• Merck & Co. (Rahway, NJ)
    …of independent problem-solving. Preferred Experience and Skills: Operations experience in a GMP clinical supply facility (intermediate scale or pilot plant) or ... clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training opportunities for improved manufacturing process development, and seamless… more
    HireLifeScience (03/26/24)
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  • Merck & Co. (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... degree with 1 years of relevant experience.Required Experience and Skills: Experience in GMP clinical supply facility.Experience with GMP facility design,… more
    HireLifeScience (03/24/24)
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  • Catalent (St. Petersburg, FL)
    …entering curricula and entering training data per employeeTracks and monitors GMP training using manual and automated systems. Individual will be responsible ... training on corporate policies, some standard operating procedures (SOPs), and GMP training modules, when requiredConducts introductory GMP training more
    HireLifeScience (03/18/24)
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  • Merck & Co. (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    HireLifeScience (03/15/24)
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  • Merck & Co. (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    HireLifeScience (03/13/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking Systems Engineer Specialist as part of the Commissioning and Qualification team based in Raritan, NJ. ... engineering support to implement and maintain computerized systems in the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be… more
    HireLifeScience (03/22/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking QA Microbiology Specialist as part of the Quality team based in Raritan, NJ. Role Overview ... The QA Microbiology Specialist is an exempt level position with responsibilities for...control of the production of autologous CAR-T products for clinical trials and commercial operations in a controlled cGMP… more
    HireLifeScience (01/19/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    clinical trials and commercial operations in a controlled GMP environment. Major Responsibilities Responsible for performing routine EM sampling, including ... the treatment of multiple myeloma. Legend Biotech is seeking a QC Microbiology Specialist , Lentivirus CAR-T Manufacturing as part of the Quality team based in… more
    HireLifeScience (01/09/24)
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  • Clinical Quality Assurance…

    ThermoFisher Scientific (Middleton, WI)
    …and participates in developing and tracking corrective actions. * Provides training for department and/or laboratory staff where required. * Reviews batch ... Handles production pre and post line clearances and in-process checks as per GMP requirements. * Provides support to the department with incoming material inspection… more
    ThermoFisher Scientific (03/24/24)
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  • QA Specialist , Training

    Catalent Pharma Solutions (St. Petersburg, FL)
    …curricula and entering training data per employee + Tracks and monitors GMP training using manual and automated systems. Individual will be responsible for ... **QA Specialist , Training ** **Position Summary** St. Petersburg...on corporate policies, some standard operating procedures (SOPs), and GMP training modules, when required + Conducts… more
    Catalent Pharma Solutions (03/18/24)
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  • Senior Specialist - Process/Facility…

    Merck (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... with 1 years of relevant experience. **Required Experience and Skills:** + Experience in GMP clinical supply facility. + Experience with GMP facility design,… more
    Merck (03/24/24)
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  • Clinical Cell Engineer Specialist II…

    MD Anderson Cancer Center (Houston, TX)
    …and/or Cellular Therapy treatment. **The ideal candidate will have GLP and/or GMP experience.** **KEY FUNCTIONS** 1. **Cell Manipulation and Processing** 1. Perform ... to procedures/policies implemented by internal or external study sponsors on various clinical trials that may differ from standard operating procedures of MDACC Cell… more
    MD Anderson Cancer Center (03/27/24)
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  • Senior Specialist , Process Engineer

    Merck (Rahway, NJ)
    …independent problem-solving. **Preferred Experience and Skills:** + Operations experience in a GMP clinical supply facility (intermediate scale or pilot plant) ... clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training opportunities for improved manufacturing process development, and seamless… more
    Merck (03/26/24)
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  • Senior Specialist - Manufacturing…

    Merck (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    Merck (03/13/24)
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  • MACS Facility Specialist - Equipment…

    Merck (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    Merck (03/15/24)
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  • Specialist , Quality Assurance

    Catalent Pharma Solutions (Princeton, NJ)
    …lives. The ** Specialist , Quality Assurance** provides Quality Assurance support for GMP Raw Materials that support the production of GMP Manufacturing ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Catalent is committed to a Patient… more
    Catalent Pharma Solutions (03/08/24)
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  • Associate Specialist - Manufacturing…

    Merck (Rahway, NJ)
    …multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, ... enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training more
    Merck (03/24/24)
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  • Cell Therapy QA Specialist IV - Melanoma…

    MD Anderson Cancer Center (Houston, TX)
    …**KEY FUNCTIONS:** * Provides administrative leadership of standard of care (SOC), clinical research and Good Manufacturing Practices ( GMP ) workflows to ensure ... Develops training and ensures laboratory follows good manufacturing practice ( GMP ) and standard operating procedures (SOPs). * Ensures compliance with quality… more
    MD Anderson Cancer Center (02/09/24)
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  • Technical Specialist

    Pfizer (Groton, CT)
    …timelines, schedules, and operational quality standards in alignment with current GMP guidelines for clinical drug product supplies.Primary responsibility ... Achieve** We are seeking a motivated individual for the role of Technical Specialist (Drug Product Manufacturing Operations Group -T3) in our GMP manufacturing… more
    Pfizer (03/20/24)
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