Contract Automation Process Engineer (BioPharma)

Morgan McKinley; Cork; Hybrid; EUR 65,000 - 90,000; Full time

Job summary

Morgan McKinley is seeking a contract Automation Process Engineer for a premier pharmaceutical site in Co. Cork. 3-5 years of experience in process control, DCS support, and GMP compliance is required to maintain uptime and support batch manufacturing.

Hybrid work arrangement: 4 days onsite with Friday work-from-home; 12-month rolling contract. You will work with Process Engineers and Maintenance to implement control updates, perform health checks, and ensure CSV/GAMP standards.

Qualifications

• 3–5 years in Process Control, Automation, or DCS support within a regulated manufacturing environment.
• Hands-on experience with automated pharmaceutical processes and batch manufacturing.
• GMP/cGMP, CSV and GAMP5 awareness are preferred.

Responsibilities

• Troubleshoot real-time control loops, sequence logic, sensor readings and valve activations to maximize uptime.
• Support DCS health checks, system backups, and architecture updates.
• Design, test and roll out minor control logic updates and alarm rationalizations.
• Collaborate with Process Engineers, Maintenance and Operations to translate requirements into automation solutions.
• Draft and execute change controls, test scripts and CSV documentation per GMP standards.

Skills

Process control troubleshooting

Team collaboration

Documentation & Change Control

GMP knowledge

Education

Bachelor's degree in Automation or Electrical Engineering

Tools

Foxboro DCS

Emerson DeltaV

Honeywell Experion

Siemens PCS7

ABB

Job description

Job Description

We are seeking a contract Automation Process Engineer with 3 - 5 years of experience to join our team supporting active production at a premier pharmaceutical manufacturing site in Co. Cork. This role focuses on maintaining daily uptime, managing process control improvements, and supporting active batch manufacturing. While knowledge of Foxboro DCS is beneficial, other major DCS platformed will be considered and hands on experience with automated pharmaceutical processes, batch manufacturing, and GMP compliance is prioritised. If you thrive on solving complex, real world technical problems, continuously building your skill set, and working alongside a supportive team that genuinely looks out for one another, this is your next move.

Why You'll Love This Role

Long-Term Stability: Enjoy the flexibility of contracting with the long-term security of a "resident" site role.

Culture of Collaboration: Work in an environment where knowledge is shared, teamwork is second nature, and people genuinely help each other succeed.

Continuous Growth: Gain hands on exposure to cutting edge biopharma automation, expand your system repertoire, and master new skills.

What You'll Be Doing

• Tackle real-time floor challenges - troubleshooting control loops, sequence logic, sensor readings, and valve activations to maintain maximum uptime.
• Support ongoing DCS health checks, system backups, and continuous architecture updates.
• Design, test, and roll out minor control logic updates, sequence modifications, and alarm rationalizations to optimize live processes.
• Work side-by-side with Process Engineers, Maintenance, and Operations to translate complex operational needs into robust automation solutions.
• Draft and execute change controls, test scripts, and CSV documentation in full alignment with GMP and site Quality standards.

Key Information

• Role: Automation / Process Control Engineer (Production Support)
• Location: Co. Cork (Hybrid: 4 days onsite, Friday WFH)
• Contract: 12-Month Rolling Contract (Long-term / Resident status)
• Hours: 40 hours/week (Occasional weekend support aligned with production cycles)

What We're Looking For

We value core process control capability, S88 batch expertise, and sharp troubleshooting skills above specific brand loyalty. If you know how biopharma/API process automation works, we want to talk to you.

• 3-5 Years Experience in Process Control, Automation, or DCS Support within a regulated manufacturing environment (Biopharma, Bulk API, Fine Chemicals, or MedTech).
• DCS/Control Platform: Solid proficiency ideally with Foxboro but will consider any major platform (Emerson DeltaV, Honeywell Experion, Siemens PCS7, ABB, or Foxboro).
• Compliance Mindset: Practical experience with GMP/cGMP, GAMP 5, and Computer System Validation (CSV).
• Strong Process Logic: Deep understanding of S88 batch processing, thermal/pressure/flow control loops, vessel sequencing, and CIP/SIP cycles.
• Education: Degree in Automation, Electrical, Electronic, Chemical, Systems Engineering, or equivalent technical experience.

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