Sanofi

biopharma

QualityControlAnalyst

$0–0k Framingham, Massachusetts, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Quality Control Analyst at Sanofi. Skills: Quality Control, cGMP, Environmental Monitoring, Critical Utility sampling. Collect Environmental Monitoring (Viable Air, Viable Surface, Non-Viable Air Samples) and Critical Utility (RO, DI, WFI, Steam Water Samples, and Compressed Air and Mixed Gases Samples) 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, r”

Industry & Context.

biopharma
Problems you'll solve

investigation; impact assessment

Eligibility Requirements

Ability to perform tasks in a Quality Control Laboratory environment, capable of lifting at least 10 pounds, May be required to pass vision exam to perform specific responsibilities, May be required to enter into controlled environments following proper gowning protocols, Work in a laboratory with minimal use of chemicals, Ability to lift at least 10lbs

What They're Looking For.

Must Have

High School Diploma or GED with a minimum of 0-2 Years of relevant industry experience, Proficient with Microsoft Office tools such as Word, Excel & PowerPoint

Nice to Have

1 Year of Experience in a GMP lab environment, Experience with lab-based data management systems, Experience in a Quality Control Laboratory

What You'll Do.

Collect Environmental Monitoring (Viable Air

Non-Viable Air Samples) and Critical Utility (RO

and Compressed Air and Mixed Gases Samples) 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

related to these tasks

Recording all expected raw data

information related to his/her tasks

to comply with cGMP and data integrity requirements

Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified

Performing the QC data review of executed tests by other analysts in a timely manner

ensuring adherence to the committed scheduled plans

Informing his/her manager of any quality or HSE event (deviations

) in a timely manner to ensure investigation and impact assessment are performed appropriately

Participating actively to any investigation

where he/she is involved

to ensure investigations and impact assessment are performed appropriately

Ensuring that his/her lab/facilities

lab instruments are kept in a quality and safety status to ensure that they can be used appropriately

How You'll Work.

Team & Collaboration

Participating actively to any investigation, where he/she is involved

Full Job Description

**Job title:** Quality Control Analyst **Location:** Framingham, MA **Shift:**_Sun - Wed or Wed- Sat 07:00 am - 5:30 pm_ **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. **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:_** * Collect Environmental Monitoring (Viable Air, Viable Surface, Non-Viable Air Samples) and Critical Utility (RO, DI, WFI, Steam Water Samples, and Compressed Air and Mixed Gases Samples) 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 the assigned analytical testing that requires to be qualified * Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans * Informing his/her manager of any quality or HSE event (deviations, OOS,) in a timely manner to ensure investigation and impact assessment are performed appropriately * Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately * Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they

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