Associate Director, GMP Quality Assurance

Structure Therapeutics is seeking an Associate Director of GMP Quality Assurance to lead and enhance our quality assurance operations within the GMP framework. This pivotal role involves overseeing quality systems, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to maintain the highest product quality.

The Associate Director will be responsible for developing and implementing quality management systems, conducting internal audits, and managing external inspections. Key duties include overseeing batch record reviews, deviation investigations, and change control processes. Additionally, the role involves providing training and guidance to staff on GMP regulations and quality standards.

Candidates should possess a Bachelor's or advanced degree in a scientific discipline, with a minimum of 10 years of experience in GMP Quality Assurance within the pharmaceutical or biotechnology industry. Strong knowledge of global GMP regulations, experience with quality management systems, and excellent leadership and communication skills are essential.

Structure Therapeutics offers a competitive compensation package, including a base salary, annual bonus, and equity awards. Employees also benefit from comprehensive health insurance, generous paid time off, and professional development opportunities.

Joining Structure Therapeutics means becoming part of a dynamic team dedicated to advancing innovative therapies. We foster a collaborative and inclusive work environment, providing opportunities for growth and the chance to make a meaningful impact in the field of biotechnology.