- ManpowerGroup (Plymouth, MN)
- …that consistently applies microbiological concepts to the manufacturing process of a medical device and understands and develops process monitoring/metrics to ... load configuration changes, design changes, etc.). * Knowledge of reusable device regulatory requirements. Develop and validate microbiological test methods.… more
- Actalent (Minneapolis, MN)
- … quality function. + Minimum of five years of related experience in medical device manufacturing. + Experience with continuous improvement, Lean Six Sigma, or ... Quality Engineer Job Description The Operations Quality...responsible for recommending and implementing process improvements to ensure regulatory compliance, with a strong focus on patient safety… more
- Danaher Corporation (Chaska, MN)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Familiarity with ISO13485, 21 CFR Part 820, ... System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Global Supplier Quality Engineer - Systems and Innovation for Beckman Coulter… more
- ManpowerGroup (Hopkins, MN)
- …equivalent with minimum of 4 years of experience in the life science or medical device industry.** + **An equivalent combination of experience and education may ... is partnering with a leader in the Pharmaceutical industry for a ** Quality Systems Coordinator.** **Job Title: Quality Systems Coordinator** **Location:… more
- Philips (Plymouth, MN)
- …discipline preferred + 5+ years of Supplier Quality Engineering experience in a medical device (Class II & III) or similar environment with manufacturing or ... that drive selection of the best suppliers based on all technical, quality and business (including cost) requirements throughout the product lifecycle. **Your… more
- Steris Corporation (Cottage Grove, MN)
- …13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. Quality Inspectors support manufacturing and servicing operations by ... ensure the proper documentation and disposition. They may also review other related Quality documentation such as device history or calibration records. Duties +… more
- Abbott (Plymouth, MN)
- …cross-functional teams, including Marketing, R&D, Field Operations, Risk Management, Reimbursement, Medical Affairs, Quality , and Regulatory Affairs. You ... Marketing, R&D, Program Management, Reimbursement, Medical Affairs, Risk Management, Quality and Regulatory Affairs, and investigational sites. + Oversee… more
- Abbott (Plymouth, MN)
- …cross-functional teams, including Marketing, R&D, Field Operations, Risk Management, Reimbursement, Medical Affairs, Quality , and Regulatory Affairs. You ... + Familiarity with relevant international regulatory requirements for medical devices including Quality Systems standards and clinical investigations.… more
- Abbott (Plymouth, MN)
- …types of product complaints + Independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory ... information into the complaint database; independently determining and filing appropriate medical devices reports with various regulatory agencies; participating… more
- US Tech Solutions (Maple Grove, MN)
- …engineering, highly preferred + Experience with design control, risk management, and medical device standards compliance + Experience with corrective and ... MN location. + This is an exciting opportunity to participate in the quality assurance of our medical electrical equipment/systems (MEE) within Interventional… more