Project Manager
- Galway
- Permanent
- Full-time
We are now hiring for a Project Manager for a leading medical device manufacturing company based in Galway, committed to delivering innovative and life-enhancing solutions in healthcare. We are currently seeking an experienced Project Manager to join our dynamic team and play a pivotal role in the successful execution of cross-functional projects.About the role:
As a Project Manager, you will lead cross-functional teams in the planning, execution, and delivery of complex and CAPEX projects within our manufacturing operations. You will be responsible for managing the full project lifecycle, from initial scoping through to execution and close-out, with a focus on equipment introduction, process improvements, and supplier/vendor coordination.Responsibilities:
- Project Leadership: Lead the planning, coordination, and execution of manufacturing and engineering projects, ensuring alignment with strategic goals.
- Scoping & Planning: Define project scope, objectives, deliverables, and timelines in collaboration with stakeholders.
- Cross-functional Collaboration: Work closely with internal departments (R&D, Quality, Manufacturing, Regulatory, and Supply Chain) to drive project success.
- Equipment Introduction: Manage the introduction and qualification of new manufacturing equipment and technologies, including FAT, SAT, IQ/OQ/PQ processes.
- Stakeholder Management: Interface with internal and external stakeholders to ensure alignment, clear communication, and timely updates on project progress.
- Supplier & Vendor Management: Source, evaluate, and manage relationships with suppliers and vendors to ensure timely delivery of project-related equipment and materials.
- Risk Management: Identify project risks and develop mitigation plans to ensure on-time and within-budget delivery.
- Reporting: Provide regular project updates, KPIs, and dashboards to senior management.
- Compliance: Ensure all activities adhere to company policies, industry standards, and applicable regulatory requirements (e.g., ISO 13485, FDA, MDR)
- Bachelor's degree in Engineering, Science, or a related technical field.
- Minimum of 5 years of experience in project management within a regulated manufacturing environment, preferably medical devices.
- Proven experience managing cross-functional projects including equipment introduction and supplier/vendor coordination.
- Strong understanding of GMP, ISO 13485, and FDA requirements.
- Project Management certification (e.g., PMP, PRINCE2) is an advantage.
- Experience with project management tools (e.g., MS Project, Smartsheet, JIRA).
- Excellent leadership, communication, and problem-solving skills.
- Ability to manage multiple priorities and work under pressure in a fast-paced environment.
Gary Keane
– 086-1030418INDCRG