Associate Director Quality Assurance

This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$/yr - $/yr

Vice President - GxP Quality Recruitment at EPM Scientific

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 better health outcomes for patients in need.

They pursue this mission through an inclusive culture of innovation, collaboration, and growth mindsets.

Responsibilities:

• Develop 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.
• Provide quality assurance oversight to ensure compliance with regulatory requirements and lead inspections and audits by regulatory agencies.
• Act as the quality liaison for clinical programs, drive process improvement initiatives, and ensure completion of regulatory commitments.
• Oversee global regulatory inspections and ensure completion of related commitments.
• Collaborate with clinical development functions to ensure compliance and act as a quality liaison.
• Identify and lead 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 outcomes and thrive in a dynamic, innovative environment, this is the next step for you. Apply now to join this dedicated team and lead the way in clinical quality compliance.

Director

Full-time

Quality Assurance

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing