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Senior Manager GVP Quality Management Lead

Regeneron Pharmaceuticals, Inc.
Tarrytown, New York
Start date
Sep 8, 2023

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Quality, Quality Control
Required Education
Bachelors Degree
Position Type
Full time
Pharm Country, Best Places to Work

Job Details

The Regeneron GVP Quality Management Lead (QML) is a key position that we believe will guide and lead all aspects of quality and compliance within global pharmacovigilance (PV) system. We expect the Sr. Manager to build strategic partnerships and direct risk-based quality management activities with key partners impacting the global Regeneron PV system. Furthermore, the GVP QML Sr. Manager will be responsible for supporting inspection readiness at all times. The GVP QML will partner with other members of the Global Development Quality Governance and Oversight (GDQGO) department to identify trends through metrics in order to diagnose and remediate systemic quality issues.

In this role, a typical day might include the following:
  • Responsible for leading GVP-compliant activities from a quality perspective in conjunction with business and Associate Director / Director, GVP QML
  • Engage with, support and liaise with multiple cross-functional collaborators whose work impacts the Regeneron global PV system, including but not limited to: Global Patient Safety (GPS), Medical Affairs, Regulatory, Commercial, etc.
  • Participate in process improvement activities, lead projects in support of quality objectives, and support inspection readiness activities
  • Act as a primary liaison to GPS to advise on any quality issues and ensure compliance
  • Provide day-to-day quality and compliance support to cross-functional team members, including Suspected Serious Non-compliance (SSN)/issue management (triage/investigation/actions), audit responses, proactive quality management, CAPA oversight, audit/issue trending
This role may be for you if:
  • You have skills in taking initiative and working independently across multiple areas.
  • You can make decisions on complex issues under minimal guidance that have a significant impact on business operations related to PV.
  • You are self-motivated with the ability to work effectively and provide mentorship to others in a dynamic environment with ambiguity.
  • You bring expertise of GVP and are a sought-out resource to evaluate novel problems and develop innovative solutions for critical organization-wide issues.
  • You have acted as a PV expert, managed quality and compliance issues related to post-marketing and clinical trial safety

To be considered, we are looking for individuals with a Bachelors degree (Masters degree preferred) or equivalent qualification with 7+ years of relevant industry experience. 5+ years proven experience working in either a PV compliance group, PV audit/QA, Quality Management/Quality Risk Management function, or PV department with expertise and/or transferrable skills with Good Pharmacovigilance Practices and Regulatory Inspections.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and equity awards, annual bonuses, and paid time off for eligible employees at all levels!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. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually)

$126,600.00 - $206,600.00


Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to seven FDA-approved treatments and numerous product candidates in development, all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye disease, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, infectious diseases, pain and rare diseases.
Regeneron is accelerating and improving the traditional drug development process through our proprietary VelociSuite® technologies, such as VelocImmune® which produces optimized fully-human antibodies, and ambitious research initiatives such as the Regeneron Genetics Center, which is conducting one of the largest genetics sequencing efforts in the world.

Stock Symbol: REGN

Stock Exchange: NASDAQ

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Company info
Corporate Headquarters
777 Old Saw Mill River Road
New York
United States

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