Automation Engineer

Automation (E /MES) Engineer - Kerry

The successful Automation / E  Design Engineer is responsible for designing, configuring, and optimizing Electronic Batch Record (E ) solutions within the Manufacturing Execution System (MES) to ensure compliant, efficient, and reliable batch documentation processes in pharmaceutical manufacturing.

Qualified with a Bachelor’s Degree in Engineering, Computer Science, Life Sciences, or related field. The successful Engineer will have 2+ years of experience in MES/E  design or pharmaceutical manufacturing IT systems.

• Collaborate with manufacturing, quality, IT, and validation teams to gather requirements and translate them into functional E  designs.
• Ensure EBRs comply with GMP, FDA 21 CFR Part 11, EU Annex 11, and other relevant regulations.
• Participate in user acceptance testing (UAT), troubleshooting, and resolution of E
  -related issues.
• Support validation activities, including authoring and executing test scripts and supporting documentation.
• Drive continuous improvement of E  templates and processes to enhance efficiency and data integrity.
• Provide training and support to end-users on E  functionality and best practices.
• Maintain documentation for E  design, configuration, and change management.
• Design, develop, and configure EBRs within the MES platform (Apprentice Tempo).

• Strong knowledge of GMP, data integrity, and regulatory requirements for electronic records.
• Experience with at least one MES platform (e.g., Apprentice TEMPO, Werum PAS-X, Emerson Syncade, Siemens Opcenter).
• Proficient in process mapping, requirements gathering, and technical documentation.
• Excellent analytical, problem-solving, and communication skills.

• Experience with batch process automation and integration with shop floor systems (PLC, SCADA, DCS).
• Familiarity with GAMP 5, validation lifecycle, and computerized system validation.
• Ability to work in a global, cross-functional team environment.
• Advanced knowledge of pharmaceutical manufacturing processes.

This role is primarily based onsite at a pharmaceutical manufacturing facility, with occasional remote work as permitted. The E  Design Engineer will interact with production, quality, and IT teams in a highly regulated, collaborative environment.

Arcadis is a leading Project Management and Engineering Company delivering Full-Service Engineering with a ‘client first’ mentality and personal touch across a range of market sectors:
Project and Programme Management, Procurement, Design, Construction Management, Health & Safety Management, Commissioning, Qualification and Start-up. We have one goal: to deliver more than our clients expect first time, every time.

Arcadis is an Equal Opportunities Employer.

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