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.

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