Job Description

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

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