• Process Expert Pharmaceutical

    PDS Tech Commercial, Inc. (Millburn, NJ)
    …impact in the world of pharmaceutical innovation? **Apply now to become a Process Expert in Millburn, NJ!** **Pay Details:** $35.71 to $39.29 per hour ... Behind Life-Changing Therapies - Join Us as a Process Expert !** **Location:** Onsite in Millburn, NJ...Commercial** , we're partnering with a leading name in ** Pharmaceutical Manufacturing ** to deliver innovation and excellence… more
    PDS Tech Commercial, Inc. (07/18/25)
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  • Lead, Manufacturing Operator - 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …production schedule, available resources, and department priorities. Engage and support manufacturing process to ensure timely completion and quality throughput. ... suite. + Actively engage in all areas of the manufacturing process . + Identify and resolve training...operator execution. + Support investigations as a subject matter expert . + Maintain process and component inventories.… more
    Integra LifeSciences (07/08/25)
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  • Lead Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …production schedule, available resources, and department priorities. Engage and support manufacturing process to ensure timely completion and quality throughput. ... suite. * Actively engage in all areas of the manufacturing process . * Identify and resolve training...operator execution. * Support investigations as a subject matter expert . * Maintain process and component inventories.… more
    Integra LifeSciences (06/27/25)
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  • Lead, Cleanroom Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …production schedule, available resources, and department priorities. Engage and support manufacturing process to assure timely completion and quality throughput. ... suite. + Actively engage in all areas of the manufacturing process . + Identify and resolve training...operator execution. + Support investigations as a subject matter expert . + Maintain process and component inventories.… more
    Integra LifeSciences (04/29/25)
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  • Vice President, Manufacturing Operations…

    Teva Pharmaceuticals (Parsippany, NJ)
    Vice President, Manufacturing Operations (Cluster Head US) Date: Jun 25, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals ... feedback and development opportunities for reports via the performance management process . + Plan, manage and deliver work plan resources (headcount, expense… more
    Teva Pharmaceuticals (06/26/25)
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  • Director, Oral Formulation Sciences

    Merck (Rahway, NJ)
    manufacturing by designing, developing, and scaling-up the formulation, device, and manufacturing process . Driving drug product design from the benchtop to ... Skills:** + Knowledge of oral drug product formulation and process development + Experience with cGMP manufacturing ... development problems + Recognized as a subject matter expert in drug delivery and/or manufacturing technology… more
    Merck (07/09/25)
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  • Principal Scientist, Upstream Process R&D

    Merck (Rahway, NJ)
    …Finite Element Analysis (FEA), Innovative Thinking, Leadership Mentoring, Pharmaceutical Process Development, Professional Collaboration, Professional ... penchant for problem-solving and expertise in upstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist. BPR&D within… more
    Merck (07/18/25)
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  • Technical Fellow (Director), Advanced Therapies…

    J&J Family of Companies (Raritan, NJ)
    …that arise when non-conforming products or deviations are generated during the manufacturing process , which can impact patient treatment. The Technical Fellow ... or Spring House, PA. **Purpose:** The Technical Fellow serves as a subject matter expert (SME) in CAR-T manufacturing and Quality Control analysis, playing a… more
    J&J Family of Companies (06/30/25)
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  • Associate Director, Quality Assurance - Third…

    Merck (Rahway, NJ)
    …Global Program Development, Good Manufacturing Practices (GMP), Management Process , Organic Chemistry, Pharmaceutical Guidelines, Pharmaceutical ... The position will be heavily involved in close partnership with Active Pharmaceutical Ingredient (API) manufacturing contractors and technical personnel and… more
    Merck (07/12/25)
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  • Director Quality Assurance

    Merck (Rahway, NJ)
    …provide compliance leadership and direction to our Company and contract manufacturing operation (CMO) sites that manufacture active pharmaceutical ingredients ... are effectively implemented. **_Primary Activities_** + Serve as a subject matter expert for current good manufacturing practice (CGMP) requirements for vaccine… more
    Merck (07/17/25)
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  • Technical Owner, MSAT

