QC Associate

Date: Oct 17, 2025

Location:

Toronto, Canada, Ontario, M1B2K9

Company: Teva Pharmaceuticals

Job Id: 64600

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

We are seeking a detail-oriented and knowledgeable QC Analyst to join our Quality Control team. Working independently under the guidance of the QC Laboratory Supervisor, the successful candidate will leverage advanced expertise in microbiology (USP/NF, BP/EP) and a strong understanding of GMP/cGMP testing requirements. This role involves coordinating audits and overseeing release activities related to microbiological test data, calibration records, and associated documentation generated within the QC laboratory.

How you’ll spend your day

Responsible for the final analytical release assessment of microbiological data including but not limited to:
Environmental monitoring and water testing results
Sterility, endotoxin, bioburden, microbial limit, and growth promotion tests
Identification and trending of microorganisms
Media and reagent preparation records
Ensure that all microbiological testing and documentation comply with GMP, GLP, and data integrity principles.
Verify that all deviations, OOS (Out of Specification), OOT (Out of Trend), and atypical results are properly investigated.
Review and approve laboratory worksheets and electronic records.
Support timely batch release by ensuring accurate and efficient data review and documentation closure.
Collaborate with analysts to provide feedback and ensure compliance with established procedures.
Ensure adherence to laboratory SOPs, quality standards, and regulatory requirements.
Perform process confirmation related to Micro Lab testing and documentation activities.
Review Water and Environmental Monitoring Trending reports.
Support internal and external audits as required.
Identify and contribute to continuous improvement initiatives in QC Microbiology.

Your experience and qualifications

Bachelor’s or Master’s degree in Microbiology, Biotechnology, or a related scientific discipline.
3 + years working experience in a QC Microbiology laboratory within a GMP-regulated pharmaceutical, biotech, or medical device industry.
Strong technical skills in Environmental Monitoring and related Pharmaceutical Microbiology Lab activities.
In-depth understanding of GMP, GLP, USP, EP, and data integrity requirements.
Excellent attention to detail, organizational, and documentation skills.
Proficiency with LIMS, TrackWise, SAP and other electronic quality systems (asset).
Strong communication and interpersonal skills with the ability to collaborate effectively across functions.
Ability to work as a member of a team and under minimum supervision.

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.