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Project Manager - Medical Devices

Infosys
Infosys
10-12 years
Not Disclosed
Pune, India
10 April 24, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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

Infosys Limited is hiring a Project Manager – Medical Devices to lead end-to-end medical device product development and lifecycle management programs. The role involves managing complex engineering projects in the healthcare and medical technology domain, ensuring delivery excellence across scope, schedule, budget, and quality parameters.

This position requires strong leadership in cross-functional global teams, deep understanding of medical device development processes, and expertise in program execution within regulated environments.


Key Responsibilities

Project & Program Management

  • Lead full lifecycle management of medical device projects from initiation to clinical evaluation and product launch

  • Define project scope, objectives, timelines, and execution strategies

  • Develop and manage project schedules, milestones, and delivery roadmaps

  • Ensure adherence to budget, scope, and quality standards

  • Prioritize tasks across multiple workstreams and project owners

Medical Device Product Lifecycle Management

  • Manage development and execution of medical device products across lifecycle stages

  • Address challenges in new therapy development and emerging medical technologies

  • Ensure compliance with engineering, clinical, and regulatory requirements

Cross-Functional Collaboration

  • Collaborate with global teams including R&D, Regulatory Affairs, Clinical, Quality, Operations, Finance, and Marketing

  • Act as liaison between project teams and senior leadership

  • Drive alignment across all stakeholders for project execution

Communication & Governance

  • Lead project core team meetings and program governance reviews

  • Present progress updates, risks, and performance reports to leadership

  • Ensure clear communication across all functional teams

Budget & Resource Management

  • Manage project budgets, forecasting, and resource allocation

  • Develop and validate cost and resource estimates

  • Ensure optimal utilization of project resources

Quality & Delivery Assurance

  • Ensure high-quality delivery of medical device engineering outputs

  • Monitor project risks and implement mitigation strategies

  • Maintain compliance with internal and external quality standards


Required Qualifications

  • Bachelor of Engineering (BE) or Bachelor of Technology (B.Tech – Honors)


Required Experience

  • 10 to 12 years of experience in project/program management

  • Experience in medical devices or healthcare engineering projects preferred


Certifications Required

  • PMP (Project Management Professional) Certification mandatory


Key Skills Required

  • Medical Device Project Management

  • Product Lifecycle Management (PLM)

  • Cross-functional Program Leadership

  • Budget & Resource Management

  • Stakeholder & Risk Management

  • Healthcare Engineering Project Execution


Preferred Skills

  • Experience in global medical device development programs

  • Strong understanding of regulatory and clinical environments

  • Excellent communication and leadership skills

  • Experience working in matrix organizations

  • Knowledge of PMP methodologies and frameworks