Job Description

About Pollogen & Lumenis

Skincare technology expert Pollogen is a dynamic subsidiary of Lumenis, a global pioneer in energy-based technology for the aesthetics and vision domains with sales in nearly 100 countries, a large and growing installed-base, and strong presence in the US, Europe, and Asia. Pollogen offers a fresh approach to innovation, specializing in professional-grade and home-use devices that provide real results. Combined with Lumenis’ six decades of market leadership, 330+ patents, 500+ clinical publications, Pollogen and Lumenis offer the perfect balance of scientific artistry and creative excellence.

Basic Job Purpose

The Project Manager is accountable for end-to-end delivery of multidisciplinary medical device development projects, ensuring alignment between business needs, technical execution, regulatory compliance, and product lifecycle objectives.

Key Responsibilities

• Full ownership of product development projects from initiation through market release and lifecycle management
• Planning and execution of project scope, budget, resources, milestones, and schedules
• Close collaboration with Product, Business Development, and Marketing to translate market and customer needs into technical deliverables
• Leadership of multidisciplinary teams, including R&D, software, regulatory, clinical, operations, and external subcontractors
• Definition and control of system-level requirements, including hardware, software, and integration aspects
• Continuous monitoring of execution, risks, dependencies, and mitigation plans, with proactive decision-making
• Enforcement of medical device development processes, quality systems, and regulatory standards across all disciplines
• Ownership of development documentation, including DHF, DMR, and software lifecycle documentation
• Accountability for verification and validation activities at system, hardware, and software levels
• Leadership of transition to manufacturing, including test strategies, production readiness, and change control
• Support of regulatory submissions, safety testing, root cause analysis, and implementation of corrective actions

Requirements

Required Qualifications

• Bachelor’s degree in Electrical Engineering, Mechanical Engineering, or equivalent engineering discipline (mandatory)
• 3-5 years of proven experience managing multidisciplinary medical device development projects (mandatory)
• Solid knowledge of medical device development processes, including design controls, V&V, documentation, and regulatory compliance
• Strong system-level engineering mindset with ability to manage complex technical trade-offs
• Practical, working understanding of software development lifecycle processes, including requirements management, architecture, implementation, testing, integration, configuration management, and change control
• Experience working with software development tools and environments, including JIRA and Linux-based systems
• High professional credibility, accountability, and data-driven decision-making capability
• Excellent communication skills with experience working directly with senior leadership and multiple stakeholders

Advantage

• Familiarity with IEC 62304 and regulated software development for medical devices
• Experience with aesthetic or energy-based medical systems
• Proven involvement in full product lifecycle and roadmap execution