Senior Engineering Manager

Bring more to life.

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

At Cytiva, one of 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.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the which makes everything possible.

The Senior Engineering Manager, Software is responsible forleadingServiceR&D Software Engineeringteamto enable remote troubleshooting and diagnostics.

Thisis a senior leadershippositionandis part of theGlobal Service R&DOrganizationlocatedinBengaluruand will beanOnsiterole.At Cytiva, our visionisto advance future therapeutics from discovery to delivery.

What you will do:

• System & Software Engineering Leadership
  Leadcross‑functionalsystem and software engineering teams to design, develop, integrate, deploy, and sustain complex, regulated product and system solutions across the full product lifecycle.
• End‑to‑EndProgram & Release Management
  Own delivery of system and software releases from requirements through production, ensuringon‑timeexecution, quality, performance, and defect metrics are met using structured project management practices.
• Planning, Estimation & Risk Management
  Develop andmaintainproject plans, schedules, resource and competency models, and risk mitigation strategies with continuous tracking and corrective action throughout execution.
• Process, Quality & Regulatory Compliance
  Implement, institutionalize, and continuously improve software and system engineering processes aligned with Agile/Lean,Continuous Delivery,DBS, ISO 13485,CyberSecurityand FDA 21 CFR Part 820 & Part 11 requirements.
• Cross FunctionalStakeholder Alignment
  Partner with product management, documentation, training, deployment, support, and other engineering teams to ensurerequirements oftraceability, technical alignment, and clear communication across the lifecycle.
• People, Capacity & Capability Management
  Lead workforce planning including hiring, onboarding,utilizationmanagement, technical mentoring, and performance development to support sustained delivery and organizational growth.
• Technical Oversight & Integration Strategy
  Provide technical direction for system architecture and integration, ensuring software compatibility with instruments, firmware, cloud platforms, DevOps pipelines, and external systems while staying current on emerging technologies.

Who you are:

• 12-15+ years of professional software development experience, with a bachelor's or master's degree in computer science, Engineering, or a related field.
• Expert-levelproficiencyin enterprise software development using C#.NET to develop Windows Services,REACT JS, HTML, Java script code on .NET core/framework including REST APIs to develop Web Services, exposure to cloud technologies (e.g., AWS) and embedded systems preferred.
• 4+ years of direct personnel management experience, including hiring, performance management, prioritization, resource allocation, and delivery accountability.
• 3+ years leading end-to-end delivery of complex, multi-team software projects, ensuring milestones, quality, and timelines are met.
• Proven delivery of software products in regulated environments (e.g., medical instruments) under FDA, ISO, or equivalent compliance frameworks.
• Demonstrated ability to translate customer insights and feedback into product design improvements and enhanced software functionality across platforms.
• Experience leading global, cross-functional teams and driving structured improvement initiatives (e.g., DBS or similar frameworks) with measurable outcomes in productivity, delivery, and compliance.

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

• Background in biotechnology or life sciences industry.
• Experience delivering software in regulated (GMP) environmentswith an understanding of Quality Management Systems (QMS) and documentation standards.

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.

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