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Job Description

Work Flexibility: Not available

Position profile


 Sr Quality Engineer


Responsibilities and duties


  • Risk Management, Design Inputs review, Design History File Document review, Design Output Document review, V&V protocols and reports review, Review and approval of CER.
  • Participate in Risk Management per ISO14971 to ensure the safety and effectiveness of product.
  • Participate in design reviews during various phases of NPD.
  • Work with team to develop robust verification, Design validation & release strategies to ensure product compliance, safety, reliability & effectiveness.
  • Sound knowledge of IEC 62304: Medical device Software – Software life cycle processes. This also includes good exposure to all the phases of Software development life cycle (SDLC).
  • Exposure to any Programming language & on Software Testing concepts.
  • Design And User Validation exposure.

Experience/skills required


  • Bachelors in Computers/ IT/ Electronics.
  • Good analytical and problem-solving skills.
  • Good understanding of Quality Management Systems. (ISO 13485, 21 CRF 820)
  • 5-7 years of relevant work experience.
  • Experience on NPD process and various phases of new product development.
  • Knowledge of ISO 14971, IEC 62366, 60601-1 family of standards.
  • Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams.
  • Expert-level knowledge of current industry standards for New Product Development and risk management practices.
Travel Percentage: None

Job Details

Job Location
India
Company Industry
Other Business Support Services
Company Type
Unspecified
Employment Type
Unspecified
Monthly Salary Range
Unspecified
Number of Vacancies
Unspecified

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