Production Operator

Sanofi; Pearl River (NY); Presencial; USD 33 000 - 44 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Parental leave and healthcare benefits

Competitive benefits package

Resumo da oferta

Sanofi in Pearl River, NY is seeking a Production Operator to operate and maintain large-scale bioreactors and associated equipment under cGMP guidelines. You will perform aseptic technique, cleaning, calibration, and documentation, contributing to the production of recombinant protein therapies.

The role requires attention to detail, adherence to safety standards, and ability to work flexible schedules including weekends/holidays as needed.

Qualificações

• Education requirements include a high school degree with 3-5 years in a cGMP manufacturing environment or a BS with 1-3 years’ experience.
• Bioreactor experience is preferred.
• Strong documentation and attention to detail required.
• Knowledge of cGMP and GMP training expected.

Responsabilidades

• Operate general manufacturing equipment under supervision in the production of Flublok Drug Substance.
• Perform operation, maintenance, cleaning and sanitization of large-scale bioreactors and related equipment.
• Document accurately and follow SOPs and GDP requirements.
• Troubleshoot equipment issues and communicate with management.

Conhecimentos

English fluent

Good communication

MS Word & Excel

Formação académica

High School degree with 3-5 years’ cGMP experience

BS degree with 1-3 years’ experience

Ferramentas

Valves

Filters

Piping systems

HMI systems

Instrumentation

Descrição da oferta de emprego

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, you’ll 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.

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.

Main Responsibilities

• 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.

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?

• high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Equal Opportunity

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

North America Applicants Only

The salary range for this position is: $24.00 - $32.00 All compensation will be determined commensurate with demonstrated experience.

We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.

Discover more about us visiting www.sanofi.com or via our movie

We are Sanofi Start a career that makes a difference. Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug‑discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.