Project Manager II - Medical Device

About the role

ECI provides professional consulting services for the life sciences industry, including full product life cycle consulting. The Project Manager leads and coordinates cross-functional projects throughout the product lifecycle within a regulated medical device environment. The role oversees project planning, execution, resource management, risk mitigation, and stakeholder communication to deliver projects on time, within scope, and in compliance with applicable quality and regulatory requirements.

Responsibilities

• Develop and manage the integrated project plan, schedule, budget, milestones, and resources.
• Coordinate Engineering, Manufacturing, Quality, Regulatory, Validation, Supply Chain, and other stakeholders.
• Manage equipment, process, documentation, tooling, and knowledge-transfer activities.
• Track validation, qualification, change control, risk management, and production-readiness activities.
• Identify and resolve project risks, issues, dependencies, and escalations.
• Coordinate pilot builds, validation activities, production ramp-up, and site readiness.
• Provide regular project status, financial updates, and risk reporting to leadership.
• Ensure successful handoff to the receiving manufacturing site and project closure.

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or a related field.
• 8 years of experience, with at least 6+ years of project management experience.

Datos clave

• The role leads cross-functional projects in a regulated medical device environment.
• A bachelor’s degree in Engineering, Life Sciences, or a related field is required.
• The source states 8 years of experience, with at least 6+ years of project management experience.