QA Compliance Specialist

Regeneron Pharmaceuticals, Inc; Munster; On-site; EUR 46,200 - 75,400; Full time

Job summary

Regeneron Pharmaceuticals, Inc is seeking a QA Compliance Specialist to join the QA Compliance & Quality Systems team in Raheen, Limerick. You will support Change Control activities, review quality systems documentation, and collaborate across functions to ensure compliance with regulatory expectations.

The role requires 3–5+ years in a regulated industry, a science/engineering degree, and strong knowledge of cGMP.

Qualifications

• Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology, or a related discipline.
• 3–5+ years of relevant experience in pharmaceutical, biotechnology, or a regulated industry.
• Experience with Quality Systems, including Change Controls, Deviations, CAPA, Audit Management and Risk Management.
• Working knowledge of cGMP requirements and regulatory expectations.

Responsibilities

• Support administration, review, and coordination of Change Control records to ensure regulatory compliance.
• Provide quality oversight of Change Control activities across the lifecycle.
• Review and approve Quality System documentation (Change Controls, Deviations, CAPA, SOPs).
• Collaborate with Manufacturing, QC, Engineering, Validation, Supply Chain, MSAT, and other functions to implement changes.
• Ensure Change Controls are categorized, assessed for impact, and progressed on time.
• Support governance activities, monitor open records, escalate risks, and drive timely actions.
• Assist in generation and trending of Quality System metrics for management review.
• Participate in investigations related to Change Controls and CAPA implementation.
• Support training development on Change Control and Quality System processes.
• Contribute to continuous improvement to enhance Quality System effectiveness.

Skills

Quality Systems

Change Control

Deviations

CAPA

Audit Management

Risk Management

Education

Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology, or related discipline

Job description

At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. Regeneron is currently seeking a QA Compliance Specialist to join our QA Compliance & Quality Systems team.

This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.

When & where:

• Location: Raheen, Limerick

What you’ll do:

• Supporting the administration, review, and coordination of Change Control records to ensure compliance with company procedures and regulatory requirements.
• Providing quality oversight of Change Control activities throughout the change lifecycle, including initiation, impact assessment, implementation, effectiveness verification, and closure.
• Reviewing and approving Quality System documentation, including: Change Control records, Deviation investigations, CAPA records, Risk assessments, Standard Operating Procedures and Work Instructions and associated quality documentation.
• Collaborating with Manufacturing, Quality Control, Engineering, Validation, Supply Chain, MSAT, and other functional areas to ensure appropriate assessment and implementation of proposed changes.
• Ensuring Change Controls are appropriately categorised, documented, assessed for impact, and progressed in accordance with established timelines.
• Supporting quality system governance activities, including monitoring open records, escalating risks, and driving timely completion of actions.
• Assisting in the generation, monitoring, and trending of Quality System metrics to support management review and continuous improvement initiatives.
• Participating in investigations related to Change Controls and supporting identification and implementation of corrective and preventive actions where required.
• Supporting the development and delivery of training on Change Control and Quality System processes.
• Actively participating in continuous improvement initiatives to enhance Quality System effectiveness, compliance, and efficiency.

The environment and physical rhythms of this role:

• Experience working with Quality Systems, including one or more of the following: Change Controls, Deviations, CAPA's, Audit Management and Risk Management
• Working knowledge of cGMP requirements and regulatory expectations.
• Strong organisational, communication, and stakeholder management skills, with the ability to effectively coordinate activities across multiple functional areas.
• Biologics manufacturing experience desirable.

Let’s find out if we’re a fit:

• Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology, or a related discipline.
• Requires 3-5+ years of relevant experience in the pharmaceutical, biotechnology, or other regulated industry.
• Relevant experience may be considered in lieu of educational requirements.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Salary Range (annually): €46,200.00 - €75,400.00