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AI-Powered Job Summary
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The candidate will be responsible for managing the following activities:
- develop detailed project plans, timelines, and budgets for R&D projects related to the relevant products and ensure successful execution;
- design and development using CAD, engineering drawings and tolerance analysis. Definition of feasibility of manufacturing and quality control inspection of the devices;
- collaborate regularly with surgeons to gather detailed clinical feedback on product designs, applying their insights to optimize product development. Direct collaboration or through marketing, reps or agents;
- collaborate with engineering, regulatory, and marketing teams to ensure project deliverables for the relevant products meet quality and regulatory requirements;
- support company presence at selected international congresses or design meetings, providing product development input and engaging with surgeons when required;
- manage communication with internal and external stakeholders for the relevant products, providing regular project updates and addressing any risks or issues;
- identify project risks for the relevant products and develop mitigation strategies to keep projects on track;
- ensure optimal use of resources for assigned projects related to the relevant products, working closely with team leads and department heads;
- maintain accurate project documentation for the relevant products and ensure compliance with regulatory requirements for medical devices;
- resolve project-related issues for the relevant products efficiently and in a timely manner, ensuring minimal impact on project deadlines;
- provide leadership and support to project teams working on the relevant products, fostering a collaborative and results-oriented environment.
Hard Skills
- Master’s or Bachelor’s degree in Engineering, Biomedical Engineering, or related field; PMP certification is a plus;
- 2+ years of experience in project management within the medical devices industry, with proven success in leading R&D projects;
- excellent knowledge of CAD systems (Solidworks), definition of tolerances and the preparation of technical drawings;
- familiar with design control documentation for Medical implants. (e.g. Risk Analysis, Verification/Validation, Design Transfer);
- fluent in English;
- strong skills in planning, execution, and resource management across multiple projects;
- solid understanding of the product development lifecycle, including working with surgeons and other stakeholders;
- experience participating in international congresses and interacting with surgeons and medical experts;
- willingness to travel for congresses and surgeon meetings.
- excellent interpersonal and communication skills to work with cross-functional teams, stakeholders, and external partners;
- strong analytical skills with the ability to identify risks and resolve project issues efficiently;
- tidy and precise person;
- pro-active and dynamic person.
- permanent contract;
- flexible working hours;
- carpooling organized by Medacta;
- incentives for mobility by public transport;
- advantageous conventions;
- growth opportunity, working in a continuously improving and expanding environment;
- annual salary review linked to performance and professional development;
- continuous training.
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