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 Improvement to join our Global Development Quality Governance and Oversight 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:

• Support oversight and maintenance of the Global Development Quality Management System.
• Lead quality-related process improvement initiatives, work groups and assigned solutions.
• Manage stakeholder engagement to identify process improvements and regulatory compliance needs.
• Oversee quality metrics, trends and reporting to support continuous improvement.
• Partner with functional teams on root cause analysis and corrective action plans.
• Facilitate governance meetings and present data on Quality Management System health.
• You influence across functions through quality expertise, collaboration and clear decision-making.

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. 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.

About Us
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories.