Carrie Berge Email & Phone Number
Contractor - Regulatory Affairs Specialist @ Sterilmed, a Johnson & Johnson Company
Carrie Berge's Location
Wyoming, MN, US
Carrie Berge's Work
- Contractor - Regulatory Affairs Specialist @ Sterilmed, a Johnson & Johnson Company
- Regulatory Affairs and Quality Systems Consultant @ Medavise
- Regulatory Affairs and Quality Systems Consultant @ Consultant
- Quality Assurance and Regulatory Compliance Manager @ Exos LLC, a DJO Global Company
- Quality Manager @ I-TEK Medical Technologies
- Quality Manager @ Enova Medical Technologies
- Project Manager @ Synovis Surgical Innovations
- Documentation Coordinator Supervisor @ CareFusion GmbH
- Sr. Process Analyst @ Qwest Communications
Carrie Berge's Education
- University of St. Thomas - Opus College of Business
Certificates (Project Management and Technical Writing)
- Gustavus Adolphus College
B. A. (Biology / Distributive Science)
- University of Minnesota-Twin Cities
M.S. (Food Science)
Carrie Berge's Skills
- Design Control
- 21 CFR
- ISO 14971
- GMP
- ISO
- Regulatory Affairs
- Supplier Quality
- Software Documentation
- Validation
- Medical Devices
Carrie Berge's Summary
Carrie Berge, based in Wyoming, MN, US, is currently a Contractor - Regulatory Affairs Specialist at Sterilmed, a Johnson & Johnson Company, bringing experience from previous roles at Medavise, Consultant, Exos LLC, a DJO Global Company and I-TEK Medical Technologies. Carrie Berge holds a Certificates in Project Management and Technical Writing @ University of St. Thomas - Opus College of Business. With a robust skill set that includes Design Control, 21 CFR, ISO 14971, GMP, ISO and more, Carrie Berge contributes valuable insights to the industry. Carrie Berge has 2 emails on RocketReach.
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