Automation Engineer

NeoDyne; Dublin; On-site; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Paid overtime

Flexible working hours

Opportunity to work on high-profile projects

Job summary

NeoDyne is seeking an Automation Engineer in Dublin to support automation projects for a pharmaceutical manufacturing facility. This role involves executing commissioning activities and ensuring compliance with GMP standards. Candidates must have a degree in Automation or Engineering and experience with automation project delivery.

The successful applicant will work closely with OEM suppliers and multidisciplinary teams, contributing to innovative automation solutions. Competitive hourly rate and flexible hours are offered.

Qualifications

• Proven experience in automation projects within GMP-regulated environments.
• Strong commissioning and start-up experience with manufacturing systems.
• Understanding of CQV methodologies and validation lifecycle.

Responsibilities

• Support delivery of automation systems for new pharmaceutical equipment.
• Work with OEM vendors on installation and commissioning.
• Execute commissioning according to project schedules.
• Ensure compliance with GMP and site change control procedures.

Skills

Automation project execution

Troubleshooting

GMP compliance

Project collaboration

Education

Degree in Automation, Electrical Engineering, Mechatronics

Tools

Rockwell Automation (ControlLogix, FactoryTalk)

Job description

Overview

NeoDyne is a leading engineering company specialising in industrial automation, digital manufacturing, and electrical engineering solutions. With a strong presence across multiple sectors, including Life Sciences, Food & Beverage, and Energy, NeoDyne delivers leading‑edge solutions that drive efficiency, safety, and performance for its customers worldwide.

With a team of 220+ skilled engineers, our expertise spans the entire project lifecycle, from design and implementation to commissioning and operations. From our offices in Ireland, the UK, Romania, and the US, we operate on a global scale, combining technical expertise with local delivery. We support customers across Europe, North America, and Asia, delivering tailored engineering services that drive long‑term success.

Our client, a leading pharmaceutical manufacturer, is undertaking a significant expansion project involving the delivery of a new drug product manufacturing facility. This role will support the implementation and commissioning of new process equipment including filling lines, lyophilisation systems, and associated utility and automation infrastructure.

The successful candidate will join a project‑focused team responsible for supporting automation, commissioning, qualification, and validation activities throughout the project lifecycle. This is a hands‑on engineering role suited to someone who enjoys working directly with systems, OEMs, and site stakeholders in a GMP‑regulated environment.

Responsibilities

• Support the delivery of automation systems associated with new pharmaceutical manufacturing equipment and facilities.
• Work closely with OEM vendors during equipment installation, integration, commissioning, and start‑up activities.
• Execute commissioning activities in accordance with site procedures and project schedules.
• Support CQV (Commissioning, Qualification and Validation) activities including protocol execution and documentation review.
• Ensure compliance with GMP requirements and site change control procedures throughout project execution.
• Assist with troubleshooting and resolution of automation, controls, and integration issues during project delivery.
• Review automation design documentation, functional specifications, test documentation, and turnover packages.
• Coordinate with multidisciplinary project teams including Process, Validation, Quality, Engineering, and Operations personnel.
• Support system handover activities and operational readiness requirements.
• Participate in FAT, SAT, commissioning, and qualification activities as required.

Required Experience

• Degree qualified in Automation, Electrical Engineering, Mechatronics, or related discipline.
• Proven experience delivering automation projects within pharmaceutical, biotechnology, or other GMP‑regulated manufacturing environments.
• Strong commissioning and start‑up experience on manufacturing systems and equipment.
• Experience working within formal GMP change control processes.
• Understanding of CQV methodologies and validation lifecycle requirements.
• Experience supporting equipment integration and commissioning activities alongside OEM suppliers.
• Strong troubleshooting and problem‑solving skills within operational manufacturing environments.
• Ability to work independently within a fast‑paced project environment.

Preferred Experience

• Experience with filling lines, aseptic processing equipment, lyophilisation systems, or packaging equipment.
• Strong knowledge of Rockwell Automation platforms including ControlLogix and FactoryTalk.
• Experience supporting capital projects within pharmaceutical manufacturing facilities.
• Familiarity with ISA‑88, ISA‑95, and pharmaceutical automation standards.
• Previous experience supporting equipment qualification and validation activities.

Characteristics

• Work well as part of a team.
• Have excellent problem‑solving and diagnostic skills.
• Can complete tasks independently, capable of self‑learning.
• Can prioritise and coordinate work.
• Have excellent customer service, interpersonal, communication and organisational skills.
• Can multitask and work well under pressure.
• Are a strategic business thinker.

What's On Offer

• Competitive hourly rate based on experience.
• Paid overtime available, depending on project demands.
• Flexible working hours may be accommodated in line with project requirements.
• Opportunity to work on a high‑profile site with a collaborative, technically strong team.
• Chance to be part of NeoDyne's network of engineering professionals, contributing to impactful automation solutions in the life sciences sector.

NeoDyne Ltd is an equal opportunity employer, and all applications will be treated in strictest confidence.

Applicants must hold a valid EU passport or have the legal right to work in Ireland (e.g. Stamp 4).