Job Market Guide: Regulatory Affairs Specialist jobs in Rochester-Mason City-Austin

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in Rochester-Mason City-Austin. Regulatory Affairs Specialists in Rochester-Mason City-Austin have between ${} and ${} years of experience, averaging $${} years of experience.

7 Regulatory Affairs Specialist jobs in Rochester-Mason City-Austin

Minneapolis, MN
Provide business and product information to to enable development of strategies and requirements, and communicate that information to the therapy management teams.
industry
Business Services
experience
5 - 7 years

PLYMOUTH, MN
The Senior Regulatory Affairs Specialist supports and improves company's regulatory position by execution of regulatory and compliance tasks to help achieve departmental and business objectives, with particular emphasis on the endoscopy division and compilation of US regulatory submissions for Korean developed product offering.
industry
Business Services
experience
5 - 7 years

Minneapolis, MN
Develop and implement regulatory strategies for Class III devices through national authorities, physicians, consultants and internal team members.
industry
Industrial Equipment & Supply
experience
5 - 7 years

PLYMOUTH, MN
Review and ensure regulatory compliance of internal operational and project documentation involved in commercial product release for all assigned projects.
industry
Medical Equipment
experience
11 - 15 years

Minneapolis, MN
Compile, author, and submit robust Regulatory submissions/technical files, and internal Regulatory file documentation, to expedite new product clearance/approval, and sustain commercial availability for all products.
industry
Life Sciences & Research
experience
8 - 10 years

Minneapolis, MN
Monitor relevant changes in scientific and regulatory environment, implement changes as necessary and communicate to cross-functional teams.
industry
Business Services
experience
5 - 7 years

Minneapolis, MN
Prepare written regulatory strategies for PMAs, clinical trials, new product development, and sustaining projects.
industry
Engineering Services
experience
11 - 15 years