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 Bachelor's 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?
We are committed to building a workplace with an inclusive culture.
Regeneron is an equal prospect 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 experience.
In 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
family support benefits
Salary Range (annually) $183,****** - $305,******
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.
Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases.
Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in ****, Fast Company's Best Workplace for Innovators in ****, and Forbes JUST companies in ****, among others.
Please be advised that at Regeneron, we believe we do our best work when we are together.
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.
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📌 Director, Gps Quality & Compliance (Western Australia)
🏢 Regeneron Pharmaceuticals
📍 Western Australia