Summary written by USA Jobs 24 from Sanofi's advert and our data on 17,030 current US jobs. How we check every job
At a glance
Sanofi is hiring a Global Head of Quality Audit Inspection & Intelligence Advocacy in Cambridge, MA; Morristown, NJ. It is a full-time role in Finance, Banking & Accounting, asking for at least 15 years of experience, first listed on November 1. The advertised pay is $247,500–$357,500 a year. The description mentions Google Cloud. Sanofi has 99 other openings in the US, 29 of them in Cambridge, MA.
How the pay compares
Sanofi advertises $247,500 to $357,500 a year, a midpoint of $302,500 a year. Where an offer lands in a range usually depends on experience and on the exact location. That is higher than about 96% of the 51 finance & banking jobs in Massachusetts that publish a yearly rate on USA Jobs 24, where the typical midpoint is $124,000 a year. To see roughly what this leaves after federal and Massachusetts tax, try our take-home pay calculator.
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Before you apply
- Check it is still open. We found this job on Sanofi's Workday site on November 1 and checked it again November 4, 5:17 AM ET. When an employer takes a job down, we remove it at our next daily update.
- Check the location works for you. This role is based in Cambridge, MA (or one of 1 other locations). If you would need to move, ask whether relocation help is offered.
- Match the experience. The advert asks for at least 15 years of experience. If you are a little short, a close match on the skills in the advert can still win an interview.
- Tailor your resume. Use the advert's own words, such as Google Cloud, wherever they are true for you. Our resume guide shows how.
- Know your number. Decide the lowest offer you would accept before the first call. Our salary negotiation guide explains how to ask for more.
- Apply only through Sanofi's own site. Our Apply button goes straight to Sanofi's Workday page. If anyone contacts you about this job and asks for money, gift cards or bank details, stop and check it with our scam checker. Read how to spot a fake job offer.
About hiring at Sanofi
Sanofi has 100 openings on USA Jobs 24 today across 28 states. Most are in healthcare & pharma (15), data & AI (12) and sales & BD (9). The biggest locations are Morristown, NJ (30), Cambridge, MA (30) and Framingham, MA (9). 2% of them are remote, 13% are open to entry-level candidates and 59% show pay. We collect Sanofi's jobs every day straight from its own careers system (Workday), never from job boards or agencies.
The employer's advert
This is Sanofi's own description of the job, copied word for word from its careers site. We have not edited it.
Show the full advert from SanofiHide the advert953 words
Job title: Global Head of Quality Audit Inspection & Intelligence Advocacy
- Location: Cambridge, MA or Morristown, NJ
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.
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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 - $357,500.00All 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.
USA Jobs 24 copied this listing from Sanofi's official careers site on November 1, 2026 and checked it again November 4, 5:17 AM ET. Sanofi will never ask you to pay to apply or to buy equipment with a check they send you. If anyone does, it is a scam.
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