Job Title: Quality Control Professional

Location: Ridgefield, NJ

HOURS: Consist of two possible shifts:

Monday - Friday from 7:00 AM to 3:30 PM, or Monday - Friday from 10:00 AM to 6:30 PM Some flex in the start and end times may be allowed; weekend work and overtime as required.

About the Job

The Quality Control Analyst I is dedicated to the Microbiology Laboratory and EM Monitoring Program. The role of the Quality Control Analyst I will be that of various Microbial testing, Environmental monitoring of the aseptic production areas, ordering and stocking supplies, creating/reviewing SOPs, investigation writing, data entry. This role is responsible for providing the day-to-day operation, testing and Environmental monitoring for the Micro team.

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 Professional within our Micro 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?

Main responsibilities:

• The candidate must have previous quality control microbiology experience. Experience in bioburden testing, membrane filtration, sterility isolator testing, conductivity, total organic carbon or endotoxin assays is preferred

• Basic knowledge of aseptic manufacturing environmental monitoring of Grade A-D Areas.

• SOP review, creation and approval is preferred

• Basic knowledge of compliance with all cGMP standards, safety and environmental regulations and company SOPs.

• Data entry of EM sampling results, LIMS, logbooks, and other miscellaneous lab data.

About you

• BA/BS in Microbiology/Biology with 2+ years’ experience in CGMP, pharma or lab environment is required.

• Environmental monitoring experience

• Practical experience in general microbiology laboratory techniques working with bacteria, yeast and mold.

• Prior experience with data review, authoring SOPS, Change Controls, out of specification investigations and report writing is recommended.

• Working knowledge of cGMPs in pharmaceuticals/biological/aseptic/medical device manufacturing

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 (https://www.youtube.com/watch?v=SkpDBZ-CJKw&t=67s) and check out our Diversity Equity and Inclusion actions at sanofi.com (https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness) !