Due to our continued success, we are now seeking a number of C&Q Specialists to work with our Cork-based client. As a member of this site-based team, you will have access to a wealth of experience and the best possible resources.

Candidates should ideally have 5+ years Pharmaceutical experience with emphasis on Biopharma, a GMP/GDP background and a degree in a science based discipline/chemical or mechanical engineering.

Responsibilities:

•Documentation preparation of Commissioning, Qualification and Validation (CQV) for process, equipment and clean & black utilities
•Field execution of Commissioning, Qualification and Validation (CQV) for process, equipment and clean & black utilities
•Co-ordination of vendor packages to achieve streamlined CQV
•Co-ordination/Review of construction packages to achieve streamlined CQV
•Knowledge of recent regulations (ICH, ASTM, FDA, ISPE) and modern CQV practices

Requirements:

•Educated to degree level in Engineering, Architectural or Science related area
•5+ year’s experience gained within a Life Sciences environment
•Experience of working in a project environment
•Hands on attitude
•Excellent oral and written communication skills in English
•High level of customer orientation/understanding
All applications will be treated in strictest confidence.