Hybrid QC Analytical Expert — GMP Method Validation

Sanofi; Waterford; Hybrid; EUR 45,000 - 65,000; Full time

Job summary

Sanofi is seeking a Quality Control Analytical Expert in Waterford, Ireland, to ensure analytical excellence across cGMP-compliant QC operations. The role blends on-site and remote work within a 12-month fixed-term contract and involves cross-functional collaboration to validate and transfer analyses.

You will lead investigations, data trends, and protocol writing while upholding safety and quality standards, contributing to a global biopharma network that delivers medicines at scale.

Qualifications

• Significant experience in quality control within the pharmaceutical industry.
• Degree in science or related discipline, or relevant experience.
• Ability to analyze complex data and laboratory results.
• Keen attention to detail for accurate testing and reporting.
• Proven ability to identify issues and implement solutions.

Responsibilities

• Provide analytical expertise for projects, troubleshooting, and investigations.
• Coordinate analytical testing on validation and transfer projects.
• Ensure tasks comply with cGMP and health, safety requirements.
• Record raw data and calculations to meet data integrity standards.
• Write and review protocols and reports for validation, transfers, and qualifications.
• Inform manager of quality or HSE deviations promptly.
• Participate in investigations and assess impact.
• Perform trend analysis on method performance to decide revalidation.
• Maintain lab facilities and instruments in a quality and safe state.
• Support QC during internal and external audits and inspections.

Skills

Quality control

GMP knowledge

Data analysis

Attention to detail

Problem solving

Education

Science degree or related field

Job description

Sanofi is seeking a Quality Control Analytical Expert in Waterford, Ireland, to ensure analytical excellence across cGMP-compliant QC operations. The role blends on-site and remote work within a 12-month fixed-term contract and involves cross-functional collaboration to validate and transfer analyses.

You will lead investigations, data trends, and protocol writing while upholding safety and quality standards, contributing to a global biopharma network that delivers medicines at scale.