• Regulatory Affairs Project

    Abbott (St. Paul, MN)
    …catheters and software, vessel closure devices and peripheral stents. **The Opportunity** This ** Regulatory Affairs Project Manager ** position is an ... the Abbott Vascular Division. As an individual contributor, the function of a Regulatory Affairs Project Manager is to combine knowledge of scientific,… more
    Abbott (04/15/25)
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  • Regulatory Affairs Program…

    Philips (Plymouth, MN)
    The Regulatory Affairs Program Manager ...and a minimum of 3+ years' experience successfully leading Regulatory Affairs program/ project teams in ... accurate and timely tracking of regulatory activities and ensures validation of regulatory affairs software tools. **You're the right fit if:** + You've… more
    Philips (05/21/25)
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  • Senior Manager , Global Regulatory

    Otsuka America Pharmaceutical Inc. (St. Paul, MN)
    …experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, quality ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed. Works… more
    Otsuka America Pharmaceutical Inc. (04/23/25)
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  • Associate Director Regulatory

    Abbott (St. Paul, MN)
    …the Vascular Division. As a manager , the function of an Associate Director Regulatory Affairs is to combine knowledge of scientific, regulatory and ... devices, peripheral stents, and atherectomy devices. **The Opportunity** This **Associate Director Regulatory Affairs ** will work on-site at our St. Paul, MN… more
    Abbott (04/03/25)
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  • Principal Regulatory Affairs

    Medtronic (Minneapolis, MN)
    …experience or familiarity with software regulations and requirements. The **Principal Regulatory Affairs Specialist** develops strategies for worldwide product ... to ensure Diagnostics and EPG portfolio is aligned with existing portfolio. Maintain Regulatory Affairs product files to support compliance with regulatory more
    Medtronic (05/17/25)
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  • Senior Manager , CMC Global…

    Otsuka America Pharmaceutical Inc. (St. Paul, MN)
    …for CMC and GMP related submissions and inquiries. + Represents CMC RA in project team meetings and provides regulatory guidance and perspective to the ... Provide CMC regulatory strategy input and expertise in the area...marketed biologic and small molecule drug products to assigned project teams, to ensure Otsuka's products are developed/maintained in… more
    Otsuka America Pharmaceutical Inc. (04/25/25)
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  • Regulatory Compliance Manager

    Cardinal Health (St. Paul, MN)
    …of internal and external regulatory policies. Leverage broad knowledge of regulatory affairs , quality management systems and business operations to develop ... + Bachelor's degree in scientific or compliance field, eg, Legal, Regulatory Affairs , Engineering discipline, or equivalent work experience, preferred… more
    Cardinal Health (05/24/25)
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  • R&D Regulatory Manager

    Grifols Shared Services North America, Inc (St. Paul, MN)
    …8 or more years of experience in positions of increasing responsibility within Regulatory Affairs or related field within the Biologics, Biotech or ... Hiring Ordinance.** Learn more about Grifols (https://www.grifols.com/en/what-we-do) **Req ID:** 527460 **Type:** Regular Full-Time **Job Category:** Regulatory Affairs more
    Grifols Shared Services North America, Inc (05/02/25)
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  • Clinical Research Manager - CRM

    Medtronic (Minneapolis, MN)
    …be assigned. + Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval. + Studies must ... from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs , and European Clinical Groups) to drive clinical… more
    Medtronic (05/17/25)
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  • Senior Manager , Clinical Supply Chain

    Sumitomo Pharma (St. Paul, MN)
    …supplies on multiple clinical programs. In addition, working closely with CMC, Regulatory Affairs , Quality Assurance, Clinical Operations, and /or SMPA external ... motivated, and experienced individual for the position of **Senior Manager , Clinical Supply Chain** . The Senior Manager...local regulations. + Collaborate closely with Clinical Operations, CMC, Regulatory Affairs , QA, and PDM to ensure… more
    Sumitomo Pharma (05/20/25)
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