- ManpowerGroup (Hendricks, MN)
- Our client, _a leader in healthcare solutions_ , is seeking a ** Medical Device Quality Associate ** to join their team in **South Brookings, SD** . As a ... Medical Device Quality Associate , you will be part of the Quality Assurance department supporting manufacturing and compliance efforts. The ideal… more
- ICON Clinical Research (Arden Hills, MN)
- Study Start Up Associate II - Medical Device - Arden Hills, MN ICON plc is a world-leading healthcare intelligence and clinical research organization. We're ... and education. + 2+ years' experience in clinical/scientific research and medical device experience, specifically clinical study site start-up experience… more
- GRAIL (St. Paul, MN)
- …development, clinical affairs, quality , or program management within the IVD, medical device , or pharmaceutical industries is required. + Regulatory affairs ... + Demonstrated knowledge of US and international regulatory frameworks and processes for medical device development and approvals is required. + Strong written… more
- GovCIO (St. Paul, MN)
- **Overview** GovCIO is seeking an Associate Service Desk Technician - Tier I to deliver exceptional first-tier technical support to our nation's Veterans. to provide ... delivering outstanding customer service while assisting users with mobile device setup, application support, login troubleshooting, and basic hardware/software… more
- Teleflex (Minneapolis, MN)
- …ability to be detail-oriented, organized, and productive with a keen interest in medical device and biologics research. **Principal Responsibilities** * Manage a ... Clinical Research Associate Manager (REMOTE) **Date:** Dec 19, 2025 **Location:**...experience. * Minimum 8 years of clinical research experience, medical device experience preferred. This should includes… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... intelligence management Standard Operating Procedures or work practices. + Review overall quality of ad hoc query research for requested regulatory topics and… more
- Cretex (Brooklyn Park, MN)
- …into the ERP system on a timely basis + Support and comply with the company Quality System, ISO, and medical device requirements + Read, understand, and ... is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in… more
- Fotona (Minneapolis, MN)
- …in the aesthetic laser market. Aesthetic Industry experience, Capital Equipment, Durable Medical Equipment, Medical Device sales experience, and high-volume ... in the Aesthetic industry preferred. + Aesthetic Industry, Capital Equipment, Durable Medical Equipment, and/or Medical Device sales experience preferred.… more
- Cretex (Dassel, MN)
- …etc. * Perform equipment set-ups as required * Support and comply with the company Quality System, ISO, and medical device requirements * Read, understand, ... contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us...engineering technician * Knowledge of Good Manufacturing Practices & Quality Systems Regulations is desirable * Medical … more
- Cretex (Coon Rapids, MN)
- …etc. + Perform equipment set-ups as required + Support and comply with the company Quality System, ISO, and medical device requirements + Read, understand, ... to prioritize and multitask Desirable Criteria & Qualifications + Associate Degree in Engineering + 3-5 years of engineering...when required - Supports and complies with the company-s Quality System, ISO, and medical device… more
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