Process Operator I, Ontario, CA

Description

Job Responsibilities:

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:

Education/Experience:

1+ year of experience in a GMP manufacturing environment (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 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

Highlights

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