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QC Analyst

Function

  • You perform Quality Control activities according to instructions, procedures and protocols in compliance with the GMP principles and the Quality Management System.
  • You validate analytical methods to support the quality control and release of drug products for use in clinical trials.
  • You plan and perform Quality Control analyses.
  • You plan and perform ICH compliant stability studies.
  • You support the preparation of the applicable protocols and reports.
  • You accurately report, document and review the analytical test results.
  • You support the maintenance, calibration and qualification of the analytical equipment. 
Profile
  • Professional Bachelor degree in biomedical laboratory technology, chemistry or pharmaceutical sciences with a minimum of 5 years relevant professional experience.
  • Experience in a regulated Quality Control laboratory and experience with pharmaceutical analytical techniques (HPLC/UPLC, Dissolution, KF, Particle sizing, etc.) is a must.
  • You are punctual and are able to work independently after a training in matters entrusted to you. 
  • You have experience with MS Office. Experience with Empower is a real asset.
  • You are flexible, problem solving and quality minded.
  • You are fluent in Dutch and English (written and spoken).
 
Offer
  • We offer a varied and challenging job with a permanent contract combined with an attractive salary package.
 
Interested in this challenging job?
  • Please send your application and CV via e-mail to Alexandrine Abbeloos (a.abbeloos@amatsigroup.com) and you will be contacted soon.