Support integration of new manufacturing equipment, process vessels, filling lines, and automated production systems.
Review control architecture, instrumentation, interlocks, alarms, and safety systems to identify opportunities for automation and operational efficiency improvements.
OEM Management, Commissioning & Qualification
Act as the site technical interface for OEMs and automation suppliers, reviewing designs, control specifications, and software configurations.
Lead or participate in Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT).
Coordinate automation activities during installation, commissioning, and start-up phases.
Collaborate with Validation teams to support IQ, OQ, and PQ, resolving technical issues before handover.
GMP Compliance & Documentation
Ensure all engineering activities comply with cGMP, GAMP 5, Good Engineering Practice (GEP), and applicable regulatory requirements.
Support change controls, risk assessments, validation documentation, and technical investigations.
Maintain software configuration control, system backups, and technical records in collaboration with QA and Validation teams.
Manufacturing Support & Continuous Improvement
Provide specialist technical support for existing automation systems and troubleshoot PLC, HMI, SCADA, and equipment control faults.
Support equipment reliability upgrades, preventative maintenance, and automation/process optimization initiatives.
Key Skills and Requirements
Education: Bachelor’s Degree in Automation, Electrical, Electronic, or Instrumentation Engineering (or equivalent technical qualifications with relevant experience).
Experience: Minimum 3 years of automation engineering experience, ideally 5-8 years in pharmaceutical or regulated manufacturing environments.
Technical Expertise
Practical PLC experience with Rockwell Studio 5000, FactoryTalk View SE, and/or Siemens TIA Portal PCS 7.
Strong understanding of HMI, SCADA, and industrial control systems.
Experience coordinating OEMs, system integrators, and engineering suppliers, including involvement in FAT, SAT, commissioning, and qualification.
Compliance Knowledge: Working knowledge of GMP, GAMP 5, GEP, change control, and pharmaceutical validation requirements.
Desirable Experience
Familiarity with DCS, Safety Instrumented Systems, batch processing, and process equipment.
Knowledge of filling equipment, automated production lines, industrial networks, and IT-OT integration.
Understanding of computerized system validation, data integrity, and electronic records.
Experience delivering automation workstreams within medium to large capital investment projects.
Key Competencies
Strong project ownership and delivery focus with the ability to manage multiple priorities.
Excellent technical problem-solving, communication, and stakeholder management skills.
Confidence in coordinating OEMs, suppliers, contractors, and cross-functional teams.
Proactive approach to resolving technical issues and driving continuous improvement.
Commitment to GMP compliance, health and safety, and engineering standards.
Salary
€75 000.00 – €80 000.00/Annum
For more information, please contact Billy O’Brien.
If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.
R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/
