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Science, bachelor*, degree, biology, chemistry, food science, Microbiology, Quality control, Laboratory, Quality assurance, Viscosity, Titration, Quality, HACCP, GMP, Food industry. Train and coach employees on GMP, HACCP, food safety and food quality standards.
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Related PhD degree with 1+ years GMP laboratory experience. Related BA/BS degree with 2+ years GMP laboratory experience. Related MA/MS degree with 1+ years GMP laboratory experience.
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Your responsibilities include orchestrating the implementation of critical systems such as enterprise and laboratory management systems, analytics, and business systems to support operational excellence and growth.
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From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.
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The scope of this role includes ensuring Good Manufacturing Processes (GMP) and Good Laboratory Practices (GLP) compliance and quality systems at Pliant and its vendors. The ideal candidate will have extensive experience leading GMP/GLP Quality Assurance activities and deep understanding and demonstrated working knowledge of Code of Federal Regulations (CFRs), ICH guidance documents, and other regulations that govern GMP/GLP compliance during clinical development and commercialization of drug candidates.
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Facilities Maintenance activities, including budget, schedule, and document management, in the design, cost estimating, procurement, installation, construction, modification, and commissioning, as applicable, of complex multi-system, multi-discipline equipment and systems for general use and GMP regulated areas.
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Enforce Kerry manufacturing standards in the areas of ingredient and product standards, process specifications, formula compliance, sanitation/GMP/pest control, and regulatory audit compliance.
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BS in Food Science, Microbiology, Chemistry - OR related work experience in a GMP manufacturing environment (2-3 years ideal) Perform laboratory analysis and prep-work which includes, but not limited to organoleptic, micro-biological (3M petri film tests and dilutions), and chemical testing (moisture, fat, etc.
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Contract - Trenton Metro Area Duties: Perform QC biochemistry laboratory assay validation and transfer activities to support GMP manufacturing, testing and release of material, intermediates and finished products under FDA/EU regulations, applicable International Regulations, and client's processes and procedures.
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The QA role is responsible for managing the plant Quality Assurance Department, and for managing all Quality Assurance, GMP, HACCP, Allergen, and food safety programs, policies, and procedures for the plant.
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Minimum of 5 years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing. Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.
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Aware of and practice Plant's Good Manufacturing Practices (GMP) as well as Good Sanitation Practices (GSP). Report out of specification results to Laboratory Supervisor, the Quality Control Office, and Production Supervision when appropriate.
$22.5 - $25 an hourInternExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Must be able to work 12 hour shift (days or nights) on a rotating scheduleMust follow GMP Policy - wear company issued shirt, hat, safety glasses, earplugs and hairnet in production areas. Quality Technician - Beverage (Nights)Responsible for executing corporate and plant specific Food Safety, Quality and Laboratory requirements.
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Confirm quality systems are applied in the performance and documentation of laboratory studies. Review and sign routine GMP reports for technical accuracy and completeness. Physical activities include sitting, walking, and standing for prolonged periods and operate laboratory equipment.
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The QA Auditor I assures the quality of data and reports generated by the GMP laboratory support teams including equipment and software validation (IQ/OQ/PQ) documentation, instrument maintenance and calibration reports and facility qualification documentation.
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