Project Manager - Class III Medical Devices
Posted 8 hours 6 minutes ago by Archer Recruitment
Lead the development of life-changing medical technology from concept to commercialisation.
Join a global medical device leader at the forefront of Class III product development, where you'll take ownership of a flagship stent graft programme that will shape the future of patient care. This is a rare opportunity to lead a complex, multi year R&D programme with significant visibility across the business, working alongside world class engineering, quality, regulatory and manufacturing teams.
If you thrive in technically challenging environments, enjoy leading cross functional teams, and want to make a tangible impact on products that improve lives, this role offers both scale and long term career growth.
As Project Manager, you'll lead a major Class III medical device development programme from early stage design through to commercialisation. You'll provide direction to a multidisciplinary R&D team while coordinating a broader network of stakeholders to ensure key milestones are delivered on time and to the highest quality standards.
Working in a highly regulated environment, you'll balance technical, commercial and regulatory priorities while proactively managing risk and keeping senior leadership informed throughout the development lifecycle.
What You'll Be Doing- Own a flagship Class III medical device programme from concept through to commercialisation.
- Lead a multidisciplinary R&D team while driving delivery across engineering, quality, regulatory and manufacturing.
- Take ownership of a complex, high profile programme with genuine autonomy and visibility.
- Shape the development of innovative products that will improve patient outcomes worldwide.
- Drive key project milestones, manage risk and keep critical development activities on track.
- Work with senior leaders to influence programme direction and strategic decision making.
- Join a global organisation with significant investment in R&D and long term product innovation.
- Proven experience leading complex product development programmes within the medical device industry.
- Strong understanding of the full product development lifecycle, ideally from concept through to commercial launch.
- Experience working with Class III medical devices or similarly regulated products.
- Strong knowledge of FDA, MDR and ISO13485 regulated environments.
- Demonstrated success leading multidisciplinary engineering teams and influencing cross functional stakeholders.
- Excellent project planning, organisational and stakeholder management skills.
- Engineering qualification (Mechanical, Biomedical or similar) preferred.
- PMP or equivalent project management certification is advantageous.
- Salary: Up to €95,000
- Bonus: Performance related bonus
- Working Model: Hybrid - 1 day per week onsite
- Pension, Healthcare + Additional Benefits