We are currently seeking a


Head of Quality Assurance 80 - 100 %

to ensure that our current high standard of compliance to quality systems is maintained and continues to develop in line with the ever changing focus of the studies performed and also the expectations of regulatory authorities.

Your profile

  • QA professional with of experience in a pharmaceutical regulatory environment.
  • Extensive QA experience in a GLP environment supporting pharmaceutical development. Knowledge of GCP and GMP is an advantage.
  • Scientific background in the biological sciences, preferably with practical experience in bioanalytics including cell-based assays.
  • Proven ability to take the lead role during regulatory inspections by Swissmedic, FDA and other regulatory agencies.
  • In addition to managing the QA programme, you also have the knowledge and experience to perform the full range of GLP inspections.
  • Ability to deliver effective training on a one-to-one basis or to the company, provide advice to all levels of staff and recommend pragmatic regulatory solutions in the face of new situations.
  • As document quality (internal and external) is of great importance, your native language is either English or you have spent some years in an English speaking environment.
  • Knowledge of German is essential despite English is the working language of the company.
  • If you are interested in working for a dynamic and highly specialized company please submit your CV.

IBR Inc., Institute for Biopharmaceutical Research
Frau Brigitte Moser
Lauchefeld 31
9548 Matzingen
+41 52 366 3520