Regulatory Affairs Manager CMC, Munich

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Location München, Bayern Salary K.A
Sector Life Sciences Type Permanent

  • You have at least 3 years' experience in the area of regulatory affairs?
  • You have experience working with EMA and the FDA?
  • You would like to work for an innovative biotech company that offers exciting career prospects?

Then I have a fantastic opportunity for you at my customer in Munich!

In this position you will have the following responsibilities:

  • Create regulatory documents (IMPD, IND, CTD Module 3)
  • Communicate with internal and external partners in the area of regulatory affairs
  • Work very closely with health authorities, partner companies and other internal departments to ensure a successful cooperation
  • Answer queries from health authorities
  • Provide regulatory expertise for clinical trials
  • Develop regulatory strategies

Required experience and qualifications for this position:

  • Master or PhD in a related field (Chemistry, Biology, Pharmacy)
  • At least 3 years' experience in the area of regulatory affairs
  • International experience
  • Fluent English and German (other languages are an advantage)

The next step:

If you are interested in this position and would like to find out more, then please contact me.

Andrew Pride - Regulatory Affairs

Principal Recruitment Consultant

T: +49 (0) 89 - 5519 7767


Progressive München - Pharma

Sthree Germany is acting as an Employment Agency in relation to this vacancy.