Program Manager - Medical Devices

Department Icon IT / Software Development & Related
102+ Applicants
Posted: 1 month ago
7-9 years
Bengaluru / Bangalore, Karnataka
work from office

Posted: 1 month ago
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Applicants: 102+
Job Description
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Job Description

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: Bachelors 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

Skills

CybersecuritySoftware Development

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About Company

Cyient is a global engineering and technology solutions company, dedicated to helping clients achieve a competitive edge through innovation and digital transformation. With a focus on industries such as aerospace and defense, healthcare, telecommunications, rail transportation, semiconductor, geospatial, industrial, and energy, Cyient offers a range of services, including engineering design, manufacturing, digital transformation, and operations. Cyient Careers presents a world of opportunities for professionals and graduates seeking growth in a challenging yet rewarding environment. The company values diversity, inclusion, and continuous learning, providing employees with the tools and support they need to develop their skills and advance their careers. At Cyient, team members contribute to projects that make a difference, leveraging cutting-edge technologies and collaborating with experts worldwide.

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Important dates & deadlines?

Application Deadline

04 Sep 26, 05:03 PM IST

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Program Manager - Medical Devices

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