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Apply engineering principles in scaling up from bench to pilot plant or GMP manufacturing scale. Knowledge of GMP working environments. Keep proper GLP lab documentation, authoring technical reports, tech transfer documents and preparing scientific presentations as needed.
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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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This position reports to the Associate Director Quality Product Testing and will oversee compliance of GMP activities for assigned Contract Testing Laboratories (CTL)/Contract Manufacturing Organizations (CMO) as it relates to QC testing of ImmunoGen products.
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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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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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Thorough understanding of GMP, GCP, and ICH standards governing IMP labeling, packaging, and global distribution, including role of QP. Thorough understanding of GMP, GCP, and ICH standards governing IMP labeling, packaging, and global distribution, including role of QP.
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He/she will work closely with the Chemistry Manufacturing and Controls (CMC) Team to ensure support of GMP manufacturing and analytical activities, as well as provide quality and compliance guidance.
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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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Experience in leading product/process support within a GMP setting: leading investigations, technology transfer, process monitoring, process validation, or routine clinical/commercial support is preferred.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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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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Comply with all HACCP/GMP and proper food handling policies and procedures. dnata catering U.S. is looking for a Receiving Clerk to join our Boston team supporting the Logan airport. Key Responsibilities as a Receiving Clerk at dnata Catering company, you will be an essential part of our supply chain operations.
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Prior knowledge of genomic medicine approaches, biopharmaceutical manufacturing process flow, and GMP. Experience working with large biopharma organizations; launching and scaling new solutions offerings in an emerging market.
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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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Experience in Quality Control roles supporting GMP testing/manufacturing of gene therapy or gene editing products, ATMPs or equivalent. The Quality Control Lead will be responsible for implementing compendia and total organic carbon methods for internal GMP testing at Tessera.
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Azzur COD is looking for a GMP Facility Manager. GMP experience in preferred. Including HVAC, Gases, Liquid Nitrogen, Tower Water, Heating Hot Water, Refrigerated Water, Etc. This employee will be a Cleanrooms On-Demand Burlington business unit (Facility Solutions) leader, who will be responsible for employees supporting the facility, client start-up, and continuous business improvement at COD. The Facility Manager will perform repairs, Maintenance, and improvement within cGMP cleanrooms, Laboratory, Warehouse, and office spaces.
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gmp job Company: Genoskin in Burlington, MA
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