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Medtronic

Medical device maker advancing therapies

Senior Research and Development Engineer

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, India

About the Job

Requirements

  • A bachelor's degree in Mechanical Engineering and 8 to 12 years of product development experience in a regulated engineering environment are required.
  • Demonstrated experience with computer-aided design (CAD) tools such as PTC Creo (Pro/ENGINEER) or SolidWorks, including robust modeling and detailed drawing creation, is required.
  • Strong expertise in Geometric Dimensioning and Tolerancing (GD&T), tolerance stack-up analysis, and mechanical engineering fundamentals is required.
  • Experience supporting medical device product development, including design controls, technical documentation, and engineering change management processes, is required.
  • Experience working independently with cross-functional and global teams to deliver engineering projects is required.

Responsibilities

  • Lead mechanical design, development, and optimization for medical device products, components, tooling, and related engineering solutions.
  • Collaborate with global cross-functional teams to execute product development and sustaining engineering projects from concept through release.
  • Conduct and lead design reviews to ensure designs meet safety, reliability, manufacturability, quality, and performance requirements.
  • Develop and release component and assembly drawings using ASME standards and applicable Product Lifecycle Management (PLM) systems.
  • Support engineering change management, product release, and sustaining engineering while ensuring compliance with applicable procedures and design controls.
  • Contribute to risk management activities, including Design Failure Mode and Effects Analysis (DFMEA), risk assessments, and related design history documentation.
  • Apply Food and Drug Administration (FDA), International Organization for Standardization (ISO), and design control requirements throughout development and sustaining projects.
  • Provide technical guidance, mentoring, and review support to engineering team members, and lead projects through milestone reviews and stage-gate approvals.

Desired Qualifications

  • Experience with Finite Element Analysis (FEA) tools such as ANSYS Workbench and modeling and simulation techniques.
  • Knowledge of Product Lifecycle Management (PLM) systems and engineering change processes, including Agile or PTC Windchill.
  • Knowledge of medical device regulations and standards, including ISO 13485, ISO 14971, and 21 CFR Part 820.
  • Experience supporting Design History File (DHF) deliverables, risk management documentation, sterilization documentation, or biocompatibility documentation.
  • Knowledge of advanced manufacturing methods, including additive manufacturing and 3D printing technologies.

About the Company

Medtronic

Medical device maker advancing therapies

Medtronic develops medical devices that diagnose, monitor, and treat chronic diseases. Its products include implantables, sensors, and therapies used in cardiovascular care, diabetes management, and neurostimulation, working by interacting with the body to regulate or monitor physiological processes. The company differentiates itself through a long history of device development, strategic acquisitions like Covidien, and a broad, diversified portfolio across therapeutic areas. Its goal is to improve patients’ health outcomes by delivering integrated medical technologies and solutions for disease management.

Company size
10,001+
Company stage
IPO
Headquarters
Fridley, MN
Founded
1949

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