• Engineering Maintenance Technician II…

    Integra LifeSciences (Braintree, MA)
    …controls. + Knowledge of regulatory requirements in the medical device or pharmaceutical industry. + Experience with cold storage validation and temperature ... Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what's possible and making headway to help improve outcomes. **Job Summary:** Integra LifeSciences is seeking a skilled and… more
    Integra LifeSciences (06/18/25)
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  • QC Scientist II/III

    Actalent (Berkeley, MO)
    …DS release, DP release, DS stability, DP stability, process validation , analytical method validation /transfer, method establishment/qualification, and other ... DS release, DP release, DS stability, DP stability, process validation , analytical method validation /transfer, and method establishment/qualification. +… more
    Actalent (08/01/25)
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  • Qualification Engineer

    Teva Pharmaceuticals (Edison, NJ)
    …and Equipment systems, with minimal supervision. + Develop and review Validation / Qualification protocols and reports that challenge the critical parameters ... needed for new products packaging, ensuring alignment with qualification and validation requirements. + Lead the development of User Requirement Specifications (URS)… more
    Teva Pharmaceuticals (07/31/25)
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  • Quality Assurance - Floor Support (Night Shift)

    Lilly (Pleasant Prairie, WI)
    …quality attributes are met (eg, deviations, procedures, technical studies, validation protocols, change controls, engineering documents) + Participates in continuous ... process team or quality organization. + Approves commissioning, qualification, and validation documents for computer systems and equipment to ensure compliance with… more
    Lilly (05/10/25)
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  • Lab Operations Specialist

    Actalent (Billerica, MA)
    …Specialist will be responsible for developing and maintaining records on pharmaceutical equipment and products, supporting the execution of documentation records on ... various equipment, aiding in the validation and calibration of the manufacturing area, and updating...Procedures (SOPs). Responsibilities + Develop and maintain records on pharmaceutical equipment and products. + Support the execution of… more
    Actalent (07/31/25)
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  • Principal Engineer - Systems

    Lilly (Branchburg, NJ)
    …+ Be responsible for and participate in the installation, configuration, and validation of LIMS applications. Develop and implement project plans, ensuring timely ... of end users, and provide end user training + Perform the pre- validation assessment of all computerized laboratory and/or manufacturing systems, ensuring that all… more
    Lilly (08/02/25)
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  • Quality Engineer

    Actalent (Minneapolis, MN)
    …you will be responsible for writing, reviewing, and approving qualification and validation protocols for new or transferred equipment and packaging designs. This ... technical reports. Responsibilities + Write, review, and approve qualification and validation protocols for equipment and packaging designs. + Support CI Engineering… more
    Actalent (07/31/25)
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  • Senior Engineer, Facilities & Maintenance CLT

    Novo Nordisk (Bloomington, IN)
    …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... team + Collaborate significantly with cross functional groups including Validation , Quality Control, Manufacturing, Process Development, and Facilities + Manage… more
    Novo Nordisk (06/30/25)
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  • Sr. Principal Manufacturing Scientist - Small…

    Lilly (Lebanon, IN)
    …new molecules. This position will interact with engineering, manufacturing, validation , quality assurance, quality control, development, and regulatory departments. ... Lilly products. This position requires comprehensive knowledge of the pharmaceutical industry, Good Manufacturing Practices (GMP), regulatory requirements, and the… more
    Lilly (06/07/25)
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  • Associate Process Engineer

    Endo International (Horsham, PA)
    …Engineer under direct supervision, performs various duties related to pharmaceutical construction, engineering, manufacturing / packaging process, and product ... Engineer will be responsible for supporting process engineering and validation initiatives as they pertain to manufacturing processes, manufacturing facilities,… more
    Endo International (07/23/25)
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