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Master Change Specialist - 16 month contract

Date: Oct 12, 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

We are currently seeking a Master Change Specialist to join our team on a contractual basis.

Tasks and responsibilities will include but are not limited to: 

Evaluate all Change Requests in line with Teva’s Change Policy to ensure holistic change review and implementation. The Change Specialist with perform creation, evaluation and assessment of a variety of Change Types.  Evaluation of all SME evaluations to ensure alignment with compliance, production, quality and business needs is also required by this role. This Candidate will update and track tasks/change progress through our validated systems to ensure that change tasks are completed to align with both Compliance and Business needs.  The Master Change Specialist has the accountability of not only processing change, but starting change, revising and implementation change from Change Owner and following thru all change controls to ensure completion.  MCS serves as a leader for change facilitation and owns the change upon creation.


  • College Diploma in related field a minimum; University Degree in related Science and  PMP Certification is preferred
  • 5 + years’ experience in a fast paced pharmaceutical manufacturing environment as a minimum
  • Capability to manage multiple priorities/ processes across multiple sites with high levels of complexity
  • Demonstrated SME knowledge of at least two of the following categories – Manufacturing Operations, Packaging Operations, Controlled Documents, Artwork, Quality Assurance, ERP Systems (Oracle and SAP required), Quality Control, Compliance Vendor Management
  • Accuracy of work, proofreading skills
  • Ability to self-lead
  • 5 + Years minimum experience in Project Management
  • SME knowledge of QMS, MS Office, LIMS, KT/EDMS, Adobe and overall pharmaceutical quality systems.
  • Strong IT skills. 



Sub Function

Quality Compliance

Reports To

Senior 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.