• NPI / Digital Specialist

    Amgen (Thousand Oaks, CA)
    …into the manufacturing plant, as well as design electronic batch records supporting these introductions. This " Specialist Manufacturing" role will serve as ... + Reviewing protocols for manufacturing activities and partnering with Quality Assurance to ensure that GMP standards...GMP standards are maintained in line with current SOPs, batch record documentation, and licenses. + Identifying… more
    Amgen (07/19/25)
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  • External Manufacturing Specialist

    Regeneron Pharmaceuticals (East Greenbush, NY)
    …Liaison between various departments within Regeneron including, but not limited to Quality Control, Quality Assurance , Supply Chain, Operations/Logistics ... We are currently looking to fill an External Manufacturing Specialist position. The External Manufacturing Specialist oversees...and business partners. * Performing reviews of pre-production master batch records and executed batch more
    Regeneron Pharmaceuticals (07/31/25)
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  • Quality Compliance Specialist

    GKN Aerospace (Garden Grove, CA)
    …+ Validate signatures, entries, dates, and part traceability across batch records + Work proactively with production, engineering, quality assurance , ... Summary We are looking for a detail-driven and collaborative Quality Compliance Specialist to support our aerospace...US ITAR regulations Preferred Qualifications: + Bachelor's degree in Quality Assurance , or field related to Document… more
    GKN Aerospace (08/09/25)
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  • Quality Compliance Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …and regulatory requirements. + Coordinates the reviews of relevant records , (eg batch records , quality control data, quality investigations, etc.) ... Quality Compliance Specialist Department: Quality...Pharmaceutical Sciences, or equivalent Experience: Minimum 3 years in Quality Assurance in the pharmaceutical, biopharmaceutical, or… more
    Glenmark Pharmaceuticals Inc., USA (05/15/25)
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  • cGMP Senior Quality Control (QC)…

    University of Southern California (Los Angeles, CA)
    …actively participate in cross-functional meetings with Manufacturing, Process Development, and Quality Assurance to ensure seamless coordination in product ... Senior Quality Control (QC) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/cGMP-Senior- Quality -Control--QC-- Specialist \_REQ20165200/apply) Keck School of Medicine Los… more
    University of Southern California (07/30/25)
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  • Senior Cleaning Validation Specialist

    Catalent Pharma Solutions (St. Petersburg, FL)
    …of drug product intended for human consumption. This validation group within the Quality Assurance department oversees all aspects of validation as they relate ... **Senior Cleaning Validation Specialist ** **Position Summary** Catalent, Inc. is a leading...and on-boarding of alternate detergents. + Development of cleaning batch records or cleaning checklists to be… more
    Catalent Pharma Solutions (06/18/25)
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  • Quality Systems Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …purposes, where applicable. + Coordinates the reviews of relevant records , (eg batch records , quality control data, quality investigations, etc.) ... Quality Systems Specialist Department: Quality...Sciences, or equivalent Experience: + Minimum 3 years in Quality Assurance in the pharmaceutical, biopharmaceutical, or… more
    Glenmark Pharmaceuticals Inc., USA (07/16/25)
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  • Medical Coding Specialist

    Weill Cornell Medical College (New York, NY)
    …to meet productivity and quality -based departmental benchmarks. Performs charge entry batch quality assurance . + Reviews and resolves charge router ... Title: Medical Coding Specialist Location: Upper East Side Org Unit: Revenue...for NYC Offices **Position Summary** Responsible for reviewing medical records for compliance with coding and documentation requirements. **Job… more
    Weill Cornell Medical College (08/08/25)
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  • Associate Specialist , Quality

    Merck (Worthington, MN)
    … systems such as change control, document management, deviation management, etc. + Review of batch records and test records + Maintenance of seed stocks + ... + Under general supervision, this position assists with: + Maintaining quality expectations and regulations for a biological vaccine manufacturing site in… more
    Merck (08/02/25)
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  • Computer Systems Validation Specialist

    Unither Pharmaceuticals (Rochester, NY)
    …duration. Obtains copies and compiles relevant documentation such as executed batch records , certificates of analysis, equipment logs, materials certificates, ... Computer Systems Validation Specialist Who we are? We are a French...including, but not limited to: Information Technology, Operations, Engineering, Quality Assurance , and Product Development to provide… more
    Unither Pharmaceuticals (08/08/25)
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