Director of QA​/RA

Join a dynamic organization leading innovation in the life sciences sector. This exciting opportunity allows you to influence quality and regulatory excellence at a high level, supporting the development of impactful solutions within the industry. You will have the chance to work alongside cross-functional teams, shape compliance strategies, and contribute to the success of groundbreaking projects—all while enjoying a collaborative environment that values growth and flexibility.

Our client is a forward-thinking life sciences organization committed to advancing health through innovative solutions and high-quality standards. Focused on ensuring safety and compliance in the development of medical products, they play a vital role in improving patient outcomes worldwide. This role is essential to maintaining their commitment to excellence and regulatory compliance across their operations.

This Director of QA/RA role is designed for an experienced leader passionate about ensuring product quality and regulatory compliance within a life sciences environment. You will drive strategic initiatives, oversee compliance programs, and partner closely with various teams to ensure adherence to industry standards and regulations. The position is on-site, offering a vital leadership presence to support operational success.

• Lead the development and implementation of quality assurance and regulatory strategies.
• Manage compliance initiatives to ensure adherence to industry standards.
• Build and implement processes to support regulatory submissions and inspections.
• Collaborate with R&D, manufacturing, and other departments to embed quality management across operations.
• Drive continuous improvement efforts within QA/RA functions to enhance efficiency and compliance.
• Partner with external agencies, auditors, and regulatory bodies to support inspections and audits.
• Mentor and develop a team of QA/RA professionals to foster a high-performance culture.

• Significant experience in quality assurance and regulatory affairs within the life sciences industry.
• Proven expertise managing compliance programs and regulatory submissions.
• Strong leadership skills with the ability to influence cross-functional teams.
• Deep knowledge of industry regulations, standards, and best practices.
• Ability to thrive in a collaborative, on-site work environment.
• Typically 10+ years of relevant experience, with a track record of strategic impact.

This role offers a competitive salary package with a range of $175,000 to $190,000, depending on experience and qualifications.