R&D Project Manager relocation to Mauritius

• Master’s degree in Biomedical Engineering, Mechanical Engineering, or related fields
• At least 8 years of experience in a Senior engineering role within the medical devices industry, particularly in catheter manufacturing 
• Proven track record of successfully managing and delivering high-impact projects from concept to market 
• Comprehensive knowledge of ISO 13485, FDA, and MDR regulations 
• Demonstrated experience in leading cross-functional teams and mentoring technical staff

The R&D Project Manager will serve as the management &technical authority in the development of new medical devices, and requires interested candidates to relocate to Mauritius for this position. Driving innovation, overseeing strategic initiatives, and ensuring successful product development. This role requires exceptional leadership, technical expertise, and strategic vision to deliver high-quality, compliant products within tight deadlines and budgets.

,[Strategic Product Development - Lead the development of advanced catheters and related medical devices from concept to commercialization. Define and oversee the product development strategy, aligning with organizational objectives and market demands. Act as the chief technical expert for product innovations, ensuring optimal design and functionality. , Technical Innovation and Expertise - Drive innovation by exploring and integrating cutting-edge technologies and methodologies into product designs. Conduct advanced material selection, product testing, and validation activities to meet client and regulatory requirements. Lead design reviews, failure mode analysis, and risk assessments for ongoing and new projects. , Cross-Functional Collaboration - Act as a liaison between R&D, Quality, Regulatory, Manufacturing, and Commercial teams to ensure cohesive project execution. Represent the R&D department in high-level meetings, contributing to organizational strategy and decision-making. Collaborate with clients and external stakeholders to translate market needs into innovative product solutions. , Compliance and Quality Assurance - Ensure that all development activities comply with ISO 13485, FDA, MDR, and other relevant regulatory standards. Partner with quality and regulatory teams to secure necessary certifications and approvals for new products. Implement robust documentation practices and technical files compliance, to meet regulatory and quality requirements. , Project and Resource Management - Lead multiple complex R&D projects simultaneously, ensuring timeline, budget, documentation practice and product performance and spec are met and resource optimization. Manage projects budgets, ensuring alignment with organizational financial targets. Identify and mitigate risks proactively, ensuring successful project outcomes.] Requirements: Ability to relocate, Degree, AutoCAD, SolidWorks, Project management, Medical Equipment , R&D Engineering, R&D Medical Equipment Experience, MS Project, Minitab, ERP systems, Analytical skills, leadership