Direct message the job poster from Cure Talent
Connecting Talent with Medical Technology to help achieve better patient outcomes!
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:
1. Lead NPD projects from concept through to product launch, managing design controls, validation, and transfer.
2. Develop and track project timelines, identifying and mitigating risks to meet key milestones.
3. Facilitate cross-functional collaboration between design, supply chain, quality, and regulatory teams.
4. Ensure compliance with ISO 13485, 21 CFR 820, and risk management regulations.
5. Implement process improvements to enhance efficiency in project execution.
Role Requirements:
1. Proven experience in project management within the orthopaedic or medical device industry.
2. Strong understanding of ISO 13485, 21 CFR 820, and design control processes.
3. Ability to manage multiple projects, ensuring alignment with commercial and regulatory goals.
4. Excellent communication and stakeholder management skills.
5. 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!
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Project Management
Industries
Medical Equipment Manufacturing
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