Global Head of Quality Audit Inspection & Intelligence Advocacy

Sanofi; Cambridge (MA); Sur place; USD 260 000 - 360 000; Plein temps

Résumé du poste

Sanofi is seeking a Global Head of Quality Audit Inspection & Intelligence Advocacy in Cambridge, MA or Morristown, NJ. Lead risk-based audits, regulatory inspections, and advocacy across GXP, data-driven intelligence, and digital strategies to safeguard product quality and compliance.

You will drive cross-functional collaboration across Manufacturing, R&D, PV, and Commercial, shaping the quality agenda globally.

Qualifications

• 15+ years relevant experience in pharma, biotech, medical devices, or regulatory bodies.
• Strong experience with regulatory and pharmaceutical policy.

Responsabilités

• Design, develop and implement the department roadmap.
• Lead risk-based auditing strategies across GXP and external intelligence efforts.
• Manage Regulatory Inspection activities and pre-approval inspections.
• Support due diligence and reverse due diligence activities.
• Use data and digital tech to drive insights and knowledge sharing.
• Represent Sanofi at industry meetings and working groups.
• Foster a culture of quality and cGMP compliance across the organization.
• Operate with independence and a compliant risk-taking mindset.
• Scope includes Manufacturing, Supply, R&D, Digital, PV, and Commercial.

Connaissances

Fluent English

Transformational leadership

Change management

Cross-functional collaboration

Formation

Bachelor's degree in related science

Description du poste

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 Aff… 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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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.