Technical Project Manager

Corin Group; Grenoble; Vor Ort; EUR 63.000 - 77.000; Vollzeit

Benefits dieser Stelle

Salary up to €70,000

Professional development

Flexible hours

Remote work options

Zusammenfassung

Corin is seeking an experienced Technical Project Manager to lead cross-functional engineering execution of a new software application for our Apollo platform. You will own day‑to‑day product development, sprint delivery, and engineering readiness across software, hardware integration and verification.

Partner with Product Owner, Systems Engineering and Quality & Regulatory to ensure the product is delivered predictably, safely and in compliance with medical device development requirements.

Qualifikationen

• Bachelor’s degree in engineering, Computer Science, or related field.
• 7+ years in regulated product development environments.
• Experience developing software‑intensive medical devices.
• Strong backlog management, traceability and defect tracking experience.
• Solid software engineering design principles understanding.
• Experience coordinating cross‑functional engineering integration activities.
• Strong English communication skills, written and spoken.
• Excellent collaboration and problem‑solving in a global team.
• Self‑motivated with ownership and commitment to quality.

Aufgaben

• Lead engineering execution for a new software application from concept to commercialization.
• Drive sprint planning, prioritization, and delivery tracking across the product team.
• Manage milestones, dependencies, risks, delivery forecasts and budgets.
• Coordinate software, mechanical, systems, and verification contributors.
• Ensure integration between application development and platform capabilities.
• Partner with Systems Engineering for system‑level coherence and interfaces.
• Ensure traceability, verification, and submission readiness of engineering deliverables.
• Support risk management, design reviews, and technical investigations.
• Follow procedures to meet ISO 13485, IEC 62304 and U.S. Title 21 CFR 820.

Kenntnisse

Project management

Regulated device development

Backlog management

Cross-functional collaboration

English communication

Ausbildung

Bachelor's degree

Tools

Jira

Jobbeschreibung

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.