• Merck & Co. (Rahway, NJ)
    …job that provides both technical and project management responsibility. The Associate Specialist - Manufacturing Automation position will report to the Director, ... production, utility systems and associated infrastructure.- Responsibilities of the Associate Specialist - Manufacturing Automation include the following: Small… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Durham, NC)
    …team culture including significant interaction with manufacturing , quality, IT, and engineering groups. - The Senior Specialist for Manufacturing ... Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible for supporting… more
    HireLifeScience (03/22/24)
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  • Merck & Co. (Rahway, NJ)
    …fast-paced job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:The automation… more
    HireLifeScience (03/19/24)
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  • Merck & Co. (Rahway, NJ)
    …fast-paced job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:Site Operations… more
    HireLifeScience (03/20/24)
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  • Merck & Co. (Rahway, NJ)
    …multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in ... Rahway, New Jersey.The Process Engineer role at the Specialist level will serve as a leader in the...leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. --This role will support formulation and process… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Rahway, NJ)
    …multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in ... Rahway, New Jersey.The Process Engineer role at the Sr. Specialist level will serve as a leader in the...as a leader in the FLEx Sterile GMP Clinical Manufacturing facility. As the facility is nearing the completion… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Rahway, NJ)
    …Associate Specialist Engineer position is within our Company's Global Engineering Solutions (GES) organization, which is responsible for the design and ... manufacturing facilities and laboratories worldwide. We provide premier engineering solutions in the pharmaceutical industry through technical innovation and… more
    HireLifeScience (03/16/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone ... The Position This position has primary responsibility to support manufacturing operations. Focus areas may include Training, Documentation, Deviations, Change… more
    HireLifeScience (02/06/24)
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  • Merck & Co. (Rahway, NJ)
    …a high degree of technical and project management responsibility. The Senior Specialist - Process/Facility Engineering position will report to the Director, ... Job DescriptionThe Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual… more
    HireLifeScience (03/24/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Rahway based Senior Specialist , Global Development Quality Operations - API, is responsible for independent review and approval of documentation ... to support Good Manufacturing Practice (GMP) - clinical supply API manufacture, testing,...worldwide regulations and our Company procedures. - The Senior Specialist will become knowledgeable in regulatory requirements, cGMPs and… more
    HireLifeScience (03/23/24)
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  • Exela Pharma Sciences, LLC (Lenoir, NC)
    The QA Specialist II - Engineering /Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other ... are adhered to as it relates to review and approval of engineering /validation specific documentation. He/she must ensure all equipment installed, qualified or… more
    HireLifeScience (02/08/24)
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  • Merck & Co. (Rahway, NJ)
    Job Description- The Rahway based Specialist , Global Development Quality Operations - API,- is responsible for review and approval of documentation to support Good ... Manufacturing Practice (GMP) clinical supply API manufacture, testing, release...and other applicable worldwide regulations and our Company procedures.--The Specialist will become knowledgeable in regulatory requirements, cGMPs and… more
    HireLifeScience (03/23/24)
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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. ... Role Overview This position will be responsible for providing engineering support to implement and maintain computerized systems in the cGMP Clinical and Commercial… more
    HireLifeScience (03/22/24)
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  • Merck & Co. (Rahway, NJ)
    …and project management responsibility. The Equipment Development and Maintenance (EDM) Facility Specialist Engineering position will report to the Director, ... Job DescriptionDescriptionThe Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated… more
    HireLifeScience (03/15/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …collaborative team setting with quality and operations counterparts that include Manufacturing Operations, Quality Assurance, Engineering and Validation, Quality ... Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in...receipt, incoming inspection and release of materials required for manufacturing and release of patient material/final product of CAR-T… more
    HireLifeScience (03/13/24)
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  • Aequor (Thousand Oaks, CA)
    …team by collaborating with diverse functional areas including Supply Chain, Manufacturing , Quality Control, Quality Assurance, Regulatory, Quality Engineering , ... with responsibility in a quality, analytical development, process development, or manufacturing environment- at least 10 years exp. Familiar with pharmaceutical… more
    HireLifeScience (03/02/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …drive projects/programs forward in a matrixed environment. Build strong partnerships with Manufacturing , Engineering and Quality to ensure seamless execution of ... multiple myeloma. Legend Biotech is seeking a MFG Technical Specialist as part of the Technical Operations team based...the development and routine operation of a new CAR-T manufacturing process. They will be a subject matter expert… more
    HireLifeScience (01/20/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionPosition Description: Senior Specialist , Business Architect Our Research & Development Division Clinical and Real - World Evidence Generation ( CRWEG ... and Architecture ( PEAAr ) group is seeking a highly motivated Senior Specialist / Business Architect responsible for developing business architectur al models and… more
    HireLifeScience (03/06/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in 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 ... Raritan, NJ. Role Overview The QC Microbiology Specialist , Lentivirus Vector (LVV) CAR-T Manufacturing is...Requirements A minimum of a Bachelor's Degree in Science, Engineering or equivalent technical discipline is required A Minimum… more
    HireLifeScience (01/09/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a CQV Specialist or CQV Associate as part of the Technical Operations team based in ... and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be responsible in handling day-to-day activities… more
    HireLifeScience (01/24/24)
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