
Biopharma Manufacturing Quality Leader
5 days ago
Lead Quality Assurance Excellence
Join our quest for quality in biopharma manufacturing.
This role offers a unique opportunity to shape the future of quality assurance in cutting-edge drug product and drug substance manufacturing.
As an 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.
Key Responsibilities:- Oversee GMP Manufacturing Operations: Ensure compliance with global regulatory requirements.
- Lead QA Support: Tech transfers, PPQ, and inspection readiness activities.
- Develop High-Performing Teams: Build, mentor, and inspire QA teams.
- Review and Approve Documentation: Safeguard data integrity and compliance.
- Drive Continuous Improvement: Elevate quality standards across the site.
- Education: A degree in Biopharma, Life Sciences, or a related field.
- Experience: 8+ years in vaccine or biopharma DP/DS manufacturing (sterile filling experience is highly desirable).
- Leadership Skills: Proven ability to coach, mentor, and motivate teams.
- Collaboration Skills: Strong collaboration skills and ability to influence across multiple functions.
- Problem-Solving: A problem-solving mindset with a track record of delivering innovative quality solutions.
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