Director, GPS Quality & Compliance

Build our future together:

At Regeneron we use science and innovation to develop life-changing medicines for people with serious diseases. Our Global Patient Safety (GPS) organization is seeking a Director GPS Quality & Compliance to support our quality event management and inspection readiness programs. This role partners closely with the Senior Director GPS leadership Global Development Quality and the QPPV Office and operates as a functional leader who coordinates and delegates work across the team to ensure consistent high-quality program delivery.

This position offers the opportunity to contribute to a fast-growing science-driven organization making a meaningful difference to patients worldwide.

When & where:
Location: Warren NJ (preferred) Armonk or Tarrytown NY or Cambridge MA
Work model: 4 days/week on-site
Travel percentage: 20% with some fluctuation expected based on onsite audit/inspection support needs.

Discover your role:
Lead functional workstreams across quality event management and inspection programs coordinating and delegating work across a team
Serve as a trusted point of contact during GCP and GVP audits and inspections guiding teams through preparation and real-time response
Bring order to complexity by maintaining inspection readiness materials and translating regulatory frameworks into practical action
Champion a culture of accountability and continuous improvement acting as an escalation point when issues arise
Turn data into direction reviewing quality metrics and trend analyses to shape clear actionable recommendations for senior leadership
Communicate with confidence and clarity presenting governance topics and quality insights to senior team members
Lead through influence coordinating across teams and functions regardless of formal reporting lines

This role requires:
A Bachelors degree required; advanced degree preferred with a minimum of 12 years of pharmaceutical industry experience; Healthcare Professional background preferred
Deep knowledge of global PV regulations quality management systems and inspection readiness frameworks (FDA CFR GVP Modules)
Demonstrated experience facilitating FDA and EMA/MHRA inspections (GCP and GVP) including direct experience as an inspection point of contact
Proven track record overseeing QMP governance metrics programs and cross-functional quality oversight
Experience managing relationships across GDQ QPPV Office Regulatory Affairs and vendors
People management experience preferred

Does this sound like you Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. 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 sexual orientation gender identity or expression gender reassignment marital or civil partnership status civil status pregnancy or parental status age disability nationality citizenship status ethnic or national origin membership of the Traveler community familial status genetic information military or veteran status or any other characteristic protected under applicable law. Where required we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process unless such accommodation would impose undue hardship.

Where necessary we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment specific role level and your skills and some countries collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include depending on country and role: annual bonuses or other incentive plans equity awards pension or retirement benefits 401(k) company match health and wellness programs fitness centers insurance benefits (e.g. medical dental vision life and disability) paid time off and family support benefits. For additional information about Regeneron benefits in the U.S. please visit For other locations additional information will be provided during the recruitment process. If you have any questions please speak with your recruiter.

Please be advised that at Regeneron we believe we do our best work when we are together. For that reason many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

As part of the recruitment process certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)