Regulatory Affairs Associate
Advanced Medical Solutions
Winsford, CheshirePosted Discovered via the company's careers siteMatch locked
Full-timeScientific & QA Jobs
About the role
Job Description Job Details Create and maintain Regulatory Technical Documentation in compliance with European, USA markets, and other global territories including 93/42/EEC, (EU) 2017/745 and 21 CFR Part 820 requirements. Maintain continued product regulatory approval for the European, USA markets, and other global territories. Contribute to regulatory strategy planning and change management. Per
Not included in the source posting: about the role, what you'll do, qualifications, benefits.
Skills
qa
Who can apply
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