QC Compliance & Process Improvement Specialist

Sanofi Inc.; Litchurch; On-site; GBP 47,000 - 73,000; Full time

Benefits offered by this job

Health benefits

Parental leave

Job summary

Sanofi Waterford, Ireland, seeks a QC Business Process Specialist to drive standardization and compliance in the QC Microbiology lab. You will manage SOPs, deviations, CAPA, and digital systems, ensuring GMP-aligned processes and regulatory readiness across the site.

The role focuses on improving laboratory business processes, training staff, and maintaining documentation to support a compliant, efficient operation within a leading biopharma environment.

Qualifications

• Experience with pharmaceutical regulations and standards (GMP).
• Experience in internal audits and regulatory inspections.
• Familiarity with SOP/procedure management and CAPA.

Responsibilities

• Contributing to the development and maintenance of an effective compliance program.
• Ensuring all operations comply with relevant regulatory requirements and other international standards.
• Providing training and guidance to employees on compliance-related topics.
• Maintaining compliance-related documentation, ensuring accuracy and completeness.
• Identifying potential compliance risks and contributing to the development of strategies to mitigate them.
• Supporting the investigation and reporting of compliance incidents.
• Managing CAPA to address compliance incidents and preventing recurrence.

Job description

Sanofi Waterford, Ireland, seeks a QC Business Process Specialist to drive standardization and compliance in the QC Microbiology lab. You will manage SOPs, deviations, CAPA, and digital systems, ensuring GMP-aligned processes and regulatory readiness across the site.

The role focuses on improving laboratory business processes, training staff, and maintaining documentation to support a compliant, efficient operation within a leading biopharma environment.