Teva Process Operator Tableting - month contract Night Shift 

Canada, Ontario 

786522481

Process Operator, Tableting - 12 month contract (Night Shift)

The Process Operator manufactures products by operating various equipment's 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 an intermediate capacity, as required per department/site.

• 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 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: Optimizes all settings, parameters and adjustment of equipment within area of responsibility or process type.
• Conducts intermediate equipment setup: Independently fully disassembles and sets up equipment within area of responsibility or process type, 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.
• Retrieves, moves and stores materials in appropriate areas of 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, support OPEX initiatives (i.e. Kaizen, SMED, OEE, 5S)
• Performs other duties as assigned.

• 1+ year experience in GMP manufacturing environment. Preferred: 1+ year of relevant pharmaceutical experience.
• Minimum completion of High School required
• Ability to wear required Personal Protective Equipment
• Demonstrated mechanical ability with high-speed machinery
• Basic working knowledge of Windows applications, SAP, MSCA
• General knowledge of Pharmaceutical or comparable GMP industry
• Good knowledge of Health & Safety procedures, including, OH&S Act & WHMIS
• Good interpersonal skills with the ability to work as part of a high-performance team
• Strong writing skills: Prepare written materials that are accurate, clear, logical and well organized
• Math skills: Demonstrated ability to perform required computations, calculations and problems
• Planning/Organizational skills: Organize and manage time to complete tasks and projects. Ability to multitask
• Problem solving: Must demonstrate ability to identify alternatives and solve routine problems, e.g., ability to troubleshoot a process or equipment issue and explain the processes to others (training)
• Candidates shall be required to demonstrate mathematical and written skills by completing an on-line assessment to be considered for interview

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