• Vice President, Perioperative Ambulatory…

    Sutter Health (Los Altos, CA)
    …Division currently generates $4.5 billion in revenue, with the Palo Alto Medical Foundation (PAMF) accounting for nearly $3.5 billion-making it the largest ... and Ambulatory Surgery. These ancillary operations represent 1/3 of the Palo Alto Medical Foundation's (PAMF) annual revenue. As the foundation enters a period of… more
    Sutter Health (08/13/25)
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  • Associate Director, Clinical Program Quality…

    Takeda Pharmaceuticals (Boston, MA)
    …of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, ... for clinical deviation management, and Serious Breaches investigation and reporting to regulatory agencies. + Act as strategic partner to Clinical Program Quality… more
    Takeda Pharmaceuticals (07/16/25)
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  • Sr. Project Manager, Project Management Office…

    Terumo Neuro (Aliso Viejo, CA)
    …Stakeholder Management + Collaborate closely with cross-functional teams, including R&D, regulatory affairs , manufacturing, quality assurance, and marketing, to ... Professional (PMP) certification is highly desirable. 3. Strong knowledge of medical device development processes, regulatory requirements, and quality… more
    Terumo Neuro (07/15/25)
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  • Scientist, Analytical Operations

    Gilead Sciences, Inc. (Oceanside, CA)
    …& Manufacturing (PDM) and partner with Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs , Clinical Development, and Technical Development to ensure ... development across all stages-from early development to commercial launch-as well as regulatory filing experience with the FDA and EMA. A deep understanding of… more
    Gilead Sciences, Inc. (09/19/25)
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  • Sr. Supplier Quality Engineer

    Teleflex (Morrisville, NC)
    …representative during acquisitions, collaborating with teams in Quality Assurance, Regulatory Affairs , Supply Chain, Design, and Manufacturing. Additionally, ... 25% **Requisition ID** :12690 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health… more
    Teleflex (09/11/25)
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  • Regional Sales Specialist

    Zimmer Biomet (Englewood, CO)
    …and shipping problems, product upgrades or price adjustments, as required. + Advise Regulatory Affairs of priority complaints or those that involve regulatory ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...Paragon 28, a Zimmer Biomet Company focused on orthopedic medical devices for the foot and ankle, is looking… more
    Zimmer Biomet (09/10/25)
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  • Materials Management Program Manager

    LifeCenter Northwest (Bellevue, WA)
    …with LifeCenter policy, applicable standards, and regulations. + Assists Quality & Regulatory Affairs with environmental monitoring of storage areas including ... + Maintains current safety data sheets for all hazardous materials. + Maintains medical waste destruction log and hazardous material disposal logs as appropriate. +… more
    LifeCenter Northwest (09/10/25)
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  • Director, Global Strategic Marketing, Tri-Specific…

    J&J Family of Companies (Raritan, NJ)
    …strategies, tactics, customer solutions and messaging. + Work closely with Medical Affairs to ensure robust publication plans and enduring/differentiating ... support/bolster reimbursement and approvals globally. + Work with R&D and Regulatory to bring commercial insight, develop/strengthen the Target Product Profile… more
    J&J Family of Companies (09/06/25)
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  • Program Manager, Robotics Surgical Technology, RPE…

    Medtronic (North Haven, CT)
    …role, you'll lead a dynamic team, collaborating across departments like R&D, Quality Affairs , and Marketing to spearhead a series of successful RPE project release. ... balancing time, schedule, cost, and quality, while adhering to safety and regulatory standards. + Manage project financials, including forecasting and tracking of… more
    Medtronic (09/05/25)
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  • Technical Writing Manager - CRM

    Medtronic (Mounds View, MN)
    …and development opportunities + Partner with marketing, geographies, clinical, legal, regulatory affairs , packaging and labeling, sales force, supply chain, ... documentation control, translation teams, regulatory agencies, etc. in support of both the CRDN...required with a minimum of 5 years of technical, medical or scientific writing/communications experience + Or Masters degree… more
    Medtronic (09/05/25)
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