Production Technician

Sanofi • Pearl River, NY

1d • Onsite

About The Position

This position is responsible for ensuring that all sampling is performed at the required frequency, including environmental monitoring and utilities sampling in cGMP areas. The role also supports manufacturing operations by preparing all necessary materials, including glassware washing, transfer assembly setup, and autoclaving. In addition, the position involves preparing media, buffers, reagents, and solutions in accordance with approved SOPs and batch records to ensure compliance and operational readiness. 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. Sanofi is an R&D-driven, AI-powered biopharma company committed to improving people’s 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 people’s lives.

Requirements

• High School Diploma plus 1-year experience or training in a cGMP manufacturing environment.
• Strong content knowledge in cGMP/regulatory compliance.
• English fluent, both written and spoken
• Good communication and social skills

Nice To Haves

• Aseptic technique sampling experience in GMP environment is preferred

Responsibilities

• Execute standard operating procedures (SOPs) in routine/non-routine sampling process in areas of the cGMP manufacturing facility.
• Prepare media, buffers, reagents, and solutions according to approved SOPs and batch records
• Perform weighing, measuring, mixing, pH adjustment.
• Perform aseptic sampling (Environmental monitoring sampling, WFI (water injection), PUW (Purified Water) and Clean Steam Sampling)
• Prepare material for manufacturing process (Glassware washing, Transfer Assembly preparation and, Autoclaving)
• Perform routine cleaning of the cGMP facility.
• Interact with other departmental personnel to assist in resolving manufacturing quality issues.
• Maintain records and documentation in accordance with a cGMP environment.
• Work a flexible work schedule, weekends and holidays as required.
• Follows instructions on notification of deviations as they occur and provides information during investigations.
• Must be able to support additional manufacturing activities as needed.

Benefits

• endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs
• at least 14 weeks’ gender-neutral parental leave.
• Company employee benefit programs.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 11-50 employees