QC Lab Lead — cGMP, Method Development & Compliance

A pharmaceutical company in New Jersey is seeking a QC Supervisor to manage daily operations of the QC Laboratory, ensuring compliance with cGMP. The candidate should have a bachelor's degree in Chemistry and at least 2 years of supervisory experience in a pharmaceutical QC lab. Responsibilities include leading a team, overseeing testing and data review, and supporting continuous improvement initiatives. The role offers competitive compensation and opportunities for growth within the organization. #J-18808-Ljbffr