Specialist, Manufacturing Automation (DeltaV Engineer)

MSD; Dunboyne; Hybrid; EUR 70,000 - 95,000; Full time

Benefits offered by this job

Hybrid work arrangement

Visa sponsorship

Job summary

MSD in Ireland (Dunboyne, Co. Meath) is seeking a Manufacturing Automation Specialist to own Emerson DeltaV DCS systems, drive optimization, and support NPIs.

You will collaborate with SIEMENS OEM Automation, PAS-X MES, Engineering, QA, Validation, and Global Technology to ensure compliant, reliable automation. The role requires a Bachelor’s in a related field and 3–5 years’ hands-on DeltaV experience in GMP pharmaceutical manufacturing, with strong knowledge of ISA S88/S95, GAMP5, 21 CFR Part

Qualifications

• Bachelor’s degree in Biotechnology, Automation, Mechatronics, Chemical Engineering, or a related field.
• 3–5 years hands‑on automation engineering with Emerson DeltaV DCS in GMP manufacturing.
• Experience in Tech Transfer, Process Design, and commissioning/qualification.
• Expertise in Batch Control Systems (ISA S88/S95), GAMP 5, 21 CFR Part 11, CSV, and SDLC.

Responsibilities

• Act as technical System Owner for the DeltaV DCS across Upstream, Downstream, Solution Prep, and utility areas.
• Develop, debug, and optimize DeltaV code and control strategies for stability.
• Lead engineering assessments, config modifications, and validation runs for NPIs.

Skills

DeltaV DCS

Batch control systems

Tech Transfer

Process Design

Root cause analysis

GMP compliance

SDLC

Education

Bachelor's degree in Biotechnology/Automation/Mechatronics/Chemical Engineering

Tools

Emerson DeltaV

PAS-X

Siemens OEM Automation

Job description

A fantastic opportunity has arisen for a Manufacturing Automation Specialist to join our state-of-the‑art, single-use multiproduct facility in Dunboyne, Co. Meath. The DeltaV Engineer is responsible for the design, implementation, support, and continuous improvement of the Emerson DeltaV DCS, providing technical expertise across all DeltaV systems and supporting both existing products and new product introductions (NPIs). As a key member of the Manufacturing Automation team, you will work closely with OEM Automation (Siemens), MES (PAS‑X), Engineering, Operations, Quality, Validation, and Global Technology teams to ensure reliable and compliant system performance. Acting as the site's DeltaV subject matter expert, you will drive automation performance while maintaining inspection‑ready systems aligned with the site's EHS, Quality, People, and Delivery objectives. This role requires strong technical expertise, cross‑functional collaboration, accountability, and a commitment to fostering a culture of dignity, respect, and continuous improvement. Based within the Digital Manufacturing Operations (DMO) team, the role involves extensive collaboration across Self‑Directed Work Teams (SDWTs) and cross‑functional groups to resolve complex automation challenges and support both sustaining operations and business‑critical projects.

Responsibilities

• System Ownership: Act as the technical System Owner for the Emerson DeltaV DCS process automation equipment supporting Upstream, Downstream, Solution Prep, and utility areas.
• Code Optimization: Develop, debug, and optimize DeltaV code and control strategies to maximize software and hardware stability.
• Tech Transfer & NPIs: Lead engineering assessments, configure automation system modifications, and support clinical/engineering validation runs for new product introductions.
• Issue Resolution: Lead complex root cause analysis (RCA), deviation investigations, and troubleshooting of electrical, instrumentation, and equipment control systems.
• Compliance & Audits: Maintain systems in a constant state of regulatory compliance and audit‑readiness; actively participate in internal and external regulatory inspections.
• Lifecycle Management: Own change control assessments, maintenance scheduling, and software development life cycle (SDLC) documentation.
• Digital Innovation: Identify, design, and implement digital, paperless manufacturing solutions that support the facility's advanced automation vision.
• Operational Excellence: Author detailed engineering specs, SOPs, and participate in continuous improvement initiatives (GEMBAs, Go-Sees).

Qualifications Required

• Bachelor’s degree in Biotechnology, Automation, Mechatronics, Chemical Engineering, or a closely related technical field.
• 3-5 years of hands‑on automation engineering experience with Emerson DeltaV DCS in a GMP‑regulated (Biotech or Pharmaceutical) manufacturing environment.
• Demonstrated success in process automation roles involving Tech Transfer, Process Design, and commissioning/qualification.
• In‑depth technical expertise in Batch Control Systems (ISA S88/S95), GAMP 5, 21 CFR Part 11, Computer System Validation (CSV), and SDLC methodologies.
• Proven capability in automation change control management, structured deviation management, and technical root‑cause analysis.

Preferred

• Multi‑Platform Exposure: Practical experience integrating with Siemens OEM Automation and MES (PAS‑X) systems.
• Work Environment: Prior experience in a site‑based Automation department or working within Self‑Directed Work Teams (SDWTs).
• Skills: Strong project planning capabilities, cross‑functional project management, and customer‑focused decision‑making.
• Auditing – exposure or involvement in Regulatory Audits.

Additional location(s) Compensation Information: Required Skills: DeltaV DCS, Emerson DeltaV, ISA88, Manufacturing Automation

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.

Employee Status: Regular

Relocation: No relocation

VISA Sponsorship: Yes

Travel Requirements: No travel required

Flexible Work Arrangements: Hybrid

Shift: Not Indicated

Valid Driving License: Yes

Hazardous Material(s): NA

Job Posting End Date: 10/31/2026

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.