Design Engineer in Gurugram bei Stryker Corporation

Datum der Veröffentlichung: 6/3/2019

Stellenauszug

Stellenbeschreibung

Education: B.Tech/B.E/M.Tech/MS. - Mechanical Engineering

Experience:  3-5 years (Preferably in Medical device)

Key Responsibilities include:

  • Solid at 3D CAD modeling on Pro/e, have good working knowledge of Windchill.
  • Change Management, including identification of problem, finding design solutions, develop prototypes for design verification and validation, executing change
  • Utilization / Management of Design/ Change Controls, NC/CAPA process
  • UDI & EU-MDR project execution
  • Standards assessment and implementation of changes in design controls
  • Technical report writing
  • Product design & development of structural components
  • Hands on experience of DFM, GD&T
  • Knowledge of ECN / ECR Process, manufacturing process & Change Control Procedures
  • Ensure continual improvement in customer satisfaction, delivering higher value services and productivity
  • Managing partnerships with vendors and other SME’s as needed
  • Manage knowledge at various spectrums appropriately to avoid losing it and help newcomers pick it up fast
  • Contribute to absorption of new technologies, processes and methods
  • Develop an open culture to instill confidence, diversity of perspectives and knowledge sharing
  • Communicating frequently across all project stakeholders to ensure project team and senior management are aware of upcoming milestones and risks/issues.
  • Knowledge of material selection, International standards (Good to have)
  • Knowledge of Design and Risk Management documents (Good to have)
  • Responsible for the timely and quality deliveries of the assigned tasks
  • Work as point of contact for all project related aspects with the stakeholders
  • Other duties assigned by manager

Particular Tasks:

  • Maintain ERP Information (i.e. Index, Status)
  • Create and maintain fixtures and inspection equipment (e.g. overlays)
  • Utilization of the Design Change Process:
    • Coordinate R&D activities pertaining to change requests
    • Gather information pertinent to the assigned product change
    • Undertake Technical assessments
    • Collaborate with BML on test plans definition
    • Define strategic plans to cover Verification & Validation activities
    • Update Interface Analysis as a result of change requests
  • Actively participate in cross functional teams
    • To address Non Conformities/Corrective-/Preventive Actions of existing medical devices
    • To support Manufacturing Transfers
    • To develop custom made devices and customized line extensions

Work From Home: No

Travel Percentage: None

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