Associate Director, Quality Assurance – Biopharma Manufacturing
Shape the Future of Quality in Biopharma Manufacturing
Are you passionate about raising the bar for Quality Assurance in cutting-edge drug product and drug substance manufacturing? This is your opportunity to step into a senior leadership role where your expertise will directly influence the success of life-changing medicines.
As
Associate Director, QA
, you'll set the standard for GMP excellence, guiding teams through critical milestones such as tech transfers, process performance qualification (PPQ), and regulatory inspections. You'll be both a strategic thinker and a hands-on leader, driving compliance, fostering a culture of quality, and ensuring operational readiness at every stage.
What you'll do
* Provide strategic oversight of GMP manufacturing operations, ensuring compliance with global regulatory requirements.
* Lead QA support for tech transfers, PPQ, and inspection readiness activities.
* Build, mentor, and inspire high-performing QA teams.
* Review and approve GMP documentation, safeguarding data integrity and compliance.
* Champion continuous improvement initiatives that elevate quality standards across the site.
What you'll bring
* A degree in Biopharma, Life Sciences, or a related field.
* 8+ years' experience in vaccine or biopharma DP/DS manufacturing (sterile filling experience is highly desirable).
* Proven leadership skills with the ability to coach, mentor, and motivate teams.
* Strong collaboration skills and the ability to influence across multiple functions.
* A problem-solving mindset with a track record of delivering innovative quality solutions.
Why join?
This is more than a QA role—it's your chance to
lead, inspire, and shape a world-class quality culture
in a growing biopharma hub. You'll work with talented colleagues, make a global impact, and grow your career in an environment that values innovation, teamwork, and excellence.