• Quality Agreement Specialist

    ThermoFisher Scientific (Pittsburgh, PA)
    …**Experience** + Minimum of 3+ years of experience in quality assurance or regulatory affairs , preferably in the pharmaceutical, biotechnology, or medical ... are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our… more
    ThermoFisher Scientific (10/12/25)
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  • Sr. Quality Engineer

    Envista Holdings Corporation (Brea, CA)
    …whether to accept the product and future purchases from the vendor. + Supports Regulatory Affairs with their activities related to submissions and notified body ... to develop, implement, and maintain quality assurance protocols that comply with regulatory requirements an industry standard. The Sr. Quality Engineer will possess… more
    Envista Holdings Corporation (11/15/25)
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  • Sr. Director Clinical Development - Lilly Gene…

    Lilly (Indianapolis, IN)
    …+ Capable of representing Lilly Gene Therapy professionally with external global opinion leaders, investigators, vendors, regulatory agencies, and others ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
    Lilly (11/07/25)
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  • Associate Product Manager (Approx. 3-6 Months)

    Kelly Services (Brea, CA)
    …implementation of changes. + Partner with internal teams-including design, planning, regulatory affairs , quality, and marketing-and external suppliers to ... Rate:** $41.34/hour - $50.48/hour **Job Summary** Reporting to the Senior Global Product Manager, the **Associate Product Manager (Temporary)** is responsible for… more
    Kelly Services (10/23/25)
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  • Senior Manufacturing Quality Engineer

    Cook Medical (Bloomington, IN)
    …with cross function teams including quality, engineering, production, clinical, and regulatory affairs .- Provide leadership in the understanding of medical ... processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements. Must work and interact effectively and professionally with and for others… more
    Cook Medical (11/22/25)
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  • Field Reimbursement Manager - Shockwave (West)

    J&J Family of Companies (Santa Clara, CA)
    …Cross-Functional Collaboration** + Collaborate with Market Access, Health Economics, Medical Affairs , and Compliance teams. + Provide field insights on reimbursement ... Perform other duties as required. + Ensure compliance with corporate and regulatory requirements. **Requirements** + Bachelor's degree in Business, Economics, or a… more
    J&J Family of Companies (11/21/25)
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  • Product Manager

    Robert Half Finance & Accounting (Newberg, OR)
    …development from design to commercialization, ensuring quality and compliance. * Partner with regulatory affairs to meet global standards and ensure ... Newberg, Oregon. This role involves driving product innovation, ensuring regulatory compliance, and collaborating with cross-functional teams to deliver high-quality… more
    Robert Half Finance & Accounting (11/08/25)
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  • Associate Manager, Clinical Trial Reimbursement

    Abbott (Austin, TX)
    …Healthcare Economics, Clinical Operations, Clinical Data Science and Analytics, Marketing, Regulatory , Legal, Clinical Affairs , Research and senior management to ... Abbott is a global healthcare leader that helps people live more...Payer) to provide coverage and reimbursement guidance for Investigational Device Exemption (IDE), Post Approval Study (PAS)/Post Market Study… more
    Abbott (10/25/25)
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  • Neuroscience LTC Specialist - Shreveport, LA/…

    Otsuka America Pharmaceutical Inc. (Jackson, MS)
    **Job Summary** Otsuka America Pharmaceutical Inc. is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better ... with other local Neuroscience Specialists and cross functional colleagues in Medical Affairs (MSLs) and Market Access (RAMs) under appropriate guardrails. You will… more
    Otsuka America Pharmaceutical Inc. (11/25/25)
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  • Project Coordinator

    Mentor Technical Group (Gurabo, PR)
    …and company SOPs. + Collaborate with cross-functional teams including R&D, QA/QC, Regulatory Affairs , and Manufacturing. Qualification: + Bachelor's degree in ... and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico,… more
    Mentor Technical Group (11/01/25)
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