• Associate Director, Global Regulatory Affairs…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... diseases and immune disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and… more
    Daiichi Sankyo Inc. (04/19/25)
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  • Global Director, Continuous Improvement

    Catalent Pharma Solutions (Bridgewater, NJ)
    …+ Coach and support the Continuous Improvement teams at key selected site Expert review and support to site projects. + Training on Continuous Improvement tools ... collaboration and influencing skills. Demonstrated knowledge as a subject matter expert and resource. Demonstrated understanding cGMP requirements related to change… more
    Catalent Pharma Solutions (05/31/25)
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  • Lead, Cleanroom Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …deficiencies and observe operator execution. + Support investigations as a subject matter expert . + Maintain process and component inventories. + Support time ... schedule, available resources, and department priorities. Engage and support manufacturing process to assure timely completion and quality throughput. Lead and… more
    Integra LifeSciences (04/29/25)
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  • Lead, Manufacturing Operator - Weekend Shift

    Integra LifeSciences (Plainsboro, NJ)
    …deficiencies and observe operator execution. + Support investigations as a subject matter expert . + Maintain process and component inventories. + Support time ... schedule, available resources, and department priorities. Engage and support manufacturing process to assure timely completion and quality throughput. Lead and… more
    Integra LifeSciences (04/29/25)
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  • Lead Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …deficiencies and observe operator execution. * Support investigations as a subject matter expert . * Maintain process and component inventories. * Support time ... schedule, available resources, and department priorities. Engage and support manufacturing process to ensure timely completion and quality throughput. Lead and… more
    Integra LifeSciences (03/28/25)
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  • FSP - Sr. Scientist - Stability

    ThermoFisher Scientific (New Brunswick, NJ)
    …the employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. Global Biologics ... sites to develop stability product requirements for annual enrollments, process changes and investigations. Determine the stability requirements for each… more
    ThermoFisher Scientific (06/06/25)
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  • Operations Technician

    Kelly Services (Rahway, NJ)
    …appropriate corrective and preventative actions (CAPAs) d. Participate as subject matter expert during internal or external audit from Quality group, safety bodies ... (GMP) principles 2. Knowledge of quality and safety requirements for pharmaceutical packaging / handling 3. Detail-oriented and organized 4. Excellent verbal… more
    Kelly Services (05/30/25)
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  • Quality Engineer Project

    Kelly Services (Parsippany, NJ)
    …Deviation Investigation) for an excellent 8 month project with a growing pharmaceutical company in Parsippany, NJ. This position offers a full benefits package ... the Kelly Engineering network. That means our team of expert engineering recruiters will have access to your profile,...the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource… more
    Kelly Services (05/29/25)
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  • Senior Analyst Medicaid Rebate Operation

    Bristol Myers Squibb (Princeton, NJ)
    …such as monitoring invoice intake and loading requirements. Act as subject matter expert related to Model N claims & payment processing and reporting functionality ... invoice intake and loading requirements + Acting as a Subject Matter Expert regarding Model N claims & payment processing and reporting functionality including:… more
    Bristol Myers Squibb (05/28/25)
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  • Sr. Director, Medical Affairs QA

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Authorities (FDA, EMA, MHRA) and other government and local agencies + Expert knowledge required for theend-to-endDrug development process in R&D space ... Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical… more
    Daiichi Sankyo Inc. (04/26/25)
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