• Quality Assurance & Compliance Specialist

    Bausch + Lomb (Tampa, FL)
    …(QMS)** Serve as a back up to for QMS elements such as Quality Change Control , Annual Product Reviews, Quality by Design initiatives and CoA/CoC creations. ... to inspections readiness initiatives. Responsible for various Quality System process improvements and Quality Assurance/System projects, which will require… more
    Bausch + Lomb (08/29/25)
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  • Director - QA Iapi

    Lilly (Indianapolis, IN)
    …supporting the oversight of Insulin or Peptide Purification Active Pharmaceutical Ingredient (API) manufactured within Indianapolis Active Pharmaceutical ... quality systems. + Review and approve deviations, procedures, protocols, and change controls with focus for improving the overall manufacturing and/or business… more
    Lilly (08/19/25)
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  • Senior Regulatory Affairs Specialist

    West Pharmaceutical Services (Exton, PA)
    …+ Advanced knowledge of product life cycle, product development process , design control and change control + Experience interacting with government ... Sr. Specialist mentors team members and ensures compliance with West Pharmaceutical Services, Inc. (West) and government requirements. This position includes… more
    West Pharmaceutical Services (10/07/25)
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  • Associate Director, Senior Architect

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …+ Experience with IP Telephony QOS and protocols including SIP + Experience with change control procedures and methodologies + 5 years experience working with ... the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as...or for payment of money during the job application process . We do not require any financial, credit card… more
    Otsuka America Pharmaceutical Inc. (09/30/25)
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  • Senior Project Manager (GxP Regulated Environment)

    CBRE (Indianapolis, IN)
    …to coordinate individual, multi-discipline real estate project solutions for a pharmaceutical client, with direct accountability for project delivery. The work will ... non-regulated areas. Candidate should have familiarity and experience with pharmaceutical GxP compliance requirements (Good Manufacturing Practices, Good Laboratory… more
    CBRE (09/13/25)
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  • Quality System Specialist

    Kelly Services (Greendale, IN)
    …to:** + Quality Systems Oversight + Support site-level quality systems such as: Change Control and Deviation processes in accordance with internal procedures and ... for supporting key compliance and quality system activities such as entry of Change Controls, Deviations, Complaints, and CAPAs into TrackWise. + The ideal candidate… more
    Kelly Services (10/04/25)
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  • Sr. Specialist, Supplier Quality Management

    Cardinal Health (San Juan, PR)
    …QA in meeting related to his/her area of responsibility (suppliers meeting, , change control , audits planning and review, budget, etc.) + Performs other ... oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on Quality policies and… more
    Cardinal Health (09/10/25)
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  • Technical Lead - Lyophilization - Global Animal…

    Merck (North Wales, PA)
    …to ensure readiness: process validation/qualification planning, batch record design, change control , deviations assessment, and regulatory file support. + ... for vaccines/biologics, and pharma technical documentation (protocols, validation reports, change control , deviations, regulatory submissions). **_Minimum qualifications_**… more
    Merck (10/17/25)
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  • Executive Director, Biologics Drug Substance…

    Bristol Myers Squibb (Devens, MA)
    …and technology transfer. The role also ensures effective development of process control strategies and specifications for manufacturing during commercialization ... industry - each of our passionate colleagues contribute to innovations that drive meaningful change . We bring a human touch to every treatment we pioneer. Join us… more
    Bristol Myers Squibb (10/19/25)
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  • Associate

    Actalent (Cambridge, MA)
    …Industry Experience: Minimum 6 months of hands-on experience in the pharmaceutical or biotech industry academic lab/internship acceptable only if candidate has ... guidelines. Job Summary Amgens Attribute Sciences AS department within the Process Development PD organization defines the favorable quality characteristics of the… more
    Actalent (10/18/25)
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