Process Operator I

Location (mandatory): Stouffville, Ontario, CAN L4A1H5 Manufacture products by operating equipment according to the Master Batch Record (MBR). Complete GMP documentation (MBRs, labels, logbooks, validation records) with accuracy and integrity

Job 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, 5S)

Skills:

1+ year of experience in a GMP manufacturing environment (pharmaceutical preferred) Ability to wear required Personal Protective Equipment Mechanical aptitude with high-speed machinery Basic knowledge of Windows applications, SAP, and MSCA Understanding GMP standards and Health & Safety procedures (OH&S Act, WHMIS)

Education/Experience:

High School diploma or equivalent