• Associate Director, Device Clinical Development

    Takeda Pharmaceuticals (Lexington, MA)
    …(CAPAs) **Clinical Trial Support:** + Develop device-specific training materials and review protocols for clinical trials + Implement train-the-trainer programs for ... input is incorporated throughout the design control processes + Review and approve user requirements, design specifications, and verification/validation plans… more
    Takeda Pharmaceuticals (09/04/25)
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  • Capital Project Engineer

    AbbVie (Worcester, MA)
    …to work on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Demonstrates judgment within defined ... procedures. + Reviews mechanical design of all vendor-fabricated equipment, including review and approval of all vendor submittals with internal stakeholders, and… more
    AbbVie (09/04/25)
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  • Lead Pharmacovigilance QC Specialist

    United Therapeutics (Concord, NH)
    …are as follows:** **Who we are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
    United Therapeutics (08/21/25)
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  • IFS ERP Financial Analyst

    Teledyne (Daytona Beach, FL)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... Assist with new implementations, requirements gathering, analysis, and support. + Review , analyze, evaluate, and document business requirements. + Configure and… more
    Teledyne (08/20/25)
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  • Director/Sr Director/Executive Director - TS/MS…

    Lilly (Indianapolis, IN)
    …Lilly, a leading innovation-driven corporation is developing a growing portfolio of pharmaceutical products by applying the latest research from its own worldwide ... process performance improvements, or control strategy effectiveness. Provide proficient data analysis and conclusions considering technical, Regulatory and Quality… more
    Lilly (08/20/25)
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  • Production Engineer I, II, III or Sr. (Days 8am…

    LSI Solutions (Victor, NY)
    …process reports by collecting, analyzing, and summarizing information and trends. + Review of component designs and identification of Design for Manufacturing and ... Able to define statistical sample sizes as related to variable and attribute data , based on established company and industry standards. + Advanced experience Design… more
    LSI Solutions (08/19/25)
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  • Principal Serialization Automation Engineer

    Takeda Pharmaceuticals (Round Lake Beach, IL)
    …production downtime. Proactively identify and implement system improvements through data analysis, technical expertise, and industry best practices to enhance ... modifications to meet design and reliability standards. + Develop and review automation strategies for manufacturing processes, support equipment, and systems. This… more
    Takeda Pharmaceuticals (08/15/25)
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  • Pharmacist

    Covenant Health Inc. (Lenoir City, TN)
    …provide care, including factors related to patients of all groups. + Provides pharmaceutical care by collaborating with physicians, nurses, and other members of the ... + Documenting medication related issues in patient chart + Interpreting laboratory data + Reviewing medication profiles + Monitoring pharmacokinetics of drug therapy… more
    Covenant Health Inc. (08/14/25)
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  • Integrated Lab Solutions Technician - Life…

    CBRE (King Of Prussia, PA)
    …As a CBRE Integrated Laboratory Solutions Technician, you will support a pharmaceutical client with maintaining and managing lab development equipment. This job is ... Manage and improve the service logging process and asset database. Create, and review supporting documentation like service reports. + Track the performance of the… more
    CBRE (08/14/25)
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  • Automation Engineer

    Hovione (East Windsor, NJ)
    …as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market. Our people ... URS and design specifications - Contribute to the design review phase of the Engineering projects to ensure that...her / his responsibility, based on multiple sources of data . - On hand-over, guarantee that deliverables were fully… more
    Hovione (08/08/25)
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