Global Head of Quality Audit and External Liaison

Posted 2 Days Ago
Be an Early Applicant
2 Locations
In-Office or Remote
248K-358K Annually
Expert/Leader
Healthtech
The Role
Leads global quality audit, regulatory inspection, surveillance, and external liaison activities across pharmaceutical, biotech, medical device, and digital technology domains. Develops risk-based GXP auditing strategies, supports regulatory inspections and due diligence, represents the company with regulators and industry groups, and drives quality, compliance, data, technology, and continuous-improvement initiatives. Oversees activities spanning manufacturing, R&D, pharmacovigilance, commercial operations, and country organizations.
Summary Generated by Built In

Job title: Global Head of Quality Audit and External Liaison

  • Location: Remote, US

 

About the Job

The team vision is to become catalysts for providing risk based, predictive & objective assurance, insight, support, intelligence & The team vision is to become catalysts for positive change by identifying the unseen, providing risk based, predictive & objective assurance, insight, support, intelligence & advocacy.


The mission is to foster best in class performance by leveraging data, technology, and diverse talents to secure product launches and support compliance through quality audits, regulatory inspections, regulatory surveillance and advocacy. Core values are integrity, collaboration, innovation and expertise.


The team is comprised of ~40 people in 7 countries in USA, Euro 

 

Scope Includes

  • All Good X Practice (GXP) domains; Current Good Manufacturing Practice (cGMP), Good Distribution Practice (GDP), Good Pharmacovigilance Practice (GVP), Good Clinical Practice (GCP), Good Clinical Laboratory Practice (GCLP), and Data Integrity. 
  • Technology, including medical devices, computerized systems, in-vitro diagnostic (IVD) and digital technologies including artificial intelligence. 
  • Diverse product portfolio; Specialty Care, Vaccines, General Medicines, Consumer Health Care (until completion of Transition Agreement). 
  • Lifecycle activities for products including pre-authorization to submission, submission to launch, commercial (including post-approval commitments and post-approval changes), additional indications (line extensions), divestments, Pharmacopoeia Affairs (USA, Europe, China). 
  • Legislative lifecycle activities including development of new legislation, evolution of existing legislation, interpretation/enforcement of legislation

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

 

About Sanofi

We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system — and innovative pipeline — enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

 

Main Responsibilities

  • Design, develop and implement the department roadmap.
  • Risk-based auditing strategies, tactics, and operations across GXP. External engagement for intelligence and benchmarking, and advocacy for Sanofi critical topics. 
  • Regulatory Inspection Activities for routine and Pre-Approval Inspections by International Regulators. 
  • Support due diligence and reverse due diligence activities. 
  • Utilize data, technology to drive efficiencies, enhance insights, facilitate knowledge sharing, and simplify. 
  • Represent Sanofi externally at key industrial and trade association meetings and in working groups. 
  • Foster a culture of quality and cGMP compliance, engaging all organizational levels to drive continuous improvement. 
  • Latitude of action: Highly independent with thoughtful risk taking and compliance mindset. 
  • Role impact: continued right to operate for marketed products. 
  • Scope: Manufacturing & Supply, Research & Development, Digital, Pharmacovigilance, Commercial, Countries, as well as interfacing with other Auditing and Compliance organizations in Sanofi.

 

About You

Basic Qualifications

  • 15+ years relevant experience in the pharmaceutical, biotech, medical device, or related industries or a major regulatory authority. Strong experience with regulatory and pharmaceutical policy.
  • Inclusive, transformational, pragmatic leadership and change management. Fluent English. 
  • Bachelors degree in a related science required.

Preferred Qualifications

  • Previous experience as an auditor, interfacing with Regulatory Authority Inspectors, and/or Regulation Intelligence/Advocacy is a plus. French speaking is a plus

 

Why Choose Us

  • Bring the miracles of science to life alongside a supportive, future-focused team.  
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.  
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.  
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave
  • Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
  • Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale.
  • Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.


#GD-SG 
#LI-GZ

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Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

North America Applicants Only

The salary range for this position is:

$247,500.00 - $357,500.00

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Skills Required

  • 15+ years of relevant experience in pharmaceutical, biotech, medical device, related industries, or a major regulatory authority
  • Strong experience with regulatory and pharmaceutical policy
  • Inclusive, transformational, pragmatic leadership and change-management experience
  • Fluent English
  • Bachelor's degree in a related science
  • Previous experience as an auditor
  • Experience interfacing with regulatory authority inspectors
  • Regulatory intelligence or advocacy experience
  • French-speaking ability

Sanofi Compensation & Benefits Highlights

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

  • Retirement Support — Retirement support stands out through a notably strong 401K matching structure (e.g., 150% match up to a 6% contribution), which materially boosts total rewards for long-tenured employees.
  • Parental & Family Support — Parental and family support is positioned as unusually robust, including a global gender-neutral paid parental leave standard (14 weeks) and added supports such as childcare assistance and adoption/surrogacy/infertility help.
  • Equity Value & Accessibility — Equity participation is made more accessible via an Employee Stock Purchase Plan that includes a meaningful purchase discount and matching/free-share mechanics, increasing perceived total compensation beyond base pay.

Sanofi Insights

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The Company
HQ: Paris
85,000 Employees
Year Founded: 1973

What We Do

We are Sanofi, an innovative global healthcare company. We chase the miracles of science to improve people’s lives. Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions. Interactions with this account must comply with the Terms: https://bit.ly/sanofi-terms

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