Sr Eng, Software V&V

6 - 10 years

6 - 11 Lacs

Posted:13 hours ago| Platform: Foundit logo

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Skills Required

Work Mode

On-site

Job Type

Full Time

Job Description

  • Review,Author, Execute, perform, summarize, report out verification & validation test activities of components to a full system device: Which includes but not limited to:
  • Test Plans, Test Procedures, User and Functional Requirements testing,
  • Design Verification,
  • Installation/Operational/Performance Qualification Protocols,
  • Traceability Matrices and
  • Final Reports.
  • Support compliance/ closure of Regulatory and Quality requirements before completing Design Outputs/ Program Deliverables.
  • Clear understanding of the elements of Risk Management, FMEA, critical / Essential parts identification, System reliability, Life / limits testing and related V&V tasks.
  • Participate in the development of Verification & Validation methodologiesin accordance withapplicable Quality/Regulatory requirements and industry bestpractices
  • Lead the qualification of lab area, productivity improvement efforts, including testing, building fixtures,calibrationand data collection.
  • Diagnose,isolateand investigate problem reports. Drive product improvements and/or bug fixes.
  • Ensure good documentation and Good Manufacturing practices are followed in the Verification and Validation Process
  • Participate in continuous improvement activities by supporting the implementation of process and product quality improvementinitiatives
  • Deep knowledge in test automation tools and realizing test automation suite.
  • Work closely with the auditees to understand the details and support with all relevant objectiveevidences
  • Adheres to Baxter Quality Management system & supportsthe qualityaudits.
  • Support on-going regulatory agency inspection readiness through the self-assessment program to include mock inspections and compliance with revised and emerging regulations.
  • Pair up with design & development team to start the testing early in the design cycle to ensure the requirements testability, design traceability & test coverage.Identifyissues early to fixthe same. Refine the test plans and procedures through pre-verifications / Dry runs.
  • Interacts with design team to resolve tests-related technical issues.
  • Presents the findings / objectiveevidencesand able to present with rationale with applicability / exclusions
  • Identifyand report any quality or compliance concerns and take immediate corrective / Preventive action as needed.

What you'llbring

  • Bachelor's degree in Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
  • 6to 10yrsof experience in Verification and validation testing ofSoftware andhardware.
  • Relevant technical testing/reliability experience in electro-mechanical, electrical, or software testing.
  • Understanding of hardware schematic diagrams and debugging tools like IC5000, CAN Analyzer,Trace 32, Keil IDE, PEAK analyzer, Oscilloscope
  • Any scripting knowledge like python, shell etc. Good programming knowledge and basic understanding of Embedded programming.
  • Understanding of modeling( MATLAB, Simulinketc)
  • Test framework development and test harness development knowledge.
  • Knowledgeonhardware in loop and software in loop testing.
  • An understanding of test methods and processes as well as the methods used to verifyproductin the realmsof;software, mechanical, electrical, functional and environmental testing environments.
  • Experience in - writing system, subsystem-level and module level verification and validation plans, procedures, Test Execution and Test reportgeneration
  • Understanding of hardware and software product design methodologies and test practices.
  • Familiarity with reliability theory and analysis as it pertains to test quantities derived from reliability.
  • Experience in medical device or similar product development, design verification/validation,softwareintegration (involving software & hardware), risk management, reliability engineering, process validation and Qualitysystems
  • Deep domain knowledge in design verification and validation of medical devices is aplus
  • Understanding of and adherence to FDA, ISO and IEC design control procedures,regulationsand standards.
  • Demonstrated experience in accomplishingobjectives. Able to deliver on multiple projectssimultaneously
  • Self-motivated with good interpersonal skills

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