Sr Principal Engineer, V&V

Vantive

11 - 15 years

35 - 40 Lacs

Bengaluru

Posted:2 days ago| Platform:

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Skills Required

Automation Medical devices Change management Compliance Analytical Quality audit product life cycle New product development Recruitment Testing

Work Mode

Work from Office

Job Type

Full Time

Job Description

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.

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