QC Auditor
Main tasks
- The QC Auditor is responsible for reviewing all raw data as part of study sample analyses and method validation, ensuring that the data are in compliance with written standard operating procedures and good laboratory practice (GLP) regulations.
Specific tasks
- Additional responsibilities include the generation and/or review of analytical and validation reports, responding to QA citations, and troubleshooting chromatographic problems.
- Further responsibilities may include analyst training and the writing of general standard operating procedures, upon request.
Qualifications
- D.E.C. and/or a B.Sc. in Chemistry, Biology, or equivalent field.
- The ideal candidate has 2 years of experience in the medical and/or pharmaceutical fields.
Remuneration
- In accordance with our salary scale.
Location