• Jt267 - Manufacturing Engineer II

    Quality Consulting Group (Villalba, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... control of Medical Devices + Equipment Commissioning / Qualification + Process Validation + Computer System Validation (CSV) + Manufacturing, Packaging and… more
    Quality Consulting Group (08/16/25)
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  • Manufacturing Scientist (R4-R5)

    Lilly (Indianapolis, IN)
    …and commercial activities within parenteral manufacturing. Drive the validation and commercialization of monoclonal antibodies, biologics, and peptide ... field followed by 5 years of progressively responsible experience with pharmaceutical manufacturing and control strategies. Experience must include a minimum of:… more
    Lilly (08/15/25)
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  • Contracts Manager

    Robert Half Management Resources (Princeton, NJ)
    …and regulatory guidelines. 2. Execute Contract Operations: + Supervise the setup, validation , and implementation of contract terms in relevant systems. + Monitor ... (eg, Model N, Revitas, Vistex, iContracts) to track contract performance, validation , and intake processes. Requirements * Extensive experience in contract… more
    Robert Half Management Resources (08/15/25)
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  • MS Digital and Data Science Lead

    Takeda Pharmaceuticals (Lexington, MA)
    …including but not limited to Manufacturing, Facilities and Engineering, Quality, Validation , Operational Excellence & Training, Supply Chain and DD&T. + Interacts ... studies, design workshops and system implementation. **Desired:** + GxP software validation ; Data governance and stewardship. + Data mining, machine learning,… more
    Takeda Pharmaceuticals (08/14/25)
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  • Senior CQV Lead : Life Sciences - Chicago, IL

    Jacobs (Milwaukee, WI)
    …know that we're making a difference. As a Senior Commissioning, Qualification, and Validation (CQV) Lead, you'll join our collaborative team providing CQV support to ... AF&IDs, etc.), developing Standard Operating Procedures (SOPs), process workflows, Validation Master Plans, User Requirement Specifications, Turnover Packages, and… more
    Jacobs (08/14/25)
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  • Quality Control Analyst

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …+ Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products. + Assist in the monitoring of changes in the ... staff + Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc. + Perform the Training Tracking Tool/Software for QUALITY… more
    Glenmark Pharmaceuticals Inc., USA (08/14/25)
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  • Sr. Specialist I, Quality Assurance - Quality…

    Abeona (Cleveland, OH)
    …Communicate lot disposition pending issues to management. + Review qualification / validation protocols and reports and ensure resolution of and discrepancies that ... to: Master Production Records, Quality Control test methods/forms, Method Qualification/ Validation records, Development Reports, etc. Authorization includes a review… more
    Abeona (08/13/25)
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  • Senior cGMP Specialist- Quality Control Analytical…

    Houston Methodist (Houston, TX)
    …+ Demonstrated knowledge and experience in analytical procedure development, validation , instrument maintenance and troubleshoot, including High Performance Liquid ... degree preferred **WORK EXPERIENCE** + Five years of biotechnology or pharmaceutical industry experience with exposure to cGMP manufacturing operations + Experience… more
    Houston Methodist (08/13/25)
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  • Quality Associate III, Operations

    Endo International (Cranbury, NJ)
    …non-conforming event support to resolve in-process issues, and process validation and qualification activities. Communicates to multiple departments and supervision ... including purging according to retention schedule. + Performs in process validation and equipment qualification activities as required. + Performs other duties… more
    Endo International (08/12/25)
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  • QC Scientist

    Astrix Technology (San Diego, CA)
    …and root cause analysis + Coordinate analytical method transfers and validation with external subcontractors + Manage relationships with subcontractors to ensure ... 3 years of QC experience in a biotech or pharmaceutical GMP environment + Prior experience in a QA...Prior experience in a QA department is advantageous, method validation + Hands-on expertise with techniques such as HPLC,… more
    Astrix Technology (08/11/25)
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