Project Manager – Medical Devices
Job ID: INFSYS-EXTERNAL-241855
Company: Infosys Limited
Location: Pune, India
Employment Type: Full-time
Experience Required: 10–12 years
Job Overview
The Project Manager – Medical Devices role focuses on end-to-end project and product lifecycle management of medical device development programs. The position requires strong expertise in project execution, cross-functional coordination, regulatory alignment, and delivery of high-quality engineering and clinical outputs within scope, schedule, and budget constraints.
This role is critical in managing complex medical device development initiatives from concept through clinical evaluation and market launch.
Key Responsibilities
Project and Program Management
Manage full project lifecycle from initiation through clinical evaluation and product launch
Define project scope, objectives, timelines, and deliverables
Develop and maintain project schedules, milestones, and execution plans
Ensure projects are delivered within approved budget, scope, and timeline
Establish operational goals and prioritize tasks across multiple workstreams
Medical Device Product Lifecycle Management
Oversee development and lifecycle activities for medical device products
Manage challenges related to new therapy development and emerging technologies
Ensure alignment with regulatory, clinical, and quality requirements
Cross-Functional Leadership
Coordinate with global teams including R&D, Regulatory Affairs, Clinical, Quality, Operations, Finance, and Marketing
Act as primary liaison between project teams and senior leadership
Lead core team meetings, phase reviews, and executive reporting sessions
Stakeholder and Communication Management
Drive clear communication across internal and external stakeholders
Present project updates, risks, and performance metrics to leadership
Ensure alignment of all stakeholders on project objectives and deliverables
Budget and Resource Management
Manage project budgets and resource allocation effectively
Prepare and validate financial and resource planning estimates
Ensure optimal utilization of resources across projects
Quality and Delivery Assurance
Ensure high-quality deliverables aligned with medical device standards
Monitor project risks and implement mitigation strategies
Ensure compliance with engineering and regulatory requirements
Required Qualifications
Bachelor of Engineering (BE) / Bachelor of Technology (B.Tech – Honors)
Required Experience
10 to 12 years of experience in project management
Strong background in medical devices or healthcare engineering projects
Certifications Required
PMP (Project Management Professional) Certification mandatory
Key Skills Required
Project Management in Medical Devices
Product Lifecycle Management (PLM)
Cross-functional Team Leadership
Budget and Resource Management
Risk and Stakeholder Management
Regulatory and Quality Compliance Awareness
Preferred Skills
Experience in global medical device development programs
Strong understanding of clinical and regulatory workflows
Excellent communication and leadership capabilities
Experience working in matrix organizational structures
Knowledge of PMP methodologies and frameworks
Role Highlights
Lead high-impact global medical device programs
Work with cross-functional engineering, clinical, and regulatory teams
Drive innovation in healthcare technology and device development
Opportunity to manage complex, multi-country product development lifecycles
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