- Owens & Minor (St. Paul, MN)
- …of statistics, Minitab and/or other statistical software experience * Experience in a medical device manufacturing environment preferred * Medical Device ... our teammates. Owens & Minor teammate benefits include: + Medical , dental, and vision insurance, available on first working...in a manufacturing environment preferred * American Society for Quality (CQA, CQBA, CQE, CQM/OE) and/or Regulatory … more
- Patterson Companies, Inc. (St. Paul, MN)
- …work experience + 2-4 years' experience with quality management systems and regulatory compliance in the medical device or related regulated field ... + Prepare metrics and provide updates related to supplier quality + Helps to interpret and apply regulatory...programs and rewards for our eligible employees: + Full Medical , Dental, and Vision benefits and an integrated Wellness… more
- Medtronic (Brooklyn Center, MN)
- …engineering + Recent experience in a regulated industry such as automotive, aerospace, or medical device + Medical device experience strongly preferred ... ensure future generations live better, healthier lives. As a member of Supplier Quality Engineering at Medtronic Energy and Component Center (MECC), you will be… more
- Olympus Corporation of the Americas (Brooklyn Park, MN)
- …components, and sub-assemblies to ensure compliance with company policies and procedures and medical device regulations. The Product Quality Engineer will ... in Quality Engineering within an FDA regulated medical device manufacturing environment. + Strong working...Notes: || United States (US) || Minnesota (US-MN) || Brooklyn Park || Quality & Regulatory Affairs… more
- Danaher Corporation (Chaska, MN)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Certifications such as CQE, CQA, Six Sigma, ... qualifications, and ongoing performance assessments to ensure adherence to internal quality standards, customer requirements, and applicable external regulatory … more
- Philips (Plymouth, MN)
- …if:** + You have a minimum of 8+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of ... have extensive experience supporting the creation and review of all medical device documentation including- Safety Classification, Design Verification… more
- Danaher Corporation (Chaska, MN)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Certifications such as CQE, CQA, Six Sigma, ... qualifications, and ongoing performance assessments to ensure adherence to internal quality standards, customer requirements, and applicable external regulatory … more
- Abbott (Plymouth, MN)
- …computer skills, including data analysis and report writing skills. **Preferred** + Prior medical device experience **Learn more about our health and wellness ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Minnetonka, MN)
- …TUV regulations, and other relevant clinical/ regulatory requirements. Class III or II medical device background in a Quality Leadership role. Quality ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Minnetonka, MN)
- …skills, as well as attention to detail **Preferred** + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more