Software Design Quality Engineer

12 - 17 years

17 - 18 Lacs

Posted:6 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

  • Ensure that appropriate project plan and quality plans are made that include all stages of the product s lifecycle, targets and strategy for a robust software products development.
  • Validates key design inputs including requirements, specifications, useability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy serviceability, sustainability, and costs.
  • Provides effective oversight during the execution of the Quality Plan and any risk management activities, and of all design related activities during the lifecycle.
  • Contribute during design and development to identify critical quality attributes (CTQ, CTS) and ensure that appropriate mitigations and design controls are applied to mitigate the risks.
  • Facilitate design failure mode and effect analysis to identify failure modes early in the design and development process and apply design, manufacturing and inspections to mitigate the risks.
  • Ensure with objective V&V evidences that design output meets the design input.
  • Leading quality related problem solving with the cross functional teams
  • Using post-market data for analytics and statistics to report on the product s performance in the market (provide feedback to manufacturing, suppliers, or design teams) and initiate field actions when required.
  • Act as a single point of contact (person assigned to) for project team(s); you re responsible to ensure the product s design quality related requirements/criteria are complete and meet the quality standards for every project milestone.
  • Make substantial contribution to integrate reliability engineering activities with the medical device development activities.
  • Effective oversight of project deliverables and provide quality input, including safety, efficacy, regulatory. Facilitate the product defect investigations and actions during defect management review meetings.
  • Participate in audits and regulatory inspection as design quality SME and guide other cross-functional stakeholders on technical aspects and audit conduct.

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Philips

Healthcare Technology

Amsterdam

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