MES Designer

QCS Staffing; Dublin; On-site; EUR 70,000 - 90,000; Full time

Job summary

QCS Staffing is sourcing a skilled MES Designer for an initial 12-month contract in Dublin, Ireland. The role focuses on master batch records, MES configuration, testing, and process improvements within a life sciences setting.

You will lead MBR design reviews with Operations, Process Development and Quality, ensure regulatory compliance, and train end-users on the Electronic Batch Record system. Join a global biotech leader.

Qualifications

• Strong MES design experience in a pharmaceutical/biotech environment.
• Experience developing, configuring and testing Master Batch Records (MBRs).
• Knowledge of GMP and EH&S regulation requirements.
• Experience with PAS-X.
• Ability and drive to learn quickly and work as part of a team.

Responsibilities

• The development, configuration and testing of Master Batch Records (MBRs) from initial to final design.
• Leading MBR development design reviews including liaising with Operations, Process Development and Quality functions.
• Drafting, executing and reviewing Application Lifecycle Management test scripts and test sets for testing MBR design.
• Support and ongoing development of the MES system in development of MBRs and improving the MES business process.
• Training of Electronic Batch Record (EBR) end-users (Supervisors, Operators, Technical/QA/Support staff).

Skills

MES design experience

MBR development

GMP & EH&S knowledge

PAS-X

Team collaboration

Pharma/Biotech industry experience

Tools

PAS-X

Job description

MES Designer - Ireland, Dublin - Initial 12-Month Contract - Life Sciences

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 support them on their global mission to better the lives of those affected by disease and illness.

What You'll Deliver

• The development, configuration and testing of Master Batch Records (MBRs) from initial to final design.


• Be 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).

Experience required

• Strong experience within a similar MES designer / MES Specialist / Manufacturing Specialist role within a pharmaceutical / biotech industry


• Strong MES design experience


• 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