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Specialist Automation Engineer

14 Mar 2025
Co. Meath, Ireland
Verified by Turrior

Content + Source + Freshness • 12 Dec 2025 • 95% confidence

79 / 100

Offer value

Engaging role for automation engineers within the biotechnology space; requires a clear understanding of complex systems.

  • Role in a leading biotech facility focusing on innovation.
  • Hands-on experience with automation systems.
  • Growth prospects in process improvement and leadership.
Pros
  • Opportunity to work in a state-of-the-art biotech facility.
  • Focus on automation, enhancing technical and leadership skills.
  • Participation in continuous improvement initiatives.
Cons
  • Demands in-depth technical knowledge of automation systems.
  • High expectations on project deliverables.
  • Possibility of less flexibility depending on project needs.

Who it's for

Mid to Senior automation engineers • Hybrid with office component

Good fit
  • Experienced automation engineers with biotech background.
  • Professionals eager to lead process improvement initiatives.
  • Candidates passionate about innovative engineering solutions.
Not recommended for
  • Entry-level applicants without technical skills.
  • Individuals uninterested in automation challenges.
  • Those seeking a less dynamic work environment.

Motivation fit

Desire to innovate and solve complex automation challenges.Interest in contributing to biotechnology advancements.Drive to collaborate with diverse teams and lead projects.

Key skills

Automation engineering, control systems.Problem-solving and troubleshooting.Project management and leadership.
Score: 79/100 AI verified analysis

About the job

Job Description

A fantastic opportunity has become available to join our facility as a Specialist Automation Engineer.

The Biologics Innovation Xceleration facility, at Dunboyne is a premier, state-of-the-art facility that enables and advances our best work. By integrating leading-edge technology with a dynamic, activity-based workspace, the facility will support seamless connection and collaboration within and across teams and functions. The facility will provide Biologics Drug Substance manufacturing for Clinical Supply, Registration & Commercial Launch.

The Process Automation team provide a strategic link between our early and late-stage pipeline which will provide Biologics Drug Substance manufacturing for Clinical Supply, Registration & Commercial Launch.

What you will do:

Bring energy, knowledge, innovation, and leadership to carry out the following:

  • Provide key automation support for various manufacturing systems such as DCS, OEM systems – in a facility operating Intensified Fed Batch and Continuous Manufacturing.
  • Support and/or Direct Continuous Improvement projects with automation review of equipment specifications, P&IDs, and System Life Cycle documentation.
  • Responsible for troubleshooting equipment/automation issues to improve manufacturing performance (e.g. yield improvements, etc.), changes to support new products, and maintaining the automation systems in compliance with cGMP.
  • Support the transfer of Process Technologies from early-stage pipeline facilities and drive to GMP Operational Status, and support line of sight to commercial supply.
  • Perform automation change controls with guidance from Sr. Automation Engineer or Automation lead to ensure that changes are raised and closed on time following the required quality standards.
  • Participate and actively support Digital Transformation initiatives involving system integrations, data connectivity, validation methods and value-based optimization of manufacturing via process control system.


Qualifications

In order to excel in this role, you will more than likely have:

  • Bachelor’s degree in a Life Science discipline or equivalent practical experience of automation control systems.
  • At least 3 years of experience in an Automation Engineering function within Biologics, Pharmaceutical, Medical Devices, or Food industries.
  • Proven experience with control systems (DeltaV, Siemens TIA, OSI PI).
  • Experience with computer system validation/SDLC and automation change control procedures. (e.g., GAMP 5).
  • Experience with DeltaV Batch is essential, including understanding of ISA S95 and S88.
  • Commissioning and qualification, test protocol development and execution.
  • Networking experience (i.e., Ethernet/IP, OPC, Profinet, and Modbus TCP protocols) is advantageous.

As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about our hybrid working model

So, if you are ready to:

Invent solutions to meet unmet healthcare needs, please apply today.

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

03/18/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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