Lead R&D Medical Devices Project Manager

Balazs; Bovezzo; On-site; EUR 28,000 - 40,000; Full time

Job summary

Air Liquide Medical Systems srl in Italy is seeking an experienced Project Manager to lead medium‑complexity R&D product development for medical devices. You will translate market needs into technical specifications and define product roadmaps while coordinating internal and external stakeholders.

The role emphasizes patient‑centric design, ergonomics and compliance with Medical Devices EU regulations to secure CE certification.

Qualifications

• Master degree in mechanical, biomechanical, biomedical or material engineer.
• Experience in R&D teams developing products.
• Knowledge of safety standards and ergonomic impact of a design.
• Basic knowledge of injection mould design for engineering polymers and elastomers.
• Ability to report to management and communicate effectively.
• Strong written and verbal communication skills.

Responsibilities

• Translate market insights into technical specifications and product roadmaps.
• Lead definition of patient-centric product requirements for ergonomics and clinical efficacy.
• Perform techno-economic feasibility analyses for product viability.
• Contribute to IP portfolio with patentable engineering solutions.
• Ensure compliance with safety standards and regulatory requirements.
• Coordinate with suppliers to prototype with additive manufacturing technologies.
• Analyze prototypes and test data; document results and insights.
• Develop technical documentation for Medical Devices EU regulations and CE certification.

Skills

R&D experience

Safety standards

Ergonomics design

Injection mould basics

Technical reporting

Communication skills

Education

Master degree in mechanical/biomedical/material engineering

Job description

Air Liquide Medical Systems srl in Italy is seeking an experienced Project Manager to lead medium‑complexity R&D product development for medical devices. You will translate market needs into technical specifications and define product roadmaps while coordinating internal and external stakeholders.

The role emphasizes patient‑centric design, ergonomics and compliance with Medical Devices EU regulations to secure CE certification.