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Job Title: Compliance Lead

Location: Framingham, MA

About the Job

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.

The Compliance Engineer organization supports the Engineering and Maintenance (EM) department by performing investigations and supporting the completion of CAPAs and change controls at the Sanofi, Framingham manufacturing facilities.

Responsible for managing a compliance EM department supporting and coordinating Compliance efforts for the EM Department consisting of Engineers and specialists. Supports manufacturing facilities and manages staff performance against department’s operational goals.

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

Management

• Ensure safety of all EM areas and work practices in accordance with site Health, Safety and Environmental program.

• Recruits and manages staff to execute department functions; ensure effective utilization of resources through consistent performance management, and rewards and recognition practices in area of responsibility.

• Provides leadership, guidance, and direction to staff in alignment cGMP requirements, department goals and corporate quality standards.

• Partners with the Manufacturing Scheduler to ensure on time closures of deviations that can impact shipment dates

• Create and maintain tracking metrics for Deviation, CAPA, and CCRs to ensure visibility to open or overdue events.

• Ensures that appropriate levels of trained resources are available to meet production schedules.

• Proactively identifies, assesses, and mitigates operational and organizational risks, escalate key risks and issues to manufacturing senior management and cross-functional support teams.

• Establishes key performance indications in alignment with department goals, maintain and report applicable area or organizational metrics.

• Escalate key risks and issues to manufacturing senior management and cross-functional support teams

Compliance/Training/Deviations

• Partners with Safety to ensure department compliance with requirements from

• Sanofi’s Safety Program including Health and Safety regulations and OSHA

• requirements.

• Ensures staff has appropriate knowledge of department processes and procedures to perform job responsibilities.

• Ensures EM documentation and EM records reflect practice, are

• aligned to cGMPs and corporate standards.

Partners with EM Managers to ensure the following:

• Design of the department training plan and manages training plan execution.

• Training materials are accurate and sufficiently detailed.

• Timely completion of investigations and deviations and CAPAs.

• Implementation of continuous improvement initiatives and changes controls as needed.

• Utilizes quality metrics to measure, analyze, and improve team performance.

Partner with Quality to ensure the following:

• Timely review of quality deliverables and “right first time”

• Ensures inspection readiness of assigned EM areas.

• Provides EM approval of department documentation changes.

• Participates in inspections conducted by external regulators

Continuous Improvement

• Identifies opportunities to improve EM processes and practices.

• Partners with cross-functional groups to troubleshoot and drive resolution of operational issues and proactively drive continuous improvement projects to completion.

• departmental projects and ensure appropriate controls, approvals, and validation requirements are implemented.

• Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs

About You

Basic Qualifications:

• Bachelor’s degree in Engineering, Automation, Life Sciences, or related discipline - preferred. A combination of education and experience will be considered.

• 5+ years of experience using various Root Cause Analysis tools (5W2H, fishbone, DMAIC, GPS3) which achieves consistent RFT (Right First Time) performance and the ability to perform Deviation Investigations - required.

• Experience leading direct reports or teams in a cGXP/cGMP environment - required.

Preferred Qualifications:

• Extended experience in EM and/or pharmaceutical manufacturing.

• Experience leading EM teams to maintain adherence to a demanding schedule.

• Experience working with cross-functional teams, including Quality, Manufacturing

• Technical Support, Operations, and Validation.

• Strong documentation practices including batch production records, SOPs, OJTs, and other controlled documents.

• Familiarity with Deviation Management Systems.

• Experienced in troubleshooting, investigation, root cause and risk analysis in a cGMP environment.

• Experienced leading the implementation of improvements to technical and business processes.

• Experienced in managing direct reports who have leadership responsibilities

• (supervisors and managers).

• Experienced in making tactical decisions on safety, process, scheduling

Special Working Conditions:

• Ability to gown and gain entry to manufacturing areas.

• Primarily day shift, with flexibility and accessibility to work with rotating shift(s)

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.

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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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.

Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.