- Actalent (Minneapolis, MN)
- Labeling Specialist Job Description * Develop and...a fast-paced environment. Hard Skills + 3-5 Years of Medical Device Labeling + Technical Writing ... Manage Labeling : Create, revise, and maintain labeling , including user manuals, quick-start guides, labels, and other technical documents. * Regulatory… more
- Medtronic (Mounds View, MN)
- …and other duties may be assigned.** + Creates, reviews, and reproduces text required for labeling medical products. + Ensures that labeling , art, film, and ... Illustrator and/or other graphic design programs * Knowledge of US and international medical device regulations and standards, especially those related to … more
- Actalent (Minneapolis, MN)
- Labeling Specialist Job Description: We are seeking a highly motivated and organized Labeling Specialist to join our team. The ideal candidate will be ... 3-5 years of experience in technical writing or technical communications within the medical device industry. + Proficiency in Adobe InDesign and Microsoft Office… more
- Abbott (Plymouth, MN)
- …help of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly with ... ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
- Medtronic (Minneapolis, MN)
- …minimum of 5 years of relevant experience + Or minimum 5 years of medical device regulatory affairs experience with Master's degree **Preferred experience:** + ... affairs support for Class I, II and Class III medical devices. The Sr Principal Regulatory Affairs Specialist...4+ years of medical device industry experience with US FDA… more
- Medtronic (Minneapolis, MN)
- …profile_ + Bachelor's degree in a technical discipline + Minimum 4 years of medical device regulatory experience with Bachelor's degree + Or minimum 2 years ... predictable procedure times and outcomes. The **Senior Regulatory Affairs Specialist ** develops strategies for worldwide product registration with global...of medical device regulatory experience with an advanced… more
- Teleflex (Maple Grove, MN)
- …Remote based **Principal Responsibilities** * Conduct regulatory review and approval of medical device marketing materials, including labeling , advertising, ... Regulatory Affairs Specialist **Date:** Sep 14, 2024 **Location:** Maple Grove,... will develop strategies, submissions, and regulatory reviews of medical device marketing materials for Teleflex … more
- Abbott (St. Paul, MN)
- …may be used in lieu of direct regulatory experience. + 5+ years' experience in Medical Device industry + 3-5 years of regulatory experience. + Think analytically ... may include (choose applicable areas and expand as appropriate). + Medical writing, Advertising and promotion, Labeling , Controlled substances (eg… more
- Cardinal Health (Roseville, MN)
- …attention to detail + Ability to lift between 30-45 lbs. + Pharmaceutical or medical device experience a plus + ISO experience a plus **_Work Environment_** ... release, facilities and equipment, material controls, laboratory controls, packaging and labeling , and production & process controls. + Establishes and reports… more