Excellent opportunity for a QA Specialist to join a newly created Vaccines company in Ireland. This role offers the opportunity to act as a QA subject matter expert across GMP and other GxP standards, driving supplier oversight, audits, and risk-based quality management. With deep knowledge of international regulations and proven expertise in supplier qualification, you will play a key role in ensuring the highest quality standards across their global operations.
Overview of your responsibilities (full job description available on request)
- Act as global QA SME for GxP supplier oversight (GMP, GLP, GCP, GDP).
- Lead and improve supplier qualification programme (risk, audits, monitoring).
- Conduct audits, issue reports, track CAPAs, verify effectiveness.
- Review/approve supplier docs: agreements, responses, changes, deviations.
- Assess supplier quality systems vs global regs (EMA, OECD GLP, VICH GCP, ISO, HACCP).
- Advise on procurement to ensure GxP compliance in supplier selection.
- Support teams (R&D, QC, Regulatory, Procurement) in supplier investigations.
- Deliver internal training on supplier qualification.
Knowledge, Skills and Experience Required for the Role:
- Degree in Life Sciences, Pharmacy, Biotech, or related field
- 7–10 years’ QA experience in pharma, biologics, or vaccines
- 5+ years hands-on in GxP supplier qualification & auditing (GMP + GLP/GCP/GDP)
- Bonus: experience with labs, contract manufacturing, or clinical service providers
- Strong knowledge of EU GMP, FDA, OECD GLP, VICH GCP & ICH guidelines
- Skilled in planning, conducting & reporting audits independently
- Deep understanding of quality systems, agreements & risk-based supplier qualification
- Experienced in investigations, CAPA management & change controls
For a confidential discussion and more information on the role contact Courtney Russell
courtney.russell@collinsmcnicholas.ie
+353 (0) 71 9108062