Direct message the job poster from European Tech Recruit
We're Hiring! MES, DCS, PLC, Automation, Robotics, Process Control, IT, OT & IIOT
A leading biopharmaceutical manufacturing site in Dublin West is seeking a skilled Automation Engineer to join their packaging operations team. This role offers the opportunity to contribute to a state-of-the-art, GMP-compliant facility supporting commercial and clinical drug product manufacturing.
About the Role
You will be part of a dynamic automation team responsible for the design, implementation, and sustaining of automation systems within a high-performance packaging environment. This includes support for automated vision systems, system upgrades, troubleshooting, and ensuring compliance with industry regulations.
Key Responsibilities
* Support the development, maintenance, and optimization of automated packaging systems
* Develop, review, and approve software standards and system documentation
* Provide automation expertise across engineering, operations, and quality teams
* Liaise with internal stakeholders to troubleshoot issues and support operational performance
* Ensure all systems operate in a validated, qualified, and compliant state in line with GMP standards
* Assist in validation activities, change controls, and investigations
* Lead or support automation efforts for new equipment, technology upgrades, and product introductions
* Deliver training and guidance to users on automated systems and procedures
* Design automation solutions aligned with site change control protocols and engineering best practices
* Create and approve project documentation to support future expansion and compliance
Candidate Profile
* 5+ years of automation experience in regulated (GMP) environments, preferably biopharma
* 3+ years supporting packaging automation or vision inspection systems
* In-depth knowledge of automation platforms and system lifecycle in a manufacturing setting
* Experience implementing change controls and supporting deviation investigations
* Solid understanding of cGMP, GAMP 5, and regulatory expectations for compliant systems
* Strong interpersonal and communication skills; ability to work cross-functionally
* Proven ability to manage vendors, system integrators, and external partners
* Background in developing project scopes, estimations, and automation documentation
* Familiarity with virtualization platforms, SQL Server, or broader IT/OT integration is a plus
Seniority Level
Mid-Senior level
Employment Type
Contract
Job Function
Biotechnology Research and Pharmaceutical Manufacturing
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