• Senior Analytical Associate II

    Kelly Services (Harleysville, PA)
    …manufacturing campaigns and requires an expert blend of 8-15+ years of pharmaceutical industry experience, especially in small molecule method development and ... validation . The position maintains a roughly 50/50 split between...scientific discipline. + 8-15+ years of experience in the pharmaceutical industry, with a focus on solid and liquid… more
    Kelly Services (12/04/25)
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  • Advisor/Senior Advisor, Analytical Chemistry…

    Lilly (Indianapolis, IN)
    …role, you will be part of a diverse team of analytical chemists, pharmaceutical scientists, and engineers delivering product and process understanding across a ... the analytical development work within a cross-functional team including process chemists, formulation scientists, and engineers. **Key Responsibilities:** + Develop… more
    Lilly (11/14/25)
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  • Principal Process Engineer (Sterile Fill…

    PCI Pharma Services (Bedford, NH)
    …the future of PCI. We're looking for a **hands-on, highly skilled Principal Process Engineer** to lead complex engineering projects from concept to completion. In ... and manufacturing systems for maximum efficiency and reliability. + **Own the Process ** - From URS and risk assessments to vendor management and factory/site… more
    PCI Pharma Services (11/11/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Cambridge, MA)
    …Proof-of-Mechanism/Proof-of-Concept, as well as natural history studies and experimental model validation to contribute building the Human Target Validation ... of multiple disciplines into a coherent translational medicine and human target validation plan is essential. We are an innovative global healthcare company with… more
    Sanofi Group (01/05/26)
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  • Engineer - Automation Engineering - Control System…

    Lilly (Lebanon, IN)
    …of Automation Servers, Network and Infrastructure and applications + Support the Process Control Validation Plan, CSV, Quality Documents, SOP's and Audit ... or related discipline and 3+ years' experience in Computerized System Validation and Data Analytics, preferably in pharmaceutical manufacturing. **Additional… more
    Lilly (01/01/26)
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  • Entry Level Commissioning & Qualification Engineer

    PACIV (Indianapolis, IN)
    Entry‑Level Commissioning & Qualification Engineer PACIV stands for Process Automation, Controls, Instrumentation, and Validation . At PACIV, we are passionate ... about delivering world-class automation & validation solutions that empower many industries and advanced manufacturing. Our teams thrive on innovation,… more
    PACIV (01/05/26)
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  • Engineer

    Mentor Technical Group (Juncos, PR)
    …of significant complexity. + Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation ... experience + Drug substance manufacturing/technical support + Working knowledge of pharmaceutical /biotech processes + Familiarity with validation processes +… more
    Mentor Technical Group (12/16/25)
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  • IT Senior Business Analyst

    Teva Pharmaceuticals (West Chester, PA)
    …Senior Business Analyst is responsible for supporting IT projects within the pharmaceutical industry, with a focus on business analysis and expertise in application ... role requires experience in projects related to computerized system implementation and validation , as well as strong business analysis skills. The Senior Business… more
    Teva Pharmaceuticals (12/05/25)
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  • Advisor - TS/MS Lab - Lebanon API Manufacturing

    Lilly (Lebanon, IN)
    … manufacturing processes. **Job Responsibilities** + Develop laboratory process and analytical expertise, provide technical oversight and stewardship ... complex laboratory experiments, data analysis, and interpretation to support process development, characterization, and optimization. + Collaborate cross-functionally with… more
    Lilly (11/21/25)
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  • Jt772 - Sr. Software Quality Engineer

    Quality Consulting Group (Juncos, PR)
    …software system requirements, traceability, and testability. + Performs and/or review process validation (not cleaning processes) and equipment documents: URS, ... QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is...Communication skills + Technical writing knowledge + Knowledge of Process validation and Computer software validation more
    Quality Consulting Group (12/31/25)
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