Overview
Barden are delighted to be supporting our Global Pharmaceutical Client in their search for an Associate Director Quality Assurance - Systems and Compliance.
In the position, you will be involved in setting and maintaining the highest standards of Quality Assurance. This includes providing QA oversight, driving compliance, and leading the Systems & Compliance team to ensure all quality systems and processes meet regulatory, global, and site requirements.
About the Role
What You will Do:
* Shape and execute the Site Quality Management Plan, driving excellence in compliance and performance.
* Provide quality insights and updates to the Site Leadership Team through governance boards and reviews.
* Drive key QA initiatives, ensuring projects are well resourced and delivered.
* Champion Quality Culture and Data Integrity across all functions.
* Oversee inspections, audits, and customer interactions with confidence.
* Manage vendor qualification, training programmes, and quality systems to ensure compliance and reliability.
* Deliver meaningful quality metrics that drive continuous improvement and strengthen overall site performance.
About the Person
* Degree in Science (Chemistry, Pharmaceutical sciences, Biochemistry, Biotechnology) or equivalent.
* 8+ years’ experience in a manufacturing site role (QA and/or Production) or equivalent in pharma/biotech.
* 4+ years of leadership experience, successfully managing teams and driving quality initiatives.
* Strong working knowledge of GMP regulations within the pharmaceutical industry.
* Experience with regulatory inspections, audits, and cross-functional quality projects.
Details
* Seniority level: Director
* Employment type: Full-time
* Job function: Quality Assurance
* Industries: Staffing and Recruiting
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