MES Engineer
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Job Type | PermanentContractor |
Area | Sligo, Ireland |
Sector | Engineering |
Start Date | |
Advertiser | Hilda Lynn |
Telephone | +353 98 33013 |
Job Ref | #1002321 |
Job Views | 137 |
- Description
- Manufacturing Execution System Engineer – Team Horizon
We are now recruiting an experienced Manufacturing Execution System Engineer who is keen to develop their career with our Pharma Client in Sligo. This is a permanent position in a team with an award-winning safety culture, that has supported a number of successful product launches and audits over the last number of years. In this role, you will contribute significantly to our continued success as we continue on our strategic journey which is underpinned by Operational Excellence and Digital solutions. We see this role as instrumental in supporting our strategic intent and will provide the opportunity for you to work with leading edge technology on exciting strategic projects.
Why you should apply:
Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
The role is generously compensated, and attracts a competitive base salary and highly attractive benefits package.
Excellent career progression opportunities.
What you will bedoing:
Design, create, write and/or make all required changes to MES & SAP Recipes, worksheets, equipment and material specifications to a high-quality standard.
Liaise with Manufacturing and Quality to close out MES execution exceptions.
Troubleshoot and provide solutions for MES & SAP problems in recipe execution and recipe authoring.
Liaise with Quality to ensure timely approval of required documentation for MES system changes.
Generate and execute system and test documentation in a GMP compliant manner.
Design, create, write and/or make all required changes to ensure manufacturing batch records, cleaning instructions and SOPs are aligned to MES processes and vice versa.
Provide training for all other site personnel on their related MES roles.
Participate in MES knowledge exchanges, MES Governance Meetings, global MES Technical Review Board (TRB) meetings, manage issues and solutions as identified.
Work closely with IT regarding upgrades, patching, hardware support, security and system access.
Liaise with global MES team on Sligo site specific MES system improvements, as required.
Provide support to other MES system users to ensure business continuity.
Participate in site projects from initiation to ensure MES system or hardware requirements are taken into consideration.
Maintain strong relationship with other team members to attain a solid understanding of team goals and objectives to ensure alignment between MES operations and production schedules.
What you need to apply:
You will have a 3rd Level qualification in suitable science/engineering course with a minimum of 2 years’ experience in Batch processing operations in an FDA / HPRA regulated industry.
Strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.
Experience in the operating in a highly automated environment and safe handling of dangerous chemicals.
Working knowledge of IT systems/MES/manufacturing processes is required for this role.