in compliance with cGMP standards. Perform room clearances in accordance with relevant Standard Operating Procedures. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification) | 10/20/2019 |
| 881 | Myriad Mason, OH Biostatiscian MS in statistics Exp: 1+ years |
The Biostatistician will provide statistical leadership in design, analysis, interpretation, and reporting of clinical trials and perform predictive modeling of a wide range of data including clinical, pharmacy claims data, electronic health records (EHR), and pharmacogenomics data that help build the business. The position will be supporting Myriad Neuroscience and based in Mason, Ohio. etc. | 10/15/2019 |
| 882 | Myriad Salt Lake City, UT Process Technician MS in a chemical, physical, or biological science Exp: 6 months |
The Process Tech III supports the clinical diagnostic lab by troubleshooting process failures, identifying and participating in continuous improvement projects in conjunction with staff and Technical Development, and participating on cross-functional teams to implement new processes into operations. This position will work with department management and quality team members to ensure that appropriate root cause is identified, corrective actions are implemented and proactive process improvements are identified. As directed by management, this role may also support Reagent Manufacturing processes, provided they are maintaining ongoing competency to perform those duties. etc. | 10/15/2019 |
| 883 | NAMSA St. Louis Park, MN Administrative Assistant AS/AA in a business field Exp: 1-3 years |
Part time. Receives and directs calls, visitors, vendors, service personnel, and all paperwork in a confidential manner. Provides clerical and administrative assistance to leadership and teams. Maintains effective working relationships with co-workers, vendors and clients. Schedules appointments and travel arrangements, as requested. etc. | 10/15/2019 |
| 884 | NAMSA Northwood, OH Associate Microbiologist BS/BA Exp: 1 year |
Independently perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs, and according to applicable work instructions. Prepare or participate in the preparation of test specifications in conjunction with the requirements of the applicable standards and/or client instructions. May have direct client contact as needed. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and for taking all concerns to management as required. Accurately collects and records raw data in logbooks and on worksheets. etc. | 10/15/2019 |
| 885 | NAMSA Northwood, OH Chemist MS Exp: None needed |
Principal Duties and Responsibilities. Independently conduct testing according to written instructions. May be requested to conduct more involved studies. May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. May conduct routine testing per NAMSA SOPs as well feasibility, protocol driven methodology, and/or method verifications on at least one of the following instrument types: HPLC, GC, or ICP, etc. Works with management to ensure large studies are completed on or before the due date. Prepare and maintain the reagents required for testing. etc. | 10/15/2019 |
| 886 | NanoString Seattle, WA Clinical Trial Assistant BS/BA Exp: 1+ years |
The Clinical Trial Assistant (CTA) is primarily responsible for supporting the clinical team. The CTA will manage coordination of activities and ensure timely flow of information to and from the team. S/he handles details of a highly confidential and critical nature, and must function efficiently and effectively in a fast-paced professional environment. S/he will have a proven ability to independently prioritize and manage multiple tasks and projects with competing priorities and deadlines, screen and prioritize communications and opportunities from external sources. etc. | 10/15/2019 |
| 887 | NanoString Seattle, WA Manufacturing Research Associate I/II BS in molecular biology, biochemistry, or related Exp: 0-2 years |
The Manufacturing Research Associate I/II, CodeSet Manufacturing 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 operate equipment, perform SOPs, navigate Document Control systems, ERP systems, etc. etc. | 10/15/2019 |
| 888 | Natera San Carlos, CA Clinical Data Operator I HS diploma or equivalent Exp: 0-1 years |
Natera is currently seeking a Clinical Data Operator to join the operations team. This position accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. PRIMARY RESPONSIBILITIES: Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. Scan test requisition forms and attached paperwork. Ensure that all paperwork belong to patient and upload to case. etc. | 10/15/2019 |
| 889 | Natera San Carlos, CA Clinical Data Operator I (5:30 -10:30 pm) HS diploma or equivalent Exp: 0-1 years |
Natera is currently seeking a Clinical Data Operator to join the operations team. This position accessions patient samples according to standard operating procedures (SOP) with high efficiency and accuracy. PRIMARY RESPONSIBILITIES: Create new orders on Laboratory Inventory Management System (LIMS) and perform necessary checks to ensure proper accessioning. Accession samples with high accuracy and efficiency. Accurately enter patient data into the Laboratory Inventory Management System (LIMS). Ensure that the information in LIMS is up-to-date. Scan test requisition forms and attached paperwork. Ensure that all paperwork belong to patient and upload to case. etc. | 10/15/2019 |
| 890 | Natera Austin, TX Clinical Laboratory Operator I BS/BA in a biological science or related field Exp: 0-2 years |
Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Provide guidance for new team members. Follows GLP (good laboratory practice): maintain clean and organized workspace. Completes training and other deadlines on time. etc. | 10/15/2019 |
| 891 | Natera Austin, TX Medical Laboratory Scientist I BS/BA in medical technology, biological sciences, or related Exp: 1-2 years |
Natera is currently seeking a licensed Medical Laboratory Scientist to analyze specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Proficient at analyzing clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Provides general oversight of personnel and the daily operations in the lab. Meet expected performance metrics within role as applicable. etc. | 10/15/2019 |
| 892 | Natera San Carlos, CA Clinical Laboratory Associate I (Temporary) BS/BA in a biological science or related field 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: 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. Follows GLP (good laboratory practice): maintain cleans and organized work space. etc. | 10/15/2019 |
| 893 | Natera San Carlos, CA Clinical Laboratory Scientist I BS/BA in medical technology, biological sciences, or related Exp: 1-2 years |
Analyzes specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Proficient at analyzing clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain clean and organized workspace. Completes training and other deadlines on time. etc. | 10/15/2019 |
| 894 | Natera San Carlos, CA Clinical Laboratory Scientist II BS/BA in medical technology, biological sciences, or related Exp: 1-2 years |
Natera is currently seeking a licensed Clinical Laboratory Scientist I to analyze clinical laboratory specimens following the standard methods and procedures. Maintain equipment and instruments in good operating condition, recognize any malfunctions and troubleshoot as needed. PRIMARY RESPONSIBILITIES: Verify the proper specimen being analyzed and perform tests that need to be completed. Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors. Responsible for maintaining updated understanding and knowledge of methods performed in the lab. Follows GLP (good laboratory practice): maintain clean and organized work space. etc. | 10/15/2019 |
| 895 | NatureWorks Blair, NE Production Technician HS diploma/AA/AS Exp: 1-2 years |
The Production Technician is responsible for the safe execution of the day to day operations of the production plant. This position will work closely with other team members and be responsible for personal and plant safety, environmental compliance, commitment to continuous improvement in the quality of our product, cost control efforts and efficient operations of the plant. This position requires working 12 hour shifts including evenings, weekends and holidays. etc. | 10/15/2019 |
| 896 | NeoGenomics Aliso Viejo, CA Accessioning Technician I HS diploma/AS/BS Exp: 1+ years |
As an Accessioning Technician I you will ensure proper handling of all specimens received and prepare specimens for laboratory testing. You will be performing functions such as matching patient information, data entry, and scanning documents. You will be responsible for reviewing all requisitions for missing information, working closely with Customer Care in order to obtain missing information in a timely fashion, and distributing new information to all departments involved. You will need to report problem holds and provide resolution in a timely fashion. etc. | 10/15/2019 |
| 897 | NeoGenomics Aliso Viejo, CA Histotechnician I Nights HS diploma/AS/BS Exp: 1+ years |
As a Histotechnician I you will work under the direct supervision of a licensed physician or surgeon, or within a training environment. You will assist with responsibilities associated with processing specimens for clinical testing and providing general support for the laboratory following established policies and procedures. Receive, organize and process clinical specimens accurately; identify worksheet, computer, and specimen problems and demonstrate ability to either resolve or elevate to licensed personnel appropriately. Prepare and organize written data, printouts, and other documents for pathologist review. etc. | 10/15/2019 |
| 898 | NeoGenomics Fort Myers, FL Histotechnologist I AS Exp: 1+ years |
As a Histotechnologist I or II, you will work under general direction to precisely and accurately conduct a variety of routine and specialized histology procedures. You will research, troubleshoot, and resolve histology related inquiries and problems within the laboratory. This position requires you to produce the highest quality of embedding, microtomy, tissue grossing, tissue processing, and H&E staining, special staining, immunohistochemistry staining and equipment maintenance. etc. | 10/15/2019 |
| 899 | Cepheid Sunnyvale, CA Associate Scientist MS in biological sciences Exp: 0-2 years |
This position is in the Biotechnology R&D group and is primarily a bench level job focusing on real time PCR assay and product development in an FDA-QSR and ISO13485 compliant organization. The ideal candidate will have experience in general molecular biology methods such as nucleic acid extraction and real-time PCR. This candidate will assist in the development of novel assays for diagnosis and monitoring of microorganisms involved in infectious diseases. In addition to technical qualifications, the ideal candidate will be highly goal-oriented, inquisitive, organized, and be able to thrive in an atmosphere of shifting demands and priorities. | 10/11/2019 |
| 900 | Phenomenex Torrance, CA Research Scientist MS in chemistry or life sciences Exp: 1-3 years |
Work with R&D team to develop, enhance or investigate new and/or existing separation products and technology. Work with synthetic and analytical chemists in developing new HPLC, SPE and Biotechnology products/methods. Take responsibility for new product development, manufacturing or analytical techniques used to create/improve products and technolo | 10/11/2019 |
| 901 | Certara Wilmington, DE Quality & Compliance Associate BS/BA Exp: 1-2 years related experience |
The Quality and Compliance Associate is a key member the company’s SOP Committee actively enforcing the company’s policies and procedures in alignment with the overall Quality Management System (QMS). Maintains and promotes company and regulatory quality standards. Conducts activities involving quality assurance and compliance with applicable requirements. Responds to compliance questionnaires | 10/11/2019 |
| 902 | Ceva Lenexa, KS R&D Technician I BS/BA in microbiology or biology Exp: 1-2 years in lab |
To assist in the development and licensure of viral, bacterial and/or recombinant vaccines as well as new label claims or product improvement research of the licensed vaccines. Propagate cell, virus, bacteria and recombinant organism stocks, perform the testing such as cell counting, titrations, ELISA and other biological and/or molecular assays. Participate in planning and executing from research to large production scale up projects | 10/11/2019 |
| 903 | Ceva Lenexa, KS R&D Technician I BS/BA in microbiology or biology Exp: 1-2 years in lab |
To assist in the development and licensure of viral, bacterial and/or recombinant vaccines as well as new label claims or product improvement research of the licensed vaccines. Propagate cell, virus, bacteria and recombinant organism stocks, perform the testing such as cell counting, titrations, ELISA and other biological and/or molecular assays. Participate in planning and executing from research to large production scale up projects | 10/11/2019 |
| 904 | Ceva Lenexa, KS Mareks Lab Technician I BS/BA preferred but not required Exp: lab experience prefered but not required |
Technicians assist in tissue and viral culture of Chicken Embryo Fibroblast (CEF) cells for Marek’s Disease vaccine production in a clean room laboratory environment. Tissue culture is currently performed using roller bottle tissue culture vessels. The production of the vaccine begins in the Marek’s laboratories with the receipt of highly concentrated primary CEF cell suspension; this suspension is then added to a growth medium made in house by technicians. Calculations are performed to reach a target cell amount per roller bottle vessel. | 10/11/2019 |
| 905 | cGMP Validation Kansas, MO Validation and Compliance Specialist Opening HS Diploma/GED Exp: 1-2 years |
Immediate need for Validation Specialist with experience in the Pharmaceutical and Biotech industry generating and executing protocols for equipment and utilities. Good writing skills a must. Overtime and some travel may be required. Submit resume along with availability | 10/11/2019 |
| 906 | Champions Oncology Rockville, MD Research Technician I, Necropsy BS in biology, pharmacology, or related Exp: 1 year related experience |
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 | 10/11/2019 |
| 907 | Champions Oncology Rockville, MD Research Technician I, Surgical Services BS in biology, pharmacology, or related Exp: 1 year related experience |
Support in vivo oncology studies in mice as a member of the MDC Team. Receive, characterize and orthotopically or heterotopically surgically implant tissue samples. Conduct tumor volume measurements and sample collection for in vitro characterization. | 10/11/2019 |
| 908 | Champions Oncology Rockville, MD Laboratory Research Associate BS or MS in biological sciences Exp: 1-2 years lab experience |
Perform laboratory tasks in support of development of immuno-oncology platform. Preparation and handling of primary specimens, including peripheral blood, ascites, other liquid biospecimens. Isolation of white blood cells by density gradient separation. Sample preparation (murine or human tissues/cells) for Flow Cytometry and Immunostaining. | 10/11/2019 |
| 909 | Champions Oncology Rockville, MD Vivarium Operations Technician I BS in biology, pharmacology, or related Exp: 1 year related experience |
Support in vivo oncology studies in mice as a member of the Vivarium Operations Team. Clean equipment, rooms and facility according to a schedule devised by senior personnel; including floor sweeping and washing, cage washing and sterilization, and waste removal. Provide animal care including feeding and watering with food and water consumption monitoring. | 10/11/2019 |
| 910 | Champions Oncology Rockville, MD Research Technician I, Study Services BS/MS in biology, pharmacology or related Exp: 1 year related experience |
Support in vivo oncology studies in mice as a member of the Study Services Team. Perform in-life technical procedures, handle, restrain, and provide care for all animals. Provide animal welfare assessments, including body weight and tumor volume measurement. Provide preoperative animal care | 10/11/2019 |
| 911 | Charles River Boston, MA Surgical Veterinary Technician BS in animal sciences/verterinary technology Exp: 1 year animal handling |
Reviews and complies with all policies pertaining to the animal care program. Cares for and maintains laboratory animals in accordance with USDA Animal Welfare Act and policies, the “Guide for the Care and Use of Laboratory Animals,” and other applicable regulations and policies. Works closely with the Veterinarian to perform daily health assessments of the large animals in the Surgical Services Program and maintain all records as needed and associated with this monitoring. Provides animal treatments as instructed by the Veterinarian. Performs technical functions required by research protocols, such as daily clinical observations, diagnostic testing, administering medications to post-operative animals and health examinations of sick animals, prior to reporting adverse findings to Veterinarian responsible for that area. | 10/11/2019 |
| 912 | Charles River Horsham, PA Research Technician 1 HS Diploma/GED Exp: 0-6 months animal research experience |
Generate data 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. Collect and record research data and biological specimens in compliance with Good Laboratory Practice Regulations (GLPs), study protocols and Standard Operating Procedures (SOPs). Perform basic in-life technical procedures upon completion and sign-off of specific skill training. (e.g., clipping, handling, binding, removals, body weight, dosing). | 10/11/2019 |
| 913 | Charles River Reno, NV Research Assistant 1 (Formulations) BS/BA in lab sciences Exp: 0-2 years related |
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. | 10/11/2019 |
| 914 | Charles River Norwich, CT Farm Technician HS Diploma/GED Exp: 1 year related experience |
We are seeking a Farm Technician to support our Avian farms located in the greater Norwich, CT area. The Farm Technician will assist where needed in the areas of hatchery, brooding, house management, egg processing, egg pickup, packing, crew and grounds. Assist in a number of different areas on the farms: hatchery, poultry houses (brooding and production), egg processing, packing, egg pickup, house recycles, vaccine bird houses, bird moves, and grounds upkeep. | 10/11/2019 |
| 915 | Charles River Ashland, OH Research Technician Assistant, Technical Operations HS Diploma/GED, BS preferred Exp: 0-1 year animal research/husbandry |
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. | 10/11/2019 |
| 916 | Charles River Mattawan, MI Quality Control Associate - Cellular Molecular Biology BS/MS Exp: 0 years |
A Quality Control Associate is responsible for verification and archival of study data and departmental records according to established Standard Operating Procedures (SOPs), protocols, methods, and processes. The individual in this role contributes to the team by working independently, completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. | 10/11/2019 |
| 917 | Charles River Boston, MA Research Technician I, Technical Operations HS Diploma/GED Exp: 0-1 years in animal research/husbandry |
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. | 10/11/2019 |
| 918 | EyeCRO Oklahoma City, OK Research Assistant-Chemistry(OKC Lab) BS/BA in chemistry, engineering, biotechnology, or pharmacy related Exp: 1 year related experience |
This Person will be responsible for participating in a wide variety of laboratory-based activities related to chemistry to advance our innovative MiDROPS platform as well as animal procedures | 10/11/2019 |
| 919 | Chemic Laboratories Canton, MA Analytical Chemists BS/BA Exp: All Levels (including Entry) |
Perform routine analytical procedures utilizing a variety of analytical techniques with minimal supervision. Perform method development under the direction of a senior level chemist. Accurately record and document raw data, observations and pharmacy usage. Ensure that work conforms to appropriate regulatory requirements, including SOP’s, Protocols, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP). | 10/11/2019 |
| 920 | Chemic Laboratories Canton, MA QAU Auditors - All levels BS/BA Exp: All Levels (including Entry) |
Review of documentation for conformance to established procedures and regulatory guidelines. Ensure that work conforms to appropriate regulatory requirements, including SOP’s, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP). Perform QA functions in support of cGMP manufacturing as necessary. | 10/11/2019 |
| 921 | Chemic Laboratories Canton, MA Analytical Technical Report Writer - All levels BS/BA Exp: All Levels (including Entry) |
Ability to write technical/scientifically detailed text reports according to established procedures and regulatory guidelines. Auditing and/or experience as an analytical chemist is preferable. Perform reporting functions for GLP/cGMP and R&D data as necessary. Ensure that work conforms to appropriate regulatory requirements, including SOP’s, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP). | 10/11/2019 |
| 922 | ChemPacific Baltimore, MD Chemist MS in chemistry or organic chemistry Exp: 1 year |
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. | 10/11/2019 |
| 923 | Cirtec Brooklyn Park, MN Assembler I HS Diploma/GED Exp: 1 year microscope experience |
This position is primarily responsible to perform assembly operations according to written procedures in the clean room environment meeting all quality standards. Be familiar with and follow operating requirements including GMPs (Good Manufacturing Practices) and specific customer defined requirements. | 10/12/2019 |
| 924 | CliniLabs West Coast, Mid-West, South, Clinical Research Associate (CRA) BS/BA in life sciences, nursing, or related Exp: 1 year or more as clinical monitor |
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. | 10/12/2019 |
| 925 | Coating Place Inc. Verona, WI QC Analytical Chemist BS/BA in chemistry or related Exp: 0-2 years |
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. In addition, support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule.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. In addition, support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule. | 10/12/2019 |
| 926 | Codexis Redwood City, CA Research Assistant/Associate (Biochemistry) BS/BA in Biochemistry, Biotechnology, Molecular Biology, Chemistry, or related field Exp: Internship experience preferred but not required |
Assist in developing relevant enzyme assays in HTP format. Execute HTP screens to evaluate enzyme performance under application-relevant conditions. Analyze HTP samples in HPLC, UV-Vis Spectrophotometry, GC, LC-MS, or GC-MS to identify and quantify small-molecule products. Grow cultures, express proteins, and test enzyme activity in high throughput and in larger scales | 10/12/2019 |
| 927 | Cogent Scientific San Diego, CA Analytical Chemist BS/MS-Chemistry Exp: 1+ years of related experience |
The position will focus on implementing and utilizing state-of-the art automation, analytical and preparative scale chromatographic systems to deliver high quality compounds for drug discovery in the first in-class Automated Life Sciences Studio facility located in La Jolla, CA. Providing new options for the continuous development of processes and chromatographic methodologies that will improve the productivity, timeliness and scientific impact of analytical support. | 10/12/2019 |
| 928 | Coloplast Minneapolis, MN Consumer Care Advisor BS/BA or AS/AA Exp: 1-6 years in healthcare customer service/sales |
You will be primarily responsible for the support and education of end-users, caregivers, and clinicians with Coloplast products and services. Acquire and demonstrate all necessary subject matter expertise to provide responses regarding product application and problem resolution to clinicians and end-users. Accurately and thoroughly document each end-user program enrollment in Coloplast systems per standard department procedures. Responsible for data quality, including self-audit of work | 10/12/2019 |
| 929 | Complete Genomics San Jose, CA Research Associate BS or MS in engineering Exp: 1-3 years |
Advanced Engineering group of BGI Research USA is seeking to bring a highly motivated fixed-term Research Associate candidate to provide aid with advanced microfluidic research and development under the direction of a project leader and/or senior engineers and scientists. Maintain and run different aspects of microfluidic systems – reagents, software, hardware. Conduct assays, fluidic and platform validation and verification tests by following defined protocols for microfluidic devices and analyze the data to generate testing reports. | 10/12/2019 |
| 930 | Complete Genomics San Jose, CA Lab Technician BS/BA in molecular biology Exp: 1-2 years |
his position provides an opportunity to work with cutting-edge technologies and contribute to BGIA’s goal of improving human health by providing genomic information to understand, prevent, diagnose, and treat diseases and conditions. As a member of the BGIA Support team, the position will support next generation processes for genome sequencing. The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing | 10/12/2019 |
| 931 | Conagen Inc Bedford, MA Scientist/ Research Associate -Protein Biochemistry MS in biochemistry, molecular biology, or related Exp: 1+ years of related experience |
We are currently seeking an associate scientist to support the projects related to metabolic engineering of plant and microbial secondary metabolites. This position will focus on protein engineering and the candidate is expected to have a strong background in protein engineering, biochemistry, molecular biology and be able to translate protein structural concepts into novel protein engineering strategies. | 10/12/2019 |
| 932 | Conagen Inc Bedford, MA Receptionist/Administrative Assistant HS Diploma/GED Exp: 1 year in office setting |
We are looking for a Receptionist/Administrative Assistant to join our team. This person would assist our Administrative team in overall office and administrative activities as well as be the first point of contact in our offices. Maintains security by following procedures; monitoring logbook; issuing badges. Maintains records by scanning documents, labeling inventory, filing packing slips, updating spreadsheets, processing online scientific journal article requests. | 10/12/2019 |
| 933 | Conformis Wilmington, MA Production Quality Engineer BS in engineering or sciences Exp: 1-3 years in QA/QE |
The Production Quality Engineer will be responsible for product quality engineering, quality assurance, and production process activities. They will be expected to provide support to Operations, interact with customers and provide support for Design Engineering, Quality Systems and Process Engineering. This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures from concept through market introduction. | 10/12/2019 |
| 934 | Conformis Wilmington, MA Manufacturing Engineer I BS/BA in engineering, MS preferred Exp: 1-3 years in manufacturing process support/development |
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. | 10/12/2019 |
| 935 | ConMed Utica , NY Quality Engineer I BS in engineering (mechanical/biomedical) Exp: 0-3 years |
We are seeking a self-driven and continuous improvement-focused Quality Engineer I to join our Utica, NY based Quality Engineering team. In this role, you will work cross-functionally to support production lines for a variety of medical devices. You will execute projects aligned with CONMED's Quality System, ISO 13485 standards, risk management, test methods, calibration and product line support. Your efforts in problem solving, innovation and cross-functional collaboration will directly contribute to taking the site's safety, quality, delivery and cost metrics to the next level. | 10/12/2019 |
| 936 | ConMed Utica , NY Associate Assembler HS Diploma/GED Exp: 3+ months work experience |
As a Team Assembler I, you will perform basic packaging and shipping functions to include basic machine and equipment operation to fabricate parts for assembly and sub-assembly. | 10/12/2019 |
| 937 | Cook Medical Bloomington, IN Quality Engineer, Non-Conformance BS in engineering or life sciences Exp: Entry Level |
The Quality Engineer, Non-Conformance at Cook Incorporated serves as the quality representative of certain product lines within product development, manufacturing, post-market surveillance, and/or CAPA. Interface with internal and external groups on quality-related issues. Perform investigation of product non-conformances and/or processes. | 10/13/2019 |
| 938 | Cook Medical Bloomington, IN Application Engineer BS/BA in computer science or related Exp: Entry Level |
The Application Engineer at Cook Medical configures, implements and documents applications that provide the technical solutions to meet specifications and business requirements defined by company objectives to promote effective, efficient, and compliant operations. Technical responsibility for all stages of solution configuration to ensure compliance with application standards, architectural standards, and achievement of documented requirements. Ensure the stability, integrity and efficient operation of the business/workflow rules that supports core integration functions. | 10/13/2019 |
| 939 | Cook Medical Bloomington, IN Manufacturing Engineer BS/BA in related field Exp: No experience required |
Responsible for providing technical support for the day-today production activities in the manufacture of custom, plastic components used in the assemblies of various medical devices. This is a hands-on position with visibility on the manufacturing floor and requires a high level of interaction with the production, product development, and quality teams. The engineer is responsible for supporting product development activities, continuous improvement, complaint resolution, CAPA investigations and other quality initiatives. | 10/13/2019 |
| 940 | Cardinal Health Reno , NV Assoc I, Assembly - Shift (6am - 6pm) HS Diploma/GED Exp: 0-6 months |
Performs a variety of tasks ranging from repetitive to non-repetitive production to put together component parts to make assemblies, sub-assemblies or completed units, using standard operating procedures. May conduct quality inspections on processing line in accordance with quality specifications. | 10/13/2019 |
| 941 | Cardinal Health Reno , NV Associate II, Warehouse Ops HS Diploma/GED Exp: 1-2 years |
Warehouse Operations is responsible for performing/controlling a combination of manual or automated tasks necessary for the receipt, storage, and shipment of product. This may include functions of receiving, picking, packing, shipping, staging, transporting, storage, delivery, etc. Also responsible for the efficient flow of products from the point of product receipt from vendors to the shipment of products (via prescribed service parameters) to a variety of internal and external customers. | 10/13/2019 |
| 942 | Cardinal Health Mansfield, MA Engineer, R&D BS/BA Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. Entry level engineer to develop new and improved Surgical Drapes and Gowns, Face Masks, Infection Control Apparel, sterilization wrap. | 10/13/2019 |
| 943 | Cardinal Health Mansfield, MA Engineer, R&D BS/BA Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. | 10/13/2019 |
| 944 | Cardinal Health Hazelwood, MO Product Development Engineer I BS/BA in mechanical/biomedical/plastics engineering Exp: 0-2 years |
Research and Development Engineering is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. This position requires an individual to be responsible for supporting the development of new medical devices and improvements to existing products in the medical disposable area. These products are mechanical in nature, and our designs serve a global market. | 10/13/2019 |
| 945 | Core RX Clearwater, FL Manufacturing Technician HS Diploma/GED Exp: 1-3 years cGMP pharma manufacturing |
