Senior Project Engineer - Medical Devices (Regulatory/Change)

Embecta Corp.; Dún Laoghaire; Híbrido; EUR 65.000 - 95.000; Jornada completa

Descripción de la vacante

embecta is a global medical device company focused on insulin delivery and diabetes care. The Senior Project Engineer will lead cross-functional programs that ensure regulatory compliance and support product changes across our injection portfolio.

Hybrid, full-time role based in Ireland, with opportunities to drive continuity and growth in a regulated manufacturing environment. The role partners with leadership and SMEs to plan, execute, and monitor projects, balancing cost, schedule, and

Formación

• Bachelor’s degree in engineering or a related technology field.
• At least 5 years’ experience in regulated medical devices or pharma.
• Experience working with cross-functional teams and project leadership.

Responsabilidades

• Lead cross-functional projects impacting compliance, form/fit/function, cost reduction, and line extensions.
• Act as primary liaison between business leadership, management, and project team members.
• Coordinate resource allocation and discretionary spending to meet schedules.
• Plan and facilitate regular project meetings with stakeholders.
• Collaborate with SMEs to define, plan, and execute tasks.
• Assess change requests for risks, costs, and schedule impact.
• Manage and, where appropriate, execute engineering change deliverables through Change Control.
• Provide regular status updates to senior management on quality, schedule, cost.
• Promote disciplined project planning and execution across activities.

Conocimientos

Product lifecycle management

Regulatory compliance

Quality systems

Cross-functional teamwork

Communication skills

Attention to detail

Educación

Bachelor's degree in engineering or technology-related discipline

Descripción del empleo

embecta is a global medical device company focused on insulin delivery and diabetes care. The Senior Project Engineer will lead cross-functional programs that ensure regulatory compliance and support product changes across our injection portfolio.

Hybrid, full-time role based in Ireland, with opportunities to drive continuity and growth in a regulated manufacturing environment. The role partners with leadership and SMEs to plan, execute, and monitor projects, balancing cost, schedule, and