We are currently looking for a Regulatory Affairs Jr. Manager to join a growing Medical Technology company West of Munich. Entering new robotic products into national and international markets within multiple medical fields.
•Registration and compiling documentation for new products
•Verification and approval of development on behalf of the Regulatory Affairs Department
•Exploring new market areas of growth
•Providing internal training about laws and standards
•1-2 years’ experience within a Regulatory Medical Device environment
•Knowledge of MDD, MDR, EN ISO 14971 and EN ISO 13485
•Involvement in technical file documentation
•Ideally 510k submission experience
•English and German fluency
•Science related or Engineering Degree
Full job description and company details are available upon application. This position is being dealt with by Georgia Blank at Meet, call on (+44)2039274277 or email directly at email@example.com to discuss further and in confidence.
Meet are good people who are great at recruitment. We’re proud to partner with the industry’s leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.
You can find out more about Meet at www.peoplewithchemistry.com