Medical Device Project Coordinator — Onsite in Sligo

PE Global; Sligo; On-site; EUR 42,000 - 66,000; Full time

Job summary

PE Global are recruiting for a Project Coordinator for a client in Sligo. This is a 12-month, fully onsite contract role. You will lead cross-functional teams to deliver new Medical Device products, manage plans, budgets and schedules, and ensure quality through established processes.

The role requires a Bachelor’s degree with 3–5 years of related experience (or a Master’s with 1–3 years). You will operate in a quality system environment and engage with internal and external stakeholders to

Qualifications

• Bachelor's degree or higher in a relevant field.
• Working knowledge within a quality system environment.
• Recognises the importance of compliance with governmental regulations.

Responsibilities

• Manages development and implementation processes for Medical Device products with cross-functional teams.
• Estimates project effort, prepares plans, schedules and budgets using MS Project.
• Directs project execution by assigning tasks and tracking schedules.
• Ensures project quality by using standard development methodologies and coordinating with SQA.
• Communicates project status through standard reports and status meetings.
• Resolves issues by coordinating with team members and customers.
• Shares project management knowledge with internal groups and supports process improvement.
• Raises Change Plans, drives impact assessment and obtains change approval up to the board.
• Prepares, edits and files reports and technical documents; maintains filing systems.
• Maintains orderly filing and records; retrieves materials on request.

Education

Bachelor's degree + 3 to 5 years of related work experience; or Master's degree + 1 to 3 years

Job description

PE Global are recruiting for a Project Coordinator for a client in Sligo. This is a 12-month, fully onsite contract role. You will lead cross-functional teams to deliver new Medical Device products, manage plans, budgets and schedules, and ensure quality through established processes.

The role requires a Bachelor’s degree with 3–5 years of related experience (or a Master’s with 1–3 years). You will operate in a quality system environment and engage with internal and external stakeholders to