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Senior Quality Engineer

Cpl Life Sciences

Switzerland · On-site Senior 1w ago

About the role

Overview

Our client a global leading Medical Device Manufacture based near Basel, Switzerland is looking for Senior QA Engineer. This is an exciting role which involves life changing operations for the patients.

Responsibilities

  • Maintain the QMS in accordance with certification standards and ensure its evolution
  • Lead quality improvements projects
  • Provide the necessary support to the controllers in order to guarantee the relevance of the
  • Quality decisions with regards to the requirements of the products
  • Implementing product development requirements
  • Support in the creation of test methods
  • Monitoring of compliance with processes and standard

Requirements

  • Bachelor’s degree in relevant field
  • 5 years’ experience in Medical Device Industry
  • Must have at least 5 years’ experience in ISO 13485 and IEC 62304
  • Must have software knowledge in Medical Devices
  • 5 years’ experience in the field of design, quality, quality management, quality assurance or in another regulated industry in compliance with regulation
  • 3 years’ experience in risk management, ideally in medical technology
  • Knowledge of the project management tools
  • Very good knