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Project Manager

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Onsite

Project Manager

Croom Medical

Project Manager

Skills

Process ImprovementComplianceRegulatory Compliance

19 days ago

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Important information


Contract type:

Permanent

Location:

Croom, Co. Limerick, Ireland

Work mode:

Onsite

Published on:

8 October 2026

What they need


Company Information and Introduction:

Croom Medical is a leading contract manufacturer of orthopaedic implants and instruments, headquartered in Croom, Co. Limerick. Operating to ISO 13485 quality management standards, we partner with global medical device companies to deliver precision-engineered products across our TALOS™ and Biofuse™ product platforms. With a growing team and expanding manufacturing capability, including our advanced ACOT facility, Croom Medical offers an exciting environment for experienced professionals to make a real impact.

Key Responsibilities and Duties:

Project Planning & Delivery

  • Lead end-to-end project management for NPI, capital investment, and process improvement initiatives
  • Develop detailed project plans, including timelines, resource requirements, risk registers, and budgets
  • Monitor and report on project progress to senior leadership, escalating issues and risks as appropriate
  • Ensure all project deliverables meet regulatory, quality, and customer requirements
  • Contribute to the development and improvement of project management frameworks and tools within the organisation

Cross-Functional Leadership

  • Facilitate project meetings, design reviews, and gate reviews in line with stage-gate processes
  • Build strong working relationships with internal stakeholders and external customers or suppliers as required

Quality & Regulatory Compliance

  • Ensure all projects are executed in accordance with ISO 13485 quality management system requirements
  • Support design history file (DHF) and device master record (DMR) development during NPI activities
  • Work with Quality and Regulatory teams to ensure compliance with applicable standards.

Key Skills and Competencies:

  • Minimum 5 years’ project management experience within the medical device manufacturing industry
  • Proven track record of successfully delivering NPI or complex engineering projects on time and within budget
  • Strong working knowledge of ISO 13485 quality management systems
  • Proficiency in project management tools and methodologies (e.g. MS Project, Smartsheet, Agile, Stage-Gate)
  • Excellent communication, presentation, and stakeholder management skills
  • Third-level qualification in Engineering, Science, Business, or a related discipline

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