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Principal Quality Engineer

Merck Life Science
Department:Healthcare
Type:ON-SITE
Region:Cork
Location:Cork, County Cork, Ireland
Experience:Associate
Estimated Salary:€70,000 - €100,000
Skills:
QUALITY ENGINEERINGQUALITY MANAGEMENT SYSTEMCAPAROOT CAUSE ANALYSISAUDITVALIDATIONPHARMABIOPHARMACOMPLIANCEOPEX
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Job Description

Posted on: March 21, 2026

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Principal Quality Engineer Reporting to the Quality Manager - Blarney Operations, the Principal Quality Engineer will be responsible for overseeing and delivering on all aspects of the Quality Functions related to Filtration Site 2, Blarney. Duties & Responsibilities

  • Supervision and talent development of Quality Engineers and Technicians with focus on compliance, issue prevention, problem solving, and team working ethic as required.
  • Support colleague engagement model to foster a positive team environment through open communication and feedback.
  • Manage performance expectations for Quality Engineers and Technicians and drive accountability as required.
  • Manage the technical quality aspects for area of responsibility and work closely with the operations team to achieve all key department metrics.
  • Ensure key quality metrics such as CAPA management, Right First Time, Complaints etc are consistently achieved.
  • Ensure effective and efficient closure of deviations, CAPAs, change controls, audit observations and customer complaints.
  • Ensure thorough investigation of Quality issues using Root Cause Analysis methodology and implementation of robust corrective and preventative actions to prevent recurrence.
  • Oversee the Quality Management System in the area to align with site QMS and to ensure effective use, compliance with relevant corporate procedures and quality standards.
  • Participate in the review of quality trends, identify opportunities for continuous improvement and complete improvement projects using OpEx tools.
  • Participate in and support the internal and external audit programmes.
  • Support the successful validation and qualification of process and raw material changes.
  • Support introduction of new products into the site as per the required standards.
  • Maintain strong communication with internal and external stakeholders.
  • Liaise with vendors and customers on quality related issues, internal and external.
  • Adhere to all company EHS guidelines and Quality procedures.
  • Additional duties as required.

Education & Experience

  • BSc qualified in appropriate scientific discipline
  • Minimum 5 years relevant experience in a similar QA role (ideally Pharma/Biopharma)
  • Excellent communication, collaboration and leadership skills
  • Results oriented
  • Good decision making and problem-solving skills

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Originally posted on LinkedIn

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