Job Title: Senior Quality Engineer

Location: Ridgefield, NJ

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.

The Senior Quality Engineer is part of the Quality Assurance Department at Ridgefield, NJ. This role is responsible for supporting the Change Control and Risk Management Quality Systems.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

 Job Responsibilities

• Perform Quality assessments on all new change controls and assist in the determination of the required actions and deliverables for implementation and closure, based on the criticality and product impact of the proposed change.
• Act as a risk facilitator in the completion of formal and less formal risk assessments.
• Represent Change Control and Risk Management programs during internal and external audits.
• Participate in Change Control Community of Practice and serve as Site Contact for Multi-site Change Control Assessments
• Collaborate with LIMS, Documentation Management, and Product Release departments for change control holds and coordinate implementation timing.
• Provide CCR Users with direction and guidance for Change Controls and on the use of the Phenix CCR Module
• Mentors site personnel in risk tool vetting process, risk strategy development, and in all other risk inquiries.
• Follow up with change control owners and task owners to ensure that required actions are completed in a timely and compliant manner.
• Assists in the oversight of the site’s Change Control and Risk Management Programs by monitoring the status of open items and compiling/reviewing program metrics.
• Perform annual review of changes to assess cumulative effect of changes on process performance, product quality or on the overall validation status of the affected process, facility, or system.
• Complete living risk reviews and determine requirement to update risk assessment documents.
• Support continuous improvement of the Change Control and Risk Management systems to simplify and streamline ways of working by trending metrics for the programs.
• Perform Product Quality Reviews
• HSE
• It is required that individuals care for their own safety and wellbeing. Individuals must promote a safe working environment for employees and contractors working in their area of responsibility.
• The individual must support all Sanofi and site HSE policies as well as ensure that work performed is compliant with local HSE regulations.

About You

Education and Experience

• A minimum bachelor’s degree is required (preferably in Life Sciences or Engineering) with 5 years of Quality experience which must include Change Control or Quality Risk Manaqement
• 7 years of Quality Systems and/or Quality Compliance experience preferred

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.

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.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.