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10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC. Hands-on experience with designing and implementing GMP Quality Systems.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. Provide drug safety and pharmacovigilance leadership to the quality and compliance team, fostering a culture of collaboration, excellence, and continuous learning.
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Manufacturing quality technician. Employee is responsible to follow and uphold all Food Safety, Food Quality, Occupational Safety, Health and Environment policies and procedures as pertains to role.
$25 - $31.12 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. Experience in assay transfer, technology transfer, validation from Analytical Developmental group to Quality Control group.
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On-Board Services is hiring a Quality Control Chemist in New Brunswick, NJ! The Quality Control Chemist for the drug product testing team reports to the Finished Product/Stability Supervisor.
$35 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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Position requires on-site presence at companies' HQ Essential Duties and Responsibilities Conducting Training: Developing and conducting training programs for personnel on GMP and GDP requirements, quality systems, and relevant procedures to ensure understanding and compliance throughout the organization.
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Developing and Maintaining Quality Systems: Establishing and maintaining comprehensive quality systems in compliance with GMP and GDP regulations. Continuous Improvement Initiatives: Leading or participating in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes, driving a culture of quality and excellence within the organization.
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Looking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization. Conducting Training: Developing and conducting training programs for personnel on GMP and GDP requirements, quality systems, and relevant procedures to ensure understanding and compliance throughout the organization.
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Job Description: Assistant QC ScientistOnsite role, Warren NJWork Schedule: Mon - Fri, AM - :PM EST Purpose:The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products.
$40.82 - $42.82ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Title : Research Associate Quality Control. Research Associate Quality Control, Somerville, NJ. a Conduct routine and non-routine analyses of test articles as assigned by supervisor by appropriate biochemical methods such as: SDS-PAGE, HPLC,CE- SDS, ELISA, Cell Based Bioassay, etc.
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Must understand and apply cGMP requirements applicable to quality control laboratory. Perform testing using HPLC, UPLC, GC, IR, UV, Malvern Mastersizer, XRD, Dissolution, Karl-Fischer titrator, analytical balances, and other instruments as required.
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Knowledgeable or familiar in quality analysis tools such as SPC, PFMEA, DMAIC, Lean Manufacturing, Acceptance Sampling, etc. Provide oversight and management of various Quality Processes such as; Internal Audit Program, Corrective and Preventive Actions System, Change Control, Supplier / Co-packer Quality Management, Non-Conforming Material, etc.
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Prepares monthly Manufacturing and Quality Related KPI’s. Proven quality and trustworthy performance have established widespread confidence in the HORIBA Brand. The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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Review and draft proposals to implement changes to the Quality System procedures/forms as needed to maintain compliance, improve effectiveness and efficiency. The Quality Compliance Engineer II is responsible for maintaining the compliance of TMCs products and processes in the changing regulatory landscape.
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Title: quality Company: Ks Engineers P C in Bridgewater, NJ
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