We are seeking an experienced Quality Auditor to join our team and support compliance with GMP/GDP regulations.
Key Responsibilities:
* To plan, schedule and conduct internal and external audits of manufacturing processes, suppliers and laboratories.
* To review and assess documentation and quality processes to ensure they meet HPRA, EU and US GMP/GDP standards.
* To identify areas for improvement in quality systems, including document control, deviations and CAPA management.
* To prepare clear audit reports and communicate results to stakeholders.
Qualifying Criteria:
* A bachelor's degree in a science-related field such as chemistry or biology.
* At least five years' experience in quality assurance or compliance in the pharmaceutical industry.
* Proven auditing experience in GMP/GDP environments.
* Strong knowledge of relevant regulatory requirements and industry best practices.
Benefits:
* The opportunity to work in a fast-paced and dynamic environment.
* Scope for impact and professional growth.
What We Offer:
* A competitive salary package.
* Ongoing training and development opportunities.