Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients

Job Title: Quality Control Biochem-Chemistry Testing 

Location: Framingham, MA

Full time - This is a 10-hour shift, workingSunday - Wednesday 7:00 a.m. - 5:30 p.m. OR 8:00 a.m. - 6:30 p.m.

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.

This Principle Quality Control Analyst is responsible for performing some routine and complex techniques associated with daily QC release and provides an in-depth investigative and technological orientation in implementing, executing and interpreting quality procedures and test methods. Successful candidate will substantially contribute to process and method improvements within the Quality Control laboratory.  

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 testing on complex laboratory equipment including HPLC, UPLC, Mass Spectrometer and Dionex Ion Chromatography instrumentation. 

• Investigate and troubleshoot Quality Control methods.  

• Review QC Data for compliance to procedures and specifications.  

• Prepare statistical analysis of results.  

• Prepare investigations related to OOS/OOT results.  

• Participate in training of less experienced staff on new procedures. 

• Transfer methods from support groups to the QC laboratory.  

• Formulate solutions to laboratory issues through testing of hypotheses.  

• Develop and author complex and explicit documentation for new and current procedures and technical reports.  

• Implement new technologies/instrumentation in the QC laboratory.  

• Provide technical leadership and guidance for the successful completion of major laboratory projects:  

• Implement new quality control procedures.  

• Transfer and develop new methods.  

• Identify deviations from QC methods and develop appropriate CAPAs.  

• Recommend method improvements.  

• Contribute substantially to the interpretation of results and subsequent impact to product/methods.  

• Represent QC as the prime technical contact for laboratory projects.  

• Work effectively with others to achieve shared goals and meet timelines.  

• Interact with internal and external personnel on technical matters requiring coordination between sites.  

• Work independently with minimal to no supervision and direction. 

About You

Basic qualifications:

• Bachelor's Degree in Life Sciences discipline and 6 years' experience in cGMP lab environment, or Master's Degree in Life Sciences discipline and 4 years' experience in cGMP lab Environment.  

• Proficient in MS Office and lab-based data management systems.  

• Ability to present technical data.  

• Ability to work independently on scientific projects.  

• Familiarity with USP and global compendial regulations.  

• Scientific technical writing ability including authoring and revising SOPs or technical reports.  

• Experience troubleshooting of assay and equipment issues. 

Preferred Qualifications

• Experience with Dionex, GC, HPLC, Gel Electrophoresis, UV Vis Spectroscopy and wet Chemistry.

• Experience with Empower software.

• Knowledge of lab-based data management systems.

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.

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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s 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, or gender identity.

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