Job Title: Quality Control Analyst - QC Raw Materials

Location: Northborough, MA

About the Job

We deliver 4.3 billon 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 Quality Control Raw Materials Department is responsible for the testing of Raw Materials and Components for use at Sanofi Massachusetts manufacturing sites. The department is responsible for the management and continuous improvement for control, testing, and inspection of raw materials. A Quality Control Analyst will be expected to successfully execute the responsibilities relating to sampling, testing, and inspection of Raw Material lots.

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?

**This is an onsite role, Monday - Friday, dayshift. **

Main Responsibilities:

• Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans

• Maintaining on time completion of all training requirements

• Performing tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks.

• Performing QC Data Review of executed tests by other analysts and external contract laboratories in a timely manner with a high attention to detail.

• Executing assigned CAPAs related to remediation plans and Continuous Improvements

• Actively participating in compliance events such as Deviations and Investigations

• Coordinating logistics and communication with contract testing laboratories for supplier certification testing.

About You

Expected Experience:

• Bachelor's Degree with 4 plus years of experience in Quality Control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements

Preferred Experience:

• Experience with laboratory instrumentation such as, but not limited to, pH, GC, UPLC, UV/VIS, FTIR, ICP-MS

• Experience working in a clean room environment with aseptic techniques

Expected Technical Skills:

• Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement

• Keen attention to detail to ensure accuracy in testing reporting, and compliance with regulatory requirements

• Proficiency in identifying issues and implementing effective solutions to resolve Quality Control problems

Special Working Conditions:

• Ability to perform tasks in a Quality Control Laboratory environment with hazardous chemicals and capable of lifting at least 10 pounds. Ability to enter into controlled environments following proper gowning protocols. May be required to pass vision exam to perform specific responsibilities.

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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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.

North America Applicants Only

The salary range for this position is:

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.