:

- 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 concerns regarding product quality.

- 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).





- Perform other duties as assigned.

Experience and Qualifications:

- 1+ year of experience in a GMP manufacturing workplace (pharmaceutical preferred).

- High School diploma or equivalent.

- Ability to wear required Personal Protective Equipment.

- Mechanical aptitude with high-speed machinery.

- Basic knowledge of Windows applications, SAP, and MSCA.

- Understanding of GMP standards and Health & Safety procedures (OH&S; Act, WHMIS).

- Strong interpersonal and teamwork skills.

- Solid math and writing skills (online assessment required for interview consideration).

- Ability to multitask, plan, and solve routine problems independently.

📌 Process Operator (Ontario)
🏢 Cynet Systems
📍 Ontario