Remote QA Specialist - Deviation & CAPA Writer (GMP)

A well-known biopharmaceutical company is seeking a remote QA Specialist for a short-term contract. This role involves leading deviation investigations and writing CAPAs, requiring 4 to 7 years of GMP quality assurance experience. Candidates should have hands-on experience in a regulated commercial environment, ideally with sterile injectables. Proficiency with Veeva EQMS is preferred. The engagement lasts approximately 4 to 6 months, with a target pay rate of $40 to $45 per hour.