Works cross functionally within the organization to facilitate the successful completion of all development projects and meets the objectives and goals of CoreRx Inc. Leads manufacturing projects applicable to the individual’s qualifications. Performs batch instructions to include dispensing of materials, operation of all minor and some major process/blending equipment. Perform physical testing, product inspection, packaging, and general support of the manufacturing operation. | 10/13/2019 |
| 946 | Cortexyme South San Francisco, CA Clinical Operations Associate BS/BA in biological sciences, health care, or life sciences research Exp: 1-2 years related experience |
The Clinical Trial Assistant provides support to the clinical operations 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. | 10/13/2019 |
| 947 | Covance Madison, WI QA Assistant I HS Diploma/GED Exp: Entry Level |
Learn to perform protocol, data and report reviews to verify conformance to applicable SOP and regulatory requirements. Learn to evaluate responses to inspection reports and performs follow-up with respondents, management, or others, if needed, to ensure resolution. Ensures that systems used in QA are properly maintained (e.g., QA audit records, training records). | 10/13/2019 |
| 948 | Covance Madison, WI Study Technician (Research Assistant) Animal Operations BS/BA in life sciences Exp: 0-2 years |
As a Research Assistant (Study Technician) in our Madison, WI In-Life department, you will monitor the research animals’ health and welfare using your experience in animal observation and your experience working with sample collections. Collection, documentation, and management of pertinent data from animal observations, test material administration, and clinical sample collection. Maintaining the facilities in accordance with the Association for Assessment and Accreditation of Laboratory Animal Care (AALAC) | 10/13/2019 |
| 949 | Millipore Sigma Burlington, MA Sales Support Specialist BS/BA in business, chemistry, biology, or related Exp: Recent graduate |
In this role as a Sales Support Specialist you will be required to interact with internal and external customers from quotation generation through the Purchase Order processing phase. You will perform research using a variety of different databases including MilliporeSigma’s customer history database, service management database, contract management database, installation database and financial database. All of which store inquiries and information that MilliporeSigma has received from a customer and/or prospective customer. etc. | 10/8/2019 |
| 950 | Millipore Sigma Burlington, MA Maintenance Contract Sales Rep. BS/BA in business, chemistry, biology, or related Exp: Recent graduate |
The role of Maintenance Contract Sales Representative will require the candidate to interact with internal and external customers from quotation generation through the Purchase Order processing phase. They will generate quotes for new and renewal of service agreements for current MilliporeSigma customers. Should be able to work independently to manage new and renewal service agreements within a defined geographical territory. etc. | 10/8/2019 |
| 951 | Millipore Sigma St. Louis, MO QC Logistics Technician AS in life or physical sciences Exp: Recent graduate |
You will assist in evaluating safety practices with regard to team activities. Work both independently and in team environment. Manage sample inventory and department stock room. Troubleshoot interruptions to the normal process flow. Manage Quality and Retain Samples. Use lean and six sigma practices to optimize efficiency and eliminate waste from process. Adhere to process requirements in a continuously changing environment. etc. | 10/8/2019 |
| 952 | Millipore Sigma St. Louis, MO Associate Production Scientist BS/BA in chemistry or other science Exp: 1+ years |
Manufacture products according to established protocols and perform operations to support a chemical manufacturing department located in St Louis, MO. Physical Attributes: Will be frequently required to wear appropriate personal protection equipment “PPE” (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes, etc.) for protection from toxic or corrosive chemicals in the forms of liquids, solids, and/or vapors. While performing the duties of this job, the employee is regularly required to sit, stand, walk, reach above the shoulder, stoop, kneel, or crouch. etc. | 10/8/2019 |
| 953 | Millipore Sigma St. Louis, MO Customer Care Associate High school diploma/AS Exp: 1+ years |
The Customer Care Associate position involves working in a dynamic, fast paced, high energy call center, and rewarding team environment focused on delivering a better customer experience. You will be responsible for ensuring each transaction is processed within customer specifications for MilliporeSigma guidelines. As a Customer Care Associate, you must be eager to learn, be respectful, honest & humble, and embrace challenges. etc. | 10/8/2019 |
| 954 | Millipore Sigma Burlington, MA Service Support Specialist High school diploma or equivalent Exp: 1+ years |
In this role you will establish and maintain service schedules with customers, prepare and process repair quotations and manage service inventory. In addition, you will support installation orders by insuring sites are prepared for service and support the service partners. You will create an efficient service schedule to maximize resources, ensure material is on site and accurate. Coordinate service-related activities as guided by service engineers and managers. etc. | 10/8/2019 |
| 955 | Miltenyl Biotec Auburn, CA Accounting Associate AS/BS/BA Exp: 1-3 years |
As a key member of the Miltenyi Biotec Accounting team, you will provide accounts payable and accounts receivable support including collecting and posting payments, assisting in debits and credits when needed, reconciling back-up documents to invoices, processing invoices through receipt and account verification, maintaining vendor and accounting files, and preparing and verifying bank deposits. Within this role, you will perform month end duties as required inclusive of GL review and journal entries, as well as providing general administrative support. etc. | 10/8/2019 |
| 956 | Miltenyl Biotec Santa Barbara, CA Assembly & Test Technician AS/AA Exp: 1-3 years |
To support this effort, we are seeking an Assembly and Test Technician to support the assembly of designed parts for the company’s core medical instruments. Within this role, you will be responsible for supporting all tasks and functions in producing interposer to chip assemblies, while inspecting incoming raw materials and maintaining inventory for all production parts. Overall, your keen ability to work with a multi-disciplinary team to lead and advance product development efforts will champion the continued success of Owl biomedical. etc. | 10/8/2019 |
| 957 | Miltenyl Biotec Sunnyvale, CA Manufacturing Associate BS in a biological science or related Exp: 1-3 years |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. etc. | 10/8/2019 |
| 958 | Miltenyl Biotec Sunnyvale, CA Process Development Associate BS in a life science Exp: 0-2 years |
As a member of Miltenyi Biotec’s Process Development team, you will have the exciting opportunity to support the development of new processes that will generate cellular therapeutic products. You will apply your GLP/GMP experience to perform and maintain cell cultures using aseptic techniques. Ideally, you will be able to order materials and maintain inventory with the goal in mind that every effort is aimed at developing and qualifying processes required for clinical cell and gene therapy products. etc. | 10/8/2019 |
| 959 | Miltenyl Biotec Gaithersburg, MD R&D Scientist, Purification & Characterization MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to develop methods for the separation of different particle types and their characterization. Also, you will develop, evaluate and implement novel analytical methods for the fine characterization of viral vectors and exosomes, in view of the distinction of viral vectors from exosomes. You will design specific experiments to test LV function, perform statistical analysis of results, and communicate results internally, for use in publications, and in scientific meetings. etc. | 10/8/2019 |
| 960 | Miltenyl Biotec Gaithersburg, MD Research and Development Scientist, RCL/HIV MS in molecular biology, immunology, or virology Exp: 0-2 years |
As a member of the Lentigen Technology team, you will have the opportunity to perform duties within the area of development of new tests, including the development of a standard RCL test and in a second instance of an automatized RCL test. This includes the set-up of a standard test based on the use of C8166 cells, the characterization of the C8166 cells with respect to susceptibility and propagation of HIV over many cell passages, etc. A very issue related to this development is that the test has to comply with FDA requirements with at the end the transfer of the test to the QC department for routine use. etc. | 10/8/2019 |
| 961 | Mizuho San Diego, CA Field Service Engineer AS in electrical or mechanical applied science Exp: 1-2 years |
The Field Service Engineer (FSE) is primarily responsible for technical support, repairing and servicing Mizuho OSI products (orthopedic equipment) in the field throughout the United States. The Field Service Engineer provides highly visible customer support through the performance of on-site installation, as well as overseeing any necessary diagnoses, troubleshooting, service, and repair of complex equipment and systems, and performing preventive maintenance as required. etc. | 10/8/2019 |
| 962 | Moderna Cambridge, MA Senior Research Associate, Drug Product Process Sciences MS in pharmaceutical science or related Exp: 1 month relevant work |
Reporting to the Principal Scientist, Process Development, the Senior Research Associate, Drug Product Process Sciences will work with in vitro bioanalytical systems to evaluate samples from in vivo studies. The successful candidate will be able to deliver reproducible and impactful results under ambitious timelines. Here’s What You’ll Do: Develop and characterize lipid nanoparticle (LNP) formulations for delivery of mRNA. etc. | 10/8/2019 |
| 963 | MP Biomedicals Irvine, CA Fine Chemicals Specialist BS/MS in chemistry, biology or related Exp: 0-3 years |
The Fine Chemicals Specialist is responsible for developing and maintaining technical documentation for industrial and pharma customers. This role works closely with our global Fine Chemicals sales team to provide rapid response to customer requests for quote of new or existing products. Principal Duties & Responsibilities: Build required product documentation. Adjust documentation per customer requirements. Manage supplier qualification in alignment with MP Bio’s ISO procedures. etc. | 10/8/2019 |
| 964 | Bio-techne Minneapolis, MN Lab Assistant 1 AA degree Exp: 0-2 years |
This is a Part-Time position. Your responsibilities as a Laboratory Assistant 1 are to maintain the animal facility at Bio-Techne and perform general lab duties. Responsible for the welfare and immunization of all rodents that are used within R & D Systems. Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. General lab duties including stocking and organizing supplies and materials and preparing reagents. | 10/3/2019 |
| 965 | Bio-techne Minneapolis, MN Inside Sales Representative - Bioprocess Service Contracts BS in sciences Exp: 1 year in telemarketing/telesales |
The Inside Sales Representative is primarily responsible for achieving sales quota for ProteinSimple products, initially, Bioprocess (Maurice/iCE/MFI) system service contracts. This person will be located at the Bio-Techne headquarters in Minneapolis, MN, interfacing primarily via the telephone and email with customers and potential end-users in the assigned territory. The secondary role is to gain proficiency on all ProteinSimple products to provide back-up support for field sales reps, and ultimately take on a full-time field sales position. | 10/3/2019 |
| 966 | Bio-techne Minneapolis, MN QC Specialist 1 BS in biological sciences/chemistry Exp: 1-2 years in vitro diagnostics |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. Assist in establishing QC specifications. Performs analysis and interpretation of test results, identifies deviations, and makes appropriate recommendations | 10/3/2019 |
| 967 | Bio-techne San Jose, CA Production Chemist I AA or BS/BA in sciences/engineering Exp: 0-3 years in wet-lab manufacturing support |
The successful applicant will work with other members of the consumable production team as well as a multidisciplinary team of engineers and scientists to support routine production activities for reagent formulation/ compounding team. Principal duties and responsibilities: Help maintain and track supplies inventory. Preparation of buffers and other biochemical formulations. Conjugation of protein solutions. Record manufacturing tasks in batch records/travelers. | 10/3/2019 |
| 968 | Bio-techne San Marcos, CA Packaging Technician HS Diploma/GED Exp: 1-2 years in vitro diagnostics |
Perform kitting, liquid / powder filling and labeling functions. Assist in the setup and running of automated liquid filling, labeling and packaging equipment. Assist in the setup and running of manual liquid and powder portable filling equipment. Comply with Good Manufacturing Practices (GMP’s) and Quality Systems Regulations (QSR). Inspect all materials being issued to and returning from shop orders. Accurately count and return all materials. | 10/3/2019 |
| 969 | Bio-techne Minneapolis, MN Research Associate, Antibody Purification BS/BA in biological sciences/chemistry or related Exp: 0-2 years |
As an Antibody Purification Research Associate you will be responsible for performing antibody purifications and conducting in process testing of product. Purify monoclonal and polyclonal antibodies following appropriate SOP’s. Prepare buffers as needed for the purification process. Document the purification processes in the appropriate computer systems. Perform routine HPLC and other equipment maintenance. | 10/3/2019 |
| 970 | Bio-techne Minneapolis, MN Equipment Technician 1 HS Diploma/GED Exp: 1-2 years in equipment maintenance |
As a Equipment Technician 1 you will perform preventative maintenance and repair malfunctioning new and existing minor equipment. Respond and log supervisory alarms on TAC Monitoring System during business hours. Act as the secondary facility maintenance mechanic responsible 24/7 on call for TAC & Security System with department personnel. Assist with installing new and existing equipment, offices furniture and shelves. Perform additional duties as assigned. | 10/3/2019 |
| 971 | Bio-Technical Resources Manitowoc , WI ASSISTANT RESEARCH SCIENTIST, ANALYTICAL SUPPORT BS/BA or MS in analytical chemistry, chemical engineering or related Exp: 1-3 years |
The position involvesimplementation of HPLC, chromatography, enzyme assays, and gel-basedanalytical methods.Common tasks include analytical separations and quantitative analyses by:1) HPLC and column chromatographyincluding affinity chromatography, IEX, HIC, and SEC; 2) spectrophotometric enzyme assays; 3) sample preparation and extraction;and 4) basic antibody and protein analyses,usingELISA, protein extraction, protein concentration assays, SDS-PAGE, and Western blot. | 10/3/2019 |
| 972 | BiOTek Winooski, VT Electro-Mechanical Assemblers AS/AA in relevant field Exp: 0-2 years |
Responsibilities include performing assembly and inspection processes, collecting report data as required by Quality standards, maintaining shop supplies, floor stock and tools and knowledge and support for Lean Manufacturing principles. Ability to lift and move units up to 35/40 lbs in weight to 5-foot high levels is required. You may perform product tests and material transaction; learn and support new products and train new employees consistently striving for efficient and effective methodologies. | 10/3/2019 |
| 973 | Biotium Fremont, CA Research Technician/Research Associate, Bioscience BS/BA or MS in biology or biochemistry Exp: 1 year research experience |
Under the supervision of Biotium scientists, perform production and quality control testing of assay kit components following standardized protocols. Under the supervision of scientists, perform R&D assays to develop new fluorescence-based products. This individual will be responsible for production and QC of products, as well as play a role in the design,optimization and assessment of novel reagents for fluorescent detection technologies. | 10/3/2019 |
| 974 | Bioventus Boise, ID Associate Sales Representative BS/BA Exp: 0-2 years |
The Associate Sales Representative (ASR) plays a critical role in helping to improve people’s lives every day, interacting directly with healthcare providers and their patients to introduce our products. ASRs also educate patients on the proper use of our products and provide invaluable support to the entire sales team. Develop and execute regional business plans to achieve quotas for assigned products, which may include cold calling to develop new customers, qualifying and following up on leads and selling to new and/or existing accounts | 10/3/2019 |
| 975 | Biovision Milpitas, CA Sales Representative BS/MS in biochemistry, or biological sciences Exp: 1-2 years in life science industry |
Meet or exceed sales objectives set by the BioVision management. Learn and master BioVision's product offering and manufacturing capabilities. Establish long-term relationships with the customers and match BioVision's capabilities with customer needs. Identify key contacts and decision makers to maximize the benefits from customer visits. Develop a customer-specific account management approach, identifying new business and growth opportunities | 10/3/2019 |
| 976 | bluebird bio Cambridge, MA Cellular Process Development & Gene Editing Specialist BS in biological sciences Exp: 0-2 years |
The cellular process development teams are responsible for developing cellular drug product processes and introducing new technologies for stem cell and T-cell therapies. The focus of this position is to contribute to the development of next generation manufacturing processes for cell therapies. We are looking for a motivated associate scientist to drive development and characterization projects. | 10/3/2019 |
| 977 | Boehringer Athens, GA Technician I, Packaging Second Shift (2:00pm-9:30pm, Monday-Friday) HS Diploma/GED Exp: 1 year manufacturing experience |
To perform the duties associated with labeling, inspecting and packaging of Boehringer Ingelheim vaccines. Performs and executes with others, all daily scheduled activities associated with packaging vaccines. Label and inspect products accurately and efficiently, to meet quality guidelines. Complete documentation in an accurate, concurrent and timely manner | 10/4/2019 |
| 978 | Boehringer Fremont, CA Engineer I, MSAT Upstream MS in engineering Exp: 0 years |
The primary purpose of the position is to execute projects, perform routine experiments and analyze data in the Upstream Manufacturing Science and Technology (MSAT) group. The position holder must live the BI values and promote a positive work environment for others. Has discretion in tactical execution of process improvement projects, investigations and experiments. Frequently executes routine and occasionally complex experiments with sound scientific and engineering principals to resolve problems with minimal oversight. The Engineer frequently executes against specific deliverables developed by the department leadership to improve operational efficiency. | 10/4/2019 |
| 979 | Boston Analytical Salem, NH Microbiologist BS/BA in microbiology or realted Exp: 0-2 years cGMP work environment |
The QC Microbiologist I 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 through compendial methods and client specific test protocols. Prepares and analyzes samples to determine microbiological quality through the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity). | 10/4/2019 |
| 980 | Boston Analytical Salem, NH Lab Technician – Microbiology HS Diploma/GED Exp: no minimal experience required |
The Lab Technician in the Microbiology Lab will perform routine laboratory tasks and assist laboratory personnel according to FDA, cGMP and Boston Analytical’s Standard Operating Procedures. Cleans and maintains laboratory glassware (including sterilization), equipment, and laboratory. Monitors and maintains water system, including sample collection for Bioburden, TOC, and Conductivity. Properly handles, stores and disposes of hazardous materials according to OSHA and Boston Analytical procedures. | 10/4/2019 |
| 981 | Boston Analytical Salem, NH Lab Technician – Chemistry HS Diploma/GED Exp: no minimal experience required |
The Lab Technician will perform routine laboratory tasks and assist laboratory personnel according to FDA, cGMP and Boston Analytical’s Standard Operating Procedures. Cleans and maintains laboratory glassware, equipment, supplies and laboratory. Properly handles, stores and disposes of hazardous materials. Assists Chemists and other company personnel on an as needed basis. | 10/4/2019 |
| 982 | Boston Analytical Salem, NH Analytical Chemist *All-Levels* BS/BA in chemistry or related Exp: 0-5 years |
he 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. | 10/4/2019 |
| 983 | Boston Analytical Salem, NH QA Specialist – All Levels BS/BA in related sciences Exp: 0-3 years QA experience |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. Auditing chemists’ routine project folders for conformance to company and customer requirements. Write, review and edit Standard Operating Procedures (SOP’s, Forms and Methods) and familiarity with internal SOPs. Alternate contact person for QA questions relating to laboratory operations and client correspondences. | 10/4/2019 |
| 984 | Boston Scientific Arden Hills, MN Quality Technician II Job AA degree or higher Exp: 1-2 years in medical device quality |
Provide Quality Technician support to Arden Hills commercial and development manufacturing lines ensuring delivery of the highest quality product to the customer while supporting continuous improvement projects and quality initiatives. This is a dynamic support role requiring cross-functional collaboration with production, manufacturing, and quality team members. This role includes responsibility for providing day-to-day quality support for manufacturing, including the processing of non-conforming product (identification, documentation, segregation evaluation and disposition), certifying builders and responding to quality signals. | 10/4/2019 |
| 985 | Boston Scientific Maple Grove, MN Quality Engineer I - Design Assurance BS in engineering or related Exp: 0-2 years in engineering |
The Design Assurance Engineer I is a quality engineer that directly supports medical device product development from concept through commercialization. This position will work with high-performance cross-functional development team to establish and maintain the design control deliverables, risk management activities, and DHF compliance within Interventional Cardiology to ensure delivery of the highest quality product to the customer. | 10/4/2019 |
| 986 | Boston Scientific Arden Hills, MN Product Performance Engineer I BS Exp: 0-3 years |
This Quality Engineer role will investigate product complaints and monitor BSC product performance. The team uses product performance data to escalate post-market field performance signals into the CAPA process in collaboration with Return Device Analysis, R & D, Design Assurance, Medical Safety and the CAPA Management teams. This role provides for significant visibility across the quality organization | 10/4/2019 |
| 987 | Boston Scientific Maple Grove, MN Technical Writer I BS/BA in technical writing or related Exp: 6 months + related |
This Technical Writer will work as a team member on product development or other technology projects to bring clarity and consistency to documents through accurate and concise writing and effective use of document format. In summary, this tech writer will write, revise, organize, plan, summarize, edit, and proofread technical engineering documents and maintain project records. | 10/4/2019 |
| 988 | Brammer Bio Somerville, MA Planner I BS/BA Exp: 1-3 years of planning/manufacturing |
Daily planning operations supporting the manufacturing facility; planning for and ensuring availability of raw materials, components, and resources per the site’s detailed manufacturing schedule. Facilitate and coordinate activities with all departments to ensure the availability of raw materials for plant operations supporting development through commercial production. Review cGMP production records and perform associated inventory transactions in the ERP system. | 10/4/2019 |
| 989 | Brammer Bio Cambridge, MA Engineer I, Process Engineering BS in automation/electrical/chemical/mechanical engineering Exp: 0-3 years |
Responsible for the support of clinical and commercial drug manufacturing in the new Viral Vector Manufacturing facility located at the Cambridge, MA campus. Scope includes designing, specifying, and supporting manufacturing equipment such as autoclaves, incubators and analytical equipment in our newly built viral vector manufacturing facility. Individual will be part of an experienced team of process and automation engineers working closely with groups such as manufacturing, quality assurance, quality control and validation. | 10/4/2019 |
| 990 | Brammer Bio Cambridge, MA Engineer I, Automation BS in automation/electrical/chemical/mechanical engineering Exp: 0-3 years |
Responsible for the support of clinical and commercial drug manufacturing in the new Viral Vector Manufacturing facility located at the Cambridge, MA campus. Scope includes designing, specifying, and supporting manufacturing systems such as DeltaV, Allen Bradley PLC and analytical equipment in our newly built viral vector manufacturing facility. Individual will be part of an experienced team of process and automation engineers working closely with groups such as manufacturing, quality assurance, quality control and validation. | 10/4/2019 |
| 991 | Brammer Bio Cambridge, MA Associate I, Process Sciences BS in biochemical/chemical engineering or related Exp: 0-2 years |
he Process Sciences (PS) Associate’s primary responsibility is to support the process establishment, pilot, and process characterization for the manufacturing of viral vectors. This position requires close interaction with the 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 therapeutics. | 10/4/2019 |
| 992 | Brammer Bio Lexington, MA Associate I, MFG Nights BS in life sciences Exp: 0-3 years |
Responsibilities include performing basic to moderately complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. Must be technically capable with a basic theoretical comprehension of general biopharmaceutical manufacturing equipment, principles and processes and have a basic understanding of current GMP and safety standards. | 10/4/2019 |
| 993 | Brammer Bio Lexington, MA Associate I, Manufacturing Downstream BS Exp: 1-3 years |
Responsible for cGMP manufacturing operations at the Brammer Lexington site Downstream Operations. Executing aseptic operations within Biosafety cabinet and cleanroom environment. Preparation of buffers to support downstream purification activities. Performing Chromatography, TFF, Viral Filtration, and Final Formulation steps. Performing various filter integrity tests throughout the process. Follows verbal and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation. | 10/4/2019 |
| 994 | Brammer Bio Cambridge, MA Associate I, Manufacturing BS in life sciences Exp: 1-3 years |
Associate I, Manufacturing is an associate with a moderate level of technical expertise and experience. Associate I may perform complex activities outside of routine manufacturing operations commensurate with their experience and training. Associate I participates in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls under limited supervision. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. | 10/4/2019 |
| 995 | Bristol-Myers Squibb Hopewell, NJ Associate Biological Technician BS/BA with ALAT certification within 12 months of hire Exp: 0-2 years |
The Associate Biological Technician performs semi-routine or diversified work that requires the ability to differentiate established principles and practices from unique occurrences which may necessitate adapting or modifying methods. May be required to breed and develop animal colonies, collect tissue samples and collect data for routine operations. Perform support duties that involve animal health maintenance, i.e. sentinel program, water and feed evaluation, sanitation sampling and testing, and other related tests, as required | 10/4/2019 |
| 996 | Bristol-Myers Squibb Syracuse, NY ASSOCIATE ENGINEER I MS in engineering Exp: 0-2 years |
The Manufacturing Technology Associate Engineer will support Manufacturing Operations (Downstream processing, column packing) on a daily basis, as well as lead or contribute to strategic projects. Support projects and identify opportunities for productivity, robustness, quality, business process, and safety improvements. Regular and frequent on-floor observation to support and improve manufacturing. | 10/5/2019 |
| 997 | Bristol-Myers Squibb Redwood City, CA Associate Research Scientist MS with background in immune-oncology Exp: 0-2 years |
This position will specifically support acquisition, processing, and analysis of human tumor tissue. The candidate will contribute to tumor tissue analysis, including drug response, phenotypic, histoloical, and genomic/transcriptomic analyses of these tissues. The candidate will be expected to effectively collaborate with colleagues in the oncology, translational medicine, biomarker and clinical groups. The successful candidate will demonstrate clear verbal and written communication skills. | 10/5/2019 |
| 998 | Essity Menasha, WI Entry Level Paper Mill Support HS Diploma/GED Exp: Entry Level |
Support Multi-Million Dollar Fiber Processing and De-inking Assets, working in a Team environment, handling raw materials and finished Tissue parent rolls as necessary. | 10/5/2019 |
| 999 | BD Salt Lake City, UT Engineer I, R&D Product Development BS in mechanical/biomedical engineering Exp: 0-2 years |
This position designs, develops, and implements new products, processes, test methods and equipment. Initiates new or revised documentation and tracks through appropriate approval cycles and implementation. Maintains a professional working relationship with internal and external customer and support staff. Participates and/or leads cross-functional teams. | 10/5/2019 |
| 1000 | BD Salt Lake City, UT R&D Technician II AA/AS in sciences, math, engineering Exp: 0-5 years |
This position reports to an engineer on the Dialysis Team. An R&D technician helps with the generation of test protocols and reports, tests products and reports results, and helps to design and maintain test fixturing. In addition, they may help with troubleshooting and test development. Assists in the execution of test protocols, methods and procedures. Sets up and operates test equipment and records measurements with limited supervision | 10/5/2019 |
| 1001 | BD Salt Lake City, UT Scientist I BS/BA or MS in molecular biology Exp: 1 year or more |
Scientist I is required to work within a team that develops automated assays using nucleic acid isolation and real-time amplification/detection technologies. Reporting to the Group Leader/Manager, the successful candidate will be responsible for assisting in the design, development, integration and/or qualification of assays on automated systems. The successful candidate may also be expected to provide support in execution of clinical studies to validate performance of the assays and assemble relevant information in support of regulatory submissions. | 10/5/2019 |
| 1002 | CaREdX Brisbane, CA Clinical Laboratory Assistant AA, BS/BA in biological sciences Exp: 1-3 years |
The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 10/6/2019 |
| 1003 | CaREdX Brisbane, CA Clinical Laboratory Assistant AA, BS/BA in biological sciences Exp: 1-3 years |
The Clinical Laboratory Assistant (CLA) performs a variety of laboratory and administrative tasks to support the clinical laboratory staff in the CLIA-certified CareDx laboratory. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed. | 10/6/2019 |
