Quality Control Chemistry Analyst

Sanofi•Framingham, MA

1d•$78,000 - $112,667•Onsite

About The Position

QC Chemistry performs testing in support of Framingham Manufacturing. The new Framingham Manufacturing facility is one of the first of its kind worldwide and puts Sanofi at the forefront of bio-manufacturing. The whole industrial process is digitalized, paperless, and is 80 times more productive than a traditional factory. Our Framingham facility leads the way in delivering the next generation of biologics manufacturing. The 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. They take time to have fun by cultivating relations with group activities and celebrating each other’s life events. 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. Who You Are: You are a dynamic Quality professional interested in providing quality support and guidance of assays to Quality Control Chemistry for release life-saving product to our patients. You are a valued influencer and mentor who has contributed to QC assay review of a Biologics or Pharmaceutical organization. You have a keen eye for improvement opportunities and the demonstrated ability to deliver on these opportunities using your personal experience.

Requirements

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-year experience in cGMP lab environment.
Proficient in Outlook and Microsoft Word and Excel and lab-based data management systems.
Experience in GMP Pharmaceutical/Biologics
Experience with HPLC, Gel Electrophoresis, UV-Vis Spectroscopy, or wet Chemistry.
Experience with Empower software.
Familiarity with USP and global compendia requirements.
Knowledge and experience with discrepancy investigation and lot disposition to meet regulatory requirement

Responsibilities

Review QC Data for compliance to procedures and specifications
Experience in HPLC/UPLC, Gel Electrophoresis, Spectrophotometric assays
Collaborate on Quality Control method investigation and corrective action implementation
Work effectively with others to achieve shared goals.

Benefits

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.
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.

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