IBR Inc. Institute for Biopharmaceutical Research is a Swiss GLP-compliant contract research organization founded in 1998 and based in Matzingen, near Zurich. The company provides bioanalytical services for preclinical and clinical studies to biotechnology and pharmaceutical companies.The services encompass method development, validation and sample analyses covering drug characterization, mode-of-action, pharmacology and preclinical safety evaluation with a broad panel of bioanalytical and immunological methods, including cell-based assays. The strength of the company lies in the ability to provide innovative solutions in the progressive environment of drug development. Method validation and sample measurement are performed to the quality standards GLP and GCP.
We are currently seeking a
Deputy Quality Assurance Manager
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.
This position, reporting to the Quality Assurance Manager, will provide an opportunity for an auditor with some expericence to progress to the next level in a small, dynamic environment. Further development to Quality Assurance Manager is anticipated for the right candidate.
QA professional with some experience in a pharmaceutical regulatory environment.
Audit 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.
Ability to participate in and, with experience, take the lead role during regulatory inspections by customers, Swissmedic, FDA and other regulatory agencies.
You will gain the knowledge and experience to perform the full range of GLP inspections. On a day-to-day basis you will manage the QA inspection programme.
You will be expected 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.
Despite English being the working language of the company, knowledge of German is desirable.
If you are interested in working for this dynamic and highly specialized company please submit your CV.
IBR Inc., Institute for Biopharmaceutical Research
Frau Brigitte Moser