MES Designer - Ireland, Dublin - 12 Months Initial Contract
Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of MES Designer.
A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions.
This is your chance to join them on their global mission to better the lives of those effected by disease and illness.
Responsibilities include:
Responsible for the development, configuration and testing of Master Batch Records (MBRs) from initial to final design.
Responsible for leading MBR development design reviews including liaising with Operations, Process Development and Quality functions.
Responsible for drafting, executing and reviewing Application Lifecycle Management test scripts and test sets for testing MBR design.
Responsible for the support and ongoing development of the Client's MES system in development of MBRs and improving the MES business process.
Responsible for training of Electronic Batch Record (EBR) end-users (Supervisors, Operators, Technical/QA/Support staff).
Responsible for the development, review and update of MES Standard Operating Procedures.
Requirements:
Strong experience within a similar MES designer / MES Specialist / Manufacturing Specialist role within a pharmaceutical / biotech industry
Experience developing, configurating and testing of Master Batch Records (MBRs)
Knowledge of regulation requirements (GMP & EH&S)
Experience with PAS-X
Ability and drive to learn quickly and work as part of a team
Aseptic Fill / Finish manufacturing environment experience highly desirable
If this role is of interest, please apply now
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