Project Management Officer

<p><strong>Robeauté</strong>&nbsp;is redefining the future of neurosurgery with self-propelled microrobots designed to navigate the human brain with unprecedented precision. Our technology enables access to deep brain regions previously unreachable without invasive surgery. These microrobots can collect biopsies, deliver cancer drugs, and implant electrodes for neurological treatments.</p><p>Since our founding in 2017, we’ve filed over 50 patents and successfully tested our technology in living animals. Human clinical trials are targeted for 2026/2027. Backed by €27M in Series A funding from Plural, Cherry Ventures, Kindred Ventures, and Brainlab, we are entering a new phase of growth.</p><p>As part of this expansion, we are looking for a&nbsp;senior&nbsp;<strong>Project Management Officer</strong>&nbsp;to lead the organisation and execution of complex projects at the core of the development of a revolutionary neurosurgical microrobotics platform.</p><p>The PMO holds strong functional authority over projects, with end-to-end accountability for delivery (timeline, quality, compliance), without direct line management responsibility over team members.</p><p>This role requires a high level of ownership, self-drive and legitimacy, built on experience, regulatory understanding, and the ability to influence multidisciplinary teams in a highly regulated medical device environment, particularly under Design Control constraints.</p><p></p><h3>What You'll Do</h3><ol><li>Supervise the design and layout of full&nbsp;project&nbsp;plans with team roadmaps/inputs, based on&nbsp;measurable&nbsp;goals,&nbsp;anticipating&nbsp;time and&nbsp;resources&nbsp;always&nbsp;with&nbsp;the highest quality level in mind</li><li>Consolidate&nbsp;inputs and contribution from all stakeholders in the&nbsp;project: Research, Development, V&amp;V,&nbsp;Product,&nbsp;Manufacturing,&nbsp;Quality, Regulatory,&nbsp;PreClinical&nbsp;&amp;&nbsp;Clinical, as well as Partners (medical, research, Industrial) and Critical Suppliers</li><li>When&nbsp;necessary,&nbsp;find out how to best breakdown large tasks&nbsp;into&nbsp;achievable, well-defined work streams</li><li>Keep time and energy to create and organize new projects</li><li>Update&nbsp;the roadmap, as in:</li><ul><li>Manage priorities based on the evolution risks (technical risks, supply chain risks, human risks, medical risks…)</li><li>Clarify second level&nbsp;dependencies&nbsp;of evolving roadmap priorities with all the parties&nbsp;impacted</li><li>Anticipate issues as&nbsp;the projects&nbsp;progress,&nbsp;identifying&nbsp;risks, deviations, and bottlenecks</li><li>Plan and&nbsp;anticipate&nbsp;the evolution of teams all&nbsp;along the&nbsp;project&nbsp;life cycle</li><li>Exercise judgment in deciding when a project&nbsp;is done and ensuring a clean, intentional close</li></ul><li>Exercise authority and&nbsp;Leadership, as in:</li><ul><li>With functional authority,&nbsp;lead&nbsp;by&nbsp;motivating teams, team&nbsp;leaders&nbsp;and individual contributors</li><li>Driving&nbsp;execution through influence rather than hierarchy</li><li>Exercise clear functional authority over project decisions (planning, sequencing, prioritization, escalation)</li><li>Foster alignment and commitment across multidisciplinary teams</li><li>Challenge teams constructively when needed, with authority, clarity, and respect</li></ul><li>Report&nbsp;on project&nbsp;advancement, as in:</li><ul><li>Serve as the central communication hub for project information</li><li>Manage both the executive overview of the project progress and the detailed version with high granularity</li><li>Present&nbsp;project&nbsp;advancement concisely, lively and with clarity to team leaders, to the whole team, to the various groups as well as to management</li><li>Prepare and lead project reviews, milestone gates, and risk reviews</li></ul><li>Maintain&nbsp;MedTech Compliance &amp; Design Control, as in:</li><ul><li>Ensure projects are executed in full compliance with medical device development processes, including:</li><ul><li>Design Control (ISO 13485 / 21 CFR 820)</li><li>Requirements management, risk management, verification &amp; validation</li></ul><li>Guarantee that all project milestones are properly documented, traceable, and&nbsp;audit-ready</li><li>Work closely with Quality and Regulatory teams to ensure alignment and compliance.</li></ul></ol> <p></p><ul><li>10+ years of experience&nbsp;in managing complex development&nbsp;projects, preferably in&nbsp;MedTech or medical devices</li><li>Proven experience working under&nbsp;Design Control&nbsp;and regulated development frameworks</li><li>Strong&nbsp;track record&nbsp;coordinating cross-functional teams (R&amp;D, Clinical, Quality, Regulatory, Manufacturing)</li><li>Strong technical and scientific background, with formal training in engineering or applied sciences (e.g., physics, mechanics, biomedical engineering)</li><li>Extensive experience in deep-tech medical device development, with a proven&nbsp;track record&nbsp;in highly innovative, complex products</li><li>End-to-end project&nbsp;experience, ideally having taken at least one medical device project from early development phases (concept, feasibility, early design), structuring the organisation from the early research focused phase to a highly structured design control phase.</li><li>Solid understanding of regulated MedTech environments, including design control, risk management, verification and validation, and interactions between technical, clinical, and regulatory constraints</li><li>Preference for candidates with experience in surgical robotics or brain-related medical devices, where technical, clinical, and safety considerations are tightly coupled</li><li>Combination of senior experience and strong personal drive, bringing both maturity in decision-making and&nbsp;a high level&nbsp;of enthusiasm, curiosity, and hands-on engagement (regardless of age)</li><li>Excellent people and communication skills, with the ability to coach, motivate, and influence teams and individual contributors across disciplines</li><li>Strong project management skillset, complemented by mastery of&nbsp;digital project management tools, including modern PM platforms and emerging&nbsp;AI-enabled tools&nbsp;to support planning, tracking, and decision-making</li><li>Professional level of both English and good level of French is required</li></ul><p></p><h3>Soft skills</h3><ul><li>Accountable and self-driven leader with great autonomy</li><li>Calm, structured leadership style</li><li>Results-driven and solution-oriented mindset</li><li>Ability to make decisions and say no when&nbsp;required</li><li>Comfortable operating in high-stakes, fast-moving environments&nbsp;requiring a good sense of&nbsp;humour</li></ul> <p><strong>A Mission That Matters:</strong>&nbsp;Join a team developing life-changing technology. Our microrobots have the potential to help over&nbsp;<strong>1 billion patients</strong>&nbsp;with neurological conditions.</p><p><strong>World-First Innovation:</strong>&nbsp;Work on pioneering microrobots that navigate the brain for diagnosis and treatment—minimally invasive, maximum impact.</p><p><strong>An Exceptional Team:</strong>&nbsp;Collaborate with leading engineers, clinicians, and researchers pushing the boundaries of medical robotics and neurotechnology.</p><p><strong>Real Ownership:</strong>&nbsp;Join a well-funded deeptech startup backed by top investors. Shape your domain, drive strategic decisions, and grow with us.</p><p><strong>Benefits:</strong></p><p><strong>Health Insurance</strong>&nbsp;— We happily cover 60% of the cost.</p><p><strong>Meal Vouchers</strong>&nbsp;— €9.25 per day, We happily cover 60% of the cost.</p><p><strong>Transportation Reimbursement</strong>&nbsp;— 50% of your commuting costs covered.</p>