• Aequor (Devers, TX)
    …have Quality Assurance experience with strong independent judgment. Job Description: Field QA Specialist Devens, MA This role is 100% Onsite Work Schedule: Mon - ... Fri, 2PM - 10PM EST JOB SUMMARY is seeking a Contractor Field QA Specialist for the QA Operations organization at the Single Use Facility (SUF) in Devens, MA. The… more
    HireLifeScience (03/28/24)
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  • Eisai, Inc (Nutley, NJ)
    …Job Summary Eisai is in the midst of an important launch of a new product in the US focused on educating HCPs on a treatment for appropriate individuals suffering ... mild cognitive impairment due to Alzheimer's disease (AD) or mild AD. TheNeurology Account Specialist (NAS) will be part of a diverse team of sales professionals who… more
    HireLifeScience (03/28/24)
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  • Aequor (Thousand Oaks, CA)
    …drug product development, manufacturing, and/or Quality Control Testing. As a Product Quality (PQ) Quality Assurance (QA) Specialist , you will actively ... at least 10 years exp. Familiar with pharmaceutical sciences, quality, compliance and regulatory requirements, associated with biologics and synthetic chemical… more
    HireLifeScience (03/02/24)
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  • Merck & Co. (Rahway, NJ)
    …high degree of technical and project management responsibility. The Senior Specialist - Process/Facility Engineering position will report to the Director, ... production, utility systems and associated infrastructure.-Responsibilities of the Senior Specialist - Process/Facility Engineer include the following:The process engineer… more
    HireLifeScience (03/24/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Senior Specialist , Process Engineer The Small Scale Organics (SSO) Pilot Plant is a Good Manufacturing Practices (GMP) facility ... operational experience to support facility operations, process development activities, compliance investigations/change management, authoring of GMP documentation, and lead… more
    HireLifeScience (03/26/24)
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  • Merck & Co. (Durham, NC)
    …issues to improve manufacturing performance, and maintaining the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must ... Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist ...system(s) to ensure a compliant, reliable supply of the product and on-time project execution. Provide production shop floor… more
    HireLifeScience (03/22/24)
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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 ... procedures, equipment and systems, and/or facilities to ensure the compliance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs)… more
    HireLifeScience (03/23/24)
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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 ... procedures, equipment and systems, and/or facilities to ensure the compliance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs)… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Rahway, NJ)
    …Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing ... in Rahway, New Jersey.The Process Engineer role at the Specialist level will serve as a leader in the...procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Rahway, NJ)
    …change management.Familiarity with United States and European Union GMP and Safety compliance regulations.Ability to convert new drug product attributes and ... is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply...Rahway, New Jersey.The Process Engineer role at the Sr. Specialist level will serve as a leader in the… 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. ... a strong, compliant program to enable robust production, testing and release of product to patients. Key Responsibilities Acts as the subject matter expert (SME) for… more
    HireLifeScience (03/22/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's products and ... Maintains up-to-date awareness in the areas of literature-related copyright compliance , adverse event reporting, and information storage and retrieval systems.-… more
    HireLifeScience (03/22/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …of multiple myeloma. Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role Overview The ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...materials required for manufacturing and release of patient material/final product of CAR-T at Raritan, NJ Legend manufacturing site.… more
    HireLifeScience (03/13/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …floor. Essential Functions Reviews all manufacturing and support records to certify compliance with specifications and procedures Releases product based on ... a global supply of our hemophilia and growth hormone product lines, as well as our next generation of...of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI… more
    HireLifeScience (03/20/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …in Monmouth Junction, New Jersey, Tris has an immediate opening for a QA Specialist I/II - Documentation. Job title and level determination will be commensurate with ... experience.The Specialist I/II, Quality Assurance (QA) Documentation supports and assists the QA function in ensuring manufacturing quality controls and procedures… more
    HireLifeScience (02/29/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking Metrology Specialist as part of the Maintenance & Metrologyteam based in Raritan, NJ. ... cross functional groups to enable robust production, testing and release of product to patients. Key Responsibilities Provides technical expertise in support of an… more
    HireLifeScience (02/15/24)
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  • Merck & Co. (North Wales, PA)
    …importance, time sensitivity, and impact which is critical to maintaining regulatory compliance . This team also monitors a list of relevant industry topics that ... Drugs, Digital Health Technologies, and/or Medical Devices for both new product development for initial registration and maintenance of registrations.- Broad… more
    HireLifeScience (02/28/24)
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  • Merck & Co. (Rahway, NJ)
    …is accountable for developing labeling content and maintaining the target product labeling for developmental products, Core Labeling documents (eg, CCDS, CCPPI, ... Providing labeling expertise and guidance to teams while ensuring compliance with applicable regulatory requirements- Serving as regulatory labeling point… more
    HireLifeScience (03/02/24)
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  • Exela Pharma Sciences, LLC (Lenoir, NC)
    Specialist II - Engineering/Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other regulatory ... Experience Requirements Must possess strong knowledge of sterile drug product manufacturing.Must be detail-oriented with exceptional planning and organizational… more
    HireLifeScience (02/08/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. We ... will reviews manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This… more
    HireLifeScience (02/29/24)
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