Quality Assurance Technician I - 2nd Shift (Pharma Lab)

Actalent; Irvine (CA); On-site; USD 33,000 - 34,000; Full time

Job summary

Actalent in Irvine, CA is seeking a Quality Assurance Technician I for 2nd shift to monitor lab process verifications and ensure compliance with GMP and FDA guidelines. Responsibilities include receiving samples, labeling control, and overseeing reinspection, with data integrity as a focus.

The role requires 2+ years in QA in pharma/medical device, a science degree preferred, and SAP experience. The position is on-site, contract-based, with a 12:00 PM–8:00 PM shift.

Qualifications

• 2+ years of QA experience in pharmaceutical or medical device industries.
• Bachelor's degree in a science-related field preferred with GMP experience.
• Proficiency in GMP, quality control inspections, and documentation writing.
• Familiarity with FDA regulations.

Responsibilities

• Monitor lab and manufacturing process verifications to ensure compliance with procedures and specs.
• Perform process monitoring, receive samples, label control, and oversee reinspection.
• Conduct monitoring and sampling for reserved samples.
• Provide quality oversight to ensure data integrity and compliance.

Skills

Quality assurance

GMP compliance

FDA regulations

SAP

Education

Bachelor's degree in a science-related field

Tools

SAP

Job description

Actalent in Irvine, CA is seeking a Quality Assurance Technician I for 2nd shift to monitor lab process verifications and ensure compliance with GMP and FDA guidelines. Responsibilities include receiving samples, labeling control, and overseeing reinspection, with data integrity as a focus.

The role requires 2+ years in QA in pharma/medical device, a science degree preferred, and SAP experience. The position is on-site, contract-based, with a 12:00 PM–8:00 PM shift.