Find a jobRecruiters

Program Manager - Medical Devices

Exclusive opportunity

Onsite

Program Manager - Medical Devices

Cyient

Program Manager - Medical Devices

Skills

Compliance

3 months ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

Important information


Contract type:

Permanent

Location:

Bengaluru, Karnataka, India

Work mode:

Onsite

Published on:

8 August 2026

What they need


Job Role: Program Manager (8–12 Years Experience)

Position Summary

We are seeking an experienced Program Manager to lead system-level documentation, architecture, and compliance activities for medical device projects. The role focuses on program high-quality while meeting business goals, Leading DHF remediation, and collaborating with cybersecurity, SAP, and software development teams to ensure successful and compliant project execution.

Key Responsibilities

  • Program Execution: Drive new product development (NPD) programs, managing the end-to-end process from design to manufacturing and launch.
  • Cross-Functional Leadership: Lead cross-functional teams comprising Engineering, Regulatory Affairs, Quality, Clinical, Marketing, and Operations.
  • Lifecycle Management: Ensure design controls are applied throughout the lifecycle, maintaining the Design History File (DHF) and ensuring compliance with QMS.
  • Risk & Issue Management: Actively identify roadblocks, assess risks, and develop mitigation strategies, ensuring project stability.
  • Phase Gate Management: Lead the team to prepare for Phase Gate reviews, facilitating Go/No-Go decisions by executive leadership.
  • Budget & Schedule Management: Develop comprehensive project plans, schedules, and budgets, tracking deliverables using [MS Project or similar software].
  • Stakeholder Communication: Provide regular updates to executive leadership regarding program status, risks, and budgetary impacts.
  • Supplier Management: Coordinate prototype development and manage external suppliers/vendors, conducting Design for Manufacturability (DFM) reviews.

Preferred Qualifications

  • Education: Bachelor’s degree in Engineering (Mechanical, Biomedical, Electrical), Life Sciences, or a related field.
  • Experience: 7+ years of experience in project/program management, with at least 3-5 years within the medical device industry.
  • Regulatory Knowledge: Deep understanding of FDA 21 CFR Part 820 (QSR), ISO 13485, and EU MDR.
  • Technical Familiarity: Experience in product development lifecycles, preferably with software, hardware, or mechatronics.
  • Certifications: PMP (Project Management Professional) or similar certification preferred.
  • Software Skills: Proficiency with PM tools (e.g., MS Project, SmartSheet) and PLM systems

Other offers great for you!

These companies are also looking for great profiles

Key4Nova

Account Manager - Medical Devices

Permanent contract

Brussels, Belgium

Hybrid

Skills

Account managementProspectingMedical devicesHospital salesProduct demonstrationsClinical training

6 months ago

Quick apply

iSupplier

Responsable de Programme IT Finance

Freelance

Paris, France

Hybrid

Skills

FinanceIT

5 months ago

Quick apply

SARIEL

Program Manager Android

Freelance

26000 Valence, France

Hybrid

Skills

AndroidAndroid POSAndroid AOSPAndroid EmulatorCuttlefish

2 days ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools