QC Analyst – Pharma Chemistry, Flexible Working

Sanofi Inc.; Christchurch; On-site; GBP 36,000 - 53,000; Full time

Job summary

Sanofi Waterford is seeking a QC Analyst on a fixed-term full-time contract. You will join the QC department, providing analytical services across manufacturing operations and contribute to continuous improvement while adhering to regulatory and safety guidelines.

Key responsibilities include maintaining methods and SOPs, interacting with QA, Production, Engineering and Planners, training analysts, trending results, and supporting new product introductions at the Waterford site.

Qualifications

• Degree in Science (Chemistry or Biochemistry preferred).
• Two years HPLC/ Empower experience.
• Operational quality laboratory experience in a fast-moving manufacturing environment.
• Detailed knowledge of quality management systems, pharmacopoeial methods and stability.
• Understand relevant quality/compliance regulations.
• Can manage projects to plan/budget.

Responsibilities

• Provide analytical chemistry services and support to 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.
• Trend results, record on COA's where required and complete OOS's investigations on a timely basis.
• Audit and review chemistry test results on a daily basis and ensure compliance with cGLP.
• Ensure all quality documentation and records are complete and current.
• Support new product introduction projects.

Skills

Quality laboratory experience

Regulatory compliance knowledge

Project management / budgeting

Analytical thinking

Education

Degree in Science (Chemistry or Biochemistry preferred)

Tools

HPLC

Empower

SOP development

Job description

Sanofi Waterford is seeking a QC Analyst on a fixed-term full-time contract. You will join the QC department, providing analytical services across manufacturing operations and contribute to continuous improvement while adhering to regulatory and safety guidelines.

Key responsibilities include maintaining methods and SOPs, interacting with QA, Production, Engineering and Planners, training analysts, trending results, and supporting new product introductions at the Waterford site.