• Manager, Parenteral Inspection and Packaging

    Bristol Myers Squibb (Manati, PR)
    …experience, or leading multidisciplinary teams. * Knowledge in product transfer validation within pharmaceutical environment. * Ability to facilitate continuous ... support the packaging processes and fast tracking for documenting and implementing process modifications. 4. Ensures budget objectives and productivity or process… more
    Bristol Myers Squibb (01/12/26)
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  • Call Plan Implementation Manager

    Novo Nordisk (Plainsboro, NJ)
    …file library and documentation: manage all files generated during the call-plan process , and ensure files are accurate, reconciled, and distributed to downstream ... and reliable for field users + Oversee the field call-plan refinement process : create project timelines, communicate milestones to stakeholders, manage inquiries and… more
    Novo Nordisk (12/19/25)
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  • Sr Utilities Engineer

    Insight Global (Sanford, NC)
    … process equipment. * Coordination with other plant engineers, validation and automation colleagues in support of manufacturing operations. Responsibilities ... availability, reliability and reduce maintenance costs through system and process continuous improvement, ie, LEAN principles and Continuous Improvement methodology.… more
    Insight Global (12/18/25)
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  • Associate Director - Engineering

    Lilly (Indianapolis, IN)
    …decisions, influencing, coaching and mentoring. + Previous equipment qualification and process validation experience. + Previous experience with deviation and ... procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, PFDs, APRs, etc. 4.… more
    Lilly (12/11/25)
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  • QC Microbiologist

    Kelly Services (West Chester, OH)
    …Microbiology department by performing quality-related activities for pharmaceutical products. Responsibilities include documenting and executing microbiological ... testing on a variety of sample types such as raw materials, in- process and finished products, stability samples, water, gas, and environmental samples, in compliance… more
    Kelly Services (01/13/26)
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  • Head of MSAT Viral and Bacterial Platform,…

    Sanofi Group (Swiftwater, PA)
    …full accountability for process internalization, development and scale up, process validation , and control strategies for new products entering Manufacturing ... drive manufacturing excellence through technical support, lifecycle management, and process optimization-all focused on delivering high-quality products to patients… more
    Sanofi Group (12/18/25)
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  • Quality Engineer

    Teledyne (Miamisburg, OH)
    …responsibilities: + Plan and manage product quality, product qualification, and design validation ; + Process analysis and improvement through the implementation ... research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an… more
    Teledyne (12/10/25)
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  • Quality Assurance Intern

    Bristol Myers Squibb (Indianapolis, IN)
    …engineering, science, or a related field. + Basic understanding of pharmaceutical manufacturing processes, validation principles and regulatory requirements is ... preferred + Prior internship or coursework in pharmaceutical manufacturing, process engineering, or quality assurance is desirable but not required + All… more
    Bristol Myers Squibb (12/06/25)
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  • Senior Automation Engineer (DeltaV)

    Bristol Myers Squibb (Devens, MA)
    …. **Responsibilities:** + Support the operations on all GMP manufacturing systems ( Process Automation System) in the Manufacturing Facilities in Devens, MA. + Lead ... development operations. The activities will involve design, configuration, integration, test process control systems. + Participate in cross functional teams (system… more
    Bristol Myers Squibb (01/12/26)
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  • Senior Quality Engineer I - Validations, Risk…

    Integra LifeSciences (Plainsboro, NJ)
    …new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & ... agencies. **Primary responsibilities are:** **(Validations, Risk Management and Statistical Process Controls)** To perform this job successfully, an individual must… more
    Integra LifeSciences (01/07/26)
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