Project Manager 1 day ago Syrma Johari MedTech Pune 10–15 years

Corporate Social; Pune District; On-site; INR 3,000,000 - 5,400,000; Full time

Job summary

Syrma Johari MedTech in Pune is seeking a Project Manager to lead complex medical device development programs. This role combines technical expertise with strong project management to drive execution across hardware, firmware, and mechanical teams while ensuring regulatory compliance.

You will define timelines, milestones and deliverables, mentor engineering teams, and coordinate with manufacturers, suppliers and design partners to ensure on-time, quality delivery in regulated environments.

Qualifications

• Bachelor’s or Master’s degree in Engineering (Mechanical, Electrical, Electronics, Biomedical, or Software).
• 10–15 years of experience in medical device development or regulated environments.
• Strong understanding of hardware, firmware, and mechanical product development lifecycle.
• Proven experience in technical project management.

Responsibilities

• Lead end-to-end planning of medical device development projects.
• Define timelines, milestones, and deliverables.
• Coordinate hardware, firmware, mechanical, and systems teams.
• Identify and mitigate risks across engineering domains.
• Ensure deliverables meet quality and regulatory standards.
• Coordinate with manufacturers, suppliers, and design partners.

Skills

Project management

Regulatory compliance

Cross-functional coordination

Technical leadership

Communication

Education

Bachelor’s or Master’s in Engineering

Tools

MS Project

Jira

Job description

Job Posted: Not specified
Role: Project Manager
Company: Syrma Johari MedTech
Location: Pune
Experience: 10–15 years in medical device / regulated product development
Work Mode: On-site
Key Focus: Lead end-to-end development of complex medical devices across hardware, firmware, and mechanical systems while ensuring regulatory compliance and timely delivery.

About the Role

We are looking for a Project Manager to lead complex medical device development programs. This role combines technical expertise with strong project management capabilities to drive execution across multidisciplinary engineering teams while ensuring compliance with global regulatory standards.

Key Responsibilities

• Project Planning & Execution
• Lead end-to-end planning of medical device development projects
• Define timelines, milestones, and deliverables
• Translate technical requirements into execution plans
• Track progress and ensure on-time delivery
• Cross-Functional Technical Coordination
• Act as a bridge between hardware, firmware, mechanical, and systems teams
• Facilitate technical discussions and design decisions
• Align cross-functional teams toward project goals
• Technical Risk & Issue Management
• Identify and mitigate risks across engineering domains
• Maintain risk registers and issue logs
• Drive timely resolution of technical blockersCoordinate with manufacturers, suppliers, and design partners
• Ensure deliverables meet quality, compliance, and performance standards

Tools & Technologies

• Project Management: MS Project, Jira
• Risk Management frameworks and tools

Required Qualifications

• Bachelor’s or Master’s degree in Engineering (Mechanical, Electrical, Electronics, Biomedical, or Software)
• 10–15 years of experience in medical device development or regulated technical environments
• Strong understanding of hardware, firmware, and mechanical product development lifecycle
• Proven experience in technical project management

Preferred Skills

• Ability to mentor and lead engineering teams
• Strong problem-solving and multitasking capabilities
• Excellent communication across technical and non-technical stakeholders
• Strategic thinking, planning, and conflict resolution skills

Compensation

Not specified