Packaging Operator I - 12 Months Contract

Date: Mar 29, 2023



Location: Toronto, Ontario, Canada, 00000



Company: Teva Pharmaceuticals



Job Id: 45661

Who are we?

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!

The Process Operator I manufacture products by operating various equipment by 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 an intermediate capacity, as required per Department/Site. Essential Duties & Responsibilities:

• Performs duties by the master batch record (MBR) and complies 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.) by Data Integrity, in their area of responsibility
• Independently runs at least two (2) process types and performs all required in-process checks (IPCs). Performs ERP data entry and transactions and verification checks as required
• Conducts intermediate troubleshooting: Optimize all settings, parameters, and adjustment of equipment within the area of responsibility or process type
• Conducts intermediate equipment setup: Independently fully disassemble and setup equipment within the area of responsibility or process type, including dismantling, cleaning, and assembly of processing equipment/rooms according to controlled procedures within the 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 the facility, as required per Department/Site
• Attends the Train the Trainer Program. Performs training on equipment, controlled procedures, and best practices as required per Department/Site and acts as a coach to Process Operators
• Understands and acts on areas of productivity losses, looks for and suggests solutions, and supports OPEX initiatives (i.e., Kaizen, SMED, OEE, 5S).

Qualifications

The Process Operator I manufactures products by operating various equipment by 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 an intermediate capacity, as required per Department/Site. Essential Duties & Responsibilities:

• Performs duties by the master batch record (MBR) and complies 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.) by Data Integrity in their area of responsibility
• Independently runs at least two (2) process types and performs all required in-process checks (IPCs). Performs ERP data entry and transactions and verification checks as required
• Conducts intermediate troubleshooting: Optimize all settings, parameters, and adjustments of equipment within the area of responsibility or process type
• Conducts intermediate equipment setup: Independently fully disassemble and setup equipment within the area of responsibility or process type, including dismantling, cleaning, and assembly of processing equipment/rooms according to controlled procedures within the 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 the facility, as required per Department/Site
• Attends the Train the Trainer Program. Performs training on equipment, controlled procedures, and best practices as required per Department/Site and acts as a coach to Process Operators
• Understands and acts on areas of productivity losses, looks for and suggests solutions, and supports OPEX initiatives (i.e., Kaizen, SMED, OEE, 5S).

Function

Manufacturing

Sub Function

Manufacturing/Operations

Reports To

In process of validation

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\xe2\x80\x99s 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.