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Medtronic

Medical device maker advancing therapies

Quality Engineer 2

Quality EngineeringPosted on Nov 10
Full-timeHyderabad, Telangana, IndiaNo salary listed

About the Job

Requirements

  • A bachelor's degree in engineering, science, or a technical discipline is required.
  • Five to eight years of quality systems experience is required.
  • Strong oral and written communication skills are required.
  • Ability to work with international and multicultural teams across different time zones is required.
  • Ability to deliver quality work accurately and on time is required.
  • Ability to work well under pressure and in a fast-paced environment is required.
  • Willingness to learn and expand responsibilities is required.

Responsibilities

  • Ensure suppliers deliver quality parts, materials, and services.
  • Work with suppliers on quality issues observed during new product introduction.
  • Complete Production Part Approval Process (PPAP) deliverables for new products and legacy product changes using a process validation approach.
  • Evaluate supplier performance periodically and take necessary action for continuous improvement.
  • Provide pre-market quality engineering support to New Product Development (NPD), partnering with Component Engineering and Post-Market Supplier Quality teams to deliver quality parts, materials, and services, prevent defects, and support high-quality, reliable products.
  • Collaborate with cross-functional teams on Supplier Quality engagement throughout the NPD lifecycle for newly qualified parts, ensuring product quality and continuous improvement.
  • Ensure purchased products and components are manufactured and qualified according to applicable industry standards, regulatory requirements, and customer requirements.
  • Collaborate with component engineers to develop and deliver product acceptance sampling strategies, approved supplier list coordination, supplier-owned quality deployment, process failure mode and effects analysis (PFMEA), measurement system analysis (MSA), control plans, and relevant quality tools and methodologies for new and legacy products.
  • Prepare receiving inspection requirements as needed and validate associated test methods for internal Medtronic test methods.
  • Support supplier audit execution and approved supplier list management.

Desired Qualifications

  • Experience in supplier management is an advantage.
  • Previous experience working with global teams in aerospace, defense, medical devices, or automobile industries is preferred.
  • Exposure to Food and Drug Administration (FDA) Quality System Regulation and ISO 13485 is preferred.
  • Quality certification such as Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA) is preferred.
  • Working knowledge of standards, guidance, and regulations is preferred.
  • Lean Six Sigma Yellow Belt or Green Belt is preferred.
  • Good interpersonal skills are preferred.

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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