Skincare technology expert Pollogen is a dynamic subsidiary of our company, 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 our companys six decades of market leadership, 330+ patents, 500+ clinical publications, Pollogen and our company 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.
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
Bachelors 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.
Required Qualifications
Bachelors 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.
This position is open to all candidates.
