Senior Project Manager - Medical Devices
Location: Dublin
Industry: Medical Devices / Regulated Manufacturing
The Opportunity
We are seeking an experienced Senior Project Manager to join a leading medical device manufacturing organisation in Dublin.
This is an exciting opportunity to lead cross-functional projects supporting a portfolio of innovative injection products, with a focus on product lifecycle management, regulatory compliance, business continuity and manufacturing improvements.
Working closely with Engineering, Quality, Regulatory, Operations and other key stakeholders, you will play a central role in delivering projects that support product changes, cost reduction, line extensions and ongoing business growth.
The successful candidate will bring strong project management experience within a regulated medical device or pharmaceutical environment, alongside the ability to coordinate technical teams and deliver complex projects to agreed timelines and quality standards.
Key Responsibilities
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Lead cross-functional projects supporting product changes, regulatory compliance, cost reduction, line extensions and business continuity.
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Manage projects from initiation through to implementation, ensuring delivery against agreed scope, timelines, budgets and quality requirements.
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Act as the primary point of contact between business leadership, functional managers and project team members.
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Coordinate technical subject matter experts to define project deliverables, activities, resources and milestones.
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Develop and maintain detailed project plans, schedules and risk assessments.
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Facilitate regular project meetings, ensuring stakeholder alignment and timely completion of actions.
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Assess change requests and evaluate their impact on project scope, cost, schedule and risk.
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Manage engineering change deliverables through formal Change Control processes.
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Work closely with Engineering, Quality, Regulatory, Operations and other functions to ensure compliance with relevant quality systems and regulatory requirements.
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Provide regular project status updates to senior management, covering progress, risks, quality, schedule and cost.
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Promote strong project planning, execution discipline and continuous improvement across project activities.
The Ideal Candidate
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Bachelor's degree in Engineering, Technology or a related discipline.
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Minimum 5 years' experience within a regulated medical device and/or pharmaceutical environment.
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Proven experience managing cross-functional technical or engineering projects.
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Experience with product lifecycle management within a manufacturing environment.
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Strong understanding of structured product development processes and engineering change control.
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Knowledge of ISO standards, GMP, FDA regulations, medical device design controls and manufacturing scale-up processes.
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Experience coordinating multidisciplinary teams and managing multiple project stakeholders.
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Strong project planning, risk management, communication and organisational skills.
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Ability to manage competing priorities while maintaining a strong focus on quality, compliance and project delivery.
What's on Offer
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Opportunity to lead projects supporting a critical medical device product portfolio.
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Exposure to cross-functional engineering, manufacturing and regulatory initiatives.
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A collaborative environment with strong technical and business stakeholder engagement.
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Competitive salary and benefits package.
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Long-term career development within the medical device industry.
