Senior QA - Documentation & Compliance Specialist

A leading biotech firm is seeking a Senior Quality Specialist for their Documentation Systems. Responsibilities include conducting quality compliance activities in accordance with GxP regulations, performing product complaint investigations, and managing documentation related to global submissions. Candidates must have a Bachelor’s degree with at least 6 years of relevant experience in quality systems, showcasing strong communication and problem-solving skills. This role is pivotal for ensuring adherence to regulatory standards and internal procedures. #J-18808-Ljbffr