Cyient
Website:
cyient.com
Company:
https://www.linkedin.com/company/cyient
Seniority: Not Applicable
Industries: IT Services and IT Consulting
Job details:
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
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