Senior Medical Device Project Lead

Morgan McKinley; Dún Laoghaire; On-site; EUR 90,000 - 130,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Career development opportunities

Job summary

Morgan McKinley in Dublin is seeking a Senior Project Manager to lead cross-functional projects for a portfolio of innovative medical devices. You will drive lifecycle management, regulatory compliance, and manufacturing improvements, coordinating Engineering, Quality, Regulatory, and Operations to deliver projects on time and within budget.

The ideal candidate will have 5+ years of experience in a regulated medical device or pharmaceutical setting, strong leadership, and a proven track record

Qualifications

• Bachelor's degree in Engineering, Technology or related discipline.
• Minimum 5 years' experience within a regulated medical device and/or pharmaceutical environment.
• Proven experience managing cross-functional technical or engineering projects.
• Experience with product lifecycle management within a manufacturing environment.
• Strong understanding of structured product development processes and engineering change control.
• Knowledge of ISO standards, GMP, FDA regulations, medical device design controls and manufacturing scale-up processes.

Responsibilities

• Lead cross-functional projects supporting product changes, regulatory compliance, cost reduction, line extensions and business continuity.
• Manage projects from initiation through to implementation, ensuring delivery against scope, timelines, budgets and quality requirements.
• Act as the primary point of contact between business leadership, functional managers and project team members.
• Coordinate technical subject matter experts to define deliverables, activities, resources and milestones.
• Develop and maintain detailed project plans, schedules and risk assessments.
• Facilitate regular project meetings, ensuring stakeholder alignment and timely completion of actions.
• Assess change requests and evaluate their impact on scope, cost, schedule and risk.
• Manage engineering change deliverables through formal Change Control processes.
• Work closely with Engineering, Quality, Regulatory, Operations to ensure compliance with quality systems and regulatory requirements.
• Provide regular project status updates to senior management, covering progress, risks, quality, schedule and cost.
• Promote strong project planning, execution discipline and continuous improvement across project activities.

Skills

Project management

Cross-functional leadership

Regulatory compliance

Quality systems

Risk management

Communication

Education

Bachelor's degree in Engineering

Job description

Morgan McKinley in Dublin is seeking a Senior Project Manager to lead cross-functional projects for a portfolio of innovative medical devices. You will drive lifecycle management, regulatory compliance, and manufacturing improvements, coordinating Engineering, Quality, Regulatory, and Operations to deliver projects on time and within budget.

The ideal candidate will have 5+ years of experience in a regulated medical device or pharmaceutical setting, strong leadership, and a proven track record