MES Designer
- Dublin
- Contract
- CAPEX Projects
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:
- Develop, configure and test MBR’s
- Lead MBR development design reviews and liaise with relevant teams
- Providing training to end users of Electronic Batch Record (EBR)
- Develop, review and test MES SOP’s
- Provide technical support
Requirements:
- Few years’ 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)
- 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 to you, please apply now!
#LI-AS3
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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