# NTO Manufacturing Associate at Sanofi

Sanofi is hiring an NTO Manufacturing Associate. It pays $27-$36/hr and Level rates it Little AI ●○○○; you can [apply on Sanofi](https://jobsbylevel.com/go/988b1490-7f55-4b4d-b0a7-086d3536bd0d?utm_medium=ai-agent).

AI Level 1, AI centrality 34 out of 100. Framingham, MA.

## Details

- Company: [Sanofi](https://jobsbylevel.com/companies/sanofi)
- AI level: AI Level 1 (score 34 out of 100)
- Location: Framingham, MA
- Salary: $27-$36/hr
- Posted: November 9, 2026
- Apply: https://jobsbylevel.com/go/988b1490-7f55-4b4d-b0a7-086d3536bd0d?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=nto-manufacturing-associate-at-sanofi-2eb128

## Description

Job title: NTO Manufacturing Associate Location: Framingham, MA Shift : 12 hrs Rotating Night Shift 7pm-7am 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. Department Description: 8 NYA is an integrated, continuous, biomanufacturing facility (ICBF). The facility is operated by upstream, downstream and support services groups which support a 24/7 large-scale therapeutic protein manufacturing facility housing multiple products. Position Overview with Key Responsibilities : This is a 12 hour, rotating nighttime position in a flexible, single-use technology, large scale cGMP biologics facility. Initial job responsibilities will include leading a team responsible for a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations. The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. About Sanofi We’re 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. Main Responsibilities: Maintains a safe working environment and reporting of incidents/accidents to Manufacturing management. Effectively demonstrates understanding of GMPs and how they apply to specific responsibilities. Follows verbal and written procedures in operating production and equipment and performing processing steps; accurately completes appropriate production documentation. Maintains cleanliness and orderliness in process area. Ensures production area is stocked with supplies. Performs batch record review, EWI (Electronic Work Instruction) revisions, and work order generation. Interacts with other support functions such as Quality Assurance, Quality Control, Manufacturing Engineering, MSIT, Validation, etc. Utilizes manufacturing knowledge to improve process operations and affect positive change. Demonstrates ability to troubleshoot basic mechanical operations. Effectively utilizes Microsoft Office applications. Mentors less experienced operators. Fulfills the role of Team Lead in the absence of the Manufacturing Sr. Associate. Escalates production floor issues related to personnel, safety, procedures, materials, process, equipment, automation, utilities, and/or information systems to Manufacturing management and/or appropriate functional area(s). Performs in process analytical testing. Demonstrates general knowledge of automation systems (INFOR, MES, ERP, DeltaV). Demonstrates general knowledge and practice of aseptic techniques. Additional Responsibilities: Cross train manufacturing personnel undefined Continuous Improvement Contributes to continual improvement of all manufacturing documentation (SOP’s, EWI’s, MBR’s, OJT’s) to ensure they are current, accurate, and clear.· Supports plant floor continuous improvement initiatives. About you Basic Qualifications: High School diploma/GED with 3-5 years of experience in a cGXP environment, or a Bachelor’s degree with 1-3 years of experience. Must have prior experience in cGMP manufacturing operations. Preferred Qualifications: Bachelor’s degree with 2-4 years of experience in bulk biologics GMP manufacturing. Effectively uses process automation systems to operate production processes (i.e. Delta V). Familiarity with deviation management systems Special Working Conditions: Ability to lift up to 50 lbs. Ability to stand on average 10 hours per shift. Ability to gown and gain entry to manufacturing areas. Ability

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/nto-manufacturing-associate-at-sanofi-2eb128

Source: https://jobsbylevel.com/jobs/nto-manufacturing-associate-at-sanofi-2eb128

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