Sterinova - Saint-Hyacinthe, QC (il y a 30+ jours)

Postuler dès maintenant

  • Drafting of protocols and stability reports
  • Coordinating of stability activities and external laboratories involved in stability activities
  • Management of stability chambers
  • Reviewing results and analytical methods
  • Investigation and documentation of any anomaly relating to the stability program
  • Monitoring of regulatory requirements and regulatory watch for stability
  • Writing trend reports by product
  • Entry of purchase / service requests in SAP
  • Knowledge of good manufacturing practices (GMP) and pharmacopoeias (USP, Ph. Eur. And BP) and their applications
  • Knowledge of instrumental analysis techniques such as high performance liquid chromatography, infrared spectrometry, ultraviolet spectrophotometry and gas chromatography.
  • Working knowledge of computers and laboratory data acquisition and analysis systems.
  • Ease of written and verbal communication.
  • Teamwork skills. Have a sense of initiative; excellent concentration; technical writing skills and analytical mind, good stress management.
  • Oral and written bilingualism (French and English).
  • Experience in the pharmaceutical industry.
  • Bachelor’s degree in chemistry or equivalent with a minimum of three (3) years of experience.
This is a permanent and full-time position. To apply, please send your resume to Mrs. Michelle De Repentigny, Quality Control Director at