Vaccines
Where
extraordinary minds
help protect  half a billion people

Job title: Manager, Quality Operations - Vaccine

Location: Waltham, MA

About the job

The Manager of Quality Operations ensures internal and external compliance to Sanofi’s Standard Operating Procedures and that current industry standards have been met throughout the development life cycle of Sanofi’s products. This position will be responsible for helping provide leadership and direction to the Operational Quality team and will be responsible to influence and help evolve the Quality mindset with the organization. This position is defined as a Manager level position reporting directly to the Head of Quality.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Main Responsibilities:

• Partner with Analytical Development, QC, Internal/External Manufacturing and Quality Operations direct reports to strategically develop and implement a phase appropriate approach to quality assurance and quality assurance systems.

• Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s).

• Assist in the development and maturation of strategic planning to meet Quality KPIs and goals, while interfacing with front line managers in the coaching and mentoring of quality related decision making.

• Help establish and maintain phase-appropriate cGMP compliance for product manufacturing, testing and stability; leading the team to ensure appropriate review and approval of master production records (internal/external) executed production records (internal), in-process and release testing, specifications, reference materials, test results, etc.

• Serve as Quality Assurance for all documentation generated during the course of execution for CoE Raw Materials, QC Lab and Manufacturing support, to include the Stability program, but not Batch Release activities.

• Quality oversite for external manufacturing of Lipids, Enzymes, pDNA and master cell banks.

• Build and successfully manage Quality to Quality relationship with CDMOs, including periodic visits to CDMOs as required, and representing Sanofi QA on CDMO project teams.

• Build the strategic platform to harmonize Ways of Working between the Waltham and France Center of Excellence facilities, aligning both sites in a common approach to Operational Excellence.

• Establish and track Quality metrics, working with internal and external stakeholders while communicating proactively to senior management any issues for resolution.

• Ensure the Waltham Quality department meet standards expected by US, global regulatory authorities and Sanofi Global Standards- for research, development and ultimately commercial activities.

• Maintain an effective Quality governance and continually improve governance to meet business and compliance needs. Determine applicable quality standards and regulations and provide guidance and quality oversight to ensure ongoing compliance with the operational team.

• Establish strong working relationships with external manufacturers of our products and assure alignment of our Quality Systems and requirements with these CDMOs. Work with global Quality and technical teams to assess and resolve discrepancies and non-compliance events to ensure the quality of the product through performance of thorough investigations and risk assessments.

• Communicate significant quality risks that may impact product suitability or regulatory compliance, in both a timely and effective manner to the Head of Quality and key business stakeholders.

• Review and edit Quality Technical Agreements, contracts, supply agreements, etc- to provide quality input to project/program plans, master service agreements and statements of work.

• Work cross functionally, representing the Quality group on discovery and development teams, line functions and to senior management for awareness of and compliance with quality/regulatory requirements.

• Collaborate with key Business Partners within the greater Sanofi organization and help build relationships for team members execution of tasks.

• Supports and improves (as needed) processes and SOPs in the area of: Deviations/Investigations, CAPAs and Change Control.

• Supports and improve (as needed) the Inspection Readiness Program.

• Support and improve (as needed) the Internal and External Audit schedules/programs.

• Promote a quality mindset within the GxP operational areas by ensuring consistent, risk based and innovative thought processes are employed to advise and make decisions.

• Ensure implementation and evaluation of corrective and preventative actions to address systemic issues.

• Motivate and coach the Quality Operations team to operational success- both in terms of quality delivery and customer satisfaction.

• Consistently promote high standards through personal example and lead the team in a manner that each member understands the standards and behaviors expected of them in relation to quality and compliance.

• Develop and maintain strong relationships with internal and external stakeholders to ensure optimal performance for Quality Operations.

• Review, implement and update company records- Policies/SOPs, performance reviews, risk assessments, etc.

• Communicate to the team Key Performance Indicators from SLT down, in a manner that each employee is in alignment with company goals and motivated to achieve success.

• Develop and maintain strong relationships with internal and external stakeholders to ensure optimal performance for Quality Operations.

About You:

• Earned Bachelor's degree (required, Master's degree preferred) within a STEM (Science, Technology, Engineering or Mathematics) discipline.

• Pharmaceutical/biotechnology industry experience (12+ years) with at least 10 years in a Quality Assurance function.

• Experience in working in compliance with US, EU and ICH GMP requirements, experience reviewing submission documentation, responses to regulatory inquiries and inspections is needed.

• Strategic experience with senior leadership team level clients, strong decision making capability and personal accountability within the organization.

• Expert knowledge and experience with data analysis, reporting, and trending is extremely valuable.

• Proven success in identifying and implementing organization-wide operational excellence/improvement initiatives is highly desired.

• Preferred experience with outsourced manufacturing and testing operations.

• Strong leadership and management experience with the ability to work in a matrix environment.

• Excellent written and verbal communication skills including the ability to communicate and negotiate across the organization, at all levels.

• Demonstrated ability to work across functions at all levels where the incumbent may not have direct authority to accomplish objectives, i.e. influence beyond your role.

• Ability and desire to work in a fast-paced, start-up environment.

• Strong collaboration, team-building skills and communication skills.

• Independently motivated and detail-oriented with good problem-solving ability

• Demonstrated effective time management skills.

• Sound judgment and commitment to ethical conduct.

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.

Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com