QC Sample and Raw Material Coordinator

Job Title: QC Sample and Raw Material Coordinator

Location: Pearl River, NY

About the Job:

The individual in the role will be in charge of sample management and shipping of drug substances, drug products, and raw material samples throughout the Contract Manufacturing sites, Sanofi Network sites, and Contract testing sites. The incumbent will also serve as the single point of contact for raw material testing, including results gathering, and serve as liaison between the release groups for timely provision of test data. The incumbent will also support the management in handling all administrative tasks related to sample test coordination between multiple sites.

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.

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 lives.

Main Responsibilities

Coordinating, packaging and shipping product test samples for contract testing at External laboratories, Sanofi Network sites, and other third parties.

Track all Raw material testing tasks and serve as the sampler for Raw materials for QC testing and other requirements at both Meriden, CT and Pearl River, NY locations.

Support testing as required.

Handle all administrative tasks related to sample/results management in a timely and compliant manner.

Serve as the single point of contact for all raw material testing and results coordination.

Alert management on testing issues including Out of Specifications, Deviations, and other laboratory events at external sites. Serve as the QC liaison for Raw Material related issues with the product release group.

Serve as the material coordinator for the QC lab, including the tracking of critical reagents and sourcing/ordering of day to supplies and chemicals/reagents.

Aggregate data for release binders for Drug Substances, Drug Products and other associated test documents for final review by QC management.

Tabulate and maintain QC data including stability data, routine release data, and serve as the data entry person for all QC and externally generated data.

Support management in data retrieval for reports and protocols.

Assist in the support and management of laboratory equipment including daily monitoring and maintenance tasks.

Promote a safe, positive, and compliance-driven work environment

Other responsibilities as assigned by the laboratory management.

About You

Basic Qualifications

Bachelor's degree in Science, Engineering or related field.

2+ Years of laboratory/manufacturing experience in a pharmaceutical or related industrial environment.

Skills

Familiarity with routine laboratory operations including handling test materials, chemicals, reagents and samples.

Prior experience in logistics is highly desirable.

Excellent organizational skills with aptitude for multi-tasking.

Strong and effective communication skills required.

Experience in Electronic systems such as LIMS is desired. A good command of Microsoft Excel as an organizational tool is highly desired.

​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 Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; colour; 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:

$90.000,00 - $130.000,00

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 .