Job Title: Senior Production Technician USP

Location: Pearl River, NY

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 a Senior Production Technician USP within our Vaccine Production Ops 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?

Position Overview:

Primary responsibility is large-scale recombinant protein production operations for commercial production through execution of SOPs, Batch Records, and all associated cGMP activities in the manufacturing facility. Duties include operation, maintenance, cleaning in place (CIP) and sterilization in place (SIP) of large-scale cell culture bioreactors and associated operations such as media preparation, infection and harvest. The incumbent is capable of identifying, troubleshooting and leading the resolution of operational and equipment problems as they arise in the large-scale Bioreactor and Media Preparation areas with minimum supervision and effective communication to management.

Leads or supports in the updating of current or new batch records for current or new processes, initiation of change controls, deviations and the closing of these documents. Leads the training of junior personnel within the large-scale Bioreactor and Media production areas. May include cross training to support other areas including cell culture, clarification, buffer preparation.

Responsibilities:

• In-depth understanding of techniques and processes being executed on routine basis.

• Understanding of the BEVS manufacturing process. Ability to manage and analyze manufacturing data to identify and support changes and improvements.

• Interacts with other departmental personnel to assist in resolving manufacturing quality issues.

• Ability to present and explain techniques and results of manufacturing processes with outside departmental personnel.

• Responsible for identifying required training and training on, understanding, and following documented procedures which apply to their departments that support the Quality System.

• Maintains records and documentation in accordance with a cGMP environment and improves as necessary.

• Participates in the cleaning of the cGMP facility in accordance with sanitary maintenance SOP.

• Cross-training as a support operator as required.

• Follows established SOPs for the flow of materials, personnel and equipment in and out of the cGMP facility.

• Work a flexible work schedule, weekends and holidays as required (estimated ≥1 weekend per month). Potential to switch to second shift or weekend shift.

• Follows instructions on notification of deviations as they occur and provides information during investigations.

• Other duties as they are required.

About you

• Education: High School degree with at least seven years of experience or training in a cGMP manufacturing environment OR

• BS degree with three years of experience OR

• MS degree with one year of experience

• Knowledge of cGMP

• English fluent, both written and spoken

• Good communication and social skills

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.

The salary range for this position is $26.32 to $32.90 USD Hourly. All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the link, www.benefits.sanofiusallwell.com

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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!