- Abbott (St. Paul, MN)
- …in the Cephea division. Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- 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
- Actalent (Minneapolis, MN)
- …of CGMP regulations. + Experience in quality engineering, particularly in the medical device sector. Additional Skills & Qualifications + Quality ... Engineer experienced with internal or external auditing to ensure compliance with internal Quality Management System (QMS)...for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… 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, ... systems throughout the product lifecycle and deliver sustained improvements in quality , delivery, cost, and compliance . The essential requirements of the… 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, ... and suppliers to develop and implement robust risk mitigation plans addressing quality , compliance , and supply continuity risks. + Collaborate with… more
- ManpowerGroup (St. Michael, MN)
- Manpower Engineering is partnering with a leader in the Medical Device industry for a Manufacturing Quality Technician. **Job Title: Manufacturing Quality ... (supplier NCR) and the NCR linked to his/her scope of activities, assuring compliance to and providing guidance regarding interpreting ISO 13485 & FDA standards in… 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, ... and suppliers to develop and implement robust risk mitigation plans addressing quality , compliance , and supply continuity risks. + Collaborate with… more
- Astrix Technology (St. Paul, MN)
- …Our client is seeking a **CMM Quality Technician I** with **2-4 years of quality experience** in manufacturing ( medical device a plus). This role offers ... results and maintain accurate records. + Support calibration, audits, and quality system compliance . **Qualifications** + 2-4 years of quality experience in… more
- ManpowerGroup (St. Paul, MN)
- …experience + Strong communication, teamwork, and organizational skills + Experience in medical device industry preferred + Knowledge of risk management, ImV/TMV, ... design verification/validation, process validation, and support for CAPA and QMS compliance . **Key Responsibilities** + Support or lead quality efforts… more
- US Tech Solutions (Maple Grove, MN)
- …Process controls + Must have experience in a regulated environment. **Preferred:** + Medical Device experience **About US Tech Solutions:** US Tech Solutions is ... Quality into all aspects of their work by maintaining compliance to all quality requirements. **Qualifications** + 4-6 Years experience with BS in… more