Contract QA Validation Specialist: cGMP Equipment

A leading pharmaceutical team is seeking a skilled QA Validation Specialist for a 6-month contract in Irvine, California. The position requires hands-on ownership of equipment and laboratory validations, ideal for professionals with 5+ years in regulated environments. Key responsibilities include executing qualification protocols and ensuring compliance with cGMP standards. This role offers $38–40/hr, medical benefits, and 401(k). #J-18808-Ljbffr