Manufacturing Quality Associate (MQA) - 2nd & 3rd shift

Role: Manufacturing Quality Associate ensuring GMP compliance and product quality in pharmaceutical manufacturing. Responsibilities: monitor manufacturing operations, conduct internal audits, investigate nonconformances, author and review GMP documentation, manage CAPAs, coordinate environmental monitoring, perform quality testing, and support manufacturing continuity. Requirements: BS in chemistry, biochemistry, or related field; 5+ years in pharma, biotech, or medical device industries; strong knowledge of GMPs, quality systems, and regulatory standards; proficiency in GMP documentation review and auditing; excellent organizational, communication, and project leadership skills. Preferred: formal quality discipline certifications (e.g., ASQ, Lean Six Sigma). High-value: focus on pharmaceutical manufacturing, GMP compliance, quality oversight, environmental monitoring, and quality testing activities. Work setup: second or third shift, off-hours and weekend availability, with potential for fast-paced environment adaptation.