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Process Operator, Compounding Specialist
2 months ago
About the Opportunity
Teva Pharmaceuticals is seeking a skilled Process Operator, Compounding to join our team on a 12-month contract basis, working night shifts. As a Process Operator, you will play a critical role in manufacturing products by operating various equipment in accordance with the master batch record (MBR) and in compliance with EH&S policies, GMPs, and controlled procedures.
Key Responsibilities
- Operate equipment in accordance with the master batch record (MBR) and in compliance with EH&S policies, GMPs, and controlled procedures.
- Perform troubleshooting and setup in an intermediate capacity, as required per department/site.
- Complete all GMP documentation (MBR, controlled procedures, labels, logbooks, validation documentation, etc.) in accordance with Data Integrity, in their area of responsibility.
- Independently run at least two (2) process types and perform all required in-process checks (IPCs). Perform ERP data entry and transactions, and verification checks as required.
- Conduct intermediate troubleshooting: Optimize all settings, parameters, and adjustment of equipment within area of responsibility or process type.
- Conduct intermediate equipment setup: Independently fully disassemble and set up equipment within area of responsibility or process type, including dismantling, cleaning, and assembly of processing equipment/rooms according to controlled procedures within area of responsibility.
- Notify Supervisor when processing issues, product quality concerns, and safety incidents occur.
- Ensure 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.
- Attend the Train the Trainer Program. Perform training on equipment, controlled procedures, and best practices as required per Department/Site and act as a coach to Process Operators.
- Understand and act on areas of productivity losses, look for and suggest solutions, support OPEX initiatives (i.e., Kaizen, SMED, OEE, 5S).
- Perform other duties as assigned.
Requirements
- 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.
