We are seeking an experienced Quality Assurance professional to fill a senior-level position in the pharmaceutical industry.
About the Role
This is a rare opportunity for a seasoned QA expert to make a significant impact at a tightly regulated GMP site. As Senior QA Associate, you will play a pivotal role in developing and refining our quality systems, culture, and operational excellence.
You will report directly to the Director of Quality and have real influence across all aspects of site QA, from audits and change control to training and cross-functional collaboration.
* Manage change control, document control, CAPAs, and deviations to ensure compliance
* E nsure data integrity, traceability, and compliance across all quality records
* Lead QA during internal/external audits and risk assessments to identify areas for improvement
* Deliver and track GMP training and mentor junior QA staff to enhance knowledge and skills
Requirements
* Bachelor's degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or similar field
* 5+ years' experience in GMP QA, preferably in API or pharmaceutical manufacturing
* Strong knowledge of GMP, HPRA regulations, quality systems, and CAPA/deviation handling
We offer a dynamic work environment and opportunities for growth and development.