Analytical QC Analyst - Biopharma GMP

Sanofi Inc.; Cambridge; On-site; GBP 30,000 - 43,000; Full time

Job summary

Sanofi Waterford seeks a QC Analyst on a fixed-term, full-time basis to provide analytical chemistry support for the site. You will interact with QA, Production, Engineering and Planners to ensure timely batch releases and maintain validated methods and SOPs in line with regulatory requirements.

The role requires a science degree and hands-on experience in QC laboratories, with proficiency in HPLC/Empower. You will contribute to continuous improvement and ensure documentation compliance across

Qualifications

• Degree in Science (Chemistry or Biochemistry preferred).
• Operational experience of quality laboratories in a fast-moving manufacturing environment.
• Detailed knowledge of quality management systems, pharmaceutical manufacturing operations, cGLP, pharmacopoeial methods and stability.

Responsibilities

• Provide analytical chemistry services and support to the Site.
• Interact with other departments on raw materials, intermediates and finished batch releases.
• Maintain, update and issue chemical methods, specifications and SOPs in compliance with pharmacopoeial and regulatory requirements.
• Assist with training of analysts in new methods, SOPs and updates.
• Audit and review chemistry test results and ensure compliance with cGLP.

Skills

HPLC/Empower

Quality labs

Education

Science degree (Chemistry/Biochemistry)

Tools

Empower LIMS

Job description

Sanofi Waterford seeks a QC Analyst on a fixed-term, full-time basis to provide analytical chemistry support for the site. You will interact with QA, Production, Engineering and Planners to ensure timely batch releases and maintain validated methods and SOPs in line with regulatory requirements.

The role requires a science degree and hands-on experience in QC laboratories, with proficiency in HPLC/Empower. You will contribute to continuous improvement and ensure documentation compliance across