Specialist - Quality Assurance
bausch-health-companies-inc
Laval, Quebec, CA
6d ago

Valeant Canada the international head office of Valeant Pharmaceuticals International, oneof the fastest growing international pharmaceutical companies dedicated to bringing quality health and wellness products to all Canadians.

Our team manufactures and markets a wide variety of pharmaceutical and health products that are distributed in pharmacies, healthcare practices and hospitals across the country.

At Valeant, we invest in our employees and we believe in the importance of cultivating performance and outdoing ourselves in finding new and better solutions with the aim of responding innovatively and effectively to current needs.

In the context of our present growth, we are seeking to fill a position as Project Responsible - Quality Assurance, based a tLaval.

SUMMARY OF THE POSITION

Reporting to QualityAssurance / quality control Manager, your mission will be to play a role of responsible for the activities of quality assurance including quality systems management such as the PONs, product’s release, and compliance of production and packaging activities.

KEY RESPONSIBILITIES :

  • Prepare andapprove the specifications of raw materials, printed and non-printed packagingcomponents and finished products;
  • Perform therelease of raw materials, printed and non-printed packaging components andfinished products manufactured internally and externally;
  • Manage thequality systems (changes control, CAPA, Investigations, Deviations, PON, etc.)prepare and update all policies and procedures in order to comply with the GoodManufacturing Practices.
  • Initiate and / orapprove GMP documents
  • Write the annualproducts review’s reports (APQR)
  • Managementof the quality systems to ensureappropriate quality control of products DIN, NPN and cosmetics;
  • Keep up-to-dateand approve the manufacture and packaging master files,
  • Analyze thecomplaints and complete the internal / external, investigations and document thecorrectives action taken;
  • Define thenecessary controls required for the manufacture and packaging of productsaccording to the Good Manufacturing Practices.
  • QUALIFICATIONS :

  • Bachelor'sdegree in chemistry, biology or equivalent
  • 5 Years ofexperience in manufacturing environment pharmaceutical or cosmetic
  • Computerskills (Microsoft Office)
  • French andEnglish reading, speaking and writing
  • Precision, rigorand judgment in the application of internal policies, standards procedures andGMP regulations of the industry.
  • Orderly,meticulous, accurate, productive
  • Team worker
  • If you are interested in this opportunity, please apply before September 18th, 2015 p.msonormal, li.msonormal * *

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