Our Client, a pharmaceuticals company, is looking for a Process Operator for their Stouffville, ON location.
Responsibilities :
- Manufacture products by operating equipment according to the Master Batch Record (MBR)
- Complete GMP documentation (MBRs, labels, logbooks, validation records) with accuracy and integrity
- Independently run at least two process types and perform all required in-process checks (IPCs)
- Conduct ERP data entry and verification checks
- Perform intermediate troubleshooting and optimize equipment settings
- Fully disassemble, clean, and reassemble equipment and rooms per controlled procedures
- Notify supervisors of any processing issues, safety incidents, or product quality concerns
- Maintain tools, equipment, and GMP areas in proper condition
- Retrieve, move, and store materials as needed
- Participate in the Train-the-Trainer program and coach other operators
- Support OPEX initiatives (Kaizen, SMED, OEE, S)
- Perform other duties as assigned
Requirements :
year of experience in a GMP manufacturing environment (pharmaceutical preferred)High School diploma or equivalentAbility to wear required Personal Protective EquipmentMechanical aptitude with high-speed machineryBasic knowledge of Windows applications, SAP, and MSCAUnderstanding of GMP standards and Health & Safety procedures (OH&S Act, WHMIS)Strong interpersonal and teamwork skillsSolid math and writing skills (online assessment required for interview consideration)Ability to multitask, plan, and solve routine problems independentlyWhy Should You Apply?
Excellent growth and advancement opportunities