Job Title: Quality Control Analyst

Location: Framingham, MA

About the Job

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 Quality Control department supports the Seprafilm (medical device) and Sodium Hyaluronate (active pharmaceutical ingredient) GMP operations at the 74/76 NYA Manufacturing Facility. The department performs analytical testing on intermediate, in-process and final product materials using a variety of equipment to include GC, FTIR, UV-VIS, and Atomic Absorption.   Additional functions include stability testing, assay transfers and the qualification of new instrumentation utilized in the Quality Control laboratory.

This Quality Control Analyst I is responsible for performing routine testing of in-process samples, stability samples and final products in accordance with SOPs for product release

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?​

Main Responsibilities:

• Perform Assays in accordance with SOP’s for release, stability and in-process samples.

• Review QC data for compliance to procedures and specification. 

• Calculate and evaluate results

• Successful completion of assigned training

• Effectively demonstrate an understanding of cGMPs and application to specific responsibilities:

• Follow accurate written procedures for testing of in-process and final product samples.

• Provide input to the technical composition of operating documentation.

• Work independently under general supervision and direction.

• Work in compliance with cGMPs

• Practice safe work habits and adhere to Sanofi’s safety procedure and guidance.

• Perform preventative maintenance on basic laboratory equipment.

Basic Qualifications:

• Bachelor's Degree in Life Sciences discipline.

• Proficient in Outlook, Microsoft Word and Excel

• 1 Year Experience in a cGMP lab environment.

Preferred Qualifications:

• ​GMP laboratory as well as technical writing. Strong attention to detail and ability to multitask.

• Experience with pH, UV Vis Spectroscopy and wet Chemistry.

Special Working Conditions:

• Requires working with hazardous chemicals.

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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