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Haleon

QC Analyst

1w

Haleon

Dungarvan, IE · Full-time · €42,000 – €48,000

About this role

Haleon is a purpose-driven consumer company putting everyday health in the hands of millions with trusted brands like Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum. We blend deep human understanding and trusted science in resilient categories. Now entering an exciting new chapter with bold ambitions through our Win as One strategy.

As a Quality Control Analyst on the QC team in Dungarvan, you ensure quality, safety, and compliance of raw materials, intermediates, stability samples, and finished products in a highly regulated environment. You support laboratory operations, continuous improvement, and site compliance with GMP, GLP, and EHS standards. Collaborative work within the QC function drives analytical accuracy and efficiency.

Day-to-day involves performing analyses, microbiological testing, peer data review, and documentation in systems like LIMS, VQMS, and M-ERP. You meet lead-time targets, support investigations, CAPAs, and audits while adhering to data integrity (ALCOA+) and EHS requirements. A safe, inspection-ready laboratory is maintained through proactive efforts.

Grow in an agile, performance-focused culture that unites and inspires through our purpose of better everyday health with humanity. Participate in CI/HAPs projects and On-The-Job Training. Unleash potential in a diverse, inclusive environment valuing different backgrounds and views.

Requirements

  • Third-level degree in Chemistry or a related science (postgraduate qualification desirable)
  • 2–3 years’ experience in a pharmaceutical or healthcare QC environment
  • Strong working knowledge of GMP, GLP, Data Integrity, and Quality Systems
  • Experience with microbiological testing
  • Familiarity with regulatory standards (EU GMP, ISO 13485, CFR, MDR, etc.)
  • Excellent communication and interpersonal skills
  • Proactive, can-do attitude with strong accountability for personal work

Responsibilities

  • Perform analysis of Raw Materials, Intermediates, Stability Samples, and Finished Products
  • Conduct peer data review and ensure analytical accuracy
  • Carry out microbiological testing, including environmental monitoring and product testing
  • Ensure sampling and testing activities comply with GLP, GMP, and data integrity (ALCOA+) requirements
  • Complete QC documentation accurately using site systems (e.g. LIMS, VQMS, M-ERP)
  • Achieve laboratory lead-time targets and address potential delays
  • Support investigations, CAPAs, and continuous improvement (CI / HAPs) projects
  • Participate in preparation for and support of internal and external audits

Benefits

  • Inclusive culture where different backgrounds and views are valued and respected
  • Agile, performance-focused culture driving continuous improvement
  • Win as One strategy uniting teams around purpose of better everyday health with humanity