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Associate Director - Quality Standards and Continuous Improvement

Regeneron Pharmaceuticals, Inc.

Build our future together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Quality Standards and Continuous Improvement to join our Global Development Quality team, supporting quality management system oversight, governance, quality events and continuous improvement across Global Development. In this role, you will help maintain effective quality standards and processes while collaborating with internal leaders, functional stakeholders and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.

When & where:

  • Location: Uxbridge, Dublin, Warren or Armonk

  • Hybrid model

Discover your role:

  • Oversee the end-to-end Issue Management framework, ensuring standardized, compliant, and inspection-ready practices.

  • Define and evolve Issue Management and Quality Event strategies to support scalability, efficiency, and consistency.

  • Drive cross-functional alignment across Quality Event Leads (QEL) and functional teams to ensure consistent and right sized approach to issue management and quality decision-making.

  • Lead QEL forums and provide SME guidance on QMS governance, continuous improvement, and inspection readiness.

  • Ensure consistency in investigations, root cause analysis, CAPAs and documentation standards.

  • Lead and Develop line reports whilst also supporting the broader QEL community through coaching, standard setting, and knowledge sharing

  • Monitor Issue Management performance through metrics and trend analysis.

This role requires:

  • Bachelor’s degree with at least 10 years of relevant healthcare or pharmaceutical industry experience.

  • Experience in quality, compliance, quality management, quality assurance or clinical development.

  • Expertise or transferable skills related to Good Clinical Practice or Good Pharmacovigilance Practice.

  • Experience training, supervising, mentoring, developing staff and leading a small team.

  • Advanced knowledge of quality management system oversight, quality governance and continuous improvement.

  • Experience participating in, managing and leading regulatory agency inspections.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit For other countries’ specific benefits, please speak to your recruiter.
Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Vacancy posted 5 days ago
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