- Fujifilm (St. Paul, MN)
- …and advertising regulations and other regulations specific to Life Sciences/Pharma and Medical Device companies. + Perform other duties as assigned. **Required ... corporate law firm and/or in-house legal department, preferably in the Life Sciences/Pharma, Medical Device or health care field. + Solid commercial contract… more
- Abbott (Maple Grove, MN)
- …**Preferred** **Qualifications** + Advanced degree + 2-5+ years' experience in medical device or pharmaceutical clinical research studies. + Experience ... analysis datasets, tables, listings, and figures (TLFs). + Conduct quality checks of datasets against source data and validate...working on medical device clinical studies in highly regulated… more
- Danaher Corporation (Chaska, MN)
- …to manage medium/large design changes and technology transfer projects in the Medical Device or Diagnostics regulatory environment, ensuring compliance ... experience leading multiple projects/a project manager + Prior experience in Medical Device manufacturing environments + Change Management Certification desired… more
- Abbott (Plymouth, MN)
- …position works out of our Plymouth MN location for our Electrophysiology Medical Device business. In Abbott's Electrophysiology (EP) business, we're advancing ... Ability to travel approximately 10%, including internationally **Preferred Qualifications** Medical device industry experience preferred Masters' degree… more
- Medtronic (Mounds View, MN)
- …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical devices. ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...for all ablation procedures at study sites for investigational device studies to guide the physician on the requirements… more
- Medtronic (Mounds View, MN)
- …specifically on ensuring the Surgical product portfolio achieves initial European Union Medical Device Regulation (EU MDR) and UK Conformity Assessed (UKCA). ... the product lifecycle. This role collaborates closely across R&D, Regulatory , Quality , Clinical, Operations, Manufacturing, and Supply...+ Knowledge in product development and commercialization in the medical device industry + PMP or PgMP… more
- Teleflex (Plymouth, MN)
- …is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades ... motivate team and supports development and experiences * Ensure Quality , Regulatory , and EHS policies and procedures...Minimum of 7+ years of experience supporting manufacturing in medical device industry or other highly regulated… more
- Medtronic (Minneapolis, MN)
- …the following tasks: + Product Security - Implement security requirements across the medical device development lifecycle by collaborating with teams to uphold ... with strong key management and the use of Hardware Security Modules (HSMs) for medical device protection. + Use of advanced methods like LLMs, Deep learning… more
- Abbott (St. Paul, MN)
- …Work with Product Development to ensure Design for Manufacturability in the electromechanical medical device space. + Analyze and solve problems from basic ... work experience. + Minimum 5 years manufacturing engineering experience. Medical device experience required. International manufacturing experience preferred.… more
- Abbott (Plymouth, MN)
- …position works out of our Plymouth MN location in the Electrophysiology medical device division. In Abbott's Electrophysiology (EP) business, we're advancing ... + Ability to maintain regular and predictable attendance **Preferred Qualifications** + Medical device experience preferred, but not required Apply Now… more