Sr Principal Engineer, V&V

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

• Lead strategy, Planning, Development and execution of Product Verification and validation deliverables for NPD (new product development) and complex sustenance projects.
• Lead the strategy for test optimization, test coverage, adequacy of testing and process simplification.
• Lead productivity improvement efforts, including design and building test fixtures etc.
• Drive automation to enhance coverage, identify more defects and reduce test efforts.
• Pair up with design & development team to start the testing early in the design cycle for NPDs.
• Lead and guide the team on test methods, Sampling and statistical techniques.
• Provide Technical direction for Systems Verification and Validation Engineering staff and programs.  Guide, mentor, and provide direction to junior verification and validation Engineers.
• Implement configuration and change management through the complete product life-cycle, including verification and validation deliverables.
• Ensure all program milestones in support of all phases of the product development lifecycle are completed on time, with appropriate quality, and in compliance with relevant laboratory standards and regulations.
• Ensure compliance to the product development process and Quality System requirements.
• Ensure good documentation are followed in the Verification and Validation Process.
• Ensure all the test methods are validated, all the analytical equipment and computer system are validated for their intended uses.
• Contribute to development of Requirements for system, derive sub system requirements, Review and Analyze requirements
• Contribute to the development and documentation systems architecture and design.
• Contribute to design and development of embedded products, particularly medical devices
• Participate and/ or lead design reviews. Guide the team in the state of art V&V practices, QMS processes and on the applicable regulations / Standards, country specific requirements.
• Participates and contributes to the roadmap discussion.
• Adheres to Vantive Quality Management system & front ends the quality audits.
• Manage the integration of deliverables from subsystem teams, cross functional teams and external partners.
• Actively communicate and advocate team’s capabilities and accomplishments.  
• Maintain an effective and collaborative working relationship with internal and external development partners across all levels and diverse cultures.
• Collaborate with other engineering teams within the organization.

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

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