| 1004 | Caribou Biosciences South San Francisco, CA In vivo Pharmacology Research Associate BS/BA in life sciences Exp: 1 or more year lab work w/rodents |
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 (IV, IP, SC, and PO) and blood draw techniques (RO bleed and cardiac puncture), 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. | 10/6/2019 |
| 1005 | Caris Life Sciences Phoenix, AZ Customer Support Representative- Oncology AS/AA in relevant field Exp: 1-3 years in client service roles |
A Customer Support Representative acts on behalf of Caris as the first tier of support for all client issues or needs. This position responds to internal and external client inquiries regarding logistics, testing, supplies, and other support needs. This position handles all incoming documentation into the department. Independent judgment is required to carry out assignments that have a significant impact on clients. | 10/6/2019 |
| 1006 | Casma Therapeutics Cambridge, MA Research Associate--Cell Lines, Biology MS in biological sciences Exp: 1-3 years |
The individual should possess strong core competencies in cell biology, molecular biology, assay development. We are seeking a qualified candidate who will share our excitement about the science, contribute to our culture, and honor our commitment to patients. Perform western blotting, FACS and imaging analysis to analyze autophagy and specific target activity in primary cells and cell lines. Cell culture and cell line development using retro- and lenti-virus, CRISPR and downstream analysis of autophagy and signaling. | 10/6/2019 |
| 1007 | Catalent Madison, WI Associate Scientist, Quality Control Microbiology BS/BA in biotechnology Exp: 0-2 years |
The Associate Scientist, Quality Control Microbiology position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained on technical procedures and once trained, execute them consistently and reliably. Additionally, this position will support Preventative Maintenance and basic Laboratory maintenance activities while maintaining a GMP quality system. The Associate will work on assignments that are primarily routine in nature but also provides support on projects and conducts lab work involving additional complexity. | 10/6/2019 |
| 1008 | Catalent Madison, WI Assistant Scientist, Upstream Process Development MS or BS/BA in biolotechnology Exp: 1-3 years lab experience |
The Assistant Scientist, Upstream Process Development will perform a variety of laboratory procedures to support Upstream Process Development. The position will perform daily work assignments accurately and in a timely and safe manner. This position 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. | 10/6/2019 |
| 1009 | Catalent Madison, WI Associate, Biomanufacturing Operations BS/BA in biotechnology Exp: 0-2 years |
Catalent has an entry level Associate, Biomanufacturing position available. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position offering enticing compensation incentives. Work hours are Wednesday to Saturday (4/10). | 10/6/2019 |
| 1010 | Catalent Madison, WI Associate, Biomanufacturing BS/BA in biotechnology Exp: 0-2 years |
Catalent has an entry level Associate, Biomanufacturing position available. As an Associate, Biomanufacturing you will perform aseptic techniques within a clean room environment. You will learn to execute and properly document current good manufacturing practices (cGMP) activities. This is a second shift position. Work hours are Sunday to Wednesday (4/10). | 10/6/2019 |
| 1011 | Catalent Madison, WI Manufacturing Associate, Drug Substance Downstream AS/AA or BS/BA Exp: 0-2 years GMP experience |
A manufacturing associate’s primary duty is to perform a variety of operational tasks in accordance with current GMP's. Operators must work effectively in a team environment to achieve company goals and must adhere to all company compliance, safety, and attendance requirements. Safely operates equipment within a preparation area (i.e. cleaning, steamings, buffer/media prep, parts washing, autoclaving, etc) | 10/6/2019 |
| 1012 | Catalent San Diego , CA Analytical Chemist I BS/BA in sciences Exp: 0-2 years |
This a great entry-level opportunity for a new grad looking to gain hands-on industry experience and learn a variety of lab techniques. The Analytical Chemist I will be expected to understand and execute basic analytical procedures in order to assess the quality of pharmaceutical API, intermediates, and final drug products under limited supervision. Duties may include the preparation of simple aqueous and organic buffered solutions, volumetric dilution of samples and standards using good laboratory techniques, clear and accurate record keeping in laboratory notebooks, use of analytical instrumentation to acquire raw data, calculation and reporting of final results. The Chemist I will begin to develop product-specific cleaning methods to support use of GMP manufacturing equipment. | 10/6/2019 |
| 1013 | Catalent Madison, WI Gold Associate: Biologics Track BS/BA Exp: Graduating in 2019-2020 |
The Catalent GOLD Program is a two-year rotational development opportunity designed for university graduates who are excited to accelerate their careers in an entrepreneurial, fast-paced and inclusive environment. If you are ready to meet new challenges head on with creative solutions and unrelenting passion to deliver on the needs of patients around the world, join us. | 10/6/2019 |
| 1014 | Celerion Lincoln, NE Laboratory Equipment Maintenance Technician AS/AA in sciences Exp: 1+ years lab experience |
As the Laboratory Equipment Maintenance Technician, you will be responsible for assisting in the maintenance of bioanalytical equipment. This position offers a chance to work on a wide variety of laboratory equipment that is vital to the clinical research process. Assists with the setup, operation, evaluation and troubleshooting all types of bioanalytical laboratory instruments, including interfacing with LCMSMS, pumps, water baths, plate washers, plate readers, incubators, etc. | 10/6/2019 |
| 1015 | Cell Signaling Technologies Danvers, MA Product Marketing Coordinator BS in lifes ciences with business concentration or related Exp: Entry Level |
We are seeking a highly organized Product Marketing Coordinator who will be responsible for supporting product marketing lifecycle management related projects, including product line discontinuations, product conversion campaigns, market research and promotions. This is an exciting opportunity for someone with strong analytical skills looking to work in a fast-paced, collaborative team setting where they can experience multiple facets of Product Marketing. | 10/6/2019 |
| 1016 | FuijiFilm Madison, WI Laboratory Technician BS/BA in biological sciences/chemistry or related Exp: 0-2 years |
FUJIFILM Cellular Dynamics, Inc in Madison, WI is recruiting for a laboratory technician. This role provides an outstanding opportunity for talented and self-motivated individuals working with our R&D teams. Ideal candidates will have exposure to cell culturing and will be interested in advancing their career to support our ongoing efforts to generate differentiated cell types from human induced pluripotent stem cells. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and life science products and tools to support research endeavors. In return we provide development and support to enhance your career development in the field of cutting edge iPSC technology. | 10/6/2019 |
| 1017 | Merz Franksville, WI Biomedical Engineer - Mechanical BS in mechanical engineering or equivalent Exp: 0-3 years |
This role is to collaboratively partner with business leaders to ensure continuity of supply for MNA device business and optimize our technical service operation to meet the global customer demands. Installed Base Support: Provide continuing product support for manufacturing, regulatory and quality on design requirements, customer needs, testing, CAPA, reliability predictions, and product documentation. etc. | 10/1/2019 |
| 1018 | MSD Rockville, MD Customer Service Representative BS/BA Exp: 1 year |
The Customer Service Representative I will provide professional, courteous, customer-centric service to the MSD customer base. This individual will directly interact with various customers and interface with multiple internal departments to facilitate the processing of quotes, orders and customer requests to allow for timely shipping of MSD products worldwide. etc. | 10/1/2019 |
| 1019 | MSD Gaithersburg, MD Quality Assurance Specialist BS/BA Exp: 1 year |
This Quality Assurance Specialist position is responsible for the operation and compliance of the training program within the Quality Management System (QMS). The incumbent will provide assistance within the department to support Document Control initiatives and the management of document change order packages. etc. | 10/1/2019 |
| 1020 | MSD Gaithersburg, MD Research Associate I BS/MS in relevant field Exp: 1+ years |
A Research Associate is responsible for independently designing and executing experiments and analyzing the resulting data in support of reagent and assay development projects. This is a laboratory based position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). The incumbent is expected to display a wide-degree of latitude, creativity and self-management. etc. | 10/1/2019 |
| 1021 | MSD Rockville, MD Production Control Tech I BS in a relevant field Exp: 1 year |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. The position will help standardize and improve documentation, manufacturing procedures and processes to increase production efficiency and ensure best practices are followed. The position will also help implement new products, projects and processes within Manufacturing Operations. Some degree of professional latitude, creativity and self-management is expected. etc. | 10/1/2019 |
| 1022 | Microbiologics Saint Cloud, MN Customer Service Representative AS/BA/BS in sales, communication, or related Exp: 1 year |
Essential Responsibilities: Manages incoming calls; respond to customer inquiries and/or direct calls accordingly. Receive and process orders received via phone, email, fax, website, Electronic Data Interchange (EDI) or other type of electronic Purchase Order system; calculates charges and process invoices. Review product availability and order status in the company ERP system (NetSuite). Open customer accounts in NetSuite. etc. | 10/1/2019 |
| 1023 | Micropoint Santa Clara, CA Quality Control Associate MS in chemistry, biology, or related Exp: None needed |
We are looking for highly motivated QC Associates (two openings) to join our quality team. These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. etc. | 10/1/2019 |
| 1024 | Micropoint Santa Clara, CA Manufacturing Operator HS diploma Exp: 0-2 years |
There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the company's disposable test cartridges. Responsibilities: Follow written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging. Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection. Prepare materials used in the cartridge production process. etc. | 10/1/2019 |
| 1025 | MicroVention-Terumo Aliso Viejo, CA Industrial Engineer I BS in industrial, mechanical or related engineering field Exp: 1-3 years |
The Industrial Engineer I supports manufacturing of products for medical devices with work including operational systems development, process flow, operational needs and process efficiencies. Capacity analysis, Layout management, Systems support, Lean programs and Improvement projects are part of the daily activities. Job duties: Analyzes Capacity for production lines including time studies and line balancing.Develops Lean Manufacturing initiatives. Designs and develops operational systems processes for new products, product changes and enhancements. etc. | 10/1/2019 |
| 1026 | MicroVention-Terumo Aliso Viejo, CA Assembler II (1st Shift) HS diploma or equivalent Exp: 1-3 years |
Performs the assembly or sub-assembly of medical devices and products in an advanced position under moderate supervision from line leaders and supervisors in accordance with manufacturing documents and verbal instructions. Using written and verbal instruction to assemble and package product. Records data associated with the building of product on builds records. Ability to meet quality standard. Perform job function within production standard on 2-5 operations. Work with engineers and supervisors to perform special assembly requests | 10/1/2019 |
| 1027 | MicroVention-Terumo Aliso Viejo, CA Engineer I/II, Process Development (with Mechanical Emphasis) BS in engineering Exp: 0-6 years |
This position will lead efforts in the creation and development of new tooling, equipment and fixtures for R&D of medical device products and mfg. processes. Provides mechanical design concepts for automated and semi-automatic equipment and machinery aimed at improving mfg. productivity, capability, and quality. Supports process development activities of new equipment/fixtures/tooling by performing tests to prove that product subassemblies or finished products meet requirements. Works proactively on projects to carry design concepts through to production release and implementation. etc. | 10/1/2019 |
| 1028 | MicroVention-Terumo Aliso Viejo, CA Engineer I/Engineer II, Mfg. Process BS in related field Exp: 0-3 years |
The Engineer I/Engineer II, Manufacturing Process is responsible for the improvement, sustaining, development, and overall support of new and existing manufacturing processes for new and existing products, product changes and enhancements, as well as related tooling and fixtures. Supports validation of product, equipment and processes. Interfaces with other departments to solve production problems. Monitor equipment maintenance program. Investigation and testing of product processes. etc. | 10/1/2019 |
| 1029 | MicroVention-Terumo Aliso Viejo, CA Scientist I BS in chemistry Exp: 0-2 years |
Under guidance and supervision, evaluates the chemical and physical properties of various organic and inorganic substances in order to investigate their applications to the medical device industry. Job duties: Primary work location is in the R&D chemistry laboratory. Secondary work location is in an office environment. Handles chemicals safely in accordance with approved processes and procedures. Performs laboratory tasks under direct supervision. etc. | 10/1/2019 |
| 1030 | 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 |
| 1031 | Baxter Round Lake, IL Quality Associate I, Receiving & Inspection AS/AA or BS/BA Exp: 1-3 years in medical devices/pharma |
Quality Associate performs daily quality review of raw material documentation to ensure that materials being received are produced in accordance to Company methodology, procedures, and standards. Quality Associate completes Change Control, Supplier Quality, and Nonconformance and Corrective Action Preventive Action (CAPA) quality records related to Receiving & Inspection. Quality Associate is SME for Receiving & Inspection procedures and manages projects. | 9/25/2019 |
| 1032 | Baxter Opelika, AL QA I -Training BS in sciences Exp: 0-3 years in manufacturing |
Conducts reviews of documentation and reports for conformance to procedures, protocols, and regulatory requirements. Ensures training effectiveness in production. Provide Quality support with assigned projects and/or audits to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. | 9/25/2019 |
| 1033 | Baxter Round Lake, IL Associate, TDP BS or MS in engineering/sciences Exp: 0-2 years |
Over the course of two years, the TDP participant will complete four x 6-month rotations, with the option to combine two rotations into a single 12 month rotation. The rotations will be based in Research and Development at Baxter’s Round Lake, IL, and Deerfield, IL, locations. Participants can optionally have the opportunity to travel to or work from other Baxter Research and Development sites across the globe. | 9/25/2019 |
| 1034 | Bayer Creve Coeur, MO Software Developer-Entry BS in computer sciences Exp: Entry Level |
The primary responsibilities of this role, Software Developer, are to: Collaborate daily with a team of Software Developers, Product Manager, Product Specialists, and Agile Coach to build and support applications; Work with team and Product Manager to manage project priorities, deadlines and deliverables; Interact directly with business customers to gather and understand requirements and how they translate in application features; | 9/25/2019 |
| 1035 | Bayer Woodland, CA Lab Tech II BS/BA in science-related field Exp: 1+ years in lab setting |
The primary responsibilities of this role, Lab Technician II, are to: Under the direction of Lab Operations Managers and/or Lab Coordinators complete the testing processes ensuring process control, accurate data management, timely escalation of problem solving, and error correction; Ability to learn and apply scientific methods and non-routine techniques for analysis as directed by protocols and work instructions to deliver quality results - which may include preparation of reagents, media, controls and sample preparation | 9/25/2019 |
| 1036 | Bayer Indianola, PA Engineer Quality BS in engineering Exp: Entry Level |
The primary responsibilities of this role, Engineer Quality, are to: Provide focused quality engineering support to develop, support and maintain quality engineering methodologies that meets Customer, Regulatory and Bayer requirements; Lead the Material Review Board cross-functional team to investigate and address all manufacturing non-conformances; Lead and support investigations by conducting problem solving and root cause analysis to address failures identified by customer complaints, internal non-conformances and manufacturing yields. | 9/25/2019 |
| 1037 | Bayer St. Louis , MO Research Associate MS in plant biology or related Exp: 0-1 year working experience |
Responsible for carrying out routine and discovery experiments in partnership with scientists. Responsible for generating highest quality research data and performing validation experiments; Responsible for organizing and recording experiment notes/best practice documents in a timely fashion to secure the company’s IP and FTO; Manage best practice documents training of new members and help onboard new team members | 9/25/2019 |
| 1038 | Beaufort Norfold, VA Clinical Trial Assistant BS/BA in science-related field Exp: Entry Level |
Beaufort is currently looking for a Clinical Trial Assistant to add to our growing Clinical Operations team! The Clinical Trial Assistant (CTA) is responsible for supporting the clinical project team in daily study activities and clinical trial conduct by providing administration and project tracking support. | 9/25/2019 |
| 1039 | Hach Loveland, CO Entry Level Firmware Engineer BS or MS in computer sciences/engineering Exp: Entry Level |
The entry level firmware engineer is an integral position within the Hach R&D team. The engineer will be part of a fast paced team, working in a collaborative environment that will drive growth and innovation within the firmware competency. The engineer will engage with SCRUM in an Agile team environment with the core responsibility of developing high quality innovative solutions. | 9/25/2019 |
| 1040 | Berg Framingham, MA Research Associate II – Neurology BS or MS in biology, neuroscience, biochemistry or related Exp: 1-2 years in lab setting |
Research Associate II is an experienced and motivated individual. The RA II will characterize novel therapeutic targets for neurodegenerative diseases and assists in the development of potency assays and phenotypic screens in vitro. | 9/28/2019 |
| 1041 | Berg Framingham, MA Laboratory Operations Specialist I AS or BS Exp: 0-2 years |
The Laboratory Operations Specialist I, in the Bioanalytical division, is an entry-level Laboratory Operations Specialist who will work primarily in our lab and they will be accessioning clinical samples, following SOPs, documenting all work performed and will assist with QA tasks. | 9/28/2019 |
| 1042 | BGI Montreal , Ca Lab Technician BS/BA in molecular biology or related Exp: 1-2 years industry expereince/training |
As a member of the BGIA Support team, the position will support next generation processes for genome sequencing. The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. | 9/28/2019 |
| 1043 | BGI San Jose, CA Lab Technician BS/BA in molecular biology or related Exp: 1-2 years industry expereince/training |
As a member of the BGIA Support team, the position will support next generation processes for genome sequencing. The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing. | 9/28/2019 |
| 1044 | 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 |
| 1045 | 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 |
| 1046 | 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 |
| 1047 | Bioclinica Princeton, NJ Pricing & Proposals Associate BS/BA Exp: 0-1 years in pharma/CRO |
Generates, analyzes, and manages accurate and timely client proposals by: Reading, analyzing, and collaboratively working with the functional team owners to understand client’s Request for Proposal (“RFP”) & protocol. Validating pricing model is within acceptable company gross margin standards, escalating to Business Lead if outside margins. Consulting on standard, variable, and value-add costing parameters based on RFP and protocol. | 9/28/2019 |
| 1048 | Bioclinica Tranklin, TN Procurement Associate Associates/Bachelors degree in business management or related Exp: 1-2 years vendor interaction |
The Procurement Associate will work directly for the Procurement Manager to assist in the operational procurement at the departmental level. He/She will own the procurement process for the department in scope and ensure compliance, budgets and corporate strategy. He/She will have responsibility for negotiating pricing arrangements. He/she will work closely with the finance, accounts payable, legal, and quality control. | 9/28/2019 |
| 1049 | Bioclinica Princeton, NJ Imaging Operations Coordinator Associates/Bachelors in engineering, information technology, or computer science Exp: 1 year computer experience |
TheImagingOperationsCoordinator performs data processing for allstudies. Review,process,trackand monitor alldata received from clinicalsites. Verify upon login that data received istheexpected data based on project protocol and previouspatientidentifiers. Review data discrepancies and resolve or route to study team as necessary/. et. | 9/28/2019 |
| 1050 | Bioclinica Princeton, NJ DXA Imaging Analysis Technican I BS/BA in health/sciences Exp: 0-1 years in clinical trials support |
Performs DXA analysis and quality control in accordance with study-specific deliverables and within study-specific turnaround times. Understands functions of software used to produce and collect DXA image analysis results. Communicates with Clinical Project Managers, Imaging Research Associates and/or Scientific Director regarding image quality, deliverables, and data discrepancies. | 9/28/2019 |
| 1051 | Biocytogen Boston, MA in vivo Pharmacology Research Associate BS or MS Exp: 1-5 years research experience |
Perform preclinical pharmacology studies in rodents. Tasks include drug administration via multiple routes (IV, IP, SC, PO etc), blood and tissue collection, and tumor volume measurement. Experience with small animal surgery is a plus. Communicate and coordinate with other scientists on project team to draft, finalize, and implement study protocols. Follow protocols and independently execute tasks. Collect and record data. Prepare summary of experimental procedures and results and present data in team meetings. | 9/28/2019 |
| 1052 | Biodesix Boulder, CO Test Support Specialist I HS Diploma/GED Exp: 1-3 years customer service/data entry |
Test Processing Support Specialist 1 duties will consist of accurately and precisely transferring and entering data from test request forms into an electronic data base. Confirmation of entered data, and confirmation that data provided meets the minimum requirements as indicated by the QMS. Timely and accurate delivery of reviewed test results. | 9/28/2019 |
| 1053 | Biodesix Boulder, CO Laboratory Technician BS/BA in chemistry/biological sciences Exp: 0-2 years lab training |
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. | 9/28/2019 |
| 1054 | Bioduro San Diego, CA Quality Assurance Associate – Analytical & Manufacturing Support BS/BA in science Exp: 6-12 months in pharma/lab |
The Senior Quality Assurance Associate assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. 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. | 9/28/2019 |
| 1055 | Bioduro San Diego, CA Associate Scientist (Analytical Development) BS in chemistry or related Exp: 1-2 years in chemistry lab |
The Analytical Development Associate Scientist facilitates and assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. Responsible for performing pharmaceutical formulation sample and finished product analysis testing and basic validation experiments using different analytical instruments (HPLC, Dissolution, and KF) and general laboratory duties. | 9/28/2019 |
| 1056 | Biogen Cambridge, MA Engineer I, Cell Culture Development BS in bio/chemical engineering Exp: 0-2 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. | 9/28/2019 |
| 1057 | Biogen Cambridge, MA Associate Scientist II, Alzheimer’s Disease and Dementia Research Unit MS in biological sciences Exp: 1+ years experience |
The successful candidate will have hands-on experience with a variety of in vitro and in vivo models relevant for neurodegenerative diseases and the ability to utilize these models for target validation, mechanism of action studies and support for drug discovery projects as a member of our world class research team in the Alzheimer’s Disease and Dementia Research Unit. As Associate Scientist II, the expectation is that the incumbent is capable of planning and executing experiments in consultation with the supervisor including the analysis and interpretation of the experimental results to achieve agreed upon objectives. | 9/28/2019 |
| 1058 | Biogen Cambridge, MA Associate Scientist I, Technical Development (Development Support) AS/AA or BS/BA in biological/chemical sciences Exp: 1 year in lab environment |
The individual will assist in the development and optimization of formulations and provide technical expertise on preparation procedures and mixing process parameters using both practical and scientific knowledge. Will work as member of dynamic team developing and following established procedures to ensure a consistent service is delivered. Management of department chemical and consumable inventories, ensuring proper levels are available. Frequent collaboration and communication with multiple line functions to develop solution formulations and preparation process instructions. | 9/28/2019 |
| 1059 | Biogen Research Triangle Park, NC Manufacturing Associate BS/BA Exp: 0-2 years work experience |
The Manufacturing Associate performs and documents manufacturing operations in a cGMP environment that involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments. The role will: Execute manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record, SLR and control system. May coordinate or lead process steps as requested. Document/Record and Review cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. Revises or creates documents as instructed. Key documentation includes batch records, SLRs, and equipment logbooks. | 9/28/2019 |
| 1060 | Biolegend San Diego, CA Research Associate- BMIA ELISA BS in chemistry/biology Exp: 0-1 years lab experience w/immunoassays |
This position is responsible for developing immunoassay products in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working closely with an experienced scientist on developing a line of product utilizing ELISA or bead-based immunoassay and flow cytometry technologies. | 9/28/2019 |
| 1061 | Biolegend San Diego, CA Process Development Associate BS/BA in biological/chemical sciences Exp: 1-3 years lab experience w/protein chemistry |
The Process Development 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 conjugated 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 | 9/28/2019 |
| 1062 | Biolegend San Diego, CA Material Coordinator BS in biological sciences Exp: 1-2 years lab experience preferred |
The Material Coordinator is an entry level role that will support corporate business development efforts to expand company product portfolio through in-licensing, in-house development, and other methods of acquisition. This position will be responsible for documenting, receiving, and distributing incoming materials to stakeholders within the facility and outside locations and will work in a collaborative environment with other internal departments including Finance, Customer Service, Research and Development, Purchasing, Facilities and Quality Assurance. | 9/28/2019 |
| 1063 | Biolegend San Diego, CA Manufacturing Associate - Tissue Culture AS/AA in biological sciences Exp: 6 months |
. 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. | 9/28/2019 |
| 1064 | Biolegend San Diego, CA Research Associate- Biomarker Immunoassay BS in chemistry/biology Exp: 1 year or more w/immunoassays |
The Research Associate will be involved in all aspects of the product development processes including designing, testing, troubleshooting, product transferring and launching. More specifically, he or she will be working closely with an experienced scientist on developing a line of product utilizing bead-based immunoassay and flow cytometry technologies. | 9/28/2019 |
| 1065 | Biolegend San Diego, CA Project Coordinator - Custom Solutions Team BS in life sciences Exp: 1-3 years in biotech/pharma |
The CST Project Coordinator will handle internal project coordination for our custom solutions team and contribute BioLegend’s mission of providing legendary customer service. They will be accountable for their own project pipeline, from the initial scoping through to manufacturing and timely delivery to the customer. | 9/28/2019 |
| 1066 | BioMarin Novato, CA Research Assistant / Research Associate at BioMarin BS in pharma sciences/biochemistry, related Exp: 1-2 years in R&D lab |
The prospective employee will work in the Formulation Development group to assist in the advancement of BioMarin’s therapeutics for clinical evaluation and potential commercialization. The candidate will be responsible characterization drug products, screening of formulation prototypes, evaluating product stability and compatibility with various container closure systems using routine and semi-routine analytical methods under limited supervision. | 9/28/2019 |
| 1067 | BioMarin San Rafael, CA Contracts Associate (TEMPORARY) BS/BA Exp: 0-2 years |
This role will support BioMarin's Legal Department and business partners by drafting, negotiating and tracking a high volume of contracts. Duties include: Drafting, primarily from templates, multiple contract types including Non-Disclosure Agreements, Master Service Agreements, Amendments, Scopes of Work, and Change Orders, using SpringCM, BioMarin's contract lifecycle management system ("SpringCM"). Monitoring and tracking a large volume of contracts from draft to final signatures using SpringCM. | 9/28/2019 |
| 1068 | BioMarin San Rafael, CA Research Associate (TEMPORARY) BS or MS in pharma sciences, biochemistry, or related Exp: 0-2 years lab experience |
The Research Associate I/II, functions to manage, coordinate, and perform activities required for the testing of drug product or human and animal specimens associated with one or more research and pre-clinical studies. In this position the candidate will work closely with Scientists in the Research group focused on mass spectrometry-based assays. | 9/28/2019 |
| 1069 | Biomerieux St. Louis , MO Engineering Technician Technical degree Exp: 0-2 years |
Provide technical support to operations engineering and instrument manufacturing with responsibilities specific to printed circuit board assemblies (PCBAs), mechanical assemblies, assembly fixtures, and test equipment. Assist engineers in projects related to manufacturing and electronic test devices used in the production and functional qualification of In vitro diagnostic laboratory equipment. Support and sustain instrument manufacturing activities and facilitate efficient operations within the production environment, optimize existing processes and ensure established production processes are achieved. | 9/29/2019 |
