Clough AMEC. is seeking a Process Operator I in Ontario, CA. The role includes operating equipment per Master Batch Record, completing GMP documentation, and troubleshooting processes. Candidates should have 1+ year in GMP manufacturing (pharmaceutical preferred), and a high school diploma. Essential skills include mechanical aptitude and knowledge of SAP and Windows applications. This position offers career development opportunities and requires adherence to health and safety standards.
Qualifications
1+ year of experience in a GMP manufacturing environment, preferably pharmaceutical.
Ability to wear required Personal Protective Equipment.
Responsibilities
Manufacture products by operating equipment according to the Master Batch Record (MBR).
Complete GMP documentation with accuracy and integrity.
Independently run at least two process types.
Conduct ERP data entry and verification checks.
Perform intermediate troubleshooting and optimize equipment settings.
Fully disassemble, clean, and reassemble equipment.
Skills
GMP manufacturing experience
Mechanical aptitude
Knowledge of Windows applications
Understanding GMP standards
Education
High School diploma or equivalent
Tools
SAP
MSCA
Job description
Process Operator I job at SGS Consulting. Ontario, CA.
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)