Cure Talent is thrilled to partner with a leading medical device manufacturer in their search for a Project Manager. This is a fantastic opportunity to play a key role in New Product Development, ensuring seamless project execution from design through to product launch within a regulated medical environment.
As a Project Manager, you will drive cross-functional collaboration, managing timelines, risk mitigation, and stakeholder alignment to successfully deliver projects under ISO 13485 and 21 CFR 820 regulatory frameworks.
Key Responsibilities:
* Lead NPD projects from concept through to product launch, managing design controls, validation, and transfer.
* Develop and track project timelines, identifying and mitigating risks to meet key milestones.
* Facilitate cross-functional collaboration between design, supply chain, quality, and regulatory teams.
* Ensure compliance with ISO 13485, 21 CFR 820, and risk management regulations.
* Implement process improvements to enhance efficiency in project execution.
Role Requirements:
* Proven experience in project management within the orthopaedic or medical device industry.
* Strong understanding of ISO 13485, 21 CFR 820, and design control processes.
* Ability to manage multiple projects, ensuring alignment with commercial and regulatory goals.
* Excellent communication and stakeholder management skills.
* Project management certification (e.g., PMP, PRINCE2) is desirable.
If you're looking for an exciting role in medical device development, where you can lead impactful projects and drive innovation, apply today