Key responsibilities include leading QA staff; maintaining QA policies, SOPs, and controlled documents; approving methods, specifications, and validation protocols; reviewing analytical data for accuracy and compliance; overseeing OOS/OOT, deviations, CAPA, and change control; trending quality events; managing internal audits; supporting client and regulatory audits; and driving GMP training and continuous improvement. Required qualifications/skills:- Bachelor’s in Chemistry (or related discipline)- 6–8 years in a regulated pharmaceutical/laboratory environment- Strong QA systems, audit, and compliance oversight experience- Proven review/approval of scientific and regulatory documentation- People leadership experience; strong knowledge of ALCOA+ and 21 CFR 210/211Apply if you can set direction, make sound quality decisions, and lead a compliant, audit-ready lab.