Hybrid QC Analyst – Analytical Quality Specialist

Sanofi; Munster; Hybrid; EUR 52,000 - 74,000; Full time

Job summary

Sanofi in Waterford, Ireland, has an opening for a Quality Control Analytical Expert on a 12-month fixed term contract. This full-time role offers a hybrid arrangement: 3 days on-site and 2 days working from home, to support analytical method validation, transfers, troubleshooting and investigations.

You will work closely with cross-functional teams to maintain cGMP compliance and data integrity, drive analytical excellence, and contribute to continuous improvement of QC operations across the

Qualifications

• Significant quality control experience in the pharmaceutical industry with GMP knowledge.
• Degree in science or related field, or equivalent relevant experience.
• Strong data analysis skills and keen attention to detail.

Responsibilities

• Provide analytical expertise for projects, troubleshooting, and investigations of analytical methods and lab technologies.
• Coordinate analytical testing on projects (validation/transfer), ensuring schedules are met.
• Perform tasks in accordance with cGMP and HSE requirements and related procedures and records.
• Record all raw data, calculations and information to ensure data integrity and traceability.
• Write/review protocols and reports for analytical validation/transfers and qualification activities.
• Write/review and maintain analytical methods procedures.
• Inform manager of quality or HSE events to ensure proper investigations.
• Participate in investigations to ensure appropriate impact assessment.
• Periodically trend method performance to determine need for revalidation or optimization.
• Ensure labs and instruments are maintained in quality/safety status for proper use.
• Support QC during internal and external audits and inspections.

Skills

QC experience

GMP knowledge

Data analysis

Attention to detail

Education

Science degree

Job description

Sanofi in Waterford, Ireland, has an opening for a Quality Control Analytical Expert on a 12-month fixed term contract. This full-time role offers a hybrid arrangement: 3 days on-site and 2 days working from home, to support analytical method validation, transfers, troubleshooting and investigations.

You will work closely with cross-functional teams to maintain cGMP compliance and data integrity, drive analytical excellence, and contribute to continuous improvement of QC operations across the