QA documentation specialist - on site Laval

Permanent Employment Date display: 30/11/2023 #Ref.:6719

Activity area : Pharmaceutical and medical

Post category : Scientific and technical positions

Province : Quebec

Region : Laval, Montreal and surroundings

Recruiter : Chantal Fillion

Contact us : cfillion@st-amour.com

Job description :

Join our dynamic team as a QA Documentation Specialist!

As a vital part of the QA department, you will be the guardian of the Quality Systems documentation. Ensure data integrity, uphold GMP standards, and be the master of official documentation.

Our client is a well-known CDMO collaborating with European and North American pharmaceutical companies.

Why join us:

  • Experience the great working atmosphere in a state-of-the-art production site.
  • Working environment where your skills are valued, and your career can flourish.
  • Team is growing and is driving excellence in quality systems.
  • Permanent role with a competitive benefit package.
  • Flexible working hours, on site work in Laval.

Skills and qualifications :

  • B.Sc  in a related field (chemistry, biology, biochemistry, or related fields)
  • 2 years of related experience or equivalent combined education with relevant work experience
  • Proficient in Microsoft applications, especially Word and Excel
  • Knowledge of GMP (Good Manufacturing Practices)
  • Bilingualism in French and English

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