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Senior Automation Engineer DeltaV Specialist

MSD -
Dunboyne, County Meath

Apply Now

Job details

Full-time
3 hours ago

Qualifications

TCP
Financial auditing
English
Analysis skills
Project management
Bachelor's degree
Team management
Communication skills
SDLC

Full job description

Job Description

At Dunboyne Biologics, an opportunity has arisen for a Senior Automation Engineer to join an existing high performance Process Automation team in our state-of-the-art, single use multiproduct facility in Dunboyne, providing Biologics Drug Substance manufacturing for Clinical Supply, Registration & Commercial Launch.

We’re hiring a Senior Automation Engineer to lead automation platform solutions, design, development, implementation and performance optimisation of Emerson DeltaV DCS in support of our biologics pipeline (early to late stage). This is a senior, site‑based role with hybrid working flexibility. The right candidate brings significant, demonstrable Emerson DeltaV experience plus proven project and team management capability.

Key responsibilities will include:

Automation Systems:

System owner of DeltaV DCS and OEM in a facility operating Intensified Fed Batch and Continuous Manufacturing.
Identify and lead Continuous Improvement projects impacting automation platform technologies.
Support troubleshooting of complex equipment/automation issues, implementing change in compliance with company policies, cGMP regulations and industry best practice while maintaining automation systems validated state.
Effectively collaborates with both internal cross functional teams, inclusive of BMSO network partners, Automation CoE, Clinical Development and commercial manufacturing facilities.
In collaboration with Process Engineering, Tech Transfer and Manufacturing Operations, maintain alignment within our network and standardize/Introduce next-gen technologies to deliver late-phase Clinical or Commercial supply. Serves as the automation technical lead for site capital projects.
Proactively participate to enhance Digital Transformation initiatives involving system integrations, data connectivity, validation methods and value-based optimization of manufacturing via process control system.
Supports business need for critical operations.
Manage automation service contract partners to ensure effective delivery adhering to cost and compliance requirements.

Compliance, Investigations & Change Control:

Support the qualification of new systems. Write, review, and/or execute test documents, maintaining automation system compliance, validated state and inspection readiness.
Own or support investigations for automation-related events or non-conformances, perform root cause analysis and CAPA implementation.
Responsible for Change management and Implementation for automation-related changes, ensuring alignment with SDLC, change control, and GMP standards.

Must‑have experience and qualifications:

Bachelor’s degree in a Life Science discipline.
10 years’ Automation experience within Biologics, Pharmaceutical, Medical Devices facilities.
Proven experience with DeltaV control system, DeltaV Batch, Siemens TIA, OSI PI.
Proven Project Management experience.
Effective communicator with strong organizational and analytical abilities.
Effective oral / written communication skills in English (C1).
Experience with computer system validation/SDLC and automation change control procedures. (e.g., GAMP 5).
Commissioning and qualification, test protocol development and execution.
Experience with Network topologies such as Ethernet/IP, OPC, Profinet, and Modbus TCP protocols is essential.
Provide examples of prioritization and planning demonstrating ability to identify opportunities, set priorities, establish timelines, define action plans for both self and others and deliver to plan.

Our facility in Dunboyne joined our network in September 2020. Our Dunboyne site is our Company’s first Biologics Drug Substance Single Use Commercialisation Facility, playing an important role in helping to commercialise key medicines. The cutting-edge innovation and collaboration between our Company’s research and manufacturing teams will significantly accelerate the time it takes to bring a medicine to market for the benefit of patients around the world.

Required Skills:

Audit Management, Automation Engineering, Automation Solutions, Business Process Improvements, Capital Projects, cGMP Regulations, Data Management, Digital Transformation, GMP Compliance, Inspection Readiness, Modbus, Prioritization, Problem Management, Project Management System, Quality Management, Real-Time Programming, Software Development Life Cycle (SDLC), System Integration, Team Management

Preferred Skills:

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:

06/16/2026

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.

Requisition ID:R403315

Apply Now

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