QC Analyst – Flexible, Impactful Chemistry Role

Sanofi Inc.

Portsmouth

On-site

GBP 36,000 - 46,000

Full time

2 days ago
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Job summary

Sanofi Waterford seeks a QC Analyst on a fixed-term, full-time basis. You will deliver analytical chemistry support to the site, maintain methods and SOPs, and work closely with QA, Engineering and Planners to ensure compliance and timely batch releases.

You will train analysts, trend results and investigate OOS issues, while ensuring equipment validation and cGLP standards are met across daily testing and documentation processes.

Qualifications

  • Degree in science (chemistry or biochemistry preferred).
  • Experience in quality laboratories within fast-moving manufacturing.
  • Knowledge of cGLP/pharmacopoeial methods and regulatory requirements.
  • Ability to manage projects to plan and budget.

Responsibilities

  • Provide analytical chemistry services and support to Site.
  • Interact with QA, Production, Engineering and Planners on materials and batch releases.
  • Maintain methods, specifications and SOPs in line with pharmacopoeial/regulatory rules.
  • Assist training of analysts in new methods and SOP updates.
  • Trend results, record on COAs and investigate OOS promptly.
  • Inform QC Team Leader of issues and potential improvements.
  • Ensure testing equipment meets IQ/OQ/PQ validation requirements.
  • Audit/Review chemistry results daily and ensure cGLP compliance.
  • Maintain complete quality documentation; support new product introductions.

Skills

HPLC/Empower
Quality labs
Regulatory knowledge
Project management
Analytical chemistry

Education

Science degree in Chemistry/Biochemistry
Post-graduate studies

Job description

Sanofi Waterford seeks a QC Analyst on a fixed-term, full-time basis. You will deliver analytical chemistry support to the site, maintain methods and SOPs, and work closely with QA, Engineering and Planners to ensure compliance and timely batch releases.

You will train analysts, trend results and investigate OOS issues, while ensuring equipment validation and cGLP standards are met across daily testing and documentation processes.

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