Pharma QC Analyst – cGMP Testing Specialist (FTC)

Sanofi; France; Sur place; EUR 42 000 - 55 000; Plein temps

Résumé du poste

Sanofi in Waterford, Ireland seeks a QC Analyst on a fixed-term contract to support analytical testing in a cGMP environment. You will record data with precision, ensure proper qualifications, and review results to support investigations and CAPA closures.

The role emphasizes data integrity, safety, and collaboration with a team of analysts in a regulated manufacturing setting at our Waterford site.

Qualifications

• Degree in Science, Chemistry, Pharmacy, or related field or equivalent practical experience.
• Experience in analytical testing within pharmaceutical, biotech, or regulated manufacturing environments.
• Fluency in English.

Responsabilités

• Carry out analytical testing in a timely and organized manner.
• Follow cGMP and HSE requirements, with proper records and procedures.
• Accurately record raw data, calculations, and related information for data integrity.
• Ensure proper qualification before testing.
• Review QC data and provide timely feedback to the manager.
• Inform management of deviations or out-of-spec results for investigations.
• Contribute to investigations and root cause analysis.
• Complete CAPAs as part of remediation and continuous improvement.
• Maintain lab facilities and instruments in safe, clean condition.

Connaissances

Attention to detail

Collaborative team player

Problem solving

Task prioritisation

Formation

Bachelors in Science/ Chemistry/ Pharmacy or related field

Outils

Quality documentation systems

Description du poste

Sanofi in Waterford, Ireland seeks a QC Analyst on a fixed-term contract to support analytical testing in a cGMP environment. You will record data with precision, ensure proper qualifications, and review results to support investigations and CAPA closures.

The role emphasizes data integrity, safety, and collaboration with a team of analysts in a regulated manufacturing setting at our Waterford site.