| 1070 | Biomerieux St. Louis , MO IRC Technician - Instrument Refurbishment Center AAS in electronics discipline Exp: 0-3 years |
Perform evaluation, refurbishment, assembly, alignment and acceptance testing of automated electro-mechanical biological test systems on an advanced level while maintaining stock levels. | 9/29/2019 |
| 1071 | Biomerieux Philadelphia, PA R&D Technician BS Exp: 1-2 years relevant experience |
Contributes, with technical and scientific expertise, to the design and development of differentiated, high quality products on time, within budget, and with a high degree of customer satisfaction. | 9/29/2019 |
| 1072 | 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 |
| 1073 | Bio-Rad San Diego or Los Angeles, CA Proteomics Sales Specialist I BS/BA Exp: 1-3 years sales experience |
Develop and Execute a Territory Sales Plan. Promote and Sell the Bio-Rad Proteomics Portfolio to Achieve the Territory Sales Goals. Build, Manage and Grow Sales Opportunity Funnel. Utilize Various Bio-Rad Departments (Technical Support, Customer Care, Marketing and other Bio-Rad Personnel) In Order to Ensure Complete Customer Satisfaction. Proactively Communicate with Regional Manager on Activities, Market Trends, Opportunities and Forecast. | 9/29/2019 |
| 1074 | LGC Alexandria, MN Laboratory Technician I AS/AA in sciences Exp: 0-2 years |
The Laboratory Technician is an integral part of the Laboratory Operations team and through collaboration with others is responsible for executing the objectives of the Research and Development group. This position will be involved in conducting lab experiments as assigned and be responsible to accurately document results. The Laboratory Technician may be asked to assist in preparing standard laboratory procedures, keep detailed record of experiments, and will report on project results to relevant stakeholders. The Laboratory Technician is expected to be familiar with the scientific background and literature relevant to the projects they are engaged. The work of a Laboratory Technician is directed and evaluated by a senior R&D laboratory member. | 9/29/2019 |
| 1075 | LGC Charleston, SC QC Chemist ( BS Exp: 1 year in production |
This is a QC chemist position where one is responsible to make check standards, routine instrument maintenance and operation of GC/MS, GC/FID, HPLC, and UHPLC/MS, validating manufactured products in a timely manner. Attention to detail, teamwork, the ability to thrive in a fast-paced work environment and organizational skills are necessary to excel in this position. | 9/29/2019 |
| 1076 | Mallinckrodt Pharmaceuticals Hobart, NY Manufacturing Assoc. I - 2nd Shift HS diploma or equivalent Exp: 3-12 months |
Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. etc. | 9/24/2019 |
| 1077 | Mallinckrodt Pharmaceuticals Hobart, NY Blending Technician I - 4on/4off (C) Shift 6pm-6am HS diploma or equivalent Exp: 3-12 months |
Blend defined quantities of designated raw materials (per specific manufacturing instructions) into final dosage blend stage. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Blending Technician is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. etc. | 9/24/2019 |
| 1078 | 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 |
| 1079 | McGuff Pharmaceuticals Santa Ana, CA Manufacturing Technician - Evening Shift BS Exp: 0-3 years |
Duties Include: Operation of pharmaceutical manufacturing equipment including automated aseptic fill lines, washers, ovens, and autoclaves. Responsible for set-up, adjustments, sanitization, minor maintenance, and operation of all machinery in the sterile filling area. Experience in using aseptic technique to conduct aseptic filtration and filling of finished product. etc. | 9/24/2019 |
| 1080 | McGuff Pharmaceuticals Santa Ana, CA Microbiology Technician BS Exp: 0-5 years |
The Microbiology Technician will be responsible for (1) Verifying that materials and products comply with microbial and/or chemical specification limits (2) Conducting laboratory testing in support of operations, (3) Maintain the laboratory operations in compliance with McGuff policies, federal regulations, state regulations, and international standards, (4) Maintain documentation, calibration, and validation of all microbial equipment, (5) conduct other duties as assigned by the laboratory supervisor and/or Microbiologist. etc. | 9/24/2019 |
| 1081 | McGuff Pharmaceuticals Santa Ana, CA Manufacturing Techician unspecified Exp: 0-3 years |
Duties include: Operation of pharmaceutical manufacturing equipment including automated aseptic fill lines, washers, ovens, and autoclaves. Responsible for set-up, adjustments, sanitization, minor maintenance, and operation of all machinery in the sterile filling area. Experience in using aseptic technique to conduct aseptic filtration and filling of finished product. etc. | 9/24/2019 |
| 1082 | MS Biosciences Oakdale, MN Quality Assurance Specialist BS Exp: 1-2 years |
This person will be responsible for assisting in the maintenance and function of the quality management systems at MD Biosciences. This person should have a background in and knowledge of quality systems in a laboratory setting and preferably have experience in aCLIA &/or GLP-regulated environment. etc. | 9/24/2019 |
| 1083 | Medicomp San Francisco, CA Cardiac Monitoring Technician HS diploma Exp: 1+ years |
Looking for an ECG interpreter, for our San Francisco, CA office, who is excited about having the front line responsibility of triaging the patients who have our life-saving products prescribed to them. That's right, I said Life-saving! This is only going to happen one way you have to have a solid work ethic and be able to focus on the clinically significant signs and symptoms of one or more patients while in a noisy environment that is full of interruptions. etc.. | 9/24/2019 |
| 1084 | 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 |
| 1085 | 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 |
| 1086 | Merieux NutriSciences Minnetonka, MN Microbiology Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 1087 | Merieux NutriSciences Minnetonka, MN Microbiology Technician - 2nd Shift unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 1088 | Merieux NutriSciences Stone Mountain, GA Microbiology Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 1089 | Merieux NutriSciences Gainesville, FL Chemistry Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 1090 | Merieux NutriSciences Columbus, Oh Lab Technician unspecified Exp: Entry level |
Mérieux NutriSciences is dedicated to improving food safety and quality though nutritional research, scientific excellence and innovation at every step of the food supply chain. Our team of scientists and technicians is committed to providing our clients with accurate results, delivered on time, with uncompromising ethics, honesty, personal integrity and confidentiality. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 1091 | Merieux NutriSciences Crete, IL Chemist I unspecified Exp: 1-2 years |
The incumbent is responsible for performing chemical analysis on food sample. The incumbent analyzes the concentration of certain components in food sample. The incumbent must accurately prepare and process the sample to obtain the needed results. etc. | 9/24/2019 |
| 1092 | Merieux NutriSciences Allentown, PA Receiving Tech unspecified Exp: Entry level |
Mérieux NutriSciences is a leader in food science and testing technology. With over 6,000 employees working in 80 labs in 21 countries, our team will stop at nothing to make sure consumers around the world are protected from foodborne illness and pathogens. Each member of our team plays a critical role in our mission. We are currently seeking a Lab Assistant to provide assistance to our technicians and scientists. NO PREVIOUS LABORATORY EXPERIENCE REQUIRED. etc. | 9/24/2019 |
| 1093 | Applied Medical Technology Brecksville, OH Mold Process Engineer AS/AA in plastics/technology Exp: 1-4 years in plastic processing |
Develop optimum molding processes for manufacturing medical components. Provide recommendations and implement improvements to production processes, methods and controls. Provide support and leadership in the development of in the injection molding processes and tools. | 9/20/2019 |
| 1094 | Applied Medical Technology Brecksville, OH Entry Level Injection Molding Machine Operator- 1st Shift HS Diploma Exp: Entry Level |
Operates injection molding machines according to specific schedules and procedures. Prepares mold inserts and reviews molded component integrity. Remove molded components from the mold once the machine has finished its cycle. When applicable test parts during machine cycle to predetermined specifications | 9/20/2019 |
| 1095 | Applied Medical Technology Brecksville, OH Associate Sales Representative BS/BA Exp: 1-2 years sales experience |
The purpose of this position is to assist sales reps in making goal. Candidate must maintain an understanding of distribution channels and key industry leaders. Must be willing to travel as needed for tradeshows, conferences and in servicing events. Duties include training and in-servicing of customers and assisting sales reps as needed. This will involve up to 75% travel throughout the United States. | 9/20/2019 |
| 1096 | Applied Molecular Transport South San Francisco, CA Research Associate BS,MS in chemistry, biochemistry, biological sciences Exp: 1-5 years |
The successful candidate will have extensive understanding of protein chemistry, protein characterization, and analytical techniques. The position will involve regular communication and collaboration with an interdisciplinary team within AMT and with outside contractors/consultants. Perform analytical method development for LC based assays such as SEC, IEX and reversed-phase HPLC, and other protein-based analysis (i.e. SDS-PAGE, western blot, A280) | 9/20/2019 |
| 1097 | Applied Stem Cell Milpitas, CA Research Associate, Molecular Biology BS/MS in biological sciences Exp: Entry Level |
We are looking for a Research Associate, Molecular Biology to join our Life Sciences department. This is a hands-on lab-based role in the Life Sciences Service program with a focus on generating engineered cells and animal models using ASC’s gene editing technologies. | 9/20/2019 |
| 1098 | Applied Stem Cell Milpitas, CA IT Support Technician AS/AA or BS/BA in computer sciences Exp: 1 or more year in IT |
We are looking for a part-time IT Support Technician to provide prompt IT support to the daily operations of various IT systems/devices. This technician is also responsible to set up new computers and systems for new hires and to decommission them when needed. This is a non-exempt role requiring an average of 20-25 hours a week. | 9/20/2019 |
| 1099 | Applied Stem Cell Milpitas, CA Microinjectionist BS in biological/animal sciences, MS preferred Exp: 1 or more year in microinjections |
We are looking for a Microinjectionist who will be responsible for the animal model division, in conducting transgenic animal production through microinjection of DNA/RNA/protein into pronuclear stage embryos or making chimeric animals with injection of targeted ESCs into morula/blastocysts. | 9/20/2019 |
| 1100 | Evotec Princeton, NJ Research Associate - Assay BS/MS in biological sciences Exp: 1-3 years in lab experience |
The successful candidate will actively contribute to ongoing and future collaborations with multiple discovery partners in the design, development and execution of novel in vitro assays to support early stage drug discovery and development. Working with a team of scientist in the design, validation and execution of in vitro assays (both biochemical and cellular) for characterization of small and large molecule drug candidates | 9/20/2019 |
| 1101 | Evotec Watertown Cyprotex, MA Associate Scientist BS in biological sciences Exp: 1-2 years in industry |
The team is looking for a highly motivated Associate Scientist that will be responsible for routine screening of compounds in various in vitro toxicology assays. Responsible for planning and conducting high and low throughput toxicology screens, processing data to a high quality of standards, and within specified time frames. | 9/20/2019 |
| 1102 | Aquestive Warren , NJ Formulation Scientist MS in sciences/chemistry Exp: 0-5 years in pharma |
A member of the R&D team responsible for the design and development of drug products for the targeted delivery of active pharmaceutical ingredients, including thin films for transmucosal delivery. Conducts laboratory activities and formulation work in support of product development, product characterization and process optimization. Prepares laboratory prototype samples for preclinical, in-vitro and stability evaluations | 9/20/2019 |
| 1103 | Abor Biotechnologies Cambridge, MA Software Engineer - Research MS or higher in engineering/sciences Exp: 1-2 years |
At Arbor, you will be at the cutting edge of biodiscovery, systematically searching through nature’s diversity to discover and engineer new technologies for improving human health and sustainability. As a Software Engineer in Research, you will focus on building a search engine from the ground up. You will have significant latitude towards ideation, problem definition, and finding novel uses of machine learning. | 9/20/2019 |
| 1104 | Archer Boulder, CO Associate BS/BA in sciences Exp: 1-2 years in manufacturing |
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. | 9/20/2019 |
| 1105 | Arcturus San Diego, CA Public Relations & Marketing Associate BS/BA in sciences or business Exp: Entry Level |
In this role, you will create PR/Marketing collateral, assist with website design, graphics, and plan publicity strategies and campaigns. You will be responsible for research, asset creation and organization to support corporate investor relations activities. | 9/20/2019 |
| 1106 | Arcturus San Diego, CA Research Associate, Translational Biology (In Vivo) Associates/Bachelors in sciences Exp: 1-3 years of small animal handling |
The successful candidate will bring hands-on experience performing in vivo experiments and with various animal handling techniques such as pharmaceutical agent dose administration (IV, PO, IP, IM) and blood/tissue collection. We seek candidates who are team oriented, diligent and meticulous, who display initiative and will be able to contribute intellectually to our science. | 9/20/2019 |
| 1107 | Arcturus San Diego, CA Research Associate, Translational Biology BS/BA in sciences Exp: 1-3 years of small animal handling |
The successful candidate will bring hands-on experience developing assays and performing in vivo, ex vivo experiments. Animal handling techniques such as pharmaceutical agent dose administration (IV, PO, IP, IM) and blood/tissue collection are required. We seek candidates who are team oriented, diligent and meticulous, who display initiative and will be able to contribute intellectually to our science. | 9/20/2019 |
| 1108 | Arcus Biosciences Hayward, CA Research Associate: Quantitative Biology BS/MS in biological sciences 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: Mammalian cell culture. Biological sample banking. Biology and tissue culture lab management, safety program support. Practical laboratory work, managing day to day tasks and ensuring timely delivery of high-quality results. | 9/20/2019 |
| 1109 | Arcus Biosciences Hayward, CA Research Associate BS/MS in chemistry or related Exp: 1-4 years |
The successful candidate will be responsible for conducting in-vitro ADME studies, qualitative and quantitative analysis of small molecules using LC-MS/MS, to support multiple drug discovery and development projects. Responsibilities include, but are not limited to: LC-MS/MS method development and quantitative analysis of in vitro and in vivo samples in various biological matrices. Perform in vitro ADME assays such as metabolic stability, CYP inhibition, plasma protein binding and blood to plasma partitioning; develop new assays as needed. | 9/20/2019 |
| 1110 | Arcus Biosciences Hayward, CA Research Associate BS/MS in chemistry or related Exp: 1-4 years |
The successful applicant will be responsible for performing bioanalysis of in vitro and in vivo samples to support discovery and development programs. Develop, troubleshoot, and validate LC-MS/MS based bioanalytical methods. Analyze, summarize and report preclinical pharmacokinetic and toxicokinetic results. Conduct in vitro ADME experiments such as metabolic stability, plasma protein binding, CYP inhibition and induction assay as necessary | 9/20/2019 |
| 1111 | Arcus Biosciences Hayward, CA Research Associate/Sr. Research Associate, Immunology BS in biological sciences Exp: 1-2 years in research |
The role will be responsible for executing a variety of experiments using in vivo models and in vitro assays in order to validate new targets and understand mechanism of action and pharmacodynamic properties of drug candidates. A successful candidate will contribute as part of a multidisciplinary team in a fast-paced environment to plan and execute experiments and subsequently collate, document, interpret, and present data internally. | 9/20/2019 |
| 1112 | Array Boulder, CO Research Associate / Associate Scientist - Medicinal Chemistry MS in organic chemistry Exp: 0-2 years |
Array’s medicinal chemistry group has openings for motivated synthetic organic chemists who are able to work in a team environment to deliver quality drug candidates with a sense of urgency. Responsibilities include: Demonstrates technical competency in reaction set-up, product isolation, purification and analysis, from milligram to multigram scale. Develop an understanding of SAR, contribute to analog design. Collaborate closely with colleagues to discuss data and generate new ideas | 9/20/2019 |
| 1113 | Go Beyond RNA Rockville, MD Lab assistant - Molecular Biology BS in biological sciences Exp: 1-2 years wet lab experience |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. | 9/20/2019 |
| 1114 | Arrowhead Madison, WI Animal Technician (Procedures) HS Diploma Exp: 6 months rodant research |
Arrowhead is seeking an experienced Animal Technician to join our Laboratory Animal Resources staff. 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. | 9/20/2019 |
| 1115 | Arrowhead Madison, WI Associate Production Chemist HS Diploma Exp: 0-5 years |
Arrowhead Pharmaceuticals is seeking a highly motivated individual to become a part of its scientific team. We have an immediate opening for an Associate Production Chemist in the Chemistry, Manufacturing, and Controls Group. The successful candidate will be expected to: Follow batch records, SOPs, and work instructions to detail. Document all operations in batch records and notebooks. Comply with GMP protocols | 9/20/2019 |
| 1116 | Arrowhead Madison, WI Research Technician, Biology BS in biological sciences Exp: 0-4 years lab experience |
Arrowhead Research seeks a full time Research Technician to join its drug targeting team at its research and development facility in Madison, WI. The candidate should be highly motivated, and enjoy working with a team of scientists in a fast-paced and highly cross-disciplinary environment. The individual will be primarily responsible for providing technical assistance in RNA and DNA isolations, cell culture, and general laboratory maintenance. | 9/20/2019 |
| 1117 | 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 |
| 1118 | Arthrex Ave Maria, FL Manufacturing Engineer I - Distal Extremities BS/BA in engineering or related Exp: 0-4 years |
Working as Manufacturing Engineer - Distal Extremities, you will responsible for supporting Engineering Manager with all support for the life cycle development of Class I, II and III medical devices, including new product development and maintenance of released products. This includes design, develop, implement and improve manufacturing processes to produce cost effective quality medical device products and systems. Provide manufacturing engineering expertise to create, document and implement required procedures and documents. Excellent analytical and communication skills, understanding of manufacturing and a Bachelors’ degree in Engineering or Engineering Technology will be essential for this position. | 9/22/2019 |
| 1119 | Arthrex Sandy Springs, SC Engineer Tech - Manufacturing AS/AA in engineering technology Exp: 0-2 years |
Support the development, implementation and improvements of manufacturing processes to produce cost effective quality products. Successful candidates for these positions will have a solid CNC Machining background, including experience with the setup, operation and troubleshooting of mills and/or Swiss lathes. Up to 5-axis machining experience is desired. The successful candidate for this position must be willing to attend initial training in the Naples, FL area if/as needed by Arthrex. | 9/22/2019 |
| 1120 | ArunaBio Athens, GA Research Associate I – Preclinical R&D Team BS/BA in biological sciencecs Exp: 1-2 years lab experience |
The Research Associate I supports the R&D efforts of ArunA Bio by aiding in the development of novel exosome therapies for a number of neurological diseases. This position must work collegially as a part of a larger team and requires the individual to carry out complex tasks. We are seeking a biologist with in vivo research experience. The successful candidate would participate in a wide variety of research activities including animal care, animal technical procedures, animal health evaluations, and research data collection. | 9/22/2019 |
| 1121 | Priamal Riverview, MI Quality Assurance Specailist I - Manufacturing BS/BA in physical/biological sciences Exp: 0-3 years in pharma operations |
The Specialist will directly support the implementation, execution, and maintenance of Quality Systems related to manufacturing to ensure the PPS-Riverview site complies with regulatory requirements as propagated by the United States Food and Drug Administration (USFDA) and other international regulatory authorities. Principle assignments related to compliance may include material release, review and implementation of new and revised documentation to support PPS-Riverview Quality Systems and operations, internal audits, and training of site personnel to meet Good Manufacturing Process (GMP) requirements. The scope of this position will support both clinical and commercial manufacturing, as well as process development, in the Riverview facility. | 9/22/2019 |
| 1122 | Myriad Genetics Salt Lake City, UT Training Specialist BS/BA in engineering or related Exp: 0-3 years |
The Training Specialist I, Prod-Ops Support administers the training program, ensuring that employee training needs are defined and met. This position works with Training Power Users and end users to ensure that job appropriate training is available and completed. Maintain training that meets all departmental needs and follows regulatory requirements for training and competency. Develop training materials for lab processes. Create a variety of training programs including e-training, computer-based, lecture, and other training formats. | 9/22/2019 |
| 1123 | Myriad Genetics South San Francisco, CA Manufacturing Associate BS in biological sciences/molecular biology Exp: 0-2 years in cGMP molecular biology |
The Manufacturing Associate is responsible for following established protocols to regularly manufacture reagents for use in the production laboratory, as well as assist in implementing upgrades to improve the quality and efficiency of manufacturing protocols and processes. They will also create, edit, and review SOPs, train junior staff, and play a key role in process scaling efforts. | 9/22/2019 |
| 1124 | Myriad Genetics Salt Lake City, UT Laboratory Technician BS or MS in biological/physical sciences or engineering Exp: 0-2 years |
The Laboratory Technician is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects. | 9/22/2019 |
| 1125 | AstraZeneca Frederick, MD Quality Control Analyst - Operations BS/BA in sciences/biotech/pharma Exp: 0-5 years |
Performs selected quality control testing activities, dependent upon assigned area, including the following: Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. Supports preparation of validation protocols, executes experiments, and provides data for validation reports. | 9/22/2019 |
| 1126 | Asuragen Austin, TX Quality Assurance Specialist I AS/AA 2- year program Exp: 6 months to 1 year |
The Quality Assurance Specialist I is responsible for helping to ensure compliance with QSR, MDSAP, ISO, GLP, and CLIA as they relate to Quality Assurance activities in Asuragen’s manufacturing facility. Provide Quality Assurance support to the Operations department with a focus on production. This is achieved though the following key duties: Develop working knowledge of quality system processes and apply this knowledge to support manufacturing operations. Assist in the management of historical files for manufactured products, including archived records stored on and off site | 9/22/2019 |
| 1127 | Alphatech Carlsbad, CA Regulatory Affairs Coordinator BS/BA in life science/engineering Exp: 1 year in research |
Maintains regulatory databases, license approvals, user fees, certificates, and establishment registrations. Submits Unique Device Identification and labeling data to regulatory agencies using various third-party applications. Responsible for post market surveillance evaluation, trending, and reporting including updates to risk management (FMEA) process.Assists in developing, maintaining, assigning, and tracking company Standard Operating Procedures (SOPs) to ensure compliance with applicable global regulatory requirements. | 9/22/2019 |
| 1128 | Alphatech Carlsbad, CA Material Handler HS Diploma Exp: 1-3 years in inventory |
Under routine supervision, this position is responsible for creating purchase orders and shipping inventory for outside processing. Counts and verify parts for outside processing. Packages parts safely for shipping. Creates purchase order for outside processing. Assists with cycle counts on raw materials, components, and distribution when needed. Conforms to all company policies and procedures and perform all duties in compliance with applicable FDA and state regulations as well as standards including but limited to ISO 13485. | 9/22/2019 |
| 1129 | Alphatech Carlsbad, CA Regulatory Affairs Specialist BS/BA in life science/engineering Exp: 1 year in FDA environment |
Collaborates as a core team member on new product development teams. Determines and documents appropriate regulatory strategy for proposed new products. Supports design control activities. Prepares regulatory submissions including 510(k) premarket notifications for US FDA. Prepares regulatory submissions including technical files/design dossiers for registration of products in European Union and interfaces as needed with Notified Bodies regarding significant changes to products. Evaluates design changes to products to determine impact to submissions and potential need for additional submissions. | 9/22/2019 |
| 1130 | Atreca South San Francisco, CA Research Associate I, In Vitro Pharmacology BS in biology or related Exp: 1-2 years in cell line research |
Oversee the growth and inventory of tumor cell panels needed for primary and secondary screens. Provide assistance with carrying out binding screens against tumor cell panels. Share and present data to team members. | 9/22/2019 |
| 1131 | AtriCure Cincinnati, OH Clinical Operations Associate HS Diploma Exp: 1-3 years in finance/accounting/admin |
The Clinical Operations Associate position will be a key contributor to AtriCure’s clinical affairs department to assist in the development, implementation, and execution of multiple key study functions. The Clinical Operations Associate primary responsibilities include but are not limited to device supply logistics, financial processes (contracts, budgets, and invoices), essential documents, trial master file (TMF), and select monitoring activities. Responsibilities will vary by study. | 9/22/2019 |
| 1132 | Boston Scientific Maple Grove, MN Machine Operator I AS/AA technical degree preferred Exp: 1 year grinding, extrusion, molding, branding operations |
Primary focus is to build quality product by following processes to meet all production goals. Responsibilities include: Responsible for quality and adheres to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Builds product by following all processes in which certified (in their most current revision), and completes other assigned work, while meeting manufacturing goals a8nd metrics. Under the direction of other maintains accurate records such as Manufacturing Execution System (MES), Shop Floor Paperwork (SFP), training Records System (TRS), Product Data Management (PDM), Systems Application & Products (SAP) and Process Equipment Optimization (PEO). | 9/22/2019 |
| 1133 | Boston Scientific Marlborough, MA Analyst I, Compliance Communications & Training Job HS Diploma Exp: 1-4 years in training/communication |
The Compliance Analyst for Global Compliance Training and Communications will be responsible for implementing and maintaining components of a comprehensive compliance training and communication program. Ideal candidates will have strong analytical, verbal and written communication and project management skills and understand risks related to regulations applicable to the medical device industry (e.g. the anti-kickback statute, Foreign Corrupt Practices Act, etc.). | 9/22/2019 |
| 1134 | Boston Scientific Coventry, RI Process Engineer I Job BS in mechanical/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 provide 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. | 9/22/2019 |
| 1135 | Boston Scientific Valencia, CA Product Analyst I Job HS Diploma minimum Exp: 1 year in regulated environment/document processing |
In this role you will work closely with Patient Care and the Complaint Call Center areas to process all customer issues and identify complaints, as required by FDA, Canadian, European, and other International regulations related to medical device manufacturers. Maintain all complaint files in accordance to Boston Scientific policies. The position will support post market and clinical studies. Must be able to work well in a team environment, foster team building, proactively communicate project and task status, and operate with a high level of initiative. Possess verbal and written communication skills to communicate effectively with various levels of management in both business and technical communities. | 9/22/2019 |
| 1136 | Avantec Vascular Sunnyvale, CA R&D ENGINEER I BS in engineering Exp: 1-3 years medical design experience |
Responsible for providing creativity to the mechanical engineering design and development of new invasive and non-invasive medical device products. Researches, develops, designs (utilizing CAD design software), and evaluates technical suitability of mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Must be able to clearly communicate designs and all requisite requirements to support personnel both verbally and in writing. | 9/22/2019 |
| 1137 | Avedro Burlington, MA Associate Research Formulation Scientist MS or BS in pharmacology, biochemistry, or analytical chemistry Exp: 0-2 y ears |
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. | 9/22/2019 |
| 1138 | Avid Bioservices Tustin, CA Associate Specialist/Specialist, Quality Assurance (GMP) BS in sciences Exp: 0-3 years |
The Quality Assurance Associate Specialist/Specialist is an individual contributor who solves a variety of issues following cGMP regulations and company standards. Assist in the release of API batches and lots. Review of Manufacturing Batch Production Records - Must have at least 6 months to 1 year or more experience. Collaborate with departments to ensure that all review activities are executed efficiently per governing SOPs. | 9/22/2019 |
| 1139 | Avion Pharmaceuticals Boston, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year in business-to-business ales |
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. | 9/22/2019 |
| 1140 | Avion Pharmaceuticals Orlando, FL Pharmaceutical Sales Representative BS/BA Exp: 1 year in business-to-business ales |
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. | 9/22/2019 |
| 1141 | Avion Pharmaceuticals Worcester, MA Pharmaceutical Sales Representative BS/BA Exp: 1 year in business-to-business ales |
