Director, GMP Compliance & Inspections

Regeneron Pharmaceuticals, Inc; Munster; On-site; EUR 102,000 - 200,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Director GMP Compliance & Inspections to join the Quality department at the IOPS Manufacturing site in Limerick. This leadership role will ensure regulatory readiness, drive continuous improvement, and coordinate inspections and audits to maintain the highest GMP standards.

The position is onsite in Limerick, with Monday–Friday work hours. The role requires a bachelor’s degree in Life Sciences and extensive experience in regulatory compliance,

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• Minimum of 12 years experience in a similar role.

Responsibilities

• Leading compliance assessments and inspection readiness initiatives across the site.
• Monitoring regulatory trends and translating them into actionable improvements.
• Developing tools, processes, metrics, and content repositories to support audit and inspection preparedness.
• Providing expert guidance on quality and regulatory matters to internal teams and external partners.
• Acting as a key liaison with regulatory agencies, customers, and partner quality organisations.
• Supporting regulatory inspections and internal audits, including coordinating responses and managing information requests.
• Benchmarking best practices and driving continuous improvement to maintain inspection readiness.

Education

Bachelor’s degree in Life Sciences

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Director GMP Compliance & Inspections to join the Quality department at the IOPS Manufacturing site in Limerick. This leadership role will ensure regulatory readiness, drive continuous improvement, and coordinate inspections and audits to maintain the highest GMP standards.

The position is onsite in Limerick, with Monday–Friday work hours. The role requires a bachelor’s degree in Life Sciences and extensive experience in regulatory compliance,