Activités Industrielles
Là où les miracles
de la science
deviennent une réalité pour les patients

Job Title: Production Technician USP

Hours: Monday - Friday 7:00 a.m. - 3:30 p.m. Overtime as needed.

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. 

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 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:

• 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 diploma or GED with 3+ years’ experience OR training in a cGMP manufacturing environment OR BS degree with 1-3 years of work experience.

• 1-3 years Single Use 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.

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.

THE FINE PRINT  -

• For influenza production roles (excluding FFIP roles): candidate must be able to be receive influenza vaccine which is required for building access

• For aseptic area production roles (excluding Flu production tech roles): candidate must be able to obtain and maintain current aseptic gowning qualification

• This position may be required to be moved or temporarily flexed to another department or building within the FFIP operation due to business needs. Additionally, candidates should expect to work in multiple buildings. Some over-time/off-shift work hours may be required based on business needs. We will attempt to provide as much advance notice as possible, two weeks where applicable if any such change is needed.

• Must be able to lift up to 25 lbs., and bend/lift/move objects as part of the job.

• •Able to stand for up to 8 hours a day (with occasional breaks)

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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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.

Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.