Technical Project Manager

Technical Project Manager

Grenoble, France

Join Corin to work within a small dynamic team that has a high impact on the quality of life of patients worldwide. We are not a startup business - we offer market-leading products that are continuously evolving for the global orthopaedic market.

Corin is looking for an experienced Technical Project Manager to lead the cross-functional engineering execution of a new application built for our Apollo surgical platform. This role owns day-to-day product development execution, sprint delivery and engineering readiness across software, hardware integration, systems engineering, and verification activities.

Working closely with Product Owner, Systems Engineering, Platform Engineering, and Quality & Regulatory, the Technical Project Manager ensures the product is delivered predictably, safely, and in compliance with medical device development requirements.

About us:

Corin is a medical device business with innovative robotically assisted platforms for joint replacement surgery. We offer a unique combination of clinically proven hip & knee solutions and world leading technologies. Our Apollo & OPS systems utilize intelligent instrumentation to give surgeons the ability to perform patient-specific procedures with high accuracy, with more consistent results and improved recovery rates.

Your role:

• Lead engineering execution for a new software application from concept through commercialization.
• Drive sprint planning, engineering prioritization, and delivery tracking across the product team.
• Manage development milestones, dependencies, technical risks, delivery forecasts and associated budget.
• Coordinate software, mechanical, systems, and verification contributors.
• Ensure effective integration between application-layer development and centralized software and hardware platform capabilities.
• Partner with Systems Engineering to ensure system-level coherence and interface integrity.
• Ensure engineering deliverables support traceability, verification, and submission readiness.
• Support risk management, design reviews, and technical investigations.
• Follow established procedures to ensure all software components, processes, and documentation meet relevant medical device regulations and standards (ISO 13485, IEC 62304 and U.S Title 21 CFR 820)

Your profile:

• Bachelor’s degree in engineering, Computer Science or a related field
• 7+ years of experience in regulated product development environments
• Experience developing software-intensive medical devices
• Strong experience with backlog management tools, traceability, work item management, and defect tracking.
• Strong understanding of software engineering design principles
• Experience coordinating cross-functional engineering integration activities
• Strong English communication skills, both written and spoken
• Excellent collaboration, problem-solving, and interpersonal skills; comfortable working in a global team
• Self-motivated with a strong sense of ownership and attention to quality

Ideally, you also bring:

• Experience with Class II or Class III medical devices.
• Experience with robotics platforms or electromechanical systems.
• Familiarity with IEC 62304, ISO 14971, IEC 60601, and cybersecurity practices.
• Experience supporting FDA submissions or design transfer activities.

What we offer:

• Salary up to €70,000 depending on experience
• Opportunities for professional development and training
• Flexible working hours and remote work options
• Collaborative and supportive work environment
• Impactful work with cutting-edge medical technology

If this appeals to you but you are in doubt about how exactly your skills match our requirements - we value personality, ambition, and an open mind. Do not hesitate to get in touch and present your personal strengths to us.