# Quality Control Microbiology testing at Sanofi

Sanofi is hiring a Quality Control Microbiology testing. It pays $69k-$100k a year and Level rates it Little AI ●○○○; you can [apply on Sanofi](https://jobsbylevel.com/go/79b23c79-97bd-439b-864a-c3a54dfb2c6c?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. Pearl River, NY.

## Details

- Company: [Sanofi](https://jobsbylevel.com/companies/sanofi)
- AI level: AI Level 1 (score 37 out of 100)
- Location: Pearl River, NY
- Salary: $69k-$100k
- Posted: November 6, 2026
- Apply: https://jobsbylevel.com/go/79b23c79-97bd-439b-864a-c3a54dfb2c6c?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=quality-control-microbiology-testing-at-sanofi-817020

## Description

Job Title: Quality Control Microbiology testing Location: Pearl River, NY About The Job: The function of this position is to perform microbiological testing and related analytical functions in the QC microbiology lab. This position includes performing microbiological and other testing following approved methodology to assure that the safety, quality, purity and stability (as appropriate) of our systems products, components and in- process stages are in compliance with approved specifications. Additionally, this position provides input for data trending and assists with or authors periodic reports as necessary, highlights problems related to technical and equipment issues, and works closely with the Microbiology Manager. The microbiology team is highly flexible and provides cross functional support as part of manufacturing processes and quality investigations. This role allows opportunity to become multi skilled with the team and gain experience/skills within all areas essential to working within an operational microbiology laboratory. 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. 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: Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and data integrity requirements Ensuring that he/she is trained and qualified to perform the assigned analytical testing on a variety of samples (e.g. raw materials, in-process drug substance samples, environmental monitoring, etc.) Performing the QC data review of executed tests by other analysts in a timely manner based on managerial delegation, ensuring adherence to the committed scheduled plans Informing his/her manager of any quality or HSE event (deviations, OOx,…) in a timely manner to ensure investigation and impact assessment are performed appropriately Participating actively in any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately Executing assigned CAPAs related to remediation plans, continuous improvements Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately Key Roles (D,A,I) Build remediation plans related to inspection readiness gaps, findings, deviations, … (A) Additional Accountabilities Contributing to trending of environmental monitoring and utilities monitoring data and assisting with/authoring periodic reports as necessary Training team members in analytical testing and documentation upon trainer qualification, ensuring adherence to local and global standard operating procedures and cGMP requirements Ensuring the laboratory is maintained in an audit-ready state at all times and represent the lab team during audits/inspections Revising and updating local procedures as necessary to align with cGMP/cGLP guidelines and enhance ease of use for laboratory activities About You: Basic Qualifications: Bachelor's degree in Life sciences, Biology, Chemistry or related field. 1+ Years of laboratory or manufacturing experience. Preferred qualifications: Experience in a pharmaceutical or related industrial environment. Why Choose Us: Bring the miracles of science to life alongside a

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