QC Method Validation Consultant

Job description

Are you an expert on Method Validation and ready to help a biopharmaceutical company in their start to produce COVID-19 vaccine? Here’s you chance to help out on this exiting project.

In order to get the QC department ready for the large-scale production of COVID-19 vaccine a number of new methods have to be Validated. You will become part of the project teams that focusses on getting this done in a challenging four-month period. Your main tasks will be:

  • HPLC Validation studies
  • Laboratory control of equipment, calibration, review of test data and quality documentation.
  • Report an act on all minor major and critical deviations.
  • Solve deviations or assist co-workers in solving.
  • Write associated quality records.

Job requirements

Does this sound like something you would want to contribute to? Then read on and see if you are a match to the requirements.

  • Bachelor or Master degree in analytical chemistry or equivalent.
  • A minimum of 5 years of experience with method validations in a pharmaceutical/GMP environment.
  • Independent, structured and flexible analyst.
  • Good oral and written communication capabilities in English, preferably also Dutch.

We offer you a 4- or 5-day workweek (the choice is yours) based in Amsterdam with flexible start times. A decent salary or hour rate if you are a consultant.

Please not that you need to be a EU citizen or have a valid EU working permit for the mentioned period.

Apply now, if you are a match to the criteria we will be in touch within 2 working days!