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Minimum of 2 years of relevant experience with materials management and/or supply chain within cGMP operations. Joining a team of highly qualified materials management and supply chain professionals, this individual will provide expert knowledge on materials resource planning strategies, develop purchase order strategies, monitor POs and invoices, maintain supplier relationships, and maintain target inventory levels to support cell therapy network.
ExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Ideal candidates should have 2+ years of Document Control and report experience with at least 1 year being in cGMP/FDA regulated environment. Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment.
ExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvote
Supply Chain - Analyst, Supply Chain Management & Systems Analyst, Supply Chain Management & Systems
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1+ years’ relevant experience with materials management and/or supply planning within cGMP operations in matrixed organization with multi-level setup. Joining a team of highly qualified materials management and supply chain professionals, this individual will be responsible for supporting the supply chain management process, systems, and software functions for MRP, ERP, data sources, testing, integrations, reporting, analytics, and more within the cell therapy network.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Manufacturing Operator/Technician II is responsible for all functions relating to the processing of drug products; consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP.
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Work directly with other departments such as Production, Quality Control, Technical Support, and IT to advise and oversee the requirements for cGMP, sampling, qualification, statistical process control analysis, software qualification, transfer of production, and other activities related to the scope of the business are met on a continuing basis.
Full-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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To lead the site cGMP system to ensure that the site meets all cGMP, IPEC requirements and FDA recommendations of good practices for glycerine (and fatty acids as needed). Must be computer literate and able to use a range of quality programs, LIMS and SQC/SPC packages.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Resolve observation / CAPAs generated from internal and external cGMP audits related to Validation, Qualification, and Commissioning studies. Understanding of validation principles, current Good Manufacturing Practices (cGMP), and applicable regulatory requirementsProficiency in equipment and process validation, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ.
$61,750 - $143,000 a yearFull-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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Must have previous experience in cGMP environment. Our client is seeking a GMP Document Coordinator to join their team in Morristown, New Jersey! Must have previous experience in cGMP environment.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The Associate Specialist is responsible for activities in accordance with corporate policies, standards, procedures, and Global cGMP in support of the QA Disposition group. Must have knowledge and experience with cGMP manufacturing, Quality, and compliance.
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Assist Center Manager in ensuring all center operations, product storage, documentation, facility maintenance, quality control, and training is current and consistent with the Company's Standard Operating Procedures Manual (the "SOP"), current State and Federal guidelines, OSHA, CLIA, cGMP, and any other internal Company procedures.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP.
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Knowledge of US and global cGMP requirements. Ability to use electronic Quality systems such as Infinity. Knowledge of quality processes, including investigations, and CAPA management. Proficient in Excel data mining and report creation.
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