Manufacturing Technical Excellence Mgr. (Solution Prep)

EyeBio; Dunboyne; On-site; EUR 90,000 - 150,000; Full time

Job summary

EyeBio seeks a Manufacturing Technical Excellence Lead to guide a dedicated IPT team in Dunboyne. The role focuses on a unit operation, compliance, and data-driven scheduling across the site for clinical to commercial supply.

The successful candidate will drive safety, quality, and efficiency, manage changeovers, lead complex investigations, and align with governance pillars while enabling Right‑First‑Time execution.

Qualifications

• Bachelor's degree in engineering or science; Master’s desirable.
• 3+ years leading teams to successful outcomes.
• 5+ years in Pharma/Biopharma or related industry preferred.
• GMP/regulated environment experience required.
• Experience with MES, SAP and DeltaV systems.

Responsibilities

• Lead, coach, and develop a high-performing technical team.
• Ensure compliance with cGMP and regulatory requirements.
• Drive CAPAs and quality events, and assess risks.
• Provide technical oversight for manufacturing operations.
• Lead cross-functional collaboration with QA, Engineering, and Supply Chain.

Skills

Leadership

Cross-functional collaboration

Problem solving

Data-driven decisions

Education

Bachelor's degree in engineering or science

Master's degree

Tools

MES

SAP

DeltaV

Job description

Job Description

A fantastic opportunity has arisen in the Integrated Process Teams (IPTs) focused on Solution Prep/Site Support. The Manufacturing Technical Excellence Lead (Mgr.) will act as a team lead and with a focus on a specific unit operation and compliance.

The successful candidate will develop, communicate, and execute a data-driven cross-enterprise schedule to ensure successful site delivery, achieving our Governance Pillars in People, Safety, Quality, Delivery, and Cost. This role is critical for managing the production schedule, planning changeovers, conducting audits, and optimizing plant operations to ensure effective and efficient production through driving a safety, compliance, and right-first-time mindset.

Our facility in 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 supports seamless connection and collaboration within and across teams and functions. Our Dunboyne facility provides Biologics Drug Substance manufacturing for Clinical Supply, Registration, and Commercial Launch.

Responsibilities

• Lead, coach, and develop a high-performing technical team.
• Foster a culture of accountability, collaboration, inclusion, and continuous learning.
• Establish clear performance expectations aligned with site and departmental goals.
• Provide regular feedback, coaching, and mentoring to team members.
• Act as a role model for company values and leadership behaviours.
• Promote a strong safety culture and lead by example in EHS performance.
• Support/Lead and participate in safety audits, investigations, and risk assessments.
• Ensure compliance with site procedures, global policies, and regulatory requirements.
• Maintain a constant state of audit and inspection readiness.
• Drive timely completion of corrective and preventative actions (CAPAs).
• Provide technical oversight and support for manufacturing operations.
• Lead and facilitate complex investigations related to safety, quality, and operational performance.
• Utilize structured problem-solving methodologies to identify root causes and implement sustainable solutions.
• Support process monitoring and execution of performance improvement initiatives.
• Ensure technical issues impacting production are escalated, acting as an escalation point throughout manufacturing and ensuring resolution appropriately as per site escalation strategy.
• Provide technical assessment and support/lead deviations, change controls, and quality events.
• Drive continuous improvement initiatives using MPS and Operational Excellence tools.
• Support site productivity, capacity, and efficiency improvements.
• Monitor and trend operational performance metrics, identify opportunities to reduce waste, improve reliability, and increase process robustness.
• Support implementation of strategic site projects and business initiatives.
• Ensure manufacturing activities are executed in accordance with cGMP requirements.
• Review and approve GMP documentation as required.
• Support Quality Management System (QMS) activities.
• Ensure adherence to approved procedures, work instructions, and quality standards.
• Promote a culture of Right First-Time execution and data integrity.
• Act as a key interface between Manufacturing, Quality, Engineering, Automation, Supply Chain, Validation, and Technical Services.
• Support and lead project execution and change management activities.
• Communicate effectively with stakeholders to ensure alignment and successful execution of priorities.
• Support site governance and escalation processes.
• Role may require some shift work/ out-of-hour support for manufacturing activities.
• On-the-floor current Good Manufacturing Practice (cGMP) manufacturing and familiarity with regulatory requirements.
• Familiar with all Safety, GMP, Environmental and Validation permits, policies, and procedures.
• Familiar with plant equipment.
• Training others and/ or leading hands‑on or instructor-led training.
• Ability to read, write and understand technical information.

Skills & Qualifications

• Minimum level 8 bachelor’s degree in engineering or science-based discipline or equivalent.
• A master’s is desirable.
• Proven leader capability in developing people and teams with at least 3 years’ experience leading teams to successful outcomes.
• Proven record of accomplishments of working for a minimum of 5 years in a Pharma/Biopharma company or related industry is desirable.
• Proven ability around working cross functionally, focusing on meeting, tracking schedules, and embracing an interdependent work culture.
• Experience working in a GMP/regulated environment is required.
• Proficiency with automated systems such as Manufacturing Execution System (MES), Systems Applications and Products (SAP), Delta V.
• Knowledge of Lean methodologies.

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. So, if you are ready to: Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology,

Required Skills:

Driving Continuous Improvement, GMP Operations, Manufacturing Operations, Operational Excellence, Process Improvements

Preferred Skills:

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

09/9/2026

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