Production Operator
Company: Sanofi
Location: Pearl River
Posted on: April 4, 2026
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Job Description:
Job Title: Production Operator Location: Pearl River, NY About
the Job Join a global network that powers how Sanofi delivers
seamlessly, purposefully, and at scale. In Manufacturing & Supply,
youll help reimagine how life-changing treatments reach people
everywhere, faster. 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.
Primary responsibility of the incumbent will be operation of
general manufacturing equipment under close supervision in
accordance with current relevant quality standards or standardized
procedures and within safety guidelines in the production of
Flublok Drug Substance in the large-scale recombinant protein
production operations of the cGMP commercial manufacturing
facility. Requires good documentation skills and attention to
detail. Duties will include the operation, maintenance, cleaning
and sanitization of large-scale cell culture bioreactors and
associated operations such as media preparation, infection, and
harvest. Activities will include executing techniques such as
large-scale bioreactor cell expansion with the use of
stainless-steel vessels and single use bioreactors (SUBs) including
transfer lines, ancillary equipment (tube welders, tube sealers,
peristaltic pumps), use of water-for-injection (WFI) point of use
taps, etc. Other duties will include the cleaning and preparation
of workspaces and biosafety cabinets. Proficiency in aseptic
technique, preventive maintenance, and changeovers for area
equipment, including biosafety cabinets, magnetic mixers,
in-process testing equipment (cell analyzer, microscope) required.
The incumbent should have the ability to identify, troubleshoot and
participate in 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. Secondary responsibilities will be to aid in the
troubleshooting of problems as they arise in the assigned areas.
Business needs may also require database entry, cross training, and
operations in flex areas. We are an innovative global healthcare
company with one purpose: to chase the miracles of science to
improve peoples lives. Were 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? About Sanofi Were an
R&D-driven, AI-powered biopharma company committed to improving
peoples lives and delivering compelling growth. Our deep
understanding of the immune system and innovative pipeline enables
us to invent medicines and vaccines that treat and protect millions
of people around the world. Together, we chase the miracles of
science to improve peoples lives. Main Responsibilities: In depth
understanding of techniques and processes being executed on routine
basis. Responsible for all aspects of large-scale bioreactor cell
expansion and protein production including equipment preparation
(CIP and SIP), appropriate use of raw materials and components
(FIFO), material sampling for applicable analytical testing, filter
integrity testing, etc. Perform cell analysis and data
interpretation of cell culture samples with the use of the cell
counter, including operation of microscope for contamination
checks. Responsible for the operation and maintenance of ancillary
equipment such as floor scales, turbidity meters, tube welder, tube
sealer, peristaltic pumps, etc. Interacts with other departmental
personnel to assist in resolving manufacturing quality issues.
Technician should have the ability to manage and analyze
manufacturing data. Ability to take initiative to identify issues,
troubleshoot, propose solutions, and keep management informed.
Ability to present and explain techniques and results of
manufacturing processes with outside departmental personnel. Ensure
good documentation practices (GDP) in execution and reviews of
production records. Responsible for all required cGMP training
including additional training assigned by their manager.
Participates in the cleaning of the cGMP facility in accordance
with sanitary maintenance SOP. 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, and as needed by department. Work with Compliance
regarding notification of deviations and CAPAs as they occur and
provides information during investigations. Other duties as they
are required. About You Requirements: Education: High School degree
with at least 3-5 years experience or training in a cGMP
manufacturing environment OR BS degree with 1-3 years of work
experience. 1-3 years Bioreactor experience preferred. Working
knowledge of manufacturing equipment and associated systems,
including but not limited to: Valves (manual, automated, control)
Filters (various types such as cartridge, bag, and membrane
filters) Piping systems (materials, fittings, layout, and flow
principles) HMI (Human-Machine Interface) systems for equipment
monitoring and control Instrumentation for pressure, temperature,
and flow monitoring Familiarity with safe startup, operation,
shutdown, and maintenance procedures for process equipment.
Experience working in a regulated manufacturing environment (e.g.,
food, pharmaceutical, chemical, or industrial) is a plus. Strong
attention to detail and adherence to safety and quality standards.
Knowledge of cGMP. English fluent, both written and spoken. Good
communication and social skills. MS Word and Excel proficiency
preferred but not required. Must be able to lift up to 50 lbs., and
bend/lift/move objects as part of the job. 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 its 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.
GD-SP LI-SP LI-Onsite vhd All compensation will be determined
commensurate with demonstrated experience. Employees may be
eligible to participate in Company employee benefit programs, and
additional benefits information can be found here.
Keywords: Sanofi, Tenafly , Production Operator, Engineering , Pearl River, New Jersey
