Senior GMP Process Technician



8 total openings: 1st Shift: 6:30am – 3pm (3 openings) 2nd Shift: 2:30pm – 11pm (3 openings) 3rd Shift: 10:30pm – 7am (2 openings) The hours will go up to 12 hour shifts until sometime in January 2025. That’s why it’s important to have flexibility across shifts. Job Description: Under limited supervision perform equipment setup operation troubleshoot to meet all standards for safety quality and efficiency. Maintain machine uptime perform any fault clearing and clear stoppages on automated equipment. Perform basic routine manufacturing process operations such as dispensing of raw materials material reconciliation line clearance basic analytics and record transactions Assist in the review of documentation for assigned areas i.e. procedures job plans logs area audits and batch records Assist as training resource on manufacturing tasks and equipment use Use human machine interfaces HMIs to identify alarms and correct line stoppages. Ensures components and products are available for a continuous operation. Carries out equipment inspections and generates emergency corrective or preventative work orders as needed in the Maximo system. Troubleshoot and identify potential solutions for mechanical errors safety issues or general operating inefficiencies within the production processes. Partner with cross-functional teams to help drive improvement opportunities. Able to use computer systems to support material inventory system SAP transactions and electronic batch records. Oversight of equipment/process validation protocols independently. Safely follow standardized operating procedures including material handling record keeping assembly and packaging. Must follow Good Manufacturing Practices GMPs. Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained. Train fellow staff on the manufacturing processes equipment and general skills.


gmp, troubleshooting, quality control, manufacturing process, pharmaceutical, inspection, quality assurance

Top Skills Details:

gmp,troubleshooting,quality control,manufacturing process,pharmaceutical

Additional Skills & Qualifications:

Associate degree preffered but open to HS Diploma 4 years of technical experience in Pharmaceutical, Medical Device, or Packaging environment in a GMP setting Experience the GMP processing/packaging/quality Must be comfortable working in a fast paced environment and willing to learn

Experience Level:

Intermediate Level

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

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