    J&J Family of Companies (Raritan, NJ)
    …for commercial manufacturing + Experience in data analytics/sciences and process automation + Expert knowledge of evolving ATMP health authority ... of the Global Technical Team, reporting to the Global Process Owner within the Advanced Therapies Manufacturing ...+ Minimum 8 Years of relevant experience in Biotech/ Pharmaceutical industry experience + Hands-on experience in Manufacturing more
    J&J Family of Companies (06/19/25)
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  • Vice President Central Quality Operations

    Gilead Sciences, Inc. (Parsippany, NJ)
    …requirements. + Strong working knowledge of relevant regulatory guidance, including pharmaceutical GMPs (Good Manufacturing Practices) and ICH (International ... implementation and delivery of systems and execution for GMP/GDP (Good Manufacturing and Distribution Practices) activities in the Global Markets organizations… more
    Gilead Sciences, Inc. (07/17/25)
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  • Associate Director, MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …CDMOs, including documentation review, gap analysis, and risk assessment. + Provide expert technical oversight of upstream manufacturing operations at CDMOs, ... biopharmaceutical industry with a strong focus on biologics upstream process development, scale-up, technology transfer, and/or manufacturing sciences/support.… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …CDMOs, including documentation review, gap analysis, and risk assessment. + Provide expert technical oversight of downstream manufacturing operations at CDMOs, ... biopharmaceutical industry with a strong focus on biologics downstream process development, scale-up, technology transfer, and/or manufacturing sciences/support.… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Qualification Engineer

    Teva Pharmaceuticals (Edison, NJ)
    …and local laws, codes, regulations and regulatory requirements + Knowledge of pharmaceutical manufacturing operations to support the approval of protocols, ... equipment qualification projects, the Qualification Engineer II acts as a subject matter expert (SME) for all qualifications at the Edison Site. This individual is… more
    Teva Pharmaceuticals (05/01/25)
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  • Scientist

    Kelly Services (New Brunswick, NJ)
    **Job Title:** QC Scientist - Pharmaceutical Manufacturing Support **Job Summary:** The primary responsibilities include routine testing and analysis of finished ... The ideal candidate will have a strong background in pharmaceutical testing and a proven track record working with...hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical… more
    Kelly Services (07/19/25)
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  • Sr. Specialist, Environmental Sustainability…

    Merck (Rahway, NJ)
    …Relationships, Management Process , Occupational Safety and Health Programs, Pharmaceutical Manufacturing , Process Safety Management, Project Management ... are not limited to:** + Serves as primary technical expert for the completion of product LCA/PCF projects, including...familiarity with WRI GHG Protocol. + Basic knowledge of pharmaceutical manufacturing and product types, especially as… more
    Merck (07/10/25)
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  • Director- Sterility Assurance

    Lilly (Branchburg, NJ)
    …role provides ad-hoc technical support to Lilly PR&D, external contract manufacturing , and non-sterile drug substance (API) manufacturing . **Responsibilities:** ... and start-up activities to ensure sterility assurance programs and process / product requirements are supported at these sites, particularly...the agenda within PR&D to ensure the needs of Manufacturing are met, and the control strategies are fit… more
    Lilly (04/21/25)
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  • Director, Pharmacometrics (Remote or Hybrid)

    Merck (Rahway, NJ)
    …clinical trial design and Go/No Go decisions + Serve as a subject matter expert and foster collaboration within QP2 and across functions to plan and execute novel ... record of increasing responsibility and independence in a similar role in pharmaceutical drug development or academia + Educational background in pharmaceutical more
    Merck (07/12/25)
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  • Sr. Manager Document Control and Training

    Integra LifeSciences (Princeton, NJ)
    …attaining the company's improvement objectives and growth strategies across Integra manufacturing facilities and a diverse portfolio of leading medical devices. This ... Medical Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical and Medical Device Agency (PMDA), and other applicable regulatory… more
    Integra LifeSciences (07/08/25)
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