Staff Engineer

Stryker

Haryana

Hybrid

INR 900,000 - 1,800,000

Full time

9 days ago

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Benefits offered by this job

Hybrid work model

Job summary

Stryker in India is seeking an experienced Mechanical/Biomedical engineer to join the device design team. You will design, develop and verify components and subsystems for medical devices, translating user needs into design inputs.

You will prototype and test, analyze complex design issues, and contribute to design controls and risk management under the Quality Management System, while collaborating with R&D, Quality and Manufacturing. Strong GD&T, CAE tools, and DFM principles are required.

Qualifications

  • Bachelor of Science in Engineering, Mechanical Engineering or BioMedical with 4+ years of work experience.
  • Experience 7–10 years in relevant field.

Responsibilities

  • Research, design, develop, modify and verify components and subsystems for medical devices.
  • Prototype, test, analyze and resolve complex design issues; contribute to design controls and risk management.

Skills

Mechanical design
GD&T
CAE tools
DFM principles

Education

B.S. in Engineering or Biomedical

Tools

CAx/CAE software

Job description

Work Flexibility: Hybrid

What you will do:
  • Independently research, design, develop, modify, and verify components, modules and sub-systems for medical devices and translate user needs to design inputs/ specifications and produce complex system level designs with some guidance.
  • Conduct or design advanced prototyping and testing and analyze and correct complex product design issues using independent judgment
  • Advance solutions by applying in-depth knowledge of customer needs, market and competitive offerings and apply detailed knowledge of clinical procedures to author design inputs
  • Support Voice of Customer sessions internally and with clinicians and demonstrate developing financial acumen
  • Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations
  • Lead creation and refinement of engineering documentation, such as the Design History file and follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System
  • Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success
  • Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology
  • Support and execute segments of complex multifunctional teams to advance projects through the design /development/launch process
  • Deliver high quality results with passion, energy and drive to meet business priorities and collaborate with cross-functional teams to build partnership to achieve business objectives
What you will need-
Required skills-
  • Bachelor of Science in Engineering, Mechanical Engineering or BioMedical & 4+ years of work experience
  • Experience- 7 years - 10 years
Preferred Qualifications-
  • Strong technical ability to develop and optimize designs for mechanical / electro-mechanical assemblies incorporating DFM principles
  • Strong technical ability in creating engineering drawings, models, applying GD&T and CAE tool
  • Adept at applying knowledge of materials and manufacturing processes to product design
  • Ability to communicate moderate complexity plans and technical information to team members

Travel Percentage: None

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