• CQV Specialist - Upstream Process Equipment

    Mentor Technical Group (Juncos, PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... America. Responsibilities: + Develop, review, and execute Commissioning, Qualification, and Validation (CQV) protocols for upstream process equipment (IQ, OQ, PQ). +… more
    Mentor Technical Group (09/07/25)
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  • Scientist, Lab Tech Services - Microbiology

    Endo International (Rochester, MI)
    …of commercial/pre-commercial materials and products, including method development, validation and transfer, pre-commercial/commercial testing of materials and ... considered an SME for these areas. Write and review SOPs, test methods, validation protocols and validation reports. The Senior Scientist also provides mentoring… more
    Endo International (08/12/25)
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  • Automation Engineer

    Amneal Pharmaceuticals (Piscataway, NJ)
    …Implement projects according to Good Automated Manufacturing Practice (GAMP) guide for validation of automated systems in pharmaceutical manufacture. + Handle ... integrating, and implementing advanced hardware and software solutions within pharmaceutical manufacturing facilities. Essential Functions: + Develop Control Systems… more
    Amneal Pharmaceuticals (09/13/25)
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  • Director, Market Access Contract Operations - Job…

    Ascendis Pharma (Princeton, NJ)
    …etc. + Purchase Order and Vendor Invoice Tracking and Reporting: Oversee the validation and payment of applicable vendor invoices. Collaborate with Finance to track ... This individual must possess an in-depth knowledge of claims processing, formulary validation processing, and dispute processes, and be able to communicate clearly… more
    Ascendis Pharma (09/09/25)
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  • Sr/Lead DeltaV Automation Engineer(remote)

    Cognizant (St. Paul, MN)
    …or equivalent experience. . 12+ years of automation experience in the pharmaceutical industry, with a strong preference for API/bulk manufacturing environments. . ... Proven experience leading cross-functional automation teams on large-scale pharmaceutical projects or programs. . Demonstrated ownership of full project lifecycle… more
    Cognizant (09/05/25)
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  • QC Scientist (pharma/micro)

    Astrix Technology (Wilmington, OH)
    …- 14/08/2025 Apply for Job _Our client, a global leader in the pharmaceutical manufacturing industry, is seeking a experienced QC Scientist to join their team!_ ... background (chemistry too is a plus) with a MS or PhD and pharmaceutical indsutry expereince! **QC Scientist I** **Background** + Lead Team in project Coordination… more
    Astrix Technology (08/15/25)
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  • Analytical Chemist

    Mallinckrodt Pharmaceuticals (Hazelwood, MO)
    …Global Technical Operations organization. Responsibilities include analytical method development, validation , and transfer to internal and external GMP laboratories; ... timely execution of project deliverables. Essential Functions + Lead the development, validation , and transfer of analytical methods using techniques such as HPLC,… more
    Mallinckrodt Pharmaceuticals (07/25/25)
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  • Scientist II; Analytical R&D

    Contract Pharmacal Corp (Hauppauge, NY)
    …of USP and FDA requirements. + Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products. + Generate method ... validation protocols. + Execute methods validation and...and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities. + Conduct… more
    Contract Pharmacal Corp (07/23/25)
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  • Sr Specialist, QC Systems Digital and Analytical…

    Pfizer (Bothell, WA)
    …quality team. As a Senior Specialist, Digital / CSV ( computer system validation ) and Analytical Equipment Management, your knowledge and skills will contribute ... and standards (ie, GxP, CFR, ICH, GDPR) + Serves as the validation lead on cross-functional technology initiatives that involve multiple lines of business.… more
    Pfizer (09/19/25)
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  • Associate Director, Quality Assurance - Site Data…

    Lilly (Pleasant Prairie, WI)
    …and integrity principles in operational processes, and Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment. The ... and integrity principles in operational processes, and Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment. The… more
    Lilly (09/10/25)
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