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A reasonable estimate of the current salary range is $86,320 - $154,960 per year for the role of Scientist - Development in Therapeutics Production & Quality. Minimum Experience:Minimum Requirement: Bachelor's degree with 7+ years experience in relevant scientific area (e.g., GMP: chemistry, biology, chemical engineering, analytical chemistry, biotechnology; ECTL: cellular biology, molecular biology, immunology, biochemistry.
$86,320 - $154,960 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Understanding of the execution process of capital projects in a GMP Biopharmaceutical Production facility including procurement, construction, startup, and validation. Understanding of safety requirements working in a GMP Biopharmaceutical Production facility.
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The QAU will support the comparable GMP production activities related to GLP toxicology lot production and technical transfer activities as it relates to clinical batch release testing conducted at GTP to support the clinical CMO. The QAU will also provide Quality Assurance support to the research-based portion of the GTP, in terms of SOP management, training, document management and archiving, and audit support.
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Provide quality oversight for commissioning, qualification, and validation activities for GxP pilot plants and GMP warehouse equipment, utilities, and automation systems. Demonstrates proficiency in understanding and applying GMP regulations related to manufacturing, GMP warehouse, test laboratories, and facility operations.
$154,020 - $199,320ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Complies with all Safety, GMP, Quality, Plant Policies and other Associate and food safety requirements. Working on the production floor to assist in the manufacture of our delicious pizza products following our standard operating procedures.
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HACCP, FSMA, GFSI, FSSC, OSHA, GMP, FDA, BRC, SQF, USDA, and AIB audit knowledge. Establishes Quality Systems and manages a Food Packaging QA Department. Bachelor's degree in Food Science, Biology, Microbiology, or Chemistry.
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Also, this role will help with ensuring the reliability, effectiveness, maintenance, and ongoing improvements of the Safe Quality Foods (SQF) System, Good Manufacturing Practices (GMP), and Product Stewardship program.
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GMP/HACCP Experience in a tooling-intensive heavy manufacturing process such as Casting, Stamping, or plastics manufacturing (Injection Molding, Blow Molding, Thermoforming, Extrusion, etc.
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The Principal PQL supports efforts to establish collaborations between Regulatory Affairs, Process Development, MS&T, Analytical Development, Site Quality (QA/QC) and Internal/External Operations to ensure regulatory compliance of GMP operations in support of the assigned program.
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Maintain damage report list, block material, add batch remarks, GMP inspections, support in compliance with standards such as GMPs, pest control, glass control, training on quality systems, sampling techniques, reversing customer returns, cut and dump unblocking for transport, communicating quality issues that they are going to see coming from the plant, customer return inspections, transportation trailer issues inspection.
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The position will support cross-functional teams across CMC, Research & Development, Preclinical & GMP Manufacturing, Quality, and Analytical Development. We’re seeking a highly skilled and motivated Research Associate to reside in Moderna’s Technical Development organization in Norwood, MA. This is a lab-based role that will support the early phase process development of Moderna’s mRNbased medicines to enable our clinical supply and pipeline.
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3+ years of experience in the pharmaceutical industry within a GMP Quality Control role; experience with cell therapy products is a plus. Minimum of 2 years experience in the pharmaceutical industry working in a GMP quality control laboratory.
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Our GMP Production Technicians work in a team-based environment and are responsible for safety, production, maintenance, and product quality. CIL separates both 13C and 18O at its Xenia, Ohio, facility and has the world's largest production capacity for both 13C and 18O. CIL also has the only large capacity nongovernmental D2O (Deuterium Oxide) enrichment columns in the world located at its CIS facility.
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Working knowledge of regulatory and quality system and sanitation requirements: Global Food Safety Initiative (GFSI), Safety Quality Food (SQF), Good Manufacturing Practices (GMP), Hazard Analysis and Critical Control Points (HACCP), Environmental Microbiological Monitoring Program (EMMP), Master Sanitation Schedule (MSS), Integrated Pest Management (IPM), CIP/COP, etc.
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Daily alignment with other PBF Sr. Management peers and fostering of a cohesive and productive leadership team at PBF.Coordination with the BD Manager, BPD Manager, VDAD Manager, Quality Lead, Operations Manager, and PBF Director on all PBF business transactions and in alignment with the CAMRIS PBF business model.
$128,603 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago
in store gmp quality jobs Title: associate production
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