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QA Associate - 14 month contact

Date: Oct 13, 2021

Location: Toronto, Ontario, CA, M1B2K9

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

QA Associate – 14 month contract
30 Novopharm

Quality Assurance Associate will coordinate DR investigations and ensure product impact is evaluated, root cause is determined and effective CAPAs are identified.  Investigate all product quality complaints and provide customer responses.  Perform trend analysis on quality deviations and complaints and evaluate CAPA effectiveness. 

Tasks and responsibilities will include but are not limited to:

  • Lead and work collaboratively with cross functional departments to resolve quality deviations and complaints to determine root cause, evaluate product impact and identify applicable CAPAs to ensure compliance with GMPs and SOPs. Working with various cross functional departments to support the completion of CAPAs and CAPAERs.           
  • Maintenance of local QTAs for the site. 
  • Evaluate excursions  (e.g environmental, temperature) for product impact.  Perform evaluation and approval of change controls and recipes/validity rules approvals if applicable. Prepare a daily summary report for Complaints and DRs.
  • Perform trend analysis for quality deviations and complaints.
  • Other duties as assigned              


  • University Degree completed in a relevant field
  • 1+ year in relevant experience in Quality Control, Quality Assurance or Operations, or proven track record within pharmaceutical industry.  Preferred: 3+ years relevant experience in Quality Control, Quality Assurance or Operations or a proven track record within pharmaceuticals.
  • Strong computer skills with good working knowledge of TrackWise, Oracle, LIMS, Smart QA, MS Office suite (Excel and Word)
  • Good working knowledge of SOPs, GMPs, and cGMP’s applicable to Quality Operations, Manufacturing and Packaging



Sub Function

Manufacturing Quality Assurance

Reports To

Sr Manager, Quality Assurance

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.