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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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Must have experience on all general housekeeping tasks-REQUIRES OPERATING A WALK BEHIND AUTO SCRUBBER AND WAREHOUSE CLEANING AS WELL AS GENERAL HOUSEKEEPING RESPONSIBILITIES.-GMP cleaning including documentation of tasks and daily floor sanitation- Floor Care, Buffing, Auto Scrubbing, Carpet Cleaning, Floor Scrub and Finish.
$13 an hourPart-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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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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.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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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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Quality assurance, Compliance, GMP, Document control, Batch Record, Batch Record Review, product release, investigations, Root cause analysis, iso 13485, audit, quality compliance. Knowledge of GMP, FDA, ISO requirements.
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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 5 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 9 days ago - UpvoteDownvoteShare Job
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Comprehensive knowledge of domestic and international GMP regulations and their application in the manufacture of biologics, cell, or gene therapy products. + 8+ years of experience in GMP regulated industry (preferably biopharmaceutical, biotechnology, cell or gene therapy industries) with roles in Supply Chain, Manufacturing or Quality.
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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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Ensure GMP processes are implemented in the Quality Management System (QMS) for clinical and commercial product process lifecycle (e.g. control strategy, technology transfer, process validation lifecycle, continuous process verification.
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gmp job Company: Genoskin in Tewksbury, MA
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