QC Compliance Specialist — Associate (Temp)

Regeneron Pharmaceuticals, Inc.; Limerick; On-site; EUR 55,000 - 75,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Temp Assoc QC Compliance Specialist to join the Quality Control team in Limerick, Ireland. You will lead investigations across Chemistry, Bioassay, Microbiology and Virology labs, writing reports and driving quality improvements.

The role requires experience in QC or analytical sciences, with strong problem-solving skills and a focus on compliant, timely CAPA implementation in a GMP environment.

Qualifications

• BS/BA in Chemistry, Biology, or a related scientific field or equivalent experience.
• Experience in QC/Analytical Sciences and laboratory investigations in a cGMP environment.
• Strong documentation and reporting skills for investigations and CAPAs.

Responsibilities

• Lead and support laboratory investigations, deviations and non-conformances.
• Write and review investigation reports and quality documentation.
• Perform root cause analysis and partner with teams to identify effective CAPAs.
• Support timely implementation and monitoring of corrective and preventative actions.
• Identify recurring trends and propose process improvements in QC operations.

Skills

Quality Control

Laboratory investigations

CAPA

Root cause analysis

Analytical Sciences

Education

BS/BA in Chemistry or Biology

Job description

Regeneron Pharmaceuticals, Inc. seeks a Temp Assoc QC Compliance Specialist to join the Quality Control team in Limerick, Ireland. You will lead investigations across Chemistry, Bioassay, Microbiology and Virology labs, writing reports and driving quality improvements.

The role requires experience in QC or analytical sciences, with strong problem-solving skills and a focus on compliant, timely CAPA implementation in a GMP environment.