Director, GPS Quality & Compliance

Posted 12 Days Ago
Be an Early Applicant
4 Locations
In-Office
183K-305K Annually
Expert/Leader
Biotech • Pharmaceutical
The Role
Leads Global Patient Safety quality event management and inspection readiness programs. Coordinates cross-functional workstreams, supports FDA and EMA/MHRA GCP and GVP inspections, maintains readiness materials, oversees quality governance and metrics, translates regulations into action, and presents recommendations to senior leadership. The role also manages stakeholder and vendor relationships, drives continuous improvement, and serves as an escalation point across quality functions.
Summary Generated by Built In

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? 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 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, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. 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 on‑site. Please speak with your recruiter and hiring manager for more information about on‑site 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)

$183,100.00 - $305,200.00

Skills Required

  • Bachelor's degree
  • Minimum 12 years of pharmaceutical industry experience
  • Deep knowledge of global pharmacovigilance regulations, quality management systems, and inspection readiness frameworks, including FDA CFR and GVP Modules
  • Demonstrated experience facilitating FDA and EMA/MHRA GCP and GVP inspections, including serving as an inspection point of contact
  • Experience overseeing QMP governance, metrics programs, and cross-functional quality oversight
  • Experience managing relationships across Global Development Quality, QPPV Office, Regulatory Affairs, and vendors
  • Advanced degree
  • Healthcare Professional background
  • People management experience

Regeneron Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Regeneron and has not been reviewed or approved by Regeneron.

  • Healthcare Strength Medical, dental, and vision coverage is positioned as comprehensive, with Regeneron prescription drugs covered at 100% for those enrolled in the medical plan. Mental health support is also emphasized through EAP access and tools like Talkspace and the Journey app.
  • Equity Value & Accessibility Stock grants are described as available to all employees, strengthening the overall total-rewards package beyond base pay. Long-term incentives and stock-related rewards are repeatedly framed as meaningful components of compensation.
  • Parental & Family Support Paid parental leave is paired with fertility/adoption assistance and childcare-related support such as discounts and nanny services. Additional family-oriented resources extend to elder care, pet care, and education support like college coaching and tutoring.

Regeneron Insights

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The Company
HQ: Tarrytown, NY
15,000 Employees
Year Founded: 1988

What We Do

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in. Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media. An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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