Quality Control Analyst I

Job title: Quality Control Analyst I

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.

You are looking for an entry level position with an opportunity to learn multiple laboratory platforms and instrumentation. You are an enthusiastic individual who believes in our common mission to release safe, high quality, life-saving products to our patients. 

Our Team is a diverse group and will be able to offer their own experiences and knowledge that others don’t possess. They communicate openly with each other, sharing their thoughts, opinions, and ideas. They offer each other support and are always happy to help others when they need a helping hand.

QC Chemistry is responsible for testing intermediate, finished product, and stability samples in support of Framingham Manufacturing. Our state-of-the-art Integrated Continuous Biomanufacturing (ICB) Facility leads the way in delivering the next generation of biologics manufacturing. 

The Quality Control Analyst 1 is responsible for testing in-process, stability, and final product samples 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:

• 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 and 1 year of laboratory experience

• Bachelor’s Degree with 0-2 years of laboratory experience

• Proficient with Microsoft Office tools such as: Word, Excel & PowerPoint.

PREFERRED QUALIFICATIONS:

• 1 Year Experience in GMP lab environment.

• Experience with lab-based data management systems such as iLIMS or BioLIMS

SPECIAL WORKING CONDITIONS:

• Ability to lift 10 lbs.

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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