Robotics Software Manager

Johnson & Johnson
Zuchwil, Switzerland
yesterday

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Senior

Job location

Zuchwil, Switzerland

Tech stack

.NET
Agile Methodologies
Computing Platforms
Systems Engineering
Build Automation
Automation of Tests
C++
Configuration Management
Static Program Analysis
Code Coverage
Computer Engineering
Continuous Integration
DevOps
Embedded C
Middleware
Embedded Software
Failure Mode Effects Analysis
Design of User Interfaces
Python
LabView
Matlab
Software Architecture
Systems Development Life Cycle
Real-Time Operating Systems
Software Safety
Requirements Management
Robotic Automation Software
SAP Product Lifecycle Management (PLM)
Software Engineering
Software Requirements Analysis
Software Systems
Software Quality Assurance (SQA)
Test Execution Engine
Jama (Software)
Scripting (Bash/Python/Go/Ruby)
Robot Operating System
DOORS (Software)
System-level Testing
Git Flow
Polarion
Software Version Control

Job description

Robotics Software Manager that will oversee the embedded software team developing next-generation surgical robotic systems This role is a critical technical and people-leadership position within Robotics R&D, combining deep hands-on expertise with strategic ownership of software architecture, execution, and quality.

The Robotics Software Manager is accountable for defining, building, and sustaining robust, scalable, and safety-critical software platforms that meet clinical, user, and regulatory requirements. Working closely with systems, robotics, hardware, clinical, manufacturing, quality, and regulatory partners, this role ensures that software solutions are architected and executed to meet system-level performance, safety, and reliability objectives.

This position requires a technical leader who can operate effectively in a highly regulated, multidisciplinary robotics environment, while mentoring teams, driving innovation, and enabling predictable, high-quality delivery., * Lead the full lifecycle development of embedded software subsystems for surgical robotic platforms, from early concept and prototyping through verification, release, and post-market support.

  • Define, own, and evolve the embedded software platform and architecture, ensuring scalability, real-time performance, safety, cybersecurity, and long-term maintainability.
  • Establish technical direction and software roadmaps aligned with product strategy and system evolution.
  • Ensure software designs are compliant with system requirements, user needs, intended use, hazard mitigations, and regulatory expectations.
  • Partner with systems engineering, robotics, hardware, clinical, usability/human factors, quality, and manufacturing teams to translate user needs into clear, testable, traceable software requirements.
  • Lead and participate in architecture reviews, design reviews, and cross-disciplinary technical trade-off discussions.
  • Collaborate on the design and implementation of safe, intuitive user interfaces with human factors and clinical teams.
  • Support regulatory submissions, audits, inspections, and DHF completeness in partnership with quality and regulatory affairs.
  • Establish and own DevOps strategies appropriate for regulated embedded robotics, including:
  • Continuous Integration (CI) with automated builds, static analysis, and test execution
  • Controlled release pipelines aligned with design controls and change management
  • Source control, branching strategies, and configuration management for safety-critical products
  • Lead adoption of automated unit-testing, integration, and system-level testing to improve quality and delivery predictability.
  • Champion metrics-driven development (build health, test coverage, defect trends) to drive continuous improvement.
  • Lead software FMEA activities, define and verify effective risk mitigation strategies, and ensure software safety levels align with system requirements and applicable risk controls.
  • Contribute to hazard analysis, risk management, and design controls in accordance with medical device regulations.
  • Ensure compliance with applicable medical device software standards (e.g., IEC 62304) and internal quality processes.
  • Investigate non-conformances, deviations, and test failures; drive root cause analysis (RCA) and corrective actions.
  • Lead software planning and execution across development phases, including prototyping, design, verification, validation, and release.
  • Support design transfer, manufacturing readiness, and product launch activities.
  • Participate in complaint investigations, post-market surveillance, and controlled software updates.
  • Build, mentor, and retain a high-performing embedded software team.
  • Identify project critical paths, proactively manage risks, and facilitate cross-functional problem solving.
  • Support resource planning, staffing, and schedule estimation.
  • Communicate risks, opportunities, and execution status clearly to senior leadership.
  • Foster a culture of technical excellence, accountability, ownership, and continuous improvement.
  • Communicate business-related issues, risks, and opportunities to senior management in a timely and effective manner.
  • Interface with regulatory, quality, and manufacturing teams to support audits and inspections.
  • Responsible for communicating business-related issues or opportunities to next management level
  • For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
  • Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
  • Performs other duties assigned as needed
  • Identify critical paths during product development, address bottlenecks and risks and facilitate problem solving across R&D teams.
  • Support project resource and schedule planning.

Requirements

Required:

  • Bachelor's or Master's degree in Software Engineering, Electrical Engineering, Computer Engineering, or a related technical discipline.
  • Minimum of 7+ years of hands-on experience developing embedded software for medical devices.
  • Deep expertise in embedded C/C++ development, including low-level drivers, middleware, and application-level software.
  • Expertise in Microsoft .NET development framework and Window based applications
  • Strong experience with real-time embedded systems, including RTOS-based environments (e.g., QNX or similar real-time operating systems).

Preferred:

  • Demonstrated experience developing software for Class II and/or Class III medical devices.
  • Strong understanding of software and systems engineering principles and product development lifecycle (e.g., V-model, waterfall, Agile).
  • Experience with requirements management tools (e.g., DOORS, Jama, Polarion).
  • Familiarity with test automation tools and scripting languages (e.g., Python, LabVIEW, MATLAB).
  • Excellent technical writing and communication skills., Compliance Management, Developing Others, Inclusive Leadership, Innovation, Leadership, Requirements Analysis, Research and Development, Researching, SAP Product Lifecycle Management, Scope Management, Scripting Languages, Software Acquisitions, Software Development Management, Software Engineering Practices, Software Quality Assurance (SQA), Systems Development Lifecycle (SDLC), Team Management, Technologically Savvy, Vendor Management

About the company

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit., Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that's reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent to join our DePuy Synthes Orthopaedics team as a Robotics Software Manager, based in U.S. (Boston, MA; Raynham, MA; Warsaw, IN; Palm Beach Gardens, FL) and EMEA (Gières, France; Oberdorf, Switzerland; Leeds-Beeston,England and Zuchwil, Switzerland).

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