Job Title: Quality Control Microbiology Analyst 1

Location: Framingham, MA

Shift Schedule: 2nd shift - Wednesday-Saturday 12 PM - 10:30 PM

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. Your job, as Quality Control Microbiology Analyst 1 within our Quality Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people.

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?

Department Description:

Quality Control Microbiology (QCM) is responsible for testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation. Quality Control is also responsible for assisting in site wide studies and projects.

Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs.

Position Summary:

This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations.

Core Responsibilities:

• Perform laboratory assays in support of Method Development, Product Release, and Stability.
• Troubleshoot assay and Instrument problems with departmental leads.
• Review data for compliance to procedures and specifications.
• Calculate and evaluate results.
• Successful completion of assigned training.
• Make detailed observations in support of Alert, Action and OOS result investigations.
• Participate in writing and revising SOP’s.
• Ensure lab areas are clean, safe and properly stocked.
• Effectively demonstrate an understanding of cGMPs and application to specific responsibilities:
• Work compliantly & independently under supervision and direction.
• Follow accurate written procedures for testing of in-process and final product samples.
• Practice safe work habits and adhere to Genzyme’s safety procedures and guidelines.
• Perform maintenance on basic laboratory equipment.

About you

Basic Qualifications:

One of the following:

• High School Diploma with minimum of 4 Years of relevant industry experience.
• Associates Degree with 2-4 Years of relevant industry experience.
• Bachelor’s Degree with 0-2 Years of relevant industry experience.
• Proficient with Microsoft Office tools such as: Word, Excel & PowerPoint

Preferred Qualifications:

• 1 Year Experience in GMP lab environment.
• Proficiency in Microsoft Office tools such as: Word, Excel & PowerPoint.
• Experience with lab-based data management systems.
• Experience in a Quality Control Laboratory.
• Experience with Environmental Monitoring, including Water Testing.

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!