On Site Project Manager Manufacturing Change Implementation
Location: Limerick, Ireland
Contract Type: Full Time
12 Month Fixed Term Contract
Start Date ASAP
About the Client: Our client is a global leader in medical technology, delivering innovative solutions that help improve patient outcomes and quality of life worldwide. Operating within a highly regulated environment, the organization is known for its strong culture of quality, compliance, and continuous improvement. The Limerick site is a key manufacturing facility supporting global production and supply.
Project Scope
* Lead the implementation of a minor raw material change within an existing manufacturing process
* Support preparation activities ahead of a planned implementation start date
* Ensure project documentation, compliance deliverables, and closure activities are completed through to end of project timeline
* Support final project wrap up and documentation completion through December 2026
Project Leadership and Execution
* Provide end to end project management for a regulated manufacturing change project
* Develop and manage detailed project plans, timelines, and milestones
* Lead cross functional project teams and chair weekly project meetings, with additional reviews as required
* Coordinate closely with global project counterparts to ensure alignment and consistency
Stakeholder and Communication Management
* Act as the primary on site point of contact for the project
* Communicate effectively across Quality, Engineering, Manufacturing, and Global teams
* Escalate risks, issues, and concerns promptly to ensure project timelines and compliance are not impacted
* Participate in global meetings with international stakeholders, primarily in the afternoon due to time zone alignment
Quality and Compliance
* Ensure all activities comply with internal quality systems and regulatory requirements
* Support change requests, bill of materials updates, and change implementation activities
* Maintain accurate project documentation throughout the project lifecycle
* Ensure strong focus on project closure and final documentation readiness
Organizational Context
* This role reports into a global Digital Product Information Compliance function
* The position works alongside existing project managers in both Ireland and the United States
* The role has been created to provide additional on site project management capacity at the Limerick facility
Required Experience and Skills
Must Have
* Minimum 5 years of Project Management experience within a heavily regulated industry, preferably medical devices
* Proven experience in a manufacturing environment
* Strong understanding of quality systems and compliance requirements
* Hands on experience with change requests, change implementations, and backend manufacturing processes
* Excellent time management skills with the ability to manage multiple priorities
* Strong ownership mindset with the ability to manage projects from initiation through closure
* Excellent cross functional communication and stakeholder management skills
Nice to Have
* No additional requirements specified
Working Model
* 100 percent on site role based in Limerick, Ireland
* Global collaboration with international teams
Recruitment Process
* One virtual meet and greet interview, approximately 30 to 60 minutes
Seniority level
* Mid‑Senior level
Employment type
* Contract
Job function
* Analyst and Project Management
Industries
* Medical Equipment Manufacturing
* Biotechnology Research
* Pharmaceutical Manufacturing
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