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Packaging Technicians are responsible for weighing, dispensing, bottling, packaging and labeling GMP, ISO and non-GMP product from bulk storage in preparation for shipping or warehousing.
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Pfizer is seeking a highly motivated and experienced candidate to support GMP activities for the validation group at the Andover site. Ample knowledge of GMP and regulatory requirements and data integrity principles.
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The Technical Operations Specialist will assume responsibility for internally overseeing the manufacture and completion of client project activities to support release of products for clinical trials and ensure the delivery of batch manufacture and documentation to GMP standards, in line with client project timelines.
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Maintain written records of all experimental work in accordance with Good Lab Practices / (Current) Good Manufacturing Practices (GLP/GMP) and departmental Standard Operating Procedures. Experience in a (Current) Good Manufacturing Practices (part of GMP) Laboratory.
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Transfers materials and equipment required by GMP Manufacturing and other departments as necessary among the warehouse, manufacturing area, and labs, adhering to relevant SOPs. Ensures changeover kits for common production equipment are maintained and available.
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The GMP Laboratory Technician will provide support to the GMP Production team through cleaning glassware, and following established safety and GMP regulations. Cambridge Isotope Laboratories, Inc. (CIL) is searching for a GMP Laboratory Technician based onsite in our Tewksbury, MA facility.
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This role involves actively participating in a collaborative team to execute manufacturing operations using disposable technologies and automation, adhering strictly to cGMPs and standard operating procedures, while demonstrating a keen understanding of bioprocess unit operations and contributing to the production of GMP mRNbased medicines for human clinical trials.
$31 - $33 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Documenting all processes accurately, per ISO and GMP. At times, work in a Clean Room environment; wearing lab coat, bouffant, gloves, and safety glasses all times while in the room. Good penmanship is required in filling out various logs, travelers, identifiers, appendices, and documents per ISO and GMP requirements.
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Work under the Production Department director to support production by performing GMP radiochemistry processes in a safe, efficient and timely manner. GMP CHEMIST (This is a hands on position with production responsibilities, not a QC position.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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2-3 years of experience working with analytical and biologic methodologies (chromatography, HPLC and ELISA in a regulated GMP/GLP Lab environment) HPLC, GC, KF, and UV/Vis. This position will also be working part of the time in the lab as the expert on HPLC and Empower in a GMP lab setting.
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The Associate Director, QC Cell Culture and Bioassay will be responsible for overseeing a testing laboratory charged with the execution of all GMP bioassay testing (release and stability) related to Sarepta' s Gene Therapy pipeline.
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The Expression group is responsible for non-GMP protein drug lead generation, supporting the various Pfizer research units and their pre-clinical therapeutic in-vitro and in-vivo needs. The Expression group is responsible for non-GMP protein drug lead generation, supporting the various Pfizer research units and their pre-clinical therapeutic in-vitro and in-vivo needs.
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The candidate will perform qualitative and quantitative analyses of organic, inorganic compounds, or biologics to determine chemical and physical properties during chemical syntheses, fermentation or drug product development process.
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Strong knowledge of engineering standards and all applicable regulatory requirements including: Building Codes, Factory Mutual, Environmental, GMP/GLP, OSHA and ADA. In this position, the ideal candidate will work independently to lead cross-functional project teams through all phases of Infrastructure-Utility, Lab-Office and GMP Manufacturing projects-from scope development, design, CQV and close-out.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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3+ Year working directly with a life science software product in a compliant environment (CLIA, GMP, IVD etc.) 3+ years of direct product management, product marketing, technical marketing, applications or pre-sales scientific support experience in life sciences or medical device industry with domain expertise in protein biomarker applications.
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gmp job in North Reading, MA
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