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Reporting to our Senior Manager, Quality Assurance CMC, this position is responsible for managing, reviewing, and approving quality documents from Contract Manufacturing Organizations and Contract Testing Laboratories for manufacturing, testing, validation, and disposition of clinical and commercial products for human use.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Our vaccine client here in Boston, MA is growing and looking to add a Manager/Senior Manager of Quality Assurance (QC Support) to their team! Provides direct Quality Assurance oversight and support for the assigned area (e.g. quality control and analytical development.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Collaborate cross-functionally with Clinical Operations, Manufacturing, Regulatory Affairs, and Quality Assurance to forecast, plan, and execute IMP supply plans including IMP utilization, labeling and packaging, inventory control, and depot management for assigned clinical studies.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Manager, QA works within the Quality department to support quality assurance, quality compliance, and daily operations. 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.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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ElevateBio is looking for a Cell Therapy Manager, QA Operations to join their growing Quality Group at our BaseCamp facility in Waltham, MA. In this role, the Manager will be primarily responsible for providing Quality oversight over execution of clinical cell and gene therapy manufacturing for cGMP compliance through on the production floor interactions, review and approval of batch related documents, and events.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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A minimum of eight (8) years of experience in pharmaceutical manufacturing, manufacturing science & technology, technical development or Quality. Perform quality review and approval of manufacturing process, aseptic process, and shipping validation protocols, performance, and final summary report.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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I have a talented group of recruiters who specifically source Technical Sales Professionals, Scientists, Regulatory Affairs, Scientific Affairs, Executive Technical professionals, Quality Assurance, Product Development, Technical Service, Nutrition, Analytical and Corporate Chefs.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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At least 3-5 years relevant experience in the pharmaceutical industry or a regulatory authority CMC review capacity, with at least 3 years of experience in Regulatory CMC and preferably 2 years professional experience in pharmaceutical manufacturing, analytical development, or quality assurance/control or related technical field.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Quality Manager - Assembly Group, LED Lighting Products Job Description: Quality Manager (LED Lighting Company) Summary: We are seeking a highly skilled and experienced Quality Manager to join our assembly group, manufacturing LED lighting products.
$110,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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You will have responsibility for Quality Assurance, and support of Quality Control, for external Oncology and Small Molecule manufacturing ( contract manufacturing organizations, or CMO ), and external testing ( contract test labs, or CTL ), inclusive of Drug Products, packaging, and labeling activities, located within the US/North American region.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Manager/Senior Manager of Quality Assurance provides oversight of GMP activities for Quality Control Release and Stability testing including method validation and transfer.
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Experience in Life Sciences practices: Clinical Operations, Regulatory Affairs, Quality, Pharmacovigilance, Data Science, Commercial, Manufacturing, Supply Chain, Medical Devices. Experience with GxP guidelines, Software Development Life Cycle (SDLC) process, Computer System Validation (CSV)/Computer Software Assurance (CSA.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Headquartered in Spain, Profand’s mission is to create a multinational company within the global fishing sector, processing and manufacturing the highest quality seafood under a fully integrated and sustainable model from extraction to sale, while also ensuring the highest safety and profitability.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Senior Audit Associate will perform and direct the broadest range of accounting tasks and will assist the supervisor, manager and/or partner in the development of audit strategy, planning, review and interpretation of audit findings for clients within various commercial industries such as architecture and engineering, manufacturing and distribution, retail and consumer products, technology and more.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Collaborate across functions such as Quality, Regulatory Affairs, Sterility Assurance, Extractables and Leachables, Analytical Chemistry, Product Design Owning teams, Project Management and Manufacturing.
Full-timeExpandApply NowActive JobUpdated 3 days ago
quality assurance manager manufacturing jobs in Cambridge, MA
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