Contract | Dublin, Ireland
Senior Automation Engineer
Overview
An excellent contract opportunity for an experienced Senior Automation Engineer to support complex biopharmaceutical and life sciences projects. The role focuses on design and delivery of GMP-compliant automation and control systems, from early concept and Basis of Design (BOD) through detailed design and project execution.
This position offers exposure to multi-million‑euro biopharma projects, working within a multidisciplinary engineering environment on regulated manufacturing and fill‑finish facilities.
Key Responsibilities
Lead the design of automation and control systems for biopharma manufacturing facilities from concept, BOD, and detailed design phases.
Develop and review control system design specifications in line with GMP and regulatory requirements.
Collaborate with cross‑functional project teams including Process, Mechanical, Electrical, CQV, Quality, and ICT.
Select, manage, and technically oversee automation vendors and system integrators throughout the project lifecycle.
Review and approve automation design documentation, software design specifications, and vendor deliverables.
Ensure automation solutions comply with GMP, data integrity, and regulatory expectations (including GAMP 5 and 21 CFR Part 11).
Support and attend hardware and software FATs, SATs, and commissioning activities.
Maintain awareness of current automation technologies and industry best practices within biopharma manufacturing.
Requirements
Degree (Level 8) in Automation, Control Systems, Mechatronics, Electronic Systems, or a related engineering discipline, or equivalent experience.
Minimum 7+ years’ experience delivering automation projects within biopharma, pharmaceutical, or regulated life sciences environments.
Strong experience in the design and implementation of PLC‑ and DCS‑based control systems.
Demonstrated experience in automation software development and system architecture design.
Solid knowledge of industry standards and frameworks including S88, GAMP 5, and 21 CFR Part 11.
Experience with industrial communication networks (Ethernet, Profinet, Profibus, ControlNet).
Ability to read and interpret P&IDs, control philosophies, and panel drawings.
Familiarity with GMP manufacturing processes such as upstream, downstream, utilities, fill‑finish, or packaging is highly desirable.
Excellent communication skills, with experience working in multidisciplinary and global project teams.
Proven ability to manage multiple priorities and deliver to tight project timelines.
Proactive, organised, and capable of working independently within a fast‑paced, regulated environment.
Seniority Level
Mid‑Senior level
Employment Type
Full‑time
Job Function
Manufacturing and Engineering
Industries
Biotechnology Research, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing
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