- ManpowerGroup (St. Paul, MN)
- …experience + Strong communication, teamwork, and organizational skills + Experience in medical device industry preferred + Knowledge of risk management, ImV/TMV, ... **Title:** Development Quality Engineer II **Location:** St. Paul, MN **Duration:**...V&V, and manufacturing reviews + Ensure DHF completeness and regulatory compliance + Review document changes and support CAPA… more
- Integer Holdings Corporation (Brooklyn Park, MN)
- …and Responsibilities 1. Adheres to Integer Core Beliefs and all safety and quality requirements including but not limited to: Quality Management Systems (QMS), ... (FDA) regulations, Company policies and operating procedures, and other regulatory requirements. 2. Uses standard measuring tools, measuring machines, and… more
- Xylem (Chaska, MN)
- …in a Science or Engineering field, or equivalent work experience * 5+ years of Medical Device Regulatory Affairs experience, domestic and international * 3 ... countries. This role ensures our products meet all applicable regulatory standards for safety, efficacy, and quality ....activities as well as other deliverables as related to medical device projects * Review and approve… more
- Medtronic (Mounds View, MN)
- …plays a critical role in ensuring the security of Medtronic Surgical Operating Unit medical device solutions. Reporting to the Director of Product Security, this ... and patients. _Make your impact by exploring a career with the world's leading Medical Device company, striving "to alleviate pain, restore health, and extend… more
- Medtronic (Mounds View, MN)
- …complying with government regulations. + Evaluate incoming information to determine Medical Device Reporting and Vigilance reporting eligibility. + Ensure ... results for Medtronic products to determine complaint status and regulatory reporting status in conjunction with US and OUS...complete, accurate, and timely submission of Medical Device Reports (MDRs), Vigilance Reports (VR)… more
- ManpowerGroup (Plymouth, MN)
- …hired on** **Summary** This position is responsible for the production of high quality medical devices within a manufacturing cell. Working under close ... on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. **Responsibilities** + Performs routine assignments… more
- ManpowerGroup (Minnetonka, MN)
- …hired on **Summary** This position is responsible for the production of high quality medical devices within a manufacturing cell. Working under close ... on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. **Responsibilities** Performs routine assignments… more
- Bausch + Lomb (St. Paul, MN)
- …Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and Clinical ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… 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 ... relevant experience in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience + OR- +… 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