About Us:
Natec Medical is a global pioneer in the design and manufacturing of life-saving medical devices. Operating as a world-class Contract Development and Manufacturing Organization (CDMO) from the state-of-the-art AVA Technopark in Mauritius, we possess nearly three decades of industry-leading expertise.
We specialize in advanced catheter and endovascular devices, handling everything from initial prototyping to high-precision cleanroom manufacturing for healthcare partners worldwide. Because the products we build directly impact patient safety every single day, our operations thrive on rigorous engineering discipline, precision, and continuous innovation. We offer a dynamic environment where technical leaders can drive impactful projects and shape the future of medical technology.
About the Role
The Senior R&D Engineer is responsible for developing projects from concept to production. These projects may be new projects, line extensions or improvements to existing production. The role purpose is to optimize the quality and the cost of the products..
Main Accountabilities
- Manage project within set schedule, and ensure that projects entrusted are completed within set timelines
- Execute the product transfer to production for projects entrusted
- Follow-up with suppliers regarding purchasing of components, tooling, equipment and services in relation to project work
- Responsible for project planning & follow-up, from kick-off to implementation
- Determine the need for resources (manpower, machine, cost) in relation to project assigned
- Work closely with other departments for improvements and project implementations
- Assist R&D engineers to provide guidance on respective projects
Technical Studies - Design and develop new test methods as needed
- Perform yearly review of R&D documents as required
- Work on the ERP system (X3) in relation to projects assigned.
- Perform benchmarking of competitors’ products
Technical Report - Define and write protocols for product validation.
- Write project report on OQ (Operational Qualification), PQ (Process Qualification), PPQ (Product Performance Qualification) & MVP (Master Validation Protocol)
- Work with CAD (autocad/solidworks) drawings in relation to project entrusted
- Complete project documentation for Design History Files of project as required.
- Write technical report and PowerPoint presentations as required
- Perform Risk analysis and FMEA in relation to product design, manufacture and usage.
Qualifications & Experience
- Bachelor degree in Mechanical Engineering
- 7 to 10 years’ experiences in medical device manufacturing company and in research and development
- Experience in R&D and product/process improvement
- Good expertise in High pressure balloon for PTCA/PTA would be
Skills & Attributes
- Good knowledge on Autocad & Solidworks
- Have a good understanding of R&D project requirements (studies CCRF, AP, CAR)
- Good knowledge on minitab
- Good knowledge on statistics analysis
- Good knowledge on pack office
- Ability to work with rigour
- Ability to manage a simple project and deliver it on time
- Good accountability
- Good communication skills in both english or/and french, in both written and verbal
How to Apply
Interested employees are encouraged to submit their applications by 03/06/2026
Please include:
- An updated resume
Submit your application by e-mail to Dominique AZA: daza@xtruline.mu with subject ”Sr R&D Engineer” as e-mail subject or by dropping the above at the HR department.
Natec Medical is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
