Senior R&D and Test Engineer MedTech
Il y a 3 jours
Greater Marseille Metropolitan Area, PAC, France
BYPASS SOLUTIONS SAS
Temps plein
Gratuit avec email ou Google
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
Gratuit avec email ou Google
En continuant, vous acceptez nos Conditions d’utilisation & Politique de confidentialité.
Bypass Solutions, a MedTech startup based in Marseille, France developping innovative vascular peripheral implants, is growing and is opening a new position in its R&D team.
You are willing to participate to the development of first-of-its-kind vascular technologies to improve patient's life? let's apply for this Senior R&D and Test Engineer position.
Responsabilities
- You will work in the field of interventional vascular devices, including among others catheters and complex implant delivery systems.
- As a technical lead, you will spearhead the design and prototyping of innovative medical devices and clinical procedures (CAD, 3D printing, prototyping, part inspection, risk management, inventory management, and proposing manufacturing improvements and tooling that meet product-related regulatory requirements) to achieve proof of concept and, subsequently design freeze.
- You apply state-of-the-art knowledge and techniques in plastics and metallurgy for the design of complex devices, covering materials, manufacturing technologies, assemblies, and design-for-manufacturing principles.
- You develop specific test methods, using test benches or other models, to verify the performance and safety of the prototypes, products and clinical implantation procedure.
- You participate in developing product V&V plans and conducting tests (in-house or outsourced) for the qualification, control, verification and validation of products and processes. Qualifications
- Mechanical or biomedical engineer
- At least 8 years of experience in the Medtech industry
- At least 3 years of experience on interventional cardiovascular devices (catheters, delivery systems, transcatheter systems)
- Proven capacities to design, develop and test complex transcatheter systems
- CAD software: SolidWorks
- Knowledge and competencies in Design Control and associated regulatory requirements (MDR, QMSR, ISO13485, ISO25539-1) and Risk Management (ISO14971)
- Fluent in spoken and written English and French
- Strong writing skills, particularly within a highly regulated environment
- High organizational, hands-on and attention to detail skills
- Autonomy, team spirit, agility, resilience and leadership are essential qualities for success in this role and for career progression within the company
- You will work in the field of interventional vascular devices, including among others catheters and complex implant delivery systems.
- As a technical lead, you will spearhead the design and prototyping of innovative medical devices and clinical procedures (CAD, 3D printing, prototyping, part inspection, risk management, inventory management, and proposing manufacturing improvements and tooling that meet product-related regulatory requirements) to achieve proof of concept and, subsequently design freeze.
- You apply state-of-the-art knowledge and techniques in plastics and metallurgy for the design of complex devices, covering materials, manufacturing technologies, assemblies, and design-for-manufacturing principles.
- You develop specific test methods, using test benches or other models, to verify the performance and safety of the prototypes, products and clinical implantation procedure.
- You participate in developing product V&V plans and conducting tests (in-house or outsourced) for the qualification, control, verification and validation of products and processes. Qualifications
- Mechanical or biomedical engineer
- At least 8 years of experience in the Medtech industry
- At least 3 years of experience on interventional cardiovascular devices (catheters, delivery systems, transcatheter systems)
- Proven capacities to design, develop and test complex transcatheter systems
- CAD software: SolidWorks
- Knowledge and competencies in Design Control and associated regulatory requirements (MDR, QMSR, ISO13485, ISO25539-1) and Risk Management (ISO14971)
- Fluent in spoken and written English and French
- Strong writing skills, particularly within a highly regulated environment
- High organizational, hands-on and attention to detail skills
- Autonomy, team spirit, agility, resilience and leadership are essential qualities for success in this role and for career progression within the company