QC Analyst - Analytical Chemist (Contract, Onsite)

Sanofi Inc.; Cardiff; On-site; GBP 31,000 - 41,000; Full time

Job summary

Sanofi Waterford is seeking a QC Analyst on a fixed-term full-time basis to provide analytical chemistry support for diverse manufacturing operations. You will interact with QA, Production, Engineering and Planners to ensure timely batch releases and maintain validated methods and SOPs.

The role requires a degree in science (chemistry or biochemistry) with 2+ years in QC labs, experience with HPLC/Empower, and strong knowledge of cGLP and regulatory standards.

Qualifications

• Operational experience in quality laboratories within a fast-moving manufacturing environment.
• Detailed knowledge of quality management systems and pharmacopoeial requirements.
• Understanding of cGLP and regulatory compliance requirements.
• Ability to manage projects with planned budgets.
• Minimum two years of HPLC/Empower experience.

Responsibilities

• Provide analytical chemistry services and support to the Site.
• Interact with departments on raw materials, intermediates and finished batch releases.
• Maintain, update and issue chemical methods, specifications, and SOPs per regulatory requirements.
• Assist with training of analysts in areas of expertise and new methods.
• Trend results, record on COAs, and complete OOS investigations timely.
• Update QC Team Leader on potential problems and improvements via standard channels.
• Ensure critical testing and related equipment meet validation requirements (IQ/OQ/PQ).
• Audit and review chemistry test results daily; ensure cGLP compliance.
• Ensure all quality documentation and records are complete and current.
• Support new product introduction projects.

Education

Degree in Science (Chemistry or Biochemistry)

Post-graduate studies

Tools

HPLC software (Empower)

Job description

Sanofi Waterford is seeking a QC Analyst on a fixed-term full-time basis to provide analytical chemistry support for diverse manufacturing operations. You will interact with QA, Production, Engineering and Planners to ensure timely batch releases and maintain validated methods and SOPs.

The role requires a degree in science (chemistry or biochemistry) with 2+ years in QC labs, experience with HPLC/Empower, and strong knowledge of cGLP and regulatory standards.