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. | 9/22/2019 |
| 1142 | Avomeen Ann Arbor, MI ANALYTICAL CHEMIST BS/MS in chemistry or related Exp: 0-5 years |
We are looking for a talented individual to fill an Analytical Chemist position at our Ann Arbor, MI facility. Learn techniques spanning across the entire spectrum of analytical chemistry from wet chemistry to HPLC, NMR, Mass Spectrometry, FTIR, GC and GC-MS. Execute projects in support of client needs including product deformulation and product development, failure analysis and problem solving, impurity identification, extractable and leachable studies, and structural characterization | 9/22/2019 |
| 1143 | Axogen Tampa , FL Quality Systems Engineer BS in engineering or sciences Exp: 1-5 years |
The Quality Compliance Engineer will provide support in the implementation, maintenance, and improvement of company-wide quality management systems, procedures and support processes. Proactively monitors the various elements of the quality system to help ensure compliance with quality system regulations and applicable national and international quality standards. Ensures processes and tools are established to ensure ongoing compliance with applicable requirements. Supports external audits by the FDA, AATB, the Notified Body, other regulatory bodies and third parties, and coordinates responses to applicable audit findings. | 9/22/2019 |
| 1144 | Axogen Vandalia, OH Quality Engineer BS in engineering, pharma sciences, life sciences, etc. Exp: 1-3 years in quality/compliance |
The Quality Engineer will provide quality engineering and quality assurance support for Manufacturing Operations to ensure new/improved and current medical products and processes are in compliance with applicable standards and regulations. Confer with external and internal departments (example Product Development, Clinical, Marketing, Sales, and Operations) concerning product design to ensure user needs are met. Implement Quality systems and processes. The Quality Engineer will write standard operating procedures, work instructions, and other Quality documentation. | 9/22/2019 |
| 1145 | Axsome New York, NY Clinical Trials Assistant BS in biological/physical sciences Exp: 1 year in clinical department |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. | 9/22/2019 |
| 1146 | Azzur Group Washington DC, DC Validation Engineer BS in engineering/sciences Exp: 1-7 years in regulated manufacturing |
Ideal candidates will exhibit, or have the willingness to develop, the following qualities: Strategic thinker with strong analytical skills who can translate client needs into actionable value-added projects/results. Understands the competitive landscape of the medical device, pharmaceutical, and biotechnology industry. Willing to work hands on, assist with building client libraries, learn from a mentor and become a mentor for others. | 9/22/2019 |
| 1147 | Bachem Torrance, CA Research Sales Representative BS in sciences Exp: 1-2 years in sales |
The Research Sales Representative will be responsible for selling the company’s products and services by contacting prospective and established customers. The Research Sales Representative will follow up on leads and establish close customer contacts to promote the company’s products to select accounts as designated by Sales Management. | 9/22/2019 |
| 1148 | Acelity South Burlington, VT Field Servive Representative I HS diploma or equivalent Exp: 1 year |
This position is responsible for providing world class customer service during the provision, return and servicing of medical equipment inclusive of responding to product inquiries or other identified customer needs. The daily responsibilities encompass the preparation of medical equipment for patient use to include sanitization and disinfection, quality control testing, preparation for use and transportation of the equipment to and from customer locations utilizing a company provided vehicle. In addition to preparation and provision of medical equipment, employees in this function are required to learn and operate within the company defined policies and procedures to maintain compliance with the regulated requirements for medical devices. Additional responsibilities include maintenance of a safe and clean service center working environment and company vehicles. etc. | 9/17/2019 |
| 1149 | 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 |
| 1150 | 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 |
| 1151 | Acella Pharmaceuticals Irvine, CA Pharmaceutical Sales Representative BA/BS Exp: 1 year |
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. etc. | 9/17/2019 |
| 1152 | Advanced Bionics Valencia, CA Quality Control Inspector I HS diploma or equivalent Exp: 1-2 years |
Responsible for performing visual, mechanical and electrical inspections at subassembly and final assembly levels. DUTIES: 1. Perform visual and mechanical inspections at sub-assembly and final assembly levels, using engineering drawings/specifications and general quality control standards. 2. Records inspection data. 3. Review manufacturing documentation to ensure that all assembly, testing and inspection steps were performed in accordance to specifications. etc. | 9/17/2019 |
| 1153 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Monday-Friday HS diploma/AA in life sciences or engineering Exp: 0-3 years |
This is a Development Technician position in the Process Development Support group. Primary responsibility will be to support the process development team processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for lab support. Under general supervision, this person carries out routine to moderately complex lab operations. Responsibilities: Lab maintenance including cleaning, autoclaving parts, stocking laboratory supplies and performing maintenance on laboratory equipment. etc. | 9/17/2019 |
| 1154 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Sun-Wed AA/BS in life science or engineering Exp: 0-3 years |
This is a Development Associates position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. etc. | 9/17/2019 |
| 1155 | AGC Biologics Bothell, WA Development Associate I-II AA/BS in life science or engineering Exp: 0-2 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. etc. | 9/17/2019 |
| 1156 | AGC Biologics Bothell, WA Downstream Manufacturing Associate HS diploma to BA/BS Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. etc. | 9/17/2019 |
| 1157 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Perform review of GMP documentation. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/17/2019 |
| 1158 | AGC Biologics Bothell, WA Manufacturing Associate III - Upstream BS in chemistry, biology, or related Exp: 1-4 years |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. PRINCIPAL RESPONSIBILTIES: Executes bioprocess operations successfully primarily in Cell Culture/Upstream manufacturing. CIP/SIP/PT operations: cleaning, assembly, sterilization, disassembly, pressure test and operation of primary process equipment. Unit operations described in standard operating procedures and batch records (50%-100% of effort). Recommends and executes projects and changes to bioprocess operations to reduce risk and increase efficiency. etc. | 9/17/2019 |
| 1159 | AGC Biologics Bothell, WA Manufacturing Support Technician HS diploma or equivalent Exp: 0-6 years |
We are seeking an experienced and highly motivated Manufacturing Support Technician to join our expanding Manufacturing team. PRINCIPAL RESPONSIBILITIES: Support product process unit operations described in standard operating procedures and batch records (100% of effort). Anticipates and minimizes deviations from support procedures. Stocking of supplies and gowning materials in GMP clean room areas. Weigh and dispensing of chemicals and processing materials. etc. | 9/17/2019 |
| 1160 | AGTC Alachua, FL QA Specialist I BS in a scientific discipline Exp: No experience |
Essential Duties and Responsibilities: Support the development, implementation, and improvement of corporate quality systems that support early, mid and late phase gene therapy clinical programs. Increase compliance awareness and promote a culture of quality throughout the company, with a focus on laboratory and manufacturing operations. Collaborate with multiple functions to perform QA oversight and ensure quality-related activities are executed efficiently. Write, review and revise standard operating procedures. etc. | 9/17/2019 |
| 1161 | AGTC Alachua, FL Pre-Clinical R&D Research Associate I - Cloning & Production MS in a biologcal science Exp: No experience |
Essential Duties and Responsibilities: Plasmid construction and large-scale plasmid DNA production. AAV vector production, purification and characterization. Design and develop new assays with minimal supervision. Maintain relevant laboratory supplies and equipment as needed. Draft SOPs, tech report and study reports. etc. | 9/17/2019 |
| 1162 | AKESOgen Peachtree Corners, GA Research Associate BS/MS in a clincal, health, or life sciences field Exp: 1+ years |
This individual is a Research Associate who will work with a team of research associates and scientist at AKESOgen. The Research Associate will work under the general direction of a Team Lead. This individual will perform extractions on a variety of sample types, genotyping on Affymetrix and/or Illumina platform equipment maintenance, solution and reagent preparation in addition to other tasks in laboratory. All duties are subject to change by managers during employment. etc. | 9/17/2019 |
| 1163 | Akorn Vernon Hills, IL Formulation Scientist II BS/MS in pharmaceutical sciences or related Exp: 0-4 years |
We seek talented Formulation Scientists at various levels to join our expanding R&D team who will be responsible for developing the final product formulation, process procedures and packaging of semisolids, suspensions and solutions, lotions, nasal sprays, inhalations, sterile injectable and ophthalmic products etc. Literature searching and review, patent searching and interpretation, performing risk assessment for formulation/process development, conducting experimental design and execution of lab scale, pilot scale developmental batches to support the final formulation and processes. Evaluation and selection of active, inactive raw materials and packaging components for various products. etc. | 9/17/2019 |
| 1164 | Akorn Cranbury, NJ Analytical Scientist I BS in chemical or life sciences Exp: 0-4 years |
We seek talented Analytical Scientists at various levels to join our expanding R&D team. You will be responsible for methods and process development for ANDA topical, suspensions and solutions, nasal sprays, inhalations, sterile injectable and ophthalmic products. You will develop and validate new analytical methods, conduct stability studies and perform sample testing to support regulatory submissions. ESSENTIAL FUNCTIONS: Independently develop analytical methods for drug substances, drug product, preservatives and degradation/impurities in the new drug products. etc. | 9/17/2019 |
| 1165 | Alamo Baltimore, MD Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in business to business sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 9/12/2019 |
| 1166 | Alamo Los Angeles, CA Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in business to business sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 9/12/2019 |
| 1167 | Alamo Austin, TX Pharmaceutical Sales Representative - Dermatology BS/BA Exp: 1 year in business to business sales |
The Specialty Dermatology Pharmaceutical Sales Representative is accountable and responsible for her/his territory achieving or surpassing sales goals on a monthly basis. Takes ownership and demonstrates the ability to drive monthly sales results through superior selling skills - meeting and exceeding all performance goals. Proven ability to observe and identify market opportunities and challenges and subsequently develop, plan, implement, and follow through with action plans to positively influence opportunities and challenges. | 9/12/2019 |
| 1168 | Alcami Charleston, SC Process Engineer BS/BA in engineering, pharma, chemistry Exp: 0-2 years in technical support |
The Process Engineer I (Sterile) for our parenteral site in Charleston, SC is accountable for driving results in a fast-paced environment by providing technical support for the manufacturing facility, including, troubleshooting validated processes, process deviations and investigations, transfers of new processes and technologies into the site and preparation of documentation to support validation and process transfer activities. | 9/12/2019 |
| 1169 | 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 |
| 1170 | Alcami Charleston, SC Material Control Tech I HS Diploma/GED Exp: 1-2 years in general warehouse |
The Materials Control Technician I is accountable for results in a fast-paced environment by following applicable SOPs and cGMPs to perform tasks for the receipt, storage, inventory and distribution of raw materials, intermediate or finished drugs or drug products and components. The Materials Control Technician I uses the electronic inventory system to track, document and control all inventory. | 9/12/2019 |
| 1171 | 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 |
| 1172 | Alcon Sinking Spring, PA Quality Engineer I BS/BA Exp: 0-2 years related experience |
Quality Engineering Complaint management and provide complaint trending analyses to support improvement of products manufactured in the facility. Maintain knowledge of product quality controls and failure modes. Evaluate complaint samples. Initiate and perform investigations, maintain & follow up on Quality Corrective Action Plans. Provide Progress Reports and trending to show product quality levels and respond to regulatory requests. | 9/12/2019 |
| 1173 | Alcon Sinking Spring, PA Engineer I BS/BA Exp: 0-2 years |
Assist engineering in identifying opportunities for change and realizing successful change in existing operations to attain quality, cost, and production requirements. Demonstrate knowledge of all equipment and processes in the areas of responsibility. Effectively and efficiently assist/lead efforts in product/process design. Coordinate detailed design efforts on process/equipment modifications and product changes. | 9/12/2019 |
| 1174 | Alcon Huntington, WV Engineer I, Manufacturing BS/BA in engineering, pharma, chemistry Exp: 0-2 years |
Develop, maintain, improve, and qualify molding and inspection processes for use in the manufacture and inspection of IOLs. Manage molding capacity and efficiency through process improvements and the fabrication, purchase, and qualification of new equipment. Lead technical personnel to maintain, troubleshoot, and repair molding equipment. | 9/12/2019 |
| 1175 | Aldevron Fargo, ND Laboratory Technician II HS Diploma/GED Exp: 1-2 years |
Our Laboratory Technicians play a critical role in our manufacturing process by managing the room changeover process or the solution preparation process. Detailed, thorough cleaning, line clearance, and segregation of GMP and GMP Source production areas and associated equipment while wearing appropriate gowning. Diagnostic Kit Production: assisting in vial weighing, capping, and labeling of vials as well as associated paperwork | 9/12/2019 |
| 1176 | Aldevron Fargo, ND Quality Systems Specialist I HS Diploma/GED Exp: 1+ years review compliance data or related |
We are currently seeking a Quality Systems Specialist I to join our team! The QS Specialist I will be responsible for reviewing data for compliance with systems within the quality department at Aldevron. These systems include but not limited to supplier management and electronic Quality Management Systesm (eQMS). | 9/12/2019 |
| 1177 | Aldevron Fargo, ND Metrology Technician HS Diploma/GED Exp: 1-3 years calibration/technical experience |
We are seeking a Metrology Technician! The Metrology Technician performs routine calibration, maintenance, troubleshooting, and repair of a variety of laboratory and manufacturing equipment in a cGMP environment. This individual will have the ability to perform a variety of routine and non-routine technical tasks and tests while having a great deal of initiative and judgement. | 9/12/2019 |
| 1178 | Abbott Pomona, CA QA Specialist I HS Diploma/GED Exp: 1-3 years in QA |
We have an exciting opportunity for a QA I within our Immunalysis group located at Pomona,CA In this role, you will be responsible for carrying out the daily operations in the batch record department. Demonstrated ability to carry out assignments in a timely, accurate manner and accomplishing tasks as required with little or no supervision. Work with groups within the organization to get corrections and clarifications to Device History Records. Demonstrates commitment to the development, implementation and effectiveness of Company Quality Management System per ISO, FDA, and other regulatory agencies. | 9/12/2019 |
| 1179 | Abbott San Diego, CA Lab Tech I (Second Shift) HS Diploma/GED Exp: 0-2 years |
We have an exciting opportunity for a Lab Tech I within our Abbott Rapid Diagnostics business located at San Diego, CA. In this role, you will be responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established QSR’s ISO, ISO 13485, CMDR, and other pertaining regulations under the direction of senior staff. | 9/12/2019 |
| 1180 | Alkermes Wilmington, OH QC Analyst I BS in chemistry Exp: 0-2 years |
The position requires the individual to perform routine/non-routine physical, chemical, and in-vitro assays of clinical, commercial, process and cleaning validation samples, and process development samples to support Manufacturing. Performs physical and/or chemical analyses of product to ensure stability. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. | 9/12/2019 |
| 1181 | Alkermes Wilmington, OH QA Associate I BS/BA in sciences Exp: 1-2 years in QA |
The Quality Assurance Associate will be responsible for performing functions including daily on the floor activities related to sterile manufacturing operations, on the floor batch record review, executed validation review, discrepancy identification, logbook review, AQL inspection of finished product, SAP transactions, room/utility walkthroughs, shutdown/incident form assessment/review and reconciliation, initiation of hold forms, training program support, and product shipping in a facility that manufactures sterile products in a GMP environment. | 9/12/2019 |
| 1182 | Alkermes Waltham, MA Process Development Associate BS in engineering Exp: 0-3 years |
The process development engineer will provide technical support in the development, scale-up and optimization of pharmaceutical process at various phases ranging from R&D to Commercial manufacturing. Specific areas of focus include material processability characterization, 1st and 2nd principle modeling knowledge. The role is expected to have a strong lab presence with the ability to design and execute experiments, interpret the data to improve process understanding. To be successful candidate in this role the candidate needs a good understanding in material characterization and statistical modeling is required | 9/12/2019 |
| 1183 | Allergan Austin, TX Accounts Receivable Administrator I BS in finance or accounting Exp: 1-2 years in related |
Responsible for analyzing and collecting past dues for specified accounts. Negotiates with customers without jeopardizing their relationship with Allergan to collect all past due invoices. Has knowledge of commonly used concepts, practices, and procedures within a particular field. Relies on experience and judgment to plan and accomplish tasks. Performs a variety of complicated tasks to minimize financial losses and obtain best possible DSO. Daily activities include establishing objectives, identifying areas of improvement internally and externally. | 9/14/2019 |
| 1184 | Allergan Livonia, MI Clinical Sales Representative BS/BA Exp: 1 year in business to business sales |
As a pharmaceutical Sales Representative, you will have the opportunity to regularly call on health care professionals (primary care physicians, clinics, hospitals and pharmacies) within a specific geographic area. Day-to-day responsibilities consist of supporting the promotional efforts behind Allergan products, which includes organizing, tracking and distributing FDA regulated sample products to health care professionals. | 9/14/2019 |
| 1185 | Allergan Mentor, OH Clinical Sales Representative BS/BA Exp: 1 year in business to business sales |
As a pharmaceutical Sales Representative, you will have the opportunity to regularly call on health care professionals (primary care physicians, clinics, hospitals and pharmacies) within a specific geographic area. Day-to-day responsibilities consist of supporting the promotional efforts behind Allergan products, which includes organizing, tracking and distributing FDA regulated sample products to health care professionals. | 9/14/2019 |
| 1186 | Alliance Spine San Antonio, TX Medical Sales Representative BS/BA Exp: 1 year operating room experience |
Responsible for working at the direction of the Chief Operating Officer and/or Managing Partner to help support the sales functions within the defined geography. Medical Sales Representative will assist in retaining and penetrating existing customers (surgeons and distributors) and finding new business. The Medical Sales Representative is responsible for field-based customer service, case coverage as necessary, and sales prospecting as assigned by the Chief Operating Officer and/or Managing Partner, generating new business, sales logistics, product knowledge, product training, and maintaining inventory assets. | 9/14/2019 |
| 1187 | Amarex Bethesda, MD IT HELP DESK TECHNICIAN LEVEL 1 BS/BA Exp: 1 year related experience |
The IT Help Desk Technician Level 1 is responsible for end user support, upgrades, customization, and system integration. First point of contact for troubleshooting of IT problems; resolving the problem if possible, with an appropriate sense of urgency. Provide IT support to end users, both on- and off-site. | 9/14/2019 |
| 1188 | Amarex Bethesda, MD CLINICAL DATA COORDINATOR (two openings) BS/BA Exp: 1 year related experience |
The Clinical Data Coordinator is responsible for timely validation of clinical trial data. Review case report forms and clinical data sets for errors, discrepancies and protocol violations. Organize and maintain clinical study databases to support regulatory submissions. Communicate orally and/or written, in a timely and effective manner, with the appropriate internal or external individuals involved in the project | 9/14/2019 |
| 1189 | Amarex Bethesda, MD PROGRAMMER ANALYST I BS/BA in computer sciences or related Exp: 1 year related experience |
The Programmer Analyst I is a computer programming position responsible for delivering technical services relating to clinical trials data. This includes working with Electronic Data Capture (EDC) and other data management applications to achieve project integrity and the delivery of on-time, quality data. The Programmer Analyst I analyzes the feasibility of program requirements to develop applications that meet FDA guidelines. | 9/14/2019 |
| 1190 | Ambry Genetics Aliso Viejo, CA Quality Assurance Engineer BS/BA in computer sciences or related Exp: 0-2 years in software quality |
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. | 9/14/2019 |
| 1191 | Ambry Genetics Aliso Viejo, CA Research Associate II, Assay Development - R&D MS in life sciences Exp: 1-2 years lab research |
Research Associate II is responsible for assisting senior R&D staffs with minimal supervision to design, develop, and validate clinical diagnostic assays spanning a wide range of Next-Generation sequencing and microarray technologies. | 9/14/2019 |
| 1192 | 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. Aid in the design and development of clinical diagnostic assays for use in a CLIA/CAP regulated setting. Perform research experiments, such as primer design and preparation, PCR, electrophoresis, gel imaging and analysis, | 9/14/2019 |
| 1193 | Ambry Genetics Aliso Viejo, CA Software Engineer, Bioinformatics MS in computational biology or related Exp: 1+ year in software development |
As a software engineer at Ambry you’ll gain industry-leading experience in AGILE software development while working at the cutting edge of clinical genetics. At Ambry, you’ll have the opportunity to develop innovative solutions and leverage the latest technologies to make our diagnostics-testing even better. The technologies we use include Perl, Python, Dancer2, MySQL, MongoDB, and Elastic Search. Knowledge of the genetics and/or genetic testing industry a huge plus and a sense of humor is a must. | 9/14/2019 |
| 1194 | Ambu Noblesville, IN Process Technician - 2nd Shift AS/AA Exp: 1 year experience |
Monitor various line and equipment functions utilizing various computer interfaces and visual observation. Perform change over, teardown, and set-up tasks. Perform, monitor, and document wastewater and lift station properties. Complete documentation to ensure compliance with relevant standards (i.e. Medical Device Directive (MDD), QSR, CMDR, ISO 13485, JPAL, production and corporate standards) | 9/14/2019 |
| 1195 | Ambu Noblesville, IN Quality Assurance Inspector - 2nd 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. | 9/14/2019 |
| 1196 | Amgen Tampa, FL Associate Data Engineer BS/BA Exp: 0-4 years |
The Associate will work with some of the brightest minds in the industry and get opportunities to solve some of the most challenging business problems. Amgen is using Enterprise Data Lake, cloud technology, and continuous deployment pipelines to produce science based insights to build new drug therapies for patients that address grievous illnesses. | 9/14/2019 |
| 1197 | Amgen Thousand Oaks, CA Automation Engineer MS Exp: 0-2 years in engineering |
The Automation Engineer reports to the Manager of the Automation group. The position is responsible for providing Automation Engineering support at the Amgen Thousand Oaks site. Provide system administration and ownership support for DeltaV and Utility systems. Work closely with multiple disciplines including: OIS network and site platform leads to support, plan and execute system roadmaps and as well as influence future improvements. Ensure optimal performance and reliability for process systems and equipment. | 9/14/2019 |
| 1198 | Amgen Tampa, FL Data Engineer MS in information systems Exp: 0-2 years |
In this role, you will work with some of the brightest minds in the industry, and you'll get an opportunity to solve some of the most challenging business problems. Amgen is using Enterprise Data Lake, cloud technology, and continuous deployment pipelines to produce science based insights to build new drug therapies for patients that address grievous illnesses. Applying specialized knowledge and understanding of principles, concepts and standards to moderately complex assignments | 9/14/2019 |
| 1199 | Amgen Thousand Oaks, CA Associate Manufacturing BS/BA Exp: 0-4 years in manufacturing or operations |
he Associate of Manufacturing will work in a dynamic production environment at the Amgen Thousand Oaks Drug Substance plant supporting development, clinical, and commercial launch activities. Under general supervision, employee will perform operations in the Manufacturing area, specifically B23 processes. Operations will be performed according to Standard Operating Procedures (SOPs). | 9/14/2019 |
| 1200 | Amgen Tampa, FL Associate Software Engineer - Regulatory Information Management BS/BA Exp: 0-4 years in information sciences |
Amgen is seeking an integration engineer with experience and interest in building scalable integrations for enterprise applications. The integration engineer will have a real passion for developing and maintaining robust integration for On-Prem and Cloud applications to support critical business functions. | 9/14/2019 |
| 1201 | Amgen Tampa, FL IS Engineer - Data Analytics (Business Intelligence) MS in computer sciences/maths Exp: 0-2 years in information sciences |
We are seeking an IS Engineer – Data Analytics in our Amgen Capability Center (ACC) Tampa, FL to join our Patient Safety IS team. The ideal candidate must be passionate about providing solutions for advanced analytics and data processing. You will collaborate with our Patient Safety business and product teams to define and build the reporting and data visualization solutions enabling faster and better-informed decision-making | 9/14/2019 |
| 1202 | Amgen Juncos, PR Associate Mfg - AML 14 BS/BA in life sciences/engineering Exp: 0-2 years |
The Associate Manufacturing role will support the Drug Product Filling operations according to Standard Operating Procedures (SOPs). Will perform and monitor critical processes, execute routine protocols, and regularly draft and revise documents such as Manufacturing Procedures and SOPs. Perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams. Employee may also have the responsibility of owning NC/CAPA’s. May identify, recommend, and implement improvements related to routine functions in a Non-Standard Shift environment. Several positions available. | 9/14/2019 |
| 1203 | Amicus Theraputics Philadelphia, PA Associate Scientist, Clinical Assay and Reagent Development MS in sciences Exp: 0-2 years |
The successful candidate will support the development and execution of in vitro and analytical biomarker assays to drive our discovery programs and provide critical support for clinical Gene Therapy programs in neurological lysosomal storage disorders. Support development of specific reagents for the characterization of lysosomal glycoproteins. Protein purification from mammalian cell lines. etc | 9/14/2019 |
| 1204 | Amneal Pharma East Hanover, NJ QA Inspector I HS Diploma/GED Exp: 1 year in QA |
The QA Inspector I monitors and ensures 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. The QA Inspector I must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run. | 9/14/2019 |
| 1205 | Amneal Pharma Branchburg, NJ QA Inspector I HS Diploma/GED Exp: 1 year in QA |
The QA Inspector I monitors and ensures 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. The QA Inspector I must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run. | 9/14/2019 |
| 1206 | ARL Bio Pharma Oklahoma City, OK Laboratory Technician - R&D Lab AS/AA or BS/BA in chemistry Exp: 0-2 years |
R&D Lab Tech performs general laboratory tasks under immediate supervision. The work involves preparation of chemical reagents/mobile phase, assistance with chemical tracking/disposal, and assistance with sample retrieval, preparation and storage. The position requires a high school diploma and some college coursework in chemistry or a related field is desired. The position also requires ability to use a personal computer, including familiarity with word processing, spreadsheet, email and database applications. | 9/14/2019 |
| 1207 | ARL Bio Pharma Oklahoma City, OK Research & Development Scientist I BS/BA in chemistry Exp: 1-2 years |
The position requires the performance of variety of task including development and validation of analytical methods and qualitatively/quantitatively testing routine and non-routine client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation (HPLC/IC) used in a chemistry laboratory. Research Scientist I work with direct supervision and reports to the lab supervisor. The Research Scientist I must be able to think and work independently, yet share ideas and work toward team goals. | 9/14/2019 |
| 1208 | Ani Pharmaceuticals Baudette, MN Distribution Worker I HS Diploma/GED Exp: Entry Level |
These responsibilities include order fulfilment, receiving, stocking of materials, replenishments, cycle counting, and returned goods within the inventory control area. Performs packing, labelling, checking and confirming in the Shipping area. Works with the parcel shipping and Bill of Lading systems. Operates an electric pallet jack, and forklift operation for loading/unloading trucks. | 9/15/2019 |
| 1209 | Ani Pharmaceuticals Baudette, MN Operator I - Production (1st, 2nd and 3rd Shift) HS Diploma/GED Exp: 1-2 years |
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. | 9/15/2019 |
| 1210 | Ani Pharmaceuticals Baudette, MN QC Chemist/Sr. QC Chemist BS/BA in chemistry, microbiology, or related Exp: 1-3 years minimum |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 9/15/2019 |
| 1211 | Ani Pharmaceuticals Baudette, MN Contracts Support Associate AS/AA Exp: 1-2 years related experience |
This position works within the Finance Department 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. | 9/15/2019 |
| 1212 | 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 |
| 1213 | 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 |
| 1214 | 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 |
| 1215 | Antech Fountain Valley, CA Float Laboratory Technician BS in medical technology or related Exp: 1 year in clinical lab |
Antech Diagnostics, the largest exclusively commercial veterinary diagnostic laboratory in the nation, is in search of a Float Laboratory Technician working out of our Lake Success, New York laboratory and reporting directly to the Lab Manager. The Ideal Candidate will have prior experience as a Medical Technician that involved performing some clinical diagnostic testing & using testing equipment. In this integral role you will perform tests in all areas of the laboratory such as: Chemistry, Hematology, Coagulation, Urinalysis, Serology, Parasitology, Histology. | 9/15/2019 |
| 1216 | Applied Meidcal Rancho Santa Margarita, CA Production Associate (Assembler/Machine Operator) HS Diploma/GED Exp: 1-2 years work experience |
As a Production Associate, you will be responsible for working within the framework of a team in a cleanroom or manufacturing environment, and performing the following activities: Perform all manufacturing operations in a cleanroom or non-cleanroom environment such as assembly, inspection, and machine operations. Comply with Applied Medical Quality Systems (QS) including SOPs, MIs, QIs and TMs. Perform manufacturing operations efficiently with or without tools and/or equipment | 9/15/2019 |
| 1217 | Applied Meidcal Rancho Santa Margarita, CA Quality Engineer I,II HS Diploma/GED Exp: 1 year in medical devices |
As a Specialist I/II or Engineer I/II on the Regulatory Affairs(RA)/Quality Systems(QS) Team, you will be responsible for working within the framework of a team and performing the following activities: Monitor and ensure conformance through the understanding of standards and regulations. Manage projects to maintain and improve the quality system by establishing or updating procedures. Participate in internal and external audits | 9/15/2019 |
| 1218 | Applied Meidcal Rancho Santa Margarita, CA Project Engineer - Construction BS/BA in construction management, engineering or related Exp: 0-3 years |
As a Project Engineer, you will be responsible for working within the framework of a team and performing the following activities: Update construction schedules based on team input. Receive, review, forward and track status of submittals. Initiate, prepare, review, track, and distribute RFIs. Assist in management of project permit process | 9/15/2019 |
| 1219 | Applied Meidcal Lake Forest, CA Mold Maintenance Technician HS Diploma/GED Exp: 1 year of mold maintenance |
As a Mold Maintenance Technician, you will be responsible for working within the framework of a team and performing the following activities: Maintain thermoplastic molds to ensure consistent quality, output and yield. Perform preventive maintenance on injection mold tooling. Communicate effectively with production team members, Team Leaders engineers, and inspectors to ensure quality installation of molds | 9/15/2019 |
| 1220 | 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 |
| 1221 | 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 |
| 1222 | 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 |
| 1223 | Accelerate Diagnostics Tuscon , AZ Quality Control Technician BS in biological sciences or chemistry Exp: 1+ years in lab/research |
The Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basisThe Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basisThe Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis | 9/6/2019 |
| 1224 | Acceleron Cambridge, MA Research Associate, Cell Culture and Media Prep BS or MS in cell biology Exp: 1 or more years in lab |
We are seeking a highly organized, motivated individual with experience in media and buffer preparation, mammalian cell culture, and recombinant protein expression. You will contribute to the development of our next-generation biologic therapeutics by generating cell lines and analyzing recombinant proteins. You will work cross-functionally with the Molecular Biology, Protein Purification, and Process Development groups and will have the opportunity to gain experience in multiple aspects of drug development. | 9/6/2019 |
| 1225 | Accuray Madison, WI Temporary Product Surveillance Specialist BS in engineering or clinical field Exp: 0-3 years |
The Product Surveillance Specialist effectively implements the complaint handling process and processes complaints in a uniform and timely manner according to regulatory requirements and company practices and policies. Evaluates complaints to determine whether an investigation is necessary and if Medical Device Reporting (MDR) is necessary in accordance with 21 CFR Part 803 Medical Device Reporting and 806 Corrections and Removals, Canadian regulations, European Vigilance Reporting and any other worldwide regulatory requirements. | 9/6/2019 |
| 1226 | KCI South Burlington, VT Field Service Representative I HS Diploma/GED Exp: 1 year work experience |
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. | 9/6/2019 |
| 1227 | 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 |
| 1228 | 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 |
| 1229 | 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 |
| 1230 | 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 |
| 1231 | Actuated Medical Bellefonte, PA Clinical Education Specialist 4 year or 2 year business degree Exp: 0-3 years |
The relevant experience required for a Clinical Education Specialist (CES) is a four year business degree or significant experience working with marketing activities, specifically digital marketing. The CES must possess a working knowledge of business principles, schedule management, organizational styles and marketing practices. The CES has the responsibility of supporting the Clinical Education Leader, President, and Director, R&D to move the company Up and Onward. The CES must assist to position Actuated Medical (AMI) as a company that Improves Patient Outcomes by developing Innovative Motion® Medical devices and providing clinical education to improve patient care. | 9/6/2019 |
| 1232 | Emergent BioSolutions Camden, MD Assistant Technician, Inspection & Packaging HS Diploma/GED Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. Execute and document procedural steps in compliance with cGMP standards. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification). Package product in final packaging components while verifying that lot information, including lot number and expiration date, are accurate | 9/6/2019 |
| 1233 | Emergent BioSolutions Camden, MD Assistant Technician, Inspection & Packaging HS Diploma/GED Exp: 0-2 years |
This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. Execute and document procedural steps in compliance with cGMP standards. Perform 100% visual inspection of product and classify rejected materials utilizing approved categories within required timelines (Qualification). Package product in final packaging components while verifying that lot information, including lot number and expiration date, are accurate | 9/6/2019 |
| 1234 | Emergent BioSolutions Bayview, MD Manufacturing Associate II HS Diploma/GED required, BS preferred Exp: 1 or more year in GMP |
The Manufacturing Associate II position reports to Manager Manufacturing at Emergent Manufacturing Operations Baltimore (EMOB). Prior experience in GMP manufacturing and operation of GMP process equipment are prerequisites. Operates manufacturing equipment such as: incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in process testing equipment | 9/6/2019 |
| 1235 | Emergent BioSolutions Lansing, MI Assistant Manufacturing Associate HS Diploma/GED Exp: 0-1 years in cGMP |
Execute tasks per cGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing qualification block training program. Actively incorporate the Core Values set out by Emergent BioSolutions while performing day to day activities. | 9/6/2019 |
| 1236 | Emergent BioSolutions Camden, MD Analyst I, QC 2nd shift BS in chemistry or related Exp: 0-2 years in GMP lab |
Perform analytical testing per cGMP in support of raw material, in-process, final product, stability. Typical hours are 2:00pm – 10:30pm, Monday through Friday. Hours may vary to meet business and training needs. Perform WFI sampling and testing as per current protocol, or validation protocols to support the WFI system. Perform various analytical testing procedures as per manufacturing/quality control batch records, stability protocols, raw material requests for testing, etc. | 9/6/2019 |
| 1237 | Emergent BioSolutions Bayview, MD Analyst I, QC AS/AA in biological sciences Exp: 1-3 years in pharma/biotech |
The Quality Control Analyst I, Microbiologist position supports the Quality Control group at EMOB to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the EMOB Microbiology, Environmental Monitoring, and Clean Utility testing programs, microbiological product testing, and supporting quality initiatives. Ensures samples are collected, tested, and reported per associated procedures and methods. Responsible for quality document generation and revision, and quality notification execution. | 9/6/2019 |
| 1238 | Emergent BioSolutions Canton, MA Analyst I, QC Microbiology BS/BA in applied sciences Exp: 0-2 years |
This is a laboratory testing position with the major responsibilities being daily routine EM and Micro testing, and laboratory maintenance/upkeep tasks. Additional responsibilities involve quality systems support which includes supporting laboratory investigations as appropriate. Works with facilities/metrology to conduct and document execution of work orders to ensure GMP compliant state of labs and equipment. Performs routine EM and Micro testing following written procedures and limited non-routine testing including validation studies with supervisory oversight. | 9/6/2019 |
| 1239 | Adaptive Biotechnologies Seattle, WA Facilities and Equipment Coordinator BS/BA in engineering/sciences Exp: 1 or more year in lab |
The Facilities and Equipment Coordinator will serve the Facilities Department at the Adaptive Biotechnologies Seattle location. The primary function of this role is to support laboratory and building services including equipment maintenance and calibrations, equipment records, qualifications (IQ/OQ/PQ), and vendor coordination’s for the regulated and non-regulated lab space. This individual will provide cross-functional support for critical revenue driving assets and departments including the Production, Clinical Development, and Research Labs. | 9/6/2019 |
| 1240 | Adaptive Biotechnologies Seattle, WA Lab Operations Compliance Specialist BS in biological sciences Exp: 1 or more year in quality management systems |
The Lab Operations QA/compliance Specialist supports activities in the Operations group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support the QA/Compliance activities for the CAP/CLIA/NYS regulated laboratory, related to the services provided. | 9/6/2019 |
| 1241 | Qdare Pharmaceuticals Vandalia, OH Operator I HS Diploma/GED Exp: Entry Level |
The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. | 9/6/2019 |
| 1242 | Qdare Pharmaceuticals Vandalia, OH Operator I HS Diploma/GED Exp: Entry Level |
The essential job function are to produce specified products by the mixing, blending, and combining of raw materials as specified by written procedures. This position is night shift working 12 hours shifts on a 2-2-3 schedule, for example working Monday and Tuesday off Wednesday and Thursday and working Friday, Saturday and Sunday then off Monday and Tuesday. | 9/6/2019 |
| 1243 | Adimab Lebanon, NH Research Associate - Protein Analytics BS in biological sciences or chemistry/engineering Exp: 0-2 years |
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 Antibody Discovery, High Throughput Expression, Molecular Core, and Computational Biology teams. Assist in in-process antibody characterization, including ForteBio kinetics and binning. Run biochemical/biophysical assays, including but not limited to, Tm and endotoxin. | 9/6/2019 |
| 1244 | ADMA Biologics Boca Raton, FL QC Lab Support Associate l BS in biology, chemistry, medical technology Exp: 1-3 years in regulated lab setting |
The QC Lab Support Associate I will Performs cGMP laboratory support activities including Sample Accessioning, Product Reserve management, Temperature Monitoring of storage chambers, Glassware Cleaning, Supply Inventory management, etc. May also assist with Stability Studies and other QC initiatives. Customer support functions for QC laboratories such as cleaning glassware and custodial services, monitoring temperature controlled chambers, shipping samples, sample preparation, administrative support. | 9/6/2019 |
| 1245 | ADMA Biologics Boca Raton, FL QC Raw Materials Specialist BS or AS in chemistry/biochemistry/biology Exp: 0-3 years |
The Raw Material Specialist I will Perform quality control raw material processing and testing. Following general instructions on routine work and detailed instructions on new assignments. Perform quality control raw material processing, sampling and testing independently according to approved Standard Operating Procedures. Complete testing documentation and data entry as required for procedures and tests performed in-house and at contract labs. | 9/6/2019 |
| 1246 | ADMA Biologics Boca Raton, FL Document Assistant - Temporary Some college Exp: 1-2 years |
The Document Assistant will Create, format, revise and proof read controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies. | 9/6/2019 |
| 1247 | ADMA Biologics Boca Raton, FL Technician I, Manufacturing Purification BS/BA in life sciences/chemistry Exp: 0-2 years |
It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. | 9/6/2019 |
| 1248 | Sonova Aurora, IL Production Associate I - 2nd shift HS Diploma/GED Exp: 1-3 years |
The Production Associate I will perform manufacturing functions associated with the following: Assembly, service and testing of BTE, RIC and FM systems. Assembly and testing of ITE custom hearing aids, Slim-tips, C-Shells and Ear Molds. Visual inspects product, identifies defects/rejects and escalates as required. Performs general routine machine maintenance and daily workstation clean-up | 9/6/2019 |
| 1249 | Sonova Valencia, CA Quality Control Inspector I HS Diploma/GED Exp: 1-2 years in inspection |
Responsible for performing visual, mechanical and electrical inspections at subassembly and final assembly levels. Perform visual and mechanical inspections at sub-assembly and final assembly levels, using engineering drawings/specifications and general quality control standards. Review manufacturing documentation to ensure that all assembly, testing and inspection steps were performed in accordance to specifications. | 9/6/2019 |
| 1250 | Sonova Warrneville, IL Customer Service Representative II HS Diploma/GED Exp: 1-2 years |
Handle customer complaints with a sense of urgency for satisfactory resolution and take ownership of that complaint. To use the current tools (SAP, Sales Force, and Cisco Finesse) to generate and maintain all customer account records and customer contacts. Handle customer requests by email and phone | 9/6/2019 |
| 1251 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician AA degree Exp: 1+ years of lab/manufacturing experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Key responsibilities include: Assemble reagents and consumables kits, Perform in-process QC and record results, Document production batch records/travelers, and computer data entry, etc. | 9/6/2019 |
| 1252 | Bio-Techne San Marcos, CA Chemist I, R&D BS/BA in chemistry, biochemistry, or biological sciences Exp: 1-5 years work in in vitro diagnostics/biotech |
Responsible for developing controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for developing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to research in a laboratory environment. | 9/6/2019 |
| 1253 | Bio-Techne Minneapolis, MN Production Assistant 1 HS Diploma/GED Exp: 0-2 years lab experience |
As a Production Assistant 1, you will be responsible for the processing of raw biological material for use in product manufacturing. You will also perform maintenance and cleaning of production equipment and containers to ensure safety and compliance, as well as completing required paperwork. | 9/6/2019 |
| 1254 | Bio-Techne Minneapolis, MN Lab Assistant I HS Diploma/GED Exp: 0-2 years |
The responsibilities of this position are to perform lab support duties and tasks for multiple departments that include: collecting and washing used labware, preparing the labware for the autoclave, running the autoclave, and harvesting and concentration of cell culture media. Perform additional duties as assigned. This position requires a Tuesday through Saturday schedule. | 9/6/2019 |
| 1255 | Bio-Techne San Jose, CA Manufacturing Laboratory Technician AA degree Exp: 1+ years of lab/manufacturing experience |
As a part of our San Jose team, the successful applicant will work with other members of Consumables Production, as well as a multidisciplinary team of engineers and scientists, to support the assembly of microfluidic cartridges for biotech products. Operate and maintain robotic and manufacturing equipment, Document production batch records/travelers, and computer data entry, Perform in-process QC and record results | 9/6/2019 |
| 1256 | 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 |
| 1257 | Bio-Techne San Marcos, CA QC Specialist 1 BS/BA in biological sciences or chemistry Exp: 1-2 years in in vitro diagnostics/biotech |
Responsible for performing QC testing for Value Assignment assays, QC release assays, stability, physical/visual inspections, any related QC function. Assists in the flow of product in the QC department. Coordinate, perform and maintain QC testing and scheduling for Stability program, Assist in establishing QC specifications, Assist in the validation testing of equipment and processes, etc. | 9/6/2019 |
| 1258 | Adverum Biotechnologies Menlo Park, CA Associate I, Quality Control BS in sciences Exp: 0-2 years in analytical, cGMP or health lab |
This individual will support the Quality Control team through development and performance Quality Control (QC) systems, policies, processes, procedures and controls as they relate to the analytical testing of clinical materials. Perform regular laboratory and equipment cleaning and maintenance according to standard operating procedures (SOPs). | 9/6/2019 |
| 1259 | 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 |
| 1260 | AGC Biologics Bothell, WA Manufacturing Associate I-IV - Upstream BS in chemistry, biology, or related Exp: 1-4 years, with experience in aseptic processing |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. | 9/6/2019 |
| 1261 | AGC Biologics Bothell, WA Manufacturing Associate I - Downstream BS in chemistry, biology, or related Exp: 1-8 years, depending on level |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/6/2019 |
| 1262 | AGC Biologics Bothell, WA Downstream Manufacturing Associate I-IV BS in chemistry, biology, or related Exp: 1-8 years, depending on level |
The Manufacturing Associate performs GMP manufacturing operations safely, reliably and in compliance with stated processes. Execute unit operations described in standard operating procedures and batch records. Perform bioprocess operations such as filtration, purification, cell culture or recovery. Clean, assemble/disassemble, sterilize and operate primary process equipment. etc. | 9/6/2019 |
| 1263 | AGC Biologics Bothell, WA Development Associate I - II A.A./B.S. in a life science or engineering Exp: 0-2 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures | 9/6/2019 |
| 1264 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Sun-Wed A.A./B.S. in a life science or engineering Exp: 0-3 years |
This is a Development Associates position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. | 9/6/2019 |
| 1265 | AGC Biologics Bothell, WA Development Associate I (Contract, Temp-to-Perm) Monday-Friday HS Diploma or Aa in life science/engineering Exp: 0-3 years |
This is a Development Technician position in the Process Development Support group. Primary responsibility will be to support the process development team processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for lab support. Under general supervision, this person carries out routine to moderately complex lab operations. | 9/6/2019 |
| 1266 | 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 |
| 1267 | Agilent Wilmington, DE R&D Electrical Engineer BS or MS in electrical engineering or related Exp: Entry Level |
As an Electrical Engineer in our R&D group, you'll be part of a team that analyze, design, prototype and test new products for Agilent's Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. Most projects require mechanical, electrical and firmware engineers, as well as chemists and software engineers, to create a complete system. As part of those projects, you will also work with our marketing, manufacturing, purchasing and service organizations to transform your designs into shipping products. | 9/6/2019 |
| 1268 | 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 |
| 1269 | 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 |
| 1270 | 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 |
| 1271 | 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 |
| 1272 | 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 |
| 1273 | 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 |
| 1274 | Akorn Decatur, IL 1st shift QA Technician I, Documentation Systems One year certificate from college/tech school Exp: 0-1 years |
Revise and maintain controlled documents including, but not limited to: Master Batch Records, Standard Operating Procedures, Active Pharmaceutical Ingredient Specifications, Finished Drug Product Specifications, Forms, and Protocols. Maintain and distribute Document Change Requests. Provide coverage for Front Desk. | 9/7/2019 |
| 1275 | Akorn Decatur, IL Technical Development Engineer BS/BA in chemical/mechanical/systems engineering Exp: Entry Level |
The full-time, Development Engineer will have an opportunity to rotate through 3 areas of engineering within our Decatur, IL facility during their first year of employment – Maintenance, Projects and Technical. | 9/7/2019 |
| 1276 | Akorn Vernon Hills, IL Formulation Scientist I BS/MS/PhD in pharma sciences or related Exp: 1 or more years |
We seek a talented Formulation Scientist to join our expanding R&D team who will be responsible for developing the final product formulation, process procedures and packaging of semisolids, suspensions and solutions, lotions, nasal sprays, inhalations, sterile injectable and ophthalmic products etc. Literature searching and review, patent searching and interpretation, performing risk assessment for formulation/process development, conducting experimental design and execution of lab scale, pilot scale developmental batches to support the final formulation and processes. | 9/7/2019 |
| 1277 | Akorn Decatur, IL 2nd shift QA Technician I, Documentation Systems One year certificate from college/tech school Exp: 0-1 years |
Revise and maintain controlled documents including, but not limited to: Master Batch Records, Standard Operating Procedures, Active Pharmaceutical Ingredient Specifications, Finished Drug Product Specifications, Forms, and Protocols. Maintain and distribute Document Change Requests. Provide coverage for Front Desk. | 9/7/2019 |
| 1278 | Akorn Decatur, IL 2nd shift Chemist I BS/BA in chemistry/chemical engineering Exp: 0-2 years, experience prefered |
The quality control chemists perform testing on raw materials, bulk formulations, finished products, stability samples, and any other samples from plant operations that require chemical analysis. The QC chemists report to the QC manager. Responsible for the laboratory testing in accordance with company SOP’s as well as cGMP’s and GLP’s. Testing involves Raw materials, In-process, Finished product, and Stability samples for potency and physical characteristics such as pH, Specific gravity, Moisture, etc. | 9/7/2019 |
| 1279 | Akoya Biosciences Menlo Park, MA Application Scientist, Contract Research Services MS in life sciences Exp: 0-2 years |
Akoyais seeking an experienced Scientist to join our Quantitative Pathology Solutions –Phenoptics Services (QPS-PS), Image Analysis teamlocatedin Hopkinton, MA. Akoyaenables staining with up to eightantibodies utilizing our OPAL™ technology to provide unparalleled cellular/tissue imaging capabilities. QPS-PS is a dynamic team that develops multiplex OPAL™ panels for clients, then performs staining, imaging, and quantitative analysis of their samples. The QPS-PS Image Analysisteam focuses on imaging of stained slides and image analysis. | 9/7/2019 |
| 1280 | 3T Biosciences Menlo Park, CA Associate Computational Biologist BS/MS Exp: 1-2 years |
TYPICAL RESPONSIBILITIES: 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. Querying and organizing an SQL database. Working with a team of consultants, data scientists, and computational biologists. | 9/10/2019 |
| 1281 | 4D Molecular Therapeutics Emeryville, CA Upstream Cell Culture Manufacturing Associate BS in bioprocessing, chemical engineering, biochemistry or related Exp: 1-3 years |
Reporting to the Upstream Supervisor, you will execute cell culture and/or solution prep unit operations in cGMP clinical pilot manufacturing plant operation. You will participate in quality, compliance and safety programs for the daily manufacturing operations of biologic products to support gene therapy clinical trial and product development. In addition, you will participate in the implementation of process improvements/scale-up. Shift/weekend work and lifting 40 lbs. unassisted is required at times. | 9/10/2019 |
| 1282 | 4D Molecular Therapeutics Emeryville, CA Research Associate (Analytical Sciences & Bioinformatics) BS in life sciences Exp: 0-3 years |
Responsibilities: Follow proper safety precautions and laboratory technique in the use of chemical compounds and reagents. Perform established analytical methods such as PCR (qPCR/ddPCR), Electrophoresis, and ELISA. Design, execute and report qualification assays under the supervision of senior group members. Write and revise documents such as SOPs and technical reports. Analyze data, identify trends and troubleshoot assays. etc. | 9/10/2019 |
| 1283 | 4D Molecular Therapeutics Emeryville, CA Research Associate I/II (Upstream Process Development) BS/MS in bioengineering, biochemistry, biology or related Exp: BS: 1-3 years, MS: 0-2 years |
Major Responsibilities: Design and execute production studies leveraging 4DMT’s vector platform processes. Collaborate with process & analytical teams to screen and evaluate drug candidates across a range of indications. Draft and update batch records, electronic lab notebooks (ELN), standard operating procedures and technical reports. Responsible for documentation that is IND-supporting and will be communicated to relevant internal/external stakeholder &/or regulatory parties. Document, consolidate, interpret and communicate scientific findings with internal/external teams. Contribute to a culture that embraces continuous learning, improvement and innovation. Can work with others to expand their technical skill base and deepen their gene therapy expertise. etc. | 9/10/2019 |
| 1284 | Abbott Plymouth, MN Operator I HS diploma or equivalent Exp: 6 months |
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. | 9/10/2019 |
| 1285 | Abbott Minnetonka, MN Operator I (2nd shift) HS diploma or equivalent Exp: 6 months |
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. | 9/10/2019 |
| 1286 | Abbott Minnetonka, MN Operator I HS diploma or equivalent Exp: 6 months |
We are seeking an experienced, high caliber Operator I. This position is responsible for the production of high quality medical devices within a manufacturing cell. | 9/10/2019 |
| 1287 | AbbVie Worcester, MA Associate Scientist II/ Scientist I, Drug Product Development (Physicochemical Characterization) MS in pharmaceutics, chemistry, or related Exp: 0+ years |
The Drug Product Development team at the AbbVie Bioresearch Center in Worcester, MA is responsible for designing and developing formulations that enable delivery of AbbVie’s candidate molecules in a dosage form suitable for preclinical or clinical studies. We are seeking a highly motivated, collaborative scientist with a proven track record in physicochemical characterization of small molecule candidates and application of drug delivery approaches in preclinical development. etc. | 9/10/2019 |
| 1288 | AbbVie Lake County, IL Associate Scientist II/Scientist I, Chemistry MS in chemistry Exp: 0+ years |
AbbVie is looking for an Associate Scientist/Scientist, Chemistry with strong synthetic skills. This individual will work under the mentorship of a supervisor discovering, developing and executing routes to compounds to treat a variety of diseases. The candidate will be a member of an integrated Process Research & Development project team consisting of synthetic, structural, and analytical chemists and engineers whose goal is to identify and develop novel practical routes to newly discovered therapeutic targets. The ideal candidate will be enthusiastic and productive, with excellent communication skills and strong functional expertise in synthetic organic chemistry and compound synthesis and characterization. | 9/10/2019 |
| 1289 | Abcam Burlingame, CA Research Associate - IVD BS in biological science Exp: 1-2 years |
Based in our Burlingame Office, this manufacturing position is a great opportunity to transition into the medical device Industry! This role will be responsible for carrying out GMP manufacturing of IVD IHC primary antibodies according to the requirements of SOP’s, batch production records, and approved protocols. etc. | 9/10/2019 |
| 1290 | Abcam Cambridge, MA Sr. Research Associate BS/MS in biology or related Exp: 1+ years |
We are seeking a dynamic Service Lab Senior Research Associate to work in our Cambridge, MA office to provide customers with quality data and analyses related to our high-throughput, multiplexed immunoassays and miRNA assays. The successful candidate will participate in every aspect of the Service Lab, from experimental design through running the assays, data analysis, report generation and supporting the customers as they interpret the results. etc. | 9/10/2019 |
| 1291 | ABEC Springfield, MO Mechanical Designer AS in CAD, drafting, or equivalent Exp: 1 year |
The Mechanical Designer works under the direction of the Design Team Leader and also utilize independent judgment to perform the day-to-day project duties of designing, developing and releasing deliverables. This includes detail & assembly drawings and related bills-of material used in the fabrication of equipment for pilot and commercial scale biopharmaceutical manufacturing (largely pressure vessel assemblies for fluid & gas handling and motorized agitation systems). Primary responsibility involves generating design plans utilizing Autodesk Inventor and AutoCAD software. etc. | 9/10/2019 |
| 1292 | Abiomed Danvers, MA Software Engineer MS in computer science, math, engineering or related Exp: 1-5 years |
We are currently hiring for a Software Engineer who has experience in digital signal processing and algorithm development. The candidate is responsible for designing, simulating, and implementing performance enhancing signal processing algorithms used in ABIOMED’s family of products. We are looking for a motivated and energetic self-starter, has a ‘make it happen’ attitude, and can thrive in a fast-paced, cutting edge environment. etc. | 9/10/2019 |
| 1293 | AbSci Vancouver, WA Research Associate I BS in molecular biology, biochemistry, microbiology or related Exp: 1-2 years |
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. | 9/10/2019 |
| 1294 | AbSci Vancouver, WA Research Associate I, Protein Purification BS/MS in biochemistry or related Exp: 1-4 years |
The Research Associate I will play a significant role in purification of protein biologics, and report to the Purification Group Leader. Core responsibilities include maintaining and operating chromatography instrumentation, conducting hands-on research for development of new techniques, and supporting ongoing protein purification activities. The ideal candidate will have a passion for scientific innovation, excellent technical skills, execute their responsibilities with high attention to detail, and work well within a team dynamic in a high-performance culture. etc. | 9/10/2019 |
| 1295 | Absorption Systems Medford, MA Research Associate - Bioanalytical BS/BA in a scientific field Exp: 1+ years |
The Research Associate will work as part of a team in a lab environment to completeclient-driven projects. Primary responsibilities 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. Ensuring the accuracy and timeliness of all laboratory-relatedprocesses. etc. | 9/10/2019 |
| 1296 | 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 |
| 1297 | Absorption Systems San Diego, CA Research Associate – Bioanalytical BS in chemistry 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. Principal Duties and Responsibilities: Execute experiments by LC-MS/MS in support of drug discovery and early development programs following the SOP. The candidate will be responsible for sample preparation from biological matrices, tissue homogenization, sample extraction techniques, and data acquisition. Perform duties in a timely manner to achieve study timelines. Perform other duties as directed by Management. etc. | 9/10/2019 |
| 1298 | Absorption Systems Exton, PA Associate Scientist / Scientist – Drug Transport & Metabolism 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. Absorption Systems also provides non-clinical testing services to pharmaceutical and biotech companies to support research and development of drugs, biologics, and medical devices. 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. etc. | 9/10/2019 |
| 1299 | Accelerate Diagnostics Tuscon, AZ Aseptic Filling Technician HS diploma/AS/BS Exp: 1+ years |
The Fill Technician will perform a variety of processing duties according to Batch Records (BRs) and Manufacturing Work Instructions (MWIs) in a cGMP environment for the Consumable Manufacturing Department including, but not limited to: Cleaning/recovery of classified area and work spaces, components preparation. Aseptic filling. Final Consumable Inspection. Labeling and packaging. Line clearance and Closeout responsibilities. etc. | 9/10/2019 |
| 1300 | Accelerate Diagnostics Tuscon, AZ Quality Control Technician BS in microbiology, chemistry, molecular and cell biology, or related Exp: 1+ years |
The Quality Control Technician will join Accelerate Diagnostics’ Consumable Operations team. This individual will be responsible for testing of incoming product both analytically and biologically in support of manufacturing. This will include, but not limited to, operation of pH/conductivity meter, spectrophotometer, refractometer and in-house biotechnology systems. This person will be part of a team that executes these tasks on a daily basis. The ideal candidate will be a team player, demonstrate excellent communication skills, be flexible, and excel in a fast-paced environment. etc. | 9/10/2019 |
| 1301 | Wright Cleveland, OH Associate Sales Representative, Upper Extremities BS/BA 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. This is a field based position. | 9/3/2019 |
| 1302 | Wright St. Louis, MO Sales Support Associate - St. Louis, MO HS diploma Exp: 0-2 years |
Wright Medical is currently hiring a Sales Support Associate. The Sales Support Associate will be responsible for assisting in the successful execution of the sales plan for their assigned territory and the achievement of quarterly and annual sales plan objectives. He/she will travel within the territory and region for development & sales support. He/she will maintain open communications with their assigned leadership team and headquarter based sales training leader. He/she will perform and excel in case coverage, sales territory support functions and sales activity. He/she will achieve success with specified individual training and development plan. etc. | 9/3/2019 |
| 1303 | Wright Alexandria, LA Sales Support Associate - Alexandria, LA HS diploma Exp: 0-2 years |
Wright Medical is currently hiring a Sales Support Associate. The Sales Support Associate will be responsible for assisting in the successful execution of the sales plan for their assigned territory and the achievement of quarterly and annual sales plan objectives. He/she will travel within the territory and region for development & sales support. He/she will maintain open communications with their assigned leadership team and headquarter based sales training leader. He/she will perform and excel in case coverage, sales territory support functions and sales activity. He/she will achieve success with specified individual training and development plan. | 9/3/2019 |
| 1304 | Wright Phoenix, AZ Associate Sales Rep, Lower Extremities and Biologics BS/BA Exp: 0 years |
This position is responsible for assisting Sales Representatives in the district with the successful execution of sales plans for their assigned areas and the achievement of quarterly and annual sales plan objectives. This role includes essential functions such as the management of field sales operations, customer acquisition, cultivation & retention, product launch execution, inventory management, surgical case coverage, and travel within the district as well as maintaining open communications with their district leader. This is a field based position. | 9/3/2019 |
| 1305 | Wright Bloomington, MN Shipping Clerk I HS diploma or equivalent Exp: 0-1 years |
The responsibilities of the Shipping Clerk I are to pull, check, pack, and ship Wright Medical products within the U.S. borders. The Shipping Clerk will operate the Fedex, UPS, and Powership stations to process packages and help protect the integrity of Wright Medical inventories. Essential Job Functions: Process orders based on the external customers preferred shipping system (e.g. USPS, UPS, FedEx, etc.) Prepare and print shipping labels corresponding to shipping needs. Assemble and fill boxes and other cartons with items that need to be shipped. etc. | 9/3/2019 |
| 1306 | Wright Portland, OR Inventory & Sales Support Handler HS diploma or equivalent Exp: 1-3 years |
The Inventory & Sales Support Handler ensures the timely processing of kits/sets in the remote location. This could include, but is not limited to, checking in sets, verifying completeness, restocking, creating new kits from sterile implant SKUs, and other basic set maintenance. The Inventory & Sales Support Handler is required to function with minimal supervision to ensure that work flow is uninterrupted and that all customer requirements are met within the functional area. The Inventory & Sales Support Handler will ensure that all relationship and delivery functions are carried out timely and as needed. Driving abstracts will be required every year to ensure certification for driving company van. etc. | 9/3/2019 |
| 1307 | WuXi AppTec Philadelphia, PA Associate Scientist - Genetic Stability MS in biological sciences or related Exp: None required for MS candidates |
Independent scientist who demonstrates innovative technical knowledge and significantly contributes to the overall operations of the lab. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and documentation. Demonstrates supervisory skills and contributes to the achievement of company and departmental goals and objectives. Performs and directs Genetic Stability assays, especially Southern Blotting, according to and in compliance with current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). etc. | 9/3/2019 |
| 1308 | 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 |
| 1309 | 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 |
| 1310 | Zoetis Salisbury, MD Production Operator HS diploma or equivalent Exp: 6 months |
This position is responsible for operating process equipment and following all site operating, Quality, cGMP, and safety procedures associated with manufacturing of bulk medicated feed additives (MFA) from raw material to finished product. Incumbent must be able to clearly and frequently communicate with various functions within the site, including production, maintenance, quality operations, fermentation development, and administration. etc. | 9/3/2019 |
| 1311 | Zoetis Kalamazoo, MI Packaging Technician Assistant (2nd and 3rd Shift) HS diploma or equivalent Exp: 6-12 months |
Work as part of a team operating pharmaceutical packaging lines. Operate packaging equipment and other related tasks. Maintain accurate and concurrent documentation of all tasks completed. Maintain a positive attitude and be able to work well with others in a team environment. Demonstrate good attendance. A Packaging Technician Assistant works as part of a team in a complex, integrated, production environment. The individual(s) selected will have attention to detail, a positive attitude, a strong work ethic, and the ability work well with others in a team environment. etc. | 9/3/2019 |
| 1312 | Zoetis Union City, CA Instrument Manufacturing Technician I HS diploma or equivalent Exp: Entry level |
Assemble and test Point of Care medical Instruments. Process instruments according to all applicable procedures and quality requirements. Major Duties and Responsibilities – including but not limited to: Follow detailed operating procedures to assemble and test point of care medical instruments. Maintain productivity and quality requirements. Operate safely within a biohazardous environment. | 9/3/2019 |
| 1313 | Zoetis Kalamazoo, MI Customer Support Associate - Technical Analyst BS/BA Exp: 1+ years |
Interface with internal and external customers from multiple departments and levels of management to achieve the business’ sales and product delivery objectives. Responsible for system support and automation to provide improved data delivery and efficiency in processes. Participate in communications with relevant breed associations and other stakeholders at an operational level to ensure seamless delivery of contracted services related to systems and reporting. Lead projects focused on Process Improvement, system integration and/or data delivery, as directed by Team Lead and/or Manager. Cooperate with the Quality and Product Delivery Team (Global Genetics) to provide support to internal investigations and new product delivery. Contribute to a team culture of continuous process improvement. etc. | 9/3/2019 |
| 1314 | Zymergen Emeryville, CA Research Associate, Microbial Genome Engineering BS/MS Exp: 0-2+ years |
Zymergen is hiring a distinctive Research Associate to develop technologies for high throughput DNA assembly and engineering of microbial genomes. The Research Associate will help create new technologies, bring in cutting edge protocols, and improve existing Zymergen protocols to provide newer and better workflows to our microbe engineering Factory. At Zymergen, the Research Associate will work together with other scientists, automation engineers, and software engineers to develop protocols for DNA cloning and microbial strain engineering, and then enable their use in high throughput workflows. etc. | 9/3/2019 |
| 1315 | Zymergen Emeryville, CA Chemist, Polymer Chemist BS/MS in chemistry, materials science, or related Exp: 1-2 years |
Zymergen is looking for a chemist with training and experience in polymer synthesis and characterization. The candidate will be a key contributor to the polymer synthesis efforts, i.e. polymer development at the discovery stage, related to our film products. He or she will be responsible for purifying and performing quality control on reagents, performing step-growth polymerizations, optimizing reaction conditions, casting films and testing basic polymer material properties. The candidate will work closely with the project scientists to help drive the overall program progress on a technical level. etc. | 9/3/2019 |
| 1316 | Zymergen Emeryville, CA Inventory Technician I HS diploma or equivalent Exp: 1-3 years |
This position requires the ability to execute daily tasks/requests with promptness and prioritize work in a fast pace environment. An ideal candidate for this position is organized, diligent, and displays excellent customer service skills. Job Description and Specific Responsibilities: Organizing and maintaining an inventory of laboratory supplies throughout the labs. Ensures material is available according to the production schedule. Performing daily cycle counts of designated inventory areas. Receive and verify material on a daily basis. etc. | 9/3/2019 |
| 1317 | Zymergen Emeryville, CA Research Associate, Fermentation Development MS Exp: None required for MS candidates |
Zymergen is hiring Research Associate into the Test Centers of Excellence team to focus on the continual improvement of both high throughput screening and fermentation workflows. These associates are required to be able to identify and implement improvements in existing processes and establish protocols for new programs. This person will need to know microbial metabolism and physiology, microbial culture techniques (including fermentation and screening methods). Assay development experience would be useful, as well as experience with Tecans, but this would be part of the training. etc. | 9/3/2019 |
| 1318 | Zymo Research Irvine, CA Research Associate/Tech Support Specialist MS in biology, biochemistry or related Exp: None required for MS candidates |
We are seeking highly-motivated and proactive individuals to join our R&D team as a Research Associate. Working side by side with some of the most talented people in biotechnology, the successful applicant will participate in independent product research efforts targeted at driving either the development of novel, cutting-edge technology or improvements to products currently in our portfolio. 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. etc. | 9/3/2019 |
| 1319 | 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 |
| 1320 | 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 |
| 1321 | 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 |
| 1322 | 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 |
| 1323 | 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 |
| 1324 | Wake Research Raleigh, NC Desktop Support Specialist AS/AA or equivalent Exp: 1-3 years |
RESPONSIBILITIES: Installing new computers/laptops and peripherals. Troubleshooting Windows operating systems. Configuring and or repairing existing computer setups. Perform routine desktop maintenance as well as refurbishing client equipment. Data Entry and answer calls for support as needed. Monitor and operate various computer systems in support of end users. Providing computer operations and support while working with the likelihood of frequent interruptions, multiple priorities, inquiries, etc. Troubleshoot and document applicable repair solutions for various systems. | 8/27/2019 |
| 1325 | 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 |
| 1326 | Waters Golden, CO Chemistry Technician I BS/BA in chemistry or related Exp: 1-2 years |
ERA, A Waters Company, has an immediate opening for a full-time Chemistry Technician within it's Process Waters Consumables Product Line. PWC team produces TOC calibration and Quality Control standards, Conductivity and Turbidity standards, and other similar products. Responsibilities: Manufacturing, analytical verification, packaging, and labeling of all PWC products. Documentation of production and packaging. Creation of product labels and Certificates of Analysis. Inventory control of PWC products. etc. | 8/27/2019 |
| 1327 | 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 |
| 1328 | 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 |
| 1329 | 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 |
| 1330 | Waters Milford, MA Concur System Support AS/AA Exp: 1+ years |
This position reports to the Concur Team Supervisor. The purpose of this role is to maintain the Global Concur Travel & Expense tool. The Concur system should reflect current Waters T&E policies and local regulatory requirements at all times and the Concur System Support is responsible for ensuring that it does. Responsibilities: Maintain the Concur system: groups, policies, roles and authorizations, negotiated rates for non-GDS suppliers. Configure Concur for changes to policies and rules. Manage data feeds to ensure: Employee data is up-to-date. etc. | 8/27/2019 |
| 1331 | Waters Milford, MA Corporate Financial Analyst II BA/BS in accounting or finance Exp: 1+ years |
Waters Corporation is seeking a Financial Analyst II to join the Corporate Accounting and Finance team. The individual will perform analytical, accounting and reporting for various corporate and division groups. Additionally, this role includes accounting and reporting responsibilities related to intercompany transactions, inventory and fixed assets. A successful candidate will need to demonstrate an ability to work and communicate well with various internal worldwide customers. etc. | 8/27/2019 |
| 1332 | Wave Life Sciences Worchester, MA Research Associate, In Vivo Biology BS/MS in biology, biochemistry, pharmacology or related Exp: 0-2 years |
WAVE Life Sciences USA seeks an experienced and highly motivated in vivo biologist. This position will primarily be based at Wave’s Worcester, MA site. This is an ideal position for an individual interested in drug discovery who would thrive in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate will be responsible for assisting in the design and execution of experiments as a member of teams focused on advancing therapeutic programs. This candidate will contribute to all levels of in vivo discovery research to support the development of nucleic acid therapies for genetic diseases. etc. | 8/27/2019 |
| 1333 | Wave Life Sciences Cambridge, MA Research Associate - Biology BS/MS in biology or related Exp: 0-3 years |
WAVE Life Sciences USA seeks a highly motivated biologist to join its research team in Boston, Massachusetts. This is an ideal position for an individual who is interested in learning cutting edge technologies and who thrives in a team-oriented, fast-paced, and crossdisciplinary biotech environment. The candidate will be responsible for designing, executing and analyzing experiments as a member of teams focused on advancing therapeutic programs and discovery research platforms. This candidate will contribute to all levels of in vitro and in vivo discovery research to support development of optimized nucleic acid therapies in multiple disease areas. Prior experience in animal handling and tissue processing are preferred, but not required. etc. | 8/27/2019 |
| 1334 | 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 |
| 1335 | Westat Rockville, MD Medical Records Abstractor HS diploma or equivalent Exp: 1 year |
Westat is seeking Medical Records Abstractors to work from our Rockville campus on a data collection effort to collect emergency department data from a sample of hospitals across the US. The primary role of the medical record abstractor (MRA) is to review medical records in a sampled hospital's emergency department(s), abstract specific information from the patient's chart following the project's case identification protocol, and entering the information into a data collection tool. etc. | 8/27/2019 |
| 1336 | Westat Rockville, MD Web Developer BS in computer science, information technology, or related Exp: 0-4 years |
Westat is seeking a highly motivated web application programmer/developer who will be responsible for the development and implementation of web applications to support a variety of projects across our research domains. You will join a technical community of developers and engineers providing intuitive, responsive systems to collect high quality data using various leading edge technologies and modern software development tools and platforms. etc. | 8/27/2019 |
| 1337 | Westat Rockville, MD Research Assistant BA/BS in health-related or social science field Exp: 1-3 years |
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. etc. | 8/27/2019 |
| 1338 | Westat Rockville, MD Research Assistant BS/MS Exp: 1 year |
Westat has an immediate opening for a research assistant with experience in data collection procedures and materials along with a background in quantitative research and data analysis. The successful candidate will work closely with a multidisciplinary research team working on an innovative longitudinal health and aging study and a caregiving study. etc. | 8/27/2019 |
| 1339 | Worldwide Clinical Trials San Antonio, TX Nutrition Technician, PRN HS diploma or GED Exp: 6-12 months |
A PRN Research Nutrition Technician, under direct supervision, provides meals for subjects in research studies. Prepares and serves food in accordance with research specifications, and food safety standards. Maintains supplies, equipment, and records as indicated. Interacts with research subjects and medical staff. The PRN Research Nutrician Technician works under the supervision and guidance of the Research Nutrition Coordinator. He/she is not responsible for supervising other staff. etc. | 8/27/2019 |
| 1340 | Worldwide Clinical Trials unspecified, Operations Associate AS/BS Exp: 1+ years |
The Operations Associate has primary responsibility for carrying out all daily aspects of the operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition, surveillance maintenance, workbook/source document, for Worldwide Clinical Trials, Inc. (WCT). The Operations Associate is responsible for ensuring all assigned projects are conducted in a timely fashion and in a manner compliant with SOPs and ICH/GCP/regulatory guidelines. The Operations Associate works under the direction of the Operations Manager, Clinical Assessment Technologies (CAT). etc. | 8/27/2019 |
| 1341 | Wright Medical San Francisco, CA Associate Sales Representative, Upper Extremities BA/BS Exp: 0-2 years |
Summary: 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. This position is a field based position. etc. | 8/27/2019 |
| 1342 | Wright Medical Charlotte, NC Associate Sales Representative, Lower Extremities & Biologics BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will support our foot & ankle and biologics 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. This is a field based position. etc. | 8/27/2019 |
| 1343 | Wright Medical Columbia, SC Associate Sales Representative, Lower Extremities & Biologics BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will support our foot & ankle and biologics 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. This is a field based position. etc. | 8/27/2019 |
| 1344 | Wright Medical Lexington, KY Associate Sales Representative, Lower Extremities & Biologics BA/BS Exp: 0-2 years |
Summary: This is an entry level sales position that will require you to learn our products, market and industry. This role will support our foot & ankle and biologics 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. This is a field based position. etc. | 8/27/2019 |
| 1345 | Wright Medical Coronado, CA Sales Support Associate HS diploma/BA/BS Exp: 0-2 years |
Wright Medical is currently hiring a Sales Support Associate. The Sales Support Associate will be responsible for assisting in the successful execution of the sales plan for their assigned territory and the achievement of quarterly and annual sales plan objectives. He/she will travel within the territory and region for development & sales support. He/she will maintain open communications with their assigned leadership team and headquarter based sales training leader. He/she will perform and excel in case coverage, sales territory support functions and sales activity. He/she will achieve success with specified individual training and development plan. etc. | 8/27/2019 |
| 1346 | Wright Medical Houston, TX Associate Sales Representative, Upper Extremities BA/BS Exp: 0-2 years |
Summary: 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. This position is a field based position. etc. | 8/27/2019 |
| 1347 | 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 |
| 1348 | 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 |
| 1349 | 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 |
| 1350 | 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 |
| 1351 | 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 |
| 1352 | 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 |
| 1353 | WuXi NextCODE unspecified, Technologist I/II BS/MS in molecular biology or related Exp: 1 year |
We are seeking a highly motivated and enthusiastic Technologist I / II to develop, optimize, and perform next-generation sequencing (NGS) assays in a CLIA/CAP laboratory. ESSENTIAL FUNCTIONS: Perform laboratory functions in accordance with standard operating procedures. Extract nucleic acids from various specimens including cell lines, human blood, fresh frozen tissue and Formalin-Fixed Paraffin Embedded tumor specimens). Participate in regular Proficiency Testing. Prepare auditing documents. Collaborate with the lab manager on all activities. etc. | 8/27/2019 |
| 1354 | 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 |
| 1355 | Zeteo Tech Sykesville, MD Electrical Engineer BS in electrical or computer engineering or related Exp: 1+ years |
Zeteo Tech, a venture-backed company developing solution for Medical and Biodefense applications, is seeking a skilled and motivated electrical or computer engineer with and interest in embedded systems. Our ideal candidate is interested in working in an entrepreneurial environment, developing game changing solutions to healthcare and national security challenges. You'll use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. etc. | 8/27/2019 |
| 1356 | Zeteo Tech Sykesville, MD Electrical Engineer - Embedded Sensors BS in electrical or computer engineering or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a highly-skilled and motivated electrical or computer engineer with and interest in embedded systems. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. etc. | 8/27/2019 |
| 1357 | Zeteo Tech Sykesville, MD Electrical Engineer - Software Systems BS in electrical or computer engineering or related Exp: 1-5 years |
Zeteo Tech, Inc, a venture backed company developing solution for Medical and Biodefense applications, is seeking a highly-skilled and motivated electrical or computer engineer with and interest in embedded systems. The ideal candidate should be interested in working in an entrepreneurial environment developing game changing solutions to healthcare and national security challenges. You will use your hands-on hardware and software engineering expertise to conceive, design, build, test and commercialize products. etc. | 8/27/2019 |
| 1358 | zPREDICTA San Jose, CA Research Associate, Cell Biology MS in life sciences Exp: 1 year |
You will join a dynamic and agile team of scientists developing patient-derived 3D tissue culture models for cancer and immunology. 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. To be successful, you have to be excited by the fast-paced environment of a start-up and possess a versatile set of technical skills. etc. | 8/27/2019 |
| 1359 | Zymo Research Irvine, CA Customer Success Associate (internal sales) BS in life science Exp: 1-3 years |
The primary responsibility of the Customer Success Associate (internal sales) is to meet sales goals and generate leads by nurturing existing clients and identifying new sales opportunities. Due to the technical nature of Zymo Research products, the ideal Customer Success Associate candidate must have a life sciences background (education/work experience) to ensure engaging and productive conversations with clients. The ideal candidate should have a passion for science, sales, and customer support. Additionally, qualified candidate should enjoy being challenged and driven by achievement. etc. | 8/27/2019 |
| 1360 | Zymo Research Irvine, CA Technical Manufacturing and QC Associate BS in related, life science field Exp: |
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. Essential Duties and Responsibilities: 1. Manufacturing: Assist the Technical Manufacturing Manager to manufacture chemicals, buffers, and cells for Zymo Research’s products. 2. Product Quality Control: Initiate and implement appropriate experiments according to the SOP in order to accept or reject the release of product(s) and other related product components. etc. | 8/27/2019 |
| 1361 | Talis Menlo Park, CA Research Associate MS in biological sciences 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. Work with senior scientists and run hands-on experiments for microbiology, sample preparation, nucleic acid extraction and amplification. Be involved in reagent QC, generating and testing of designed controls and standards. | 8/20/2019 |
| 1362 | Tandem San Diego, CA Product Development Engineer I BS in mechanical/biomedical engineering Exp: 0-1 years in product development |
A team member responsible for technical contributions to the development, documentation, testing, analysis, troubleshooting, and debugging of the Company’s new medical devices, test and assembly fixtures, and data collection systems. Participates in the research and development of components and systems for the Company’s medical devices, utilizing knowledge of engineering theory and materials or component properties. Works within design controls and contributes to the design history file for medical devices by reviewing product requirements and specifications, documenting the design process, participating in formal design reviews and verifying the product performance with formal test methods, protocols and reports. | 8/20/2019 |
| 1363 | Tanvex San Diego, CA Temporary Research Associate, R&D Cell Culture BS in chemical/biomedical engineering Exp: 0-2 years in cell culture |
The Temporary Research Associate is responsible for executing individual experiments related to all aspects of cell culture process development from process definition to process characterization for support of pipeline projects. The Research Associate contributes to technology transfer from process development to clinical cGMP manufacturing and performs experiments related to mammalian cell culture development and scale up such as media selection, feed strategy development, bioreactor operations, process optimization, and metabolite analysis | 8/20/2019 |
| 1364 | Tanvex San Diego, CA Research Associate, Analytical Sciences BS or MS in chemistry/biochemistry/engineering 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. | 8/20/2019 |
| 1365 | TE Various Locations, na Product Engineering Early Career Development Program BS in mechanical/biomedical engineering Exp: Recent Graduate (August 2019-June 2020) |
Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership. During your time this Program you may rotate into a variety of Mechanical Engineering positions throughout our organization, which may include, but is not limited to Mechanical Design Engineer, Mechanical Development Engineer, Mechanical Engineer, and Operations Rotational Engineer – Mechanical Engineering. | 8/20/2019 |
| 1366 | TE Various Locations, na Manufacturing & Process Engineering Early Career Development Program BS in mechanical/electrical engineering Exp: Recent Graduate (August 2019-June 2020) |
During your time this Program you may rotate into a variety of General Engineering positions throughout our organization, which may include, but is not limited to Manufacturing Engineering, Engineering – Stamping, Engineering Test Lab and Product Development Engineering. Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership | 8/20/2019 |
| 1367 | TE Various Locations, na Supply Chain Early Career Development Program BS in supply/industrial engineering Exp: Recent Graduate (August 2019-June 2020) |
Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership. Supply Chain professionals are an integral part of our organization and we are committed to hiring the right talent to grow and develop. During your time in Supply Chain Program you may rotate into a variety of Supply Chain positions throughout our organization, which may include, but is not limited to Materials Planning, Operations Associate, Supply Chain Analyst, and Supply Chain Associate. | 8/20/2019 |
| 1368 | TE Various Locations, na Electrical Engineering Early Career Development Program BS in electrical engineering Exp: Recent Graduate (August 2019-June 2020) |
Designed for graduating seniors and early career professionals, this 2-year program accelerates participant’s development by combining intensive on-the-job training, rotations across business units, locations and roles, and exposure to senior leadership. During your time in Electrical Engineering Program you may rotate into a variety of EE positions throughout our organization, which may include, but is not limited to Operations, Electrical/Plating Engineer, Electrical Testing Engineer, Electrical Component Engineer. | 8/20/2019 |
| 1369 | TE San Francisco, CA R&D/PRODUCT DVL ENGINEER I BS in electrical/computer engineering Exp: 0-1 years (recent graduate) |
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. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. Typical fields of expertise include: materials, mechanics and systems, electrical, optics, chemistry, software, automation systems, packaging, testing and measurement, and manufacturing of electrical, mechanical and electronic components, products, and their integration into systems. | 8/20/2019 |
| 1370 | Tedor Cumberland, RI Production Technician HS Diploma/GED Exp: 1-2 years production environemtn |
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. | 8/21/2019 |
| 1371 | Teligent Buena, NJ QC Chemist I BS in chemistry or related Exp: 0-3 years pharma/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. 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. | 8/21/2019 |
| 1372 | Teligent Buena, NJ 2nd Shift Compounder AA/AS Exp: 1 or more year |
Perform functions relating to the processing of Topical products (creams, ointments, lotions, solutions) ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements, and in conjunction with all Standard Operating Procedures (SOPs). Perform functions relating to the cleaning and sanitization of compounding process equipment and compounding facility to facilitate GMP compliance, quality, safety, and schedule attainment. Follow standard operating procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. | 8/21/2019 |
| 1373 | Terumo Elkton, MD Engineer I - Test and Evaluation BS in engineering Exp: 0-3 years (entry level) |
The Test & Evaluation Engineer 1 is responsible for providing engineering support for planning and execution of NPD test and evaluation activities. Testing activities may include new product concept testing, competitive benchmarking, marketing claim substantiation, formal design verification testing (including accelerated and real time aging), usability testing, and root cause analyses. The Test & Evaluation Engineer 1 may serve as an extended project team member and will typically coordinate with marketers, development engineers, process engineers, manufacturing and quality engineers. | 8/21/2019 |
| 1374 | Terumo Elkton, MD NPD Test & Evaluation Technician HS Diploma/GED Exp: 1-5 years |
The NPD Test & Evaluation Test Technician position is responsible for the preparation and testing of pre-production devices to support the product development process. The position is also responsible for testing support of competitor product evaluations for marketing information. Assisting in preparing the lab for simulated clinical evaluations and new product pilot lines is also included in the position. An additional responsibility is supporting the acquisition, calibration and validation of lab equipment. | 8/21/2019 |
| 1375 | Teva Pharmaceuticals Salt Lake City, UT Production Support II HS Diploma/GED Exp: 1+ years |
Set up and operate packaging equipment in accordance with current good manufacturing practices and standard operating procedures. Package finished goods according to batch record format. Maintain inventory of job materials. ssue and reconcile data in the batch record required per batch. Clean production equipment or work areas. | 8/24/2019 |
| 1376 | Teva Pharmaceuticals Salt Lake City, UT Quality Control Analyst I BS in sciences Exp: 1 or more 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. 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. | 8/24/2019 |
| 1377 | Teva Pharmaceuticals Salt Lake City, UT Pharmaceutical Technology Specialist I BS in sciences Exp: 1-2 years |
Under general supervision, the Pharm Tech Specialist I determines the critical aspects of manufacturing equipment with regard to product and process, and writes protocols and other records related test results. Prepares final reports that identify the results of protocol testing and the conditions of release. Assists in conducting efficiency studies and in the identification of process improvement opportunities. Participates in project coordination activities. | 8/24/2019 |
| 1378 | Teva Pharmaceuticals Salt Lake City, UT Process Operator I HS Diploma/GED Exp: 0-2 years in manufacturing |
This position is responsible for performing operations related to the manufacturing and/or packaging of drug products through equipment set-up, operation, clean-up and maintenance in compliance with all regulatory requirements and company policies and procedures. Responsible for learning the manufacturing and/or packaging process as assigned by following approved batch records (BR), work instructions (WI), standard operating procedures (SOP), etc. | 8/24/2019 |
| 1379 | 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 |
| 1380 | TRC Columbia, SC Multi-Craft Technician 2-year technical degree Exp: 0-2 years |
Multi-Craft Technician will maintain and trouble-shoot equipment within the manufacturing department. The technician will be fully trained in the operation of all manufacturing equipment before being trained specifically on the technical maintenance and repair Standard Operating Procedures (SOP’s). Responsible for electrical and mechanical troubleshooting of fluid delivery, extrusion, hydraulic, electrical, mechanical, and conveyance systems in a clean room manufacturing environment. The technician will be required to maintain Operating Technician proficiency and in case of emergency, may be required to assist starting and ending of batch processing | 8/24/2019 |
| 1381 | West Pharmaceuticals Kinston, NC Lab Analyst BS in microbiology or sciences Exp: 1-3 years in lab |
In this role you will perform all required routine testing (Bioburden Silicone, Particle, Endotoxin) to support product release, including water testing, environmental monitoring. Support other laboratory functions as needed. Perform product release routine testing including, but not limited to, bacterial endotoxin, bioburden, particulate and silicone testing, etc. Perform routine testing to support the plant functions including but not limited to environmental monitoring in Clean Rooms, water testing etc. | 8/24/2019 |
| 1382 | West Pharmaceuticals Bangalore, IN Associate Data Scientist, D&T BS in computer/math/stats Exp: 0-3 years |
The Associate Data Scientist, Digital and Transformation will work with a multidisciplinary team to design and develop innovative data-driven analytical products and solutions for complex business problems using advanced analytics, data mining, and machine learning. Work with stakeholders throughout the organization to identify opportunities for leveraging novel statistical and machine learning techniques on data problems to solve strategic business questions. Should have a strong background and skill-sets related to programming and software development | 8/24/2019 |
| 1383 | Teravance Biopharma South San Francisco, CA Research Associate I/II BS/MS in sciences Exp: 1 or more year in drug discovery |
The successful candidate will work collaboratively with senior scientists to develop and execute pharmacodynamic and disease mechanism models designed to assess the pharmacological activity of novel molecules. Research Associate should have strong in vitro / in vivo skills. Ability to provide scientific inputs for new assay/ experimental model development. | 8/24/2019 |
| 1384 | Thermo Fisher West Hills, CA Scientist I, Manufacturing Sciences HS Diploma/GED Exp: 1-2 years lab experience |
The Scientist I, Manufacturing Sciences is responsible to manage and prioritize assigned projects related to development and improvement of DNA-based diagnostic reagents with supervision. Simultaneously manage and prioritize multiple projects and products across multiple functional groups while meeting target due dates with guidance of supervisor/lead. Design, create experimental task, run tests and be able to look at data and complete analysis using Fusion, Orchid, or equivalent software. Can provide experimental task(s) to designated Scientist with Supervisor approval. | 8/24/2019 |
| 1385 | Thermo Fisher Tewksbury, MA Manufacturing Technician HS Diploma/GED Exp: 0 years |
Component assembly with UV cured epoxy. Adhere to ISO9000 requirements including ESD, work area cleanliness, maintenance and calibration of equipment and work instruction adherence. Responsible for processing work orders for the manufacture of optical components | 8/24/2019 |
| 1386 | Thermo Fisher Tewksbury, MA Depot Repair Technician HS Diploma/GED Exp: 1-3 years |
Diagnose and repair, customer and in-process units. Keep accurate and ISO auditable records of product repairs, test results and other data as required. Adhere to ISO9000 requirements including ESD, work area cleanliness, maintenance and calibration of equipment and work instruction adherence | 8/24/2019 |
| 1387 | Thermo Fisher Florence, SC Scientist 1 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. 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. Laboratory personnel will be responsible for disposing of any hazardous waste they generate in accordance with Patheon’s Hazardous Waste Training | 8/24/2019 |
| 1388 | Tolmar Windsor, CO Manufacturing Operator I HS Diploma/GED Exp: 1 or more years of experience in a GMP manufacturing environment. |
Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Assist in the set-up of semi-automatic filling equipment used to fill dermatological products. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Perform facility cleaning of manufacturing areas as required to maintain a cGMP environment and by Tolmar Standard Operating Procedures. | 8/24/2019 |
| 1389 | Tolmar Fort Collins, CO Manufacturing Operator I HS Diploma/GED Exp: 1 or more years of experience in a GMP manufacturing environment. |
Perform job responsibilities in accordance with standard operating procedures (SOPs) and production records with an expectation of "Right the First Time". Assist in the set-up of semi-automatic filling equipment used to fill dermatological products. Perform routine sampling and inspections for product attributes (fill weights, product sealing, labeling) of filled products. Perform facility cleaning of manufacturing areas as required to maintain a cGMP environment and by Tolmar Standard Operating Procedures. | 8/24/2019 |
| 1390 | Tolmar Windsor, CO Packaging Development Engineer I BS in packaging engineering or related Exp: 1 or more years in packaging |
Under general supervision, develops the packaging components and packaging requirements for existing commercial products and for development projects. Develops, maintains and monitors packaging components to ensure compliance with Quality, Safety, Manufacturing and Regulatory guidelines and procedures. Conducts testing activities that influence selection of primary, secondary and tertiary packaging components. | 8/24/2019 |
| 1391 | Texikon Bedford, MA Laboratory Assistant, In-Vivo HS Diploma/GED Exp: Entry Level |
The successful candidate will haveinteraction with In Vivo Research Associates, In Vivo Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. Additionally, you will be responsible to ensure the technical conduct and regulatory compliance of your duties comply with FDA GLP and ISO regulatory guidelines. | 8/24/2019 |
| 1392 | Texikon Bedford, MA Histology Laboratory Assistant HS Diploma/GED Exp: Entry Level |
The successful candidate will have interaction with Histology Research Associates, Histology Study Directors, Vet Care staff and interface with laboratory management regarding all day-to-day activities of the studies. They will be responsible for providing logistical support for the studies being conducted. As a laboratory assistant, you will be responsible for preparing animals for the studies conducted, including shaving, weighing and identification. Additionally, you will be responsible to ensure the technical conduct and regulatory compliance of your duties comply with FDA GLP and ISO regulatory guidelines. | 8/24/2019 |
| 1393 | Tris Pharma Monmouth Junction , NJ Quality Control Chemist BS/BA in chemistry or related Exp: 1 or more years in lab |
QC Chemists perform analytical testing of raw materials, packaging component, in-process, finished product, stability samples, cleaning verification/validation, and process validation samples following Analytical Methods, Protocols, Procedures (SOP’s) and company policies. He/she follows and maintains adherence to current industry standards (cGMP’s, GLP’s, etc.) to meet production and customer demand. Qualified candidates will be expected to work either independently or as a team to achieve company goals and initiatives. | 8/24/2019 |
| 1394 | Tris Pharma Monmouth Junction , NJ Product Development/Formulation Scientist I MS in pharma sciences or related Exp: 1+ year in pharma |
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. | 8/24/2019 |
| 1395 | 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 |
| 1396 | 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 |
| 1397 | Tunnell na, PA Tech Transfer Specialist - Upstream Process MS Exp: 1+ years |
The Vaccine Process Development and Commercialization group within our client's manufacturing division focuses on late stage process development, technology transfer, and support of established vaccine products. Our client is seeking an energetic, people-oriented professional with strong scientific and technical skills to execute the tech transfer activities of multiple vaccine programs with a focus on upstream manufacturing process ( Drug Substance ). | 8/24/2019 |
| 1398 | 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 |
| 1399 | 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 |
| 1400 | United Therapeutics Research Triangle Park, NC Associate Test Engineer, Medical Device BS in engineering Exp: 0-5 years |
The Associate Test Engineer – Medical Device will manage the investigation of device product complaints. This individual will develop, document, and execute medical device test protocols; Enhance/automate test processes; Support the engineering team with testing, prototyping, and reworking activities; Responsible for equipment calibration and general lab organization. | 8/25/2019 |
| 1401 | United Therapeutics Research Triangle Park, NC Bioprocess Technician - Cell Biology AAS/BS/BA in biological sciences Exp: 1+ year in industry/cell culture |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. Routinely perform large-scale primary lung cell culture in 2D and 3D to support process development activities for a tissue engineered product. Routinely perform bioanalytical assays to phenotypically and functionally characterize cells (such as flow cytometry and plate-based assays). | 8/25/2019 |
| 1402 | United Therapeutics Silver Spring, MD Process Engineer BS in sciences Exp: 1+ years of research |
We are currently looking for a Process Engineer to join our API team. In this role, you will support the process engineering team in the specification, installation, maintenance and operation of small-molecule API production equipment and processes. Additionally, you will partner with members of the API Production and R&D team on activities as required to help internal customers efficiently produce the best medicines possible. | 8/25/2019 |
| 1403 | Unum Cambridge, MA Associate Scientist - Bioassay MS in biological sciences Exp: 1-3 years |
The primary role as an Associate Scientist will be to use and develop immunoassays and bioassays to enhance understanding of key attributes in support of cell therapy process and product development and characterization. Participate in activities to support Unum’s pipeline within established timelines and ensure data quality and integrity. | 8/25/2019 |
| 1404 | Unum Cambridge, MA Associate Scientist, Translational Medicine MS in biology, immunology or oncology Exp: 1-4 years |
Support the development, execution and analysis of assays in early clinical studies to assess ACTR T cell persistence and phenotype, target expression/occupancy, cytokine levels and immunogenicity. Explore predictive biomarkers of ACTR manufacturing and clinical success across various patient populations. Prepare data packages for technical reports, SOPs, and regulatory submissions | 8/25/2019 |
| 1405 | 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 |
| 1406 | 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 |
| 1407 | 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 |
| 1408 | Barry Wehmiller East Brunswick, NJ Validation Engineer (Design Group) BS in sciences/engineering/manfacturing technology Exp: 0-2 years |
The Validation Engineer will interface with our clients and be responsible for preparing and executing commissioning and qualification documents for a variety of utility, facility and process equipment. This role will include both document development and field execution of test protocols, including FATs, SATs, CTPs, IQs, OQs, PQs, PVs. Required experience with good documentation practices, cGMP, & FDA CQV methods and systems, ability to read engineering documents, set priorities, and work on multiple projects simultaneously. | 8/25/2019 |
| 1409 | Varian Palo Alto, CA HW Verification Engineer MS in engineering Exp: 1+ years |
As a Hardware Verification Engineer, you will own verification activities on new and released products. Your responsibilities will include: Collaborate with cross functional teams to ensure that Varian’s complex devices are thoroughly tested. Collaborate on requirements definition and test acceptance criteria. Develop manual and automated test methods to characterize performance of new devices from prototype to production. | 8/25/2019 |
| 1410 | Varian Palo Alto, CA Dosimetry Coordinator/Rad Safety Tech MS Exp: 0 years |
As needed for compliance with state and country regulatory requirements (North and Latin America), act as the coordinator for the Varian radiation dosimetry program that includes 1400+ permanent participants, including individuals who work at Varian sites in Palo Alto, Milpitas, and Las Vegas and Varian service personnel who receive dosimeters at individual addresses. Using Varian’s Learning Management System, ensure applicable radiation safety training requirements have been met for individuals to be added to the dosimetry program. | 8/25/2019 |
| 1411 | Varian Palo Alto, CA QA Engineer MS in related Exp: 1+ years |
We currently have an opportunity for a Quality Assurance Engineer for our Palo Alto facility. In this key role, the Quality Assurance Engineer will manage implementation, support, and maintenance of company-wide quality objectives, including analysis and trending of key quality system elements on a periodic basis. | 8/25/2019 |
| 1412 | Varian Richmond, VA Field Service Rep I HS Diploma/GED Exp: 0-1 years |
Performs client-site servicing, repair and/or installation of company product(s). This job may include any aspect of product field support, including system hardware and software, medical or laboratory devices and equipment, and systems networking. Provides technical support to customers on operational or maintenance aspects of system equipment. Serves as customer contact on technical and service related problems. Diagnoses mechanical, hardware, software and systems failures using established procedures. Determines most cost effective repair/resolution to minimize customer downtime. Prepares reports for analysis of product failure trends and service ability issues. | 8/25/2019 |
| 1413 | Vector Labs Burlingame, CA Technical Sales Representitive BS or MS Exp: 1+ years in sales |
Using NetSuite and web-based research to understand customer organizations and working with colleagues at Vector Laboratories and at each account to understand buying trends and purchasing mechanisms. Meeting and exceeding sales targets by establishing strong business relationships with current and future customers and aggressively pursuing new sales opportunities. Engaging with purchasing decision-makers at each account, establishing relationships, evaluating, prioritizing, and uncovering sales opportunities and customer concerns. | 8/26/2019 |
| 1414 | Veeva Pleasanton, CA Associate Software Engineer BS in computer sciences or related Exp: Recent Graduate |
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 | 8/26/2019 |
| 1415 | Veeva Columbus, OH Associate Software Engineer BS in computer sciences or related Exp: Recent Graduate |
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 | 8/26/2019 |
| 1416 | Veeva Toronto, Ca QA Engineer - Safety BS in math/computer sciences Exp: 1-4 years in QA/Development |
Veeva Systems is looking for a QA Engineer that likes to figure out how things work and make sure they are working correctly. This is a hands-on position for delivering a quality SaaS product. Create testing-related documentation, including test plans, test cases/scripts, and bug reports assessing quality and associated risk. Work closely with the automation group to automate features for better regression coverage, automate production issues, execute scripts, and triage automation runs | 8/26/2019 |
| 1417 | Veeva Pleasanton, CA Associate QA Engineer BS/BA; GPA > 3.0 Exp: Recent Graduate |
Work with product managers and developers using Agile methods to identify/refine test cases from requirements and design. Work with developers and other QA engineers in a team environment to ensure product quality. Document test cases and outcomes within a test case management application. Conduct QA tests and verify outcomes within schedules/timelines. Clearly document and explain defects found in defect tracking system. | 8/26/2019 |
| 1418 | SevenBridges San Francisco, CA Technical Support Engineer BS/BA in computer science or related Exp: 1+ years |
Your main role will be to work with our developers, bioinformaticians as well as our clients, on removing obstacles and helping users troubleshoot issues, resolving or escalating problems to engineering teams. Technical Support Engineers will work with our cross-functional team as a part of our Product division in Seven Bridges. Working on production database/microservices (e.g. making mass changes using Seven Bridges API, scripts or SQL) independently and confidently . | 8/16/2019 |
| 1419 | 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 |
| 1420 | 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 |
| 1421 | 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 |
| 1422 | 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 |
| 1423 | 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 |
| 1424 | SightLife Seattle, WA Research Associate BS in related field Exp: 1 or more years in lab |
Responsible for aiding in the continued research and development of current and future activities and projects related to corneal transplantation and cell therapy following GCP and GMP guidelines. Design and execute laboratory processes according to established protocols. Maintain records of observations and interpret findings. Continually assess procedures and look for process improvements. Organize and store all chemical substances, fluids and compressed gases according to safety instructions. | 8/16/2019 |
| 1425 | SightLife Seattle, WA Operations Business Analyst BS/BA in related field Exp: 0-2 years in operations |
This position is responsible for collaborating with Operations teams and Technology Services to plan, design, develop and deploy new technology solutions while maintaining and enhancing existing systems for Operations. This includes gathering and analyzing data, process flows and business requirements in support of business cases and proposed projects and working closely with management and staff across Operations in all SightLife locations to maximize use of resources and technology solutions. | 8/16/2019 |
| 1426 | SightLife Boston, MA Laboratory Support Technician AS/AA in allied health fields Exp: 0-2 years |
Under the direction of the Technical Program Manager and Director at CorneaGen - Boston, the Laboratory Support Technician will assist in tissue processing and distribution related operations, and tissue suitability activities. The incumbent will be expected to steward each donor’s Gift by ensuring standardized operational practices are effectively executed at the local level and by seeking continual improvement opportunities to maximize the value of the Gift | 8/16/2019 |
| 1427 | Sinclair Research Auxvasse, MO Veterinary Technician BS/BA, Registered Vet Tech or HS Diploma Exp: BS/BA: 0 years, HS: 1 year |
Our Veterinary Technicians are critical in bridging study procedures from Operations to Veterinary Services. They will participate in activities relating to both departments by assisting in blood collections, catheter placement, anesthesia monitoring, collecting samples and administering dosing, and supporting veterinary staff in overseeing herd health. More advanced technicians will also assist during surgical procedures or perform minor procedures themselves, administer advanced dosing, and perform advanced collection procedures. | 8/16/2019 |
| 1428 | Smith Nephew Columbia, MD Donor Eligibility Associate BS/BA in life sciences Exp: 1 or more year in hospital/biotech/GTP environment |
The primary purpose of this position is to receive, assemble, review, and assess the donor recovery records (donor chart) against current tissue bank standards, applicable tissue regulations, and Osiris criteria in order to help determine donor eligibility. | 8/16/2019 |
| 1429 | Smith Nephew Columbia, MD Manufacturing Technician AS/AA in life sciences Exp: 1-2 years in GMP environment |
Responsible for hands-on execution of all activities in the manufacturing area including the processing and packaging of human tissue products for transplantation. All duties are performed in compliance with FDA cGMP/cGTP requirements, American Association of Tissue Banks (AATB) standards, and Osiris Therapeutics Inc. standard operating procedures (SOPs). | 8/16/2019 |
| 1430 | Smith Nephew Fort Worth, TX Quality Engineer I BS in engineering, biomedical or industrial engineering Exp: |
Responsible for assisting to improve the Quality Compliance of Fort Worth and TJ Smith & Nephew QMS. Primary responsibilities include assisting with Risk Management, Design History Files, Product Release, and revision of documents in the DMS. Works within the quality management systems and ensuring functional compliance to the applicable FDA’s cGMPs, international standards, Good Distribution Practices and state requirements (Smith & Nephew and outsource suppliers). | 8/16/2019 |
| 1431 | Smith Nephew Memphis, TN Quality Assurance Inspector 1 HS Diploma/GED Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. | 8/16/2019 |
| 1432 | Smith Nephew Columbia, MD Quality Assurance Inspector 1 HS Diploma/GED Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions. | 8/16/2019 |
| 1433 | Smith Nephew Columbia, MD Quality Assurance Inspector 1 HS Diploma/GED Exp: 0-2 years |
The Quality Assurance Inspector 1 shall be responsible for performing basic visual/dimensional/functional inspections of incoming purchased product as well as product manufactured/assembled in-house, determining whether or not product meets specifications and documenting these decisions | 8/16/2019 |
| 1434 | Smithers Wareham, MA Laboratory Assistant HS Diploma/GED Exp: 0 years required |
Individual is expected to perform a variety of routine tasks in support of the conduct of normal laboratory operations and similar duties as assigned. Also responsible for cleaning laboratory glassware and equipment, as well as stocking and requesting laboratory supplies. Maintains the cleanliness of the laboratory including but not limited to sweeping and washing the floor, cleaning bench tops, fume hoods. Individual disposes of chemical and solid waste. Responsible for the development of familiarity with routine assignments and laboratory practices. | 8/16/2019 |
| 1435 | Smithers Wareham, MA Entry Level Technical Report Writer BS/BA in environmental sciences Exp: 0-2 years lab experience |
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. | 8/16/2019 |
| 1436 | Smithers Lansing MI, MA Product Testing Technician HS Diploma/GED Exp: 1-5 years of mechanical background/training |
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. Perform testing in accordance with relevant specification(s). Follow daily work assignments relative to test schedule. | 8/16/2019 |
| 1437 | SomaLogic Boulder, CO Research Associate II MS in biology,biochemistry, chemistry or related Exp: 1 year |
The Analytical Sciences team is seeking a Research Associate to assist in the identification and characterization of SOMAmer® reagents. This position works in a fast-paced, team-oriented research group. The individual will primarily perform sample preparation of protein pulldown samples for LC-MS analysis and also generate new SOMAmer reagents using the SELEX process. Detailed documentation, critical evaluation and communication of results are essential traits for this position. Level will be commensurate with experience. | 8/17/2019 |
| 1438 | Sorrento Theraputics San Diego, CA Quality Control Microbiology Associate BS in microbiology or related Exp: 1-2 years industry experience |
This individual contributes to general operations and testing for the Quality Control and Microbiology Laboratories. This position supports in-process testing and drug substance and drug product release and stability testing programs. Environmental monitoring of cGMP cleanrooms per FDA and USP guidelines. Sampling of utilities (i.e. water, clean compressed air) | 8/17/2019 |
| 1439 | Sorrento Theraputics San Diego, CA Manufacturing Associate I BS/BA in biological/chemical sciences Exp: 0-1 year in manufacturing |
We are currently seeking a Downstream Manufacturing Associate I. This position is tasked with supporting all aspects of downstream manufacturing processes. For GMP-qualified campaigns this involves large scale buffer preparation, column chromatography using the Akta Process system and large bed volume columns, various filtration methods, ultrafiltration/diafiltration methods, and formulation. This position will also be responsible for supporting the inventory control for the downstream group. | 8/17/2019 |
| 1440 | Sorrento Theraputics San Diego, CA Manufacturing Associate I BS in life sciences, chemistry, or chemical engineering Exp: 1-3 years in cGMP environment |
We are currently seeking a Manufacturing Associate who will be responsible for performing Upstream manufacturing tasks. Including but not limited to: Tracking & control of raw material inventory. Maintenance and operation of equipment in cGMP facilities. Preparation of buffer and media. Assistance in operation of single use bioreactors for production of clinical and commercial products. | 8/17/2019 |
| 1441 | Sorrento Theraputics San Diego, CA Research Associate / Associate Scientist, Antibody Analytics MS in chemical sciences Exp: 1-2 years |
As an Associate Scientist you will work in the Antibody Analytics group and be responsible for the development, implementation and maintenance of a variety of analytical assays to support R&D in protein therapeutics including monoclonal antibodies, bispecific antibodies, antibody-drug conjugates (ADC) and CAR-T. These assays include but not limited to chromatography (SEC, IEX, HIC and RP), electrophoresis (SDS-PAGE and CE-SDS), and icIEF | 8/17/2019 |
| 1442 | Sepectrum Pharmaceuticals Irvine, CA Clinical Trials Assistant HS Diploma/GED Exp: 1-2 years clinical study experience |
Provide support to the Clinical Trial Managers and Clinical Research Associates in clinical trial conduct via preparation, distribution, and tracking of study supplies, mass mailings, copying, data entry, etc. Recognize the urgency of meeting established schedules and be able to prioritize tasks and time to meet those schedules. Develop materials that supp |