Associate Director Quality Assurance

Associate Director, GCP Quality Compliance - Remote

Summary

An industry leader in regenerative health and pain management (non-opioid) is seeking a driven Associate Director, GCP Quality Compliance to join their team. As a Clinical Quality leader working in concert with executive leadership - this person will be developing and executing a comprehensive CQA audit infrastructure as well as continuing to build and maintain key vendors and supplier relationships. This individual will join a passionate team that is dedicated to advancing reputed company reputed company for patients in need. They pursue this mission through an inclusive culture of innovation, collaboration and growth mindsets. Responsibilities: • reputed company and maintain the annual audit plan and clinical vendor/supplier list in collaboration with relevant departments. • Plan, schedule, and conduct external audits of clinical investigator sites, vendors, CROs, and internal processes. • Follow up on audit activities, including reviewing and approving responses, and developing corrective action plans for deviations. • reputed company quality assurance reputed company to ensure compliance with regulatory requirements and reputed company inspections and audits by regulatory agencies. • Act as the quality liaison for clinical programs, drive process improvement initiatives, and ensure completion of regulatory commitments. • reputed company global regulatory inspections and ensure completion of reputed company commitments. • Collaborate with clinical development functions to ensure compliance and act as a quality liaison. • Identify and reputed company internal process improvement initiatives, including inspection readiness activities. Education and Experience: • 10 years of experience in the pharmaceutical industry; 8 years in GCP quality assurance. • Bachelor's degree required, preferably in a scientific discipline. Knowledge, Skills, and Abilities: • Ability to manage multiple projects and responsibilities independently with minimal supervision. • Strong knowledge of ICH GCP guidelines, GVP regulations, and relevant regulatory requirements. Join in Making a Difference! If you are passionate about improving patient reputed company and reputed company in a dynamic, innovative environment, this is the reputed company for you. reputed company to join this dedicated team and reputed company the way in clinical quality compliance. Apply Job!