Senior Manager - Device Software Development

Department Icon Risk Management & Compliance
Posted: 3 months ago
15-17 years
Bengaluru / Bangalore, Karnataka
Risk Management & Compliance
work from office
Full Time

Posted: 3 months ago
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Job Description

Purpose of this position / Position summary:

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, re-lease, 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.

Primary duties and responsibilities:

  • Device Software Development Leadership
  • Lead full lifecycle development and maintenance of device software, including requirement, 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 :

  • Bachelors or masters degree in computer science, Software Engineering, Electronics, Bio-medical 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, diagno

Skills

ComplianceRegulatoryRisk Management

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About Company

ZEISS is an internationally leading technology enterprise operating in the fields of optics and optoelectronics. In the previous fiscal year, the ZEISS Group generated annual revenue totaling 8.8 billion euros in its four segments Semiconductor Manufacturing Technology, Industrial Quality & Research, Medical Technology and Consumer Markets (status: 30 September 2023). For its customers, ZEISS develops, produces and distributes highly innovative solutions for industrial metrology and quality assurance, microscopy, medical technology, and eyeglass lenses, as well as camera and cinema lenses. ZEISS stands for continuous innovation, sustainability and a future-oriented approach. With more than 43,000 employees in almost 50 countries, ZEISS is contributing to technological progress and helping to improve the quality of life of many people around the world. The foundation of the success of ZEISS lies in its outstanding employees, its strong innovative strength and its exceptional portfolio of technologies, products and solutions. Founded in 1846 in Jena, the company is headquartered in Oberkochen, Germany. The Carl Zeiss Foundation, one of the largest foundations in Germany committed to the advancement of science, is the sole owner of the holding company, Carl Zeiss AG.
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