# Document Coordinator at Sanofi

Sanofi is hiring a Document Coordinator. It pays $27-$36/hr and Level rates it Little AI ●○○○; you can [apply on Sanofi](https://jobsbylevel.com/go/a9e3f6db-0d27-43f5-863a-920188613a77?utm_medium=ai-agent).

AI Level 1, AI centrality 33 out of 100. Swiftwater, PA.

## Details

- Company: [Sanofi](https://jobsbylevel.com/companies/sanofi)
- AI level: AI Level 1 (score 33 out of 100)
- Location: Swiftwater, PA
- Salary: $27-$36/hr
- Posted: November 5, 2026
- Apply: https://jobsbylevel.com/go/a9e3f6db-0d27-43f5-863a-920188613a77?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=document-coordinator-at-sanofi-87ea24

## Description

Job title: Document Coordinator Location: Swiftwater, PA 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: Test Data Review: 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, OOx,…) 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 Support root cause analysis investigations for testing deviations Document coordination: Coordinate quality control documentation lifecycle activities Manage document workflows, including review, approval, and distribution processes Ensure documentation compliance with good documentation practices (GDP) Create, maintain, and update QC technical documentation and SOPs Monitor document revision schedules and coordinate periodic reviews Liaise with subject matter experts (SMEs) for document content development Support metadata management and document control activities in quality systems (e.g., QualiPSO) Coordinate stakeholder reviews and consolidate feedback Other accountabilities: 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. 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 Supporting laboratory and deviation investigations Typical Activities: Review test data for accuracy, completeness, and compliance Coordinate the creation, review, and approval of QC SOPs and technical documents Manage document change requests and assess impact on testing operations Facilitate document review meetings with cross-functional teams Maintain document control records and ensure proper version management Support regulatory inspections by providing documentation and technical expertise Participate in CAPA investigations related to testing or documentation issues Monitor documentation metrics and report on completion status Train laboratory personnel on new or revised procedures About you Key Qualifications: Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field 3-5 years of experience in QC laboratory operations. Working in a pharmaceutical environment is preferred. Strong understanding of GxP requirements and/or pharmaceutical quality systems Experience with analytical testing methods and equipment Proficiency in document management systems (e.g., QualiPSO, electronic document management systems) Knowledge of test data review processes and data integrity principles Experience coordinating documentation workflows and managing stakeholder reviews Excellent attention to detail and organizational skills Strong written and verbal communication skills Knowledge of iShift

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Source: https://jobsbylevel.com/jobs/document-coordinator-at-sanofi-87ea24

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