- Teleflex (Minneapolis, MN)
- …Cardiology environment. - Medical Device industry supporting Clinical and Medical Affairs , strongly preferred. - Proficient in Microsoft Word, Excel, and ... with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which… more
- Oracle (St. Paul, MN)
- …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
- Philips (Plymouth, MN)
- **Intern - Regulatory Affairs - Minneapolis, MN - Summer 2026** We welcome individuals who are currently pursuing an undergraduate degree in engineering to join ... Philips as a Regulatory Affairs Intern in our Minneapolis location...**Your role** Join Philips Image Guided Therapy (IGT), a medical device manufacturer offering healthcare solutions in… more
- Abbott (Plymouth, MN)
- …of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly ... affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device , pharmaceutical, or… more
- Medtronic (Mounds View, MN)
- …**A Day in the Life** Join the Medtronic Cardiac Ablation Solutions (CAS) regulatory affairs team of innovators who bring their worldview, unique backgrounds, ... be based in Mounds View, MN The ** Associate Regulatory Affairs Specialist** will work under the...health profession, science and/or engineering field + Experience in medical device industry + Demonstrated technical writing… more
- Medtronic (Mounds View, MN)
- …Have: Minimum Requirements** + Bachelors degree with 4+ years of regulatory affairs experience in the medical device , biotech or pharmaceutical industry ... OR a Masters degree with 2+ years of regulatory affairs experience in the medical device , biotech or pharmaceutical industry. **Nice to Have** +… more
- Abbott (Plymouth, MN)
- …etc.), math, engineering, or medical fields. + Master's degree in Regulatory Affairs . + Regulatory experience with capital equipment including ... on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced ** Regulatory Affairs Specialist II** to join our team on-site in Plymouth,… more
- Medtronic (Fridley, MN)
- …seeking a dynamic and experienced communications professional to join our Clinical Research, Medical Science, and Regulatory Affairs organization. As a ... biotech) + Experience with global regulatory requirements + Experience with medical device industry groups **Physical Job Requirements** The above statements… more
- Bausch + Lomb (St. Paul, MN)
- …+ Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device , cosmetics or ... and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
- Bio-Techne (Minneapolis, MN)
- …disease worldwide.** Pay Range: $62,300.00 - $102,350.00 **POSITION SUMMARY** Responsible for regulatory affairs activities to assist in regulatory ... submission, annual reports, registrations, and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance, and standards.… more
- Stryker (Bloomington, MN)
- …out Stryker's mission to make healthcare better. **Opportunities Available** As a Regulatory Affairs Intern, you will gain exposure to regulatory and ... legal frameworks, requirements, and processes that guide medical device development and compliance. In this role, you will support activities such as gathering… more
- Edwards Lifesciences (Minneapolis, MN)
- …the ground up. **How you'll make an impact:** + As a key member of the Medical Affairs Clinical Science team, the Senior Manager (formal internal title is Senior ... Manager, Medical Affairs ) is responsible for providing scientific...across TMTT. The Senior Manager will be an experienced medical device professional with strong scientific acumen… more
- Teleflex (Minneapolis, MN)
- …Cardiology environment. * Medical Device industry supporting Clinical and Medical Affairs , strongly preferred. * Proficient in Microsoft Word, Excel, and ... with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which… more
- Fujifilm (St. Paul, MN)
- …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to healthcare… more
- Veterans Affairs, Veterans Health Administration (Minneapolis, MN)
- …soft goods, as deemed appropriate and prescribed by VA and medical facility policies, procedures and treatment plans. Responsibilities This position involves ... the full performance level without further competition when all regulatory , qualification, and performance requirements are met. Selection at...Whole Health System of care in each of the Medical Centers. This is an approach to healthcare that… more
- Abbott (Maple Grove, MN)
- … Affairs departmental responsibilities and processes + Familiarity of medical device regulatory requirements and submission/registration activities. + ... Regulatory Services managing projects related to harmonized regulatory processes in Abbott's Medical Device...Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) + 5+ years'… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory… more
- Abbott (Maple Grove, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives… more
- Abbott (Plymouth, MN)
- …cross-functional teams, including Marketing, R&D, Field Operations, Risk Management, Reimbursement, Medical Affairs , Quality, and Regulatory Affairs ... communication between Sales and Marketing, R&D, Program Management, Reimbursement, Medical Affairs , Risk Management, Quality and Regulatory Affairs , and… more
- Abbott (Maple Grove, MN)
- …stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs , medical affairs as well ... clinical studies. . Familiarity with quality system environments. . Strong background in medical device clinical trials. . Knowledge of MDR requirements and… more
