About Amgen Dun Laoghaire (ADL):
Amgen is a global biotechnology leader committed to discovering, developing, and delivering innovative human therapeutics. Our Dun Laoghaire site is a state-of-the-art aseptic drug product operations facility specializing in secondary manufacturing activities, including Formulation, Vial/Syringe Filling, Lyophilisation, Inspection and Packaging.
We foster a culture of continuous improvement and innovation, striving to improve health outcomes and ensure the continuity of supply for our medicines to over 50 countries worldwide.
About the Role:
The Sr. Automation Engineer is a member of the ADL Plant Automation Team responsible for supporting drug product manufacturing, maintaining automation systems in a GMP environment and implementing optimisation projects. The role is a System Owner for critical automation assets, leading troubleshooting, lifecycle management, and continuous improvement initiatives across multiple automation platforms.
Key Responsibilities
System Ownership & Reliability
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Act as System Owner for automation systems in a GMP-regulated manufacturing setting, overseeing lifecycle maintenance and validation.
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Manage Change Controls, Deviations, and CAPAs associated with Automation Systems.
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Maintain robust system documentation, configuration control, and software versioning.
Support & Troubleshooting
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Provide on-the-floor and remote technical support to operations and engineering during production, shutdowns, and technology transfers.
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Lead or support incident investigations and root cause analyses for automation-related issues.
Continuous Improvement & Innovation
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Implement CAPAs, including software changes and updates to design documentation and SOPs.
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Analyse current system designs and recommend improvements aligned with the latest technology and regulatory standards.
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Champion Industry 4.0 initiatives, including data integration, advanced analytics, and digital twin technologies.
Project & Technology Integration
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Support new product or technology introductions by performing engineering assessments, implementing automation system changes, and supporting engineering runs.
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Work closely with cross-functional teams, stakeholders, and vendors to achieve common goals and deliver projects efficiently.
Safety & Compliance
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Promote a culture of safety and regulatory compliance across all activities.
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Always Ensure adherence to EHS and GMP policies.
Preferred Qualifications and Experience:
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Bachelor’s Degree in Automation Engineering, Electrical Engineering, Computer Science, Chemical Engineering, Biotech Engineering, or related life science engineering with minimum 5+ years’ experience in operations/manufacturing environment.
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Background in automation design, installation, validation, lifecycle management, testing and programming.
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Experience in one the following automation specialties is an advantage:
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Biopharmaceutical Formulation or Vial/Syringe Filling
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Inspection or Packaging facilities
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Siemens and Rockwell PLC/HMI.
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iFix, InTouch, Zenon, Process Control Systems, and Rockwell FTView SCADAs.
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Fieldbus systems such as ControlNet, DeviceNet, Profibus, ProfiNet, AS-I, BACnet etc.
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Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards, 21 CFR Part 11 and Annex 11.
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Working knowledge of network architecture technologies including TCP/IP and Firewalls.
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Independent, self-motivated, organised, and able to multi-task in a manufacturing environment.
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Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
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Solid technical writing, and communication/presentation skills.
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Proficient in managing relationships with stakeholders; coordinating and collaborating with teams from different departments to achieve common goals.
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Travel at various times may be required to support training and vendor visits.
