JO-***********
Global Supplier Quality Specialist
Cpl is partnering with a leading global pharmaceutical/biologics organisation to recruit a QA Specialist with expertise in supplier and vendor oversight.
This is a high-profile position offering the opportunity to shape supplier compliance programs and ensure quality excellence across a global network of partners.
Get in touch for further information: Deirdre Murphy on *********** /************* or ******
Please note - applicants need to have a Stamp 4 or to have unrestricted full working rights for Ireland
Key Responsible:
As QA Specialist, you will:
Lead supplier qualification and monitoring programs across GxP areas (GMP, GLP, GCP, GDP).
Conduct supplier audits (initial, routine, and for-cause), prepare reports, and oversee CAPA effectiveness.
Review and approve supplier quality documentation (agreements, deviations, change controls).
Assess supplier systems against EU, FDA, OECD, ICH, and other global standards.
Provide QA support to cross-functional teams and procurement decisions.
Deliver internal training on supplier qualification and compliance expectations.
Represent QA on outsourced projects to safeguard GxP data integrity.
Maintain supplier records in eQMS and quality systems.
Candidate profile:
Degree in Life Sciences, Pharmacy, Biotechnology, or related discipline.
7–10 years' QA experience within pharma, biologics, or vaccines.
Minimum 5 years in supplier qualification & auditing (GMP expertise required; additional GLP/GCP/GDP an advantage).
Strong knowledge of international GxP regulations and quality systems.
Experienced in audits, CAPA, and change control.
Excellent communication and stakeholder engagement skills.
Fluent English (other languages desirable).
Willingness to travel internationally (up to 25%).
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