Pharma Manufacturing Systems Specialist

Viatris; Sutton; On-site; EUR 55,000 - 75,000; Full time

Job summary

Viatris is seeking a Manufacturing System Technician to support MES, SAP and LIMS across manufacturing operations in Ireland. The role requires strong technical knowledge and a proactive approach to process improvement and compliance with regulatory standards.

You will collaborate with cross-functional teams, deliver system enhancements, and provide training and validation support to ensure product quality and operational efficiency. This is a full-time on-site position based in Sutton.

Qualifications

• Third level qualification in a relevant discipline (Mechanical/Mechatronic/Engineering preferred).
• If no degree, path to qualification with manufacturing and systems experience.
• Five years+ experience in Pharma/Medical Device or related industries.
• Willingness to develop across MES, SAP, LIMS, validation, automation.
• Lean/Six Sigma certification would be advantageous.
• Provide shift support across 1–4 shifts as required.

Responsibilities

• Develop knowledge across MES, SAP, LIMS, and manufacturing processes.
• Specify, design and implement MES projects with handover and post-implementation support.
• Measure, analyse and improve manufacturing process outputs.
• Support preparation of product and process reports including quality deviations.
• Deliver improvement initiatives across products and processes.
• Assure product and process quality and optimize manufacturing processes.
• Provide training and qualification/validation support.
• Promote Safe Working in all areas and projects.

Skills

MES

SAP

LIMS

Manufacturing processes

Validation

Automation

Quality

Project management

Education

Bachelors in Mechanical/Mechatronic/Engineering

Job description

Viatris is seeking a Manufacturing System Technician to support MES, SAP and LIMS across manufacturing operations in Ireland. The role requires strong technical knowledge and a proactive approach to process improvement and compliance with regulatory standards.

You will collaborate with cross-functional teams, deliver system enhancements, and provide training and validation support to ensure product quality and operational efficiency. This is a full-time on-site position based in Sutton.