C&Q Engineer

A global pharmaceutical organisation, based in Ireland, is looking for a C&Q Engineer for an initial 6 month contract role. Our client is a multinational organisation with a sales turnover of €1.3billion. Dedicated to the discovery and development of innovative drugs for patient care in targeted therapeutic areas such as oncology, endocrinology and neurological disorders.

Key Responsibilities:
* Execution of commissioning protocols which have already been written
* Create documentation and execute the qualification protocols through IQ/OQ
* Work to support the 2 Project Managers on this role
* Work closely with the Quality department to execute some or their preapproved protocols

IDEAL SKILLS AND EXPERIENCE:

* An experienced pharmaceutical C&Q equipment engineer - API experience is a bonus, may even consider Bio people
* Good knowledge of the GMP standards to which they will need to work
* Experience of lyophilises or bio reactors (specifically synthesis reactors ideally) a big bonus
* Key is the knowledge of the process of compilation and development of equipment Commissioning & Qualification documentation in line with GMP standards.
* As you will be joining a small team the ability to communicate with you team and be a team player are key, and so know when to ask for direction and update your colleagues

Please apply now for more information!