- 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 (Plymouth, MN)
- …Good Manufacturing Practices (GMP) standards and navigate the complexity of government and medical device industry regulations including FDA 21 CFR Part 820, ISO ... close on - 9 Sep 2025 **Position Description:** Sr. Quality Engineer for Covidien, LP, (a Medtronic company) located...us. We advance healthcare, society, and equity with every design , inside and outside our walls. **Insight-driven care** .… more
- Abbott (Plymouth, MN)
- …for providing engineering leadership in the creation and the development of new medical device products (invasive and non-invasive). You will be accountable for ... Our business purpose is to restore health and improve quality of life by designing and providing device...primarily in R&D or clinical engineering. **Preferred Qualifications** + Medical device experience.. + Master's Degree in… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …in applying FDA design control requirements (21 CFR ) as applied to medical device software and medical device regulation (IEC-62304) ... new technology adoption. Therefore, a commitment to collaborative problem solving, sophisticated design , and the creation of quality products are essential. Your… more
- Actalent (Dassel, MN)
- …with Cretex Medical Quality System, ISO 13485 and when required medical device requirements. - Monitor the utilization of employee safety and OE programs ... - Support and comply with the company's Quality System, ISO, and medical ...fixture design , machine shop, fabrication machine shop, medical device Additional Skills & Qualifications -… more
- Medtronic (MN)
- …experience in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience -OR- + Associate's ... curriculum build utilizing the ADDIE model of adult instructional design . + Strongly influence the design of...a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience… more
- Actalent (Minneapolis, MN)
- …new product development for disposable medical devices. The role requires expertise in medical device design , focusing on Class II and Class III ... medical devices. + Ensure compliance with FDA Design Controls and ISO Quality Management Systems....Apply risk management practices as per ANSI/AAMI/ISO standards in medical device development. + Collaborate with cross-functional… more
- ManpowerGroup (Plymouth, MN)
- …that consistently applies microbiological concepts to the manufacturing process of a medical device and understands and develops process monitoring/metrics to ... maintain microbiological quality of the final device **.** *...**Qualifications:** Bachelors degree with 5+ years of experience with Medical device /pharmaceutical, or related industry with work… more
- Olympus Corporation of the Americas (Brooklyn Park, MN)
- …degree (Supply Chain Management, Engineering, Finance or equivalent) + Supply Chain and/or Medical Device quality certifications or training is desired. + ... years of experience in New Product Development support, Vendor negotiations, Purchasing and/or Quality functions, preferably in medical device or other… more
- Teleflex (Minneapolis, MN)
- …is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades ... with new and existing OEM customers to explain/recommend Teleflex Medical OEM's products, design capabilities, and production...* 1+ years of engineering experience with a leading medical device company preferred * Minimum of… more