Stryker—Senior Advance Quality Engineer

Job description

Description: Work Flexibility: Hybrid What you will do- - Serve as the Quality representative on New Product Development (NPD) and sustenance engineering projects. - Defining the quality and compliance requirements for development of SaMD and ensuring the requirements are communicated to the stakeholders and met. - Development of process and procedures for development, testing and deployment of SaMD or Non Med SW and ensure software development activities comply with established SDLC processes. - Participate in requirements, architecture, design, code, verification, and validation reviews and drive risk management activities including software hazard analysis and FMEA reviews. - Review and Approve quality deliverables required throughout the development lifecycle; requirements for traceability, completeness, and testability and E2E test coverage and compliance. - Develop and execute software quality strategies, test plans, and validation approaches. - Ensure appropriate verification and validation activities are performed and documented. - Ensure compliance with industry standards and regulations (e.g., ISO 13485, FDA regulations, IEC 62304, cybersecurity requirements, company quality procedures). - Support internal and external audits and ensure the SW bugs (pro-prod and prod) and properly addressed and review CAPAs, non-conformances, deviations, and change controls related to software products. - Validation of SW tools used in development, testing and deployment. - Ensuring the deployment compliance per customer requirements in collaboration with R&D and deployment teams. - Maintain Design History File (DHF) and software quality documentation - Partner with Software Engineering, Systems Engineering, Product Management, Regulatory Affairs, Clinical Affairs, and Manufacturing teams and provide guidance on software quality best practices. - Mentor junior quality engineers and support organizational capability building What you will need- Required Skills- - Experience on Medical Device Development process; New Product Development process and various phases of new product development; experience on Risk Management, different Risk Analysis tools and techniques and experience on ISO 14971 - Understanding of Quality Management Systems. (ISO 13485, 21 CRF 820, ISO 9001) and well versed with change control process - Experience in following technical areas is recommended - Software Development Life Cycle (SDLC); Risk Management / FMEA; Verification & Validation (V&V); Defect Management Systems (Jira, Azure DevOps, etc.); Requirements Traceability; Root Cause Analysis (RCA); Cybersecurity and Product Security concepts and change control process; Jira, Testrail, TrackWise, Salesforce, slack - Education- Bachelor's degree in Computer Science, Software Engineering, Electronics Engineering, Biomedical Engineering, or related discipline/ Master's degree preferred - Experience- 5 years- 7 years; 4 years in relevant Software Quality Assurance, Software Engineering, or Quality Engineering. - Experience working in regulated environments (Medical Devices, Healthcare Software, Automotive, Aerospace, etc.). Preferred Skills- - Should be ready to travel to divisions as required. - Effective interpersonal, communications skills. - Good understanding of Agile and traditional SDLC methodologies Travel Percentage: 10%