• Director, Commercial Manufacturing…

    Sumitomo Pharma (Trenton, NJ)
    … of the following activities - equipment and utilities qualification/ validation , process development, process validation , continued process ... 8 - 12 years (with Master's) of relevant experience in biotech or pharmaceutical industry Validation experience with multiple therapeutic modalities (eg API,… more
    Sumitomo Pharma (12/12/25)
    - Related Jobs

  • Validation Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …criterion from a quantitative standpoint. The candidate must be familiar with process flow of a medical device organization, including the regulatory impact of ... change and the documentation path of a compliant process . The candidate must possess technical writing experience in protocol generation and procedure generation.… more
    Integra LifeSciences (01/20/26)
    - Related Jobs

  • DeltaV Tech Lead - ( Pharmaceutical…

    Cognizant (Trenton, NJ)
    …in cross-functional program leadership meetings, ensuring alignment between automation, process engineering, digital/MES, and quality teams + Serve as the ... software testing strategies + Identification of any remediation effort required on process control software + Identify and analyze risks of technical nature… more
    Cognizant (01/06/26)
    - Related Jobs

  • IVR Validation Specialist

    Insight Global (Hopewell Township, NJ)
    …Description Our top Pharmaceutical client is seeking a Documentation and Validation specialist to join their External Call Center team within their Patient ... resource will have experience with Salesforce Service Cloud, Visio, PPT, and other process documentation tools to document workflows and validation . We are a… more
    Insight Global (12/09/25)
    - Related Jobs

  • Specialist, Quality Assurance Validation

    Bristol Myers Squibb (New Brunswick, NJ)
    …Perform independent review and approval of initial Commissioning, Qualification, and Validation (CQV) lifecycle documents and subsequent changes. + Review and ... -Experience as a CQV, QA, and/or QC representative within Pharmaceutical /Drug Substance Manufacturing (API, Sterile, Non-Sterile or Biological products) or… more
    Bristol Myers Squibb (01/21/26)
    - Related Jobs

  • Manager, CSV - Equipment and Instrumentation

    Bristol Myers Squibb (Summit, NJ)
    …qualification and support requests. + Provides technical support and guidance on Validation , Quality Process , and equipment qualification issues. Interfaces with ... documentation practices relating to systems, equipment, and instrumentation within the pharmaceutical industry. + Strong working knowledge of ISPE guidance, 21 CFR… more
    Bristol Myers Squibb (01/12/26)
    - Related Jobs

  • Manager, QC Biochemistry (Hopewell, NJ)

    BeOne Medicines (Pennington, NJ)
    …Biochemistry laboratory routine operations, including but not limited to validation , SOP revisions, specification updates, testing records, personnel training and, ... Health and Safety (EHS) standards. + Ensure timely completion of testing (eg, in- process , DS release, DP release, and stability testing) to ensure timely generation… more
    BeOne Medicines (12/18/25)
    - Related Jobs

  • Process Engineer

    Amneal Pharmaceuticals (Piscataway, NJ)
    …and plans, executes and functionally directs Process /Cleaning Validation /Study assignments and projects, which require sound pharmaceutical /engineering ... the organization. Managing the post approval projects. Essential Functions: + Prepare validation protocols & reports for manufacturing process and cleaning … more
    Amneal Pharmaceuticals (12/13/25)
    - Related Jobs

  • Sterile Specialist, Engineering (Onsite)

    Merck (Rahway, NJ)
    …center, for sterile operations within Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group ... products, including critical program needs related to new products undergoing process development, new products undergoing scale-up, launch and transfer to the… more
    Merck (01/15/26)
    - Related Jobs

  • Associate Director, Process Operations Lead

    Merck (Rahway, NJ)
    …(GMP), Leadership, Lean Manufacturing, Manufacturing Process Validation , Operational Excellence, Operations Management, People Leadership, Pharmaceutical ... **Job Description** The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance… more
    Merck (01/08/26)
    - Related Jobs