Director, Systems Engineering

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology

At Cepheid, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you'll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world's most complex health challenges. Together, we bring MORE change to the world.

Learn about the Danaher Business System which makes everything possible.

We are seeking a highly influential and experienced Director of Systems Engineering to lead the technical conscience of our R&D organization. This critical leadership role owns the holistic technical vision and execution for our diagnostic platforms. You will be responsible for leading the teams that define, integrate, verify, and ensure the reliability of our complex products. You will lead our System Architects, System Integration Engineers, Verification & Validation (V&V) Engineers, and Reliability Engineers. Your primary mission is to ensure that we build the right product and that we build the product right, meeting all user needs, technical requirements, and stringent regulatory standards.

This position reports to the Senior Director Systems Engineering and is part of the Research & Development department, located in Bengaluru, IDC, India, and will be based on-site.

In this role, you will have the opportunity to :

• Direct the systems engineering function across architecture, integration, verification, validation, and reliability, ensuring alignment with ISO 13485 and FDA QSR (21 CFR 820) standards
• Oversee end-to-end requirements management, translating clinical workflows into technical specifications using tools such as IBM DOORS or Jama Connect
• Lead system architecture development, including trade-off analysis and platform scalability decisions, with proficiency in model-based systems engineering (MBSE) frameworks
• Manage integration of multidisciplinary subsystems-hardware, software, firmware, and biochemical assays-using structured integration plans and risk-based methodologies
• Own the V&V strategy and execution, including authoring and approving test protocols and reports for regulatory submissions under FDA and CE marking requirements
• Implement reliability engineering practices including FMEA, HALT / HASS, and predictive analytics to meet product lifetime targets and reduce field failure rates
• Administer product risk management activities per ISO 14971, ensuring traceable mitigation strategies across the full product lifecycle using validated risk analysis tools

The essential requirements of the job include :

It would be a plus if you also possess previous experience in :

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit .

Skills Required

Polarion, Iso 13485, Iso 14971, halt, Fmea, Predictive Analytics, HASS