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Process Operator - PM shift, 1 year contract (Capsulating)

Date: Dec 31, 2021

Location: Markham, Ontario, CA, L3R 4E1

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

The Process Operator I manufactures products by operating various equipment in accordance with the master batch record (MBR) and in compliance with EH&S policies, GMPs, and controlled procedures (SOP, EM, WI, JA, etc.) and performing troubleshooting and setup in a basic capacity,  as required per Department/Site.

Essential Duties & Responsibilities:          

  • Performs duties in accordance with the master batch record (MBR) and in compliance with EH&S policies, GMPs, and controlled procedures (SOP, EM, WI, JA, etc.)              
  • Completes all GMP documentation (MBR, controlled procedures, labels, logbooks, validation documentation, etc.) in accordance with Data Integrity, in their area of responsibility       
  • Independently runs at least one (1) process type and performs all required in process checks (IPCs). Performs ERP data entry and transactions, and verification checks as required        
  • Conducts basic troubleshooting: Identifies issues and reacts to resolve (i.e. reset and fine tune equipment) within area of responsibility
  • Conducts basic equipment setup: Programming batch information, setup and configuration of equipment) includes dismantling, cleaning, and assembly of processing equipment/rooms according to controlled procedures within area of responsibility
  • Notifies Supervisor when processing issues, product quality concerns and safety incidents occur 
  • Ensures the proper care, use and condition of tools, equipment, rooms, and GMP area   
  • Retrieve, move and store materials in appropriate areas of facility, as required per Department/Site
  • Supports and engages in OPEX activities/ initiatives (OEE, SMED, RCPS, Kaizen, 5S, etc.)  
  • Acts as a coach and supports training of new employees


  • Minimum successful completion of High school diploma or equivalent. Preferred: Pharmaceutical Manufacturing Technologist Diploma  or a university degree in a related science field
  • 1+ year experience in manufacturing environment. Preferred: 1+ year of experience in either dispensing, compounding, coating, tableting or encapsulation
  • Basic working knowledge of Windows applications, Oracle MSCA
  • Demonstrated knowledge of GMPs, EH&S procedures, including OH&S Act, WHMIS
  • General knowledge of Pharmaceutical or comparable GMP industry



Sub Function


Reports To

Site Production Head

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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.