Senior Manager – Device Software Development

Posted:
6/28/2026, 8:11:16 PM

Location(s):
Bengaluru, Karnataka, India ⋅ Karnataka, India

Experience Level(s):
Senior

Field(s):
Software Engineering

ZEISS in India

ZEISS in India is headquartered in Bengaluru and present in the fields of Industrial Quality Solutions, Research Microscopy Solutions, Medical Technology, Vision Care and Sports & Cine Optics.

ZEISS India has 3 production facilities, R&D center, Global IT services and about 40 Sales & Service offices in almost all Tier I and Tier II cities in India. With 2200+ employees and continued investments over 25 years in India, ZEISS’ success story in India is continuing at a rapid pace. 

Further information at ZEISS India.

The Senior Manager – Device Software Development (Refraction and Centration) leads the end-to-end software development of ZEISS refraction and centration devices, ensuring delivery of high-quality, reliable, and compliant solutions. The role combines strong technical expertise in medical device software with people leadership, driving architecture, development, testing, release, and lifecycle management. It collaborates with cross-functional teams to translate product and clinical needs into scalable solutions, supporting innovation, usability, and long-term product reliability within a regulated global environment.

  • Device Software Development Leadership

• Lead full lifecycle development and maintenance of device software, including requirements, architecture, implementation, integration, testing, release, and support.
• Define and evolve scalable, reliable, and maintainable software architectures.
• Ensure seamless integration between software, hardware, sensors, and optical systems.
• Drive best practices in design, coding, cybersecurity, data privacy, and defect prevention aligned with medical device standards.

  • Cross-Functional Product Development and Systems Integration

Collaborate with product management, systems engineering, hardware, optics, usability, and quality teams.
• Translate customer, clinical, and business needs into clear requirements and implementation plans.
• Ensure alignment with timelines, product goals, and system architecture.
• Emphasize traceability, risk management, and disciplined change control in a regulated environment.

  • Quality, Compliance, and Delivery Excellence

• Establish and maintain high standards for quality, compliance, and engineering discipline.
• Drive robust testing strategies, documentation, configuration management, and traceability.
• Ensure secure development practices and regulatory adherence.
• Balance delivery speed with product reliability, maintainability, and service readiness.

  • People Leadership and Engineering Culture

Build and lead a high-performing software engineering team.
• Foster a culture of ownership, collaboration, continuous learning, and quality.
• Provide coaching, technical guidance, and career development support.
• Align individual growth with team and product objectives.

  • Stakeholder Engagement & Global Collaboration

• Partner with global R&D, quality, regulatory, service, manufacturing, and product teams.
• Translate product strategies into scalable and supportable software solutions.
• Drive effective collaboration across geographies and disciplines.
• Strengthen software development as a key enabler of innovation and customer value.

  • Education requirements / Experience / Job Specifications

• Bachelor’s or master’s degree in computer science, Software Engineering, Electronics, Biomedical Engineering, or related field.

• 15+ years of experience in software engineering for medical devices, including leadership roles.
• Proven track record delivering complex product software across the lifecycle
• Experience in regulated environments such as medical technology or diagnostics preferred.
• Strong background in software interacting with hardware, sensors, and user interfaces.
• Experience working in cross-functional and global teams.

  • Technical Skills:
    • Strong expertise in Windows-based device software (Linux is a plus).
    • Proficiency in requirements engineering, architecture, development, integration, and testing.
    • Knowledge of medical device lifecycle processes, risk management, and documentation.
    • Experience in cybersecurity, data privacy, and secure development practices.
    • Strong focus on product quality, diagnostics, serviceability, and maintainability.

Your ZEISS Recruiting Team:

Itishree Pani