Quality Systems Internal Auditor

Haleon

Dungarvan, Ireland
**
Lead internal audits
Supplier and service provider audits
Medical device and medicinal sites
** Haleon is seeking a Quality Systems Internal Auditor for its Dungarvan, Ireland facility, responsible for leading internal audits, managing the auditing process, and supporting regulatory compliance within the medical device and pharmaceutical sectors. The ideal candidate will have at least five years of audit experience and a deep understanding of global pharmaceutical regulations. This position offers competitive pay, excellent training, and a community-focused workplace. **

Job Summary

  • This role is responsible for leading internal/ service provider and supplier audits and managing the Internal Audit (Independent Business Monitoring) Process at Haleon Dungarvan.
  • You will be the key point of contact / Subject Matter Expert for the Internal Audit process in both Medical Device and Medicinal sites.
  • Employees highlight great teamwork, fair management, valuable learning opportunities and competitive pay supported by union-negotiated increases.

Matching Summary

Match Score: 75

** Haleon is seeking a Quality Systems Internal Auditor for its Dungarvan, Ireland facility, responsible for leading internal audits, managing the auditing process, and supporting regulatory compliance within the medical device and pharmaceutical sectors. The ideal candidate will have at least five years of audit experience and a deep understanding of global pharmaceutical regulations. This position offers competitive pay, excellent training, and a community-focused workplace. **

Skills & Requirements

Must-have

  • Lead internal audits
  • Supplier and service provider audits
  • Medical Device and Medicinal sites
  • Regulatory requirements, GMP, Haleon Quality Standards
  • Audit procedures, tools, methodologies
  • Site representative for audit readiness
  • Monitor and report audit metrics

Nice-to-have

  • Deep human understanding and trusted science
  • Agile, performance-focused culture
  • Support site HAPs projects
  • Continuous improvement in Right First Time/compliance

Key Requirements

  • Minimum 5 years audit experience
  • Degree in science or equivalent discipline
  • In-depth understanding of global pharmaceutical regulations
  • Understanding of supplier qualification and auditing requirements
  • Experience with EU Medical Device Regulation 2017/745
  • Experience with FDA 21 CFR Parts 210, 211 and 820

Work Rights

Not specified

Tailored Resume

Cover Letter