QC Analyst: Analytical Chemistry Specialist (Contract)

Sanofi Inc.; West Carr; On-site; GBP 36,000 - 46,000; Full time

Job summary

Sanofi Waterford seeks a QC Analyst on a fixed-term, full-time basis to support analytical chemistry across diverse manufacturing operations and ensure adherence to cGLP and pharmacopoeial standards.

With a science degree and 2+ years of HPLC/Empower experience, you’ll collaborate with QA, Engineering, and Production to update methods and SOPs, maintain quality documentation, and contribute to new product introductions.

Qualifications

• Degree in Science (Chemistry or Biochemistry preferred).
• Post-graduate studies as appropriate to augment primary degree.
• Operational experience of quality laboratories in a fast-moving manufacturing environment.
• Detailed knowledge of quality management systems, pharmaceutical manufacturing operations, requirements for cGLP, pharmacopoeial methods and stability.
• Understand relevant quality/compliance regulations.
• Can manage projects to plan/budget.
• Minimum two years HPLC/Empower experience.

Responsibilities

• Provide analytical chemistry services and support to the Site.
• Effective interaction with other departments on matters related to raw materials, intermediates and finished batch releases.
• Maintain, update and issue chemical methods, specifications and SOPs in compliance to pharmacopoeial and regulatory requirements.
• Assist with training of the analysts in areas of expertise and knowledge and in new methods, SOPs and updates.
• Audit and review chemistry test results on a daily basis and ensure compliance with cGLP.
• Support new product introduction projects.

Skills

HPLC experience

Quality management systems knowledge

Project management

Regulatory compliance understanding

cGLP awareness

Education

Degree in Science (Chemistry or Biochemistry preferred)

Post-graduate studies

Tools

Empower

Job description

Sanofi Waterford seeks a QC Analyst on a fixed-term, full-time basis to support analytical chemistry across diverse manufacturing operations and ensure adherence to cGLP and pharmacopoeial standards.

With a science degree and 2+ years of HPLC/Empower experience, you’ll collaborate with QA, Engineering, and Production to update methods and SOPs, maintain quality documentation, and contribute to new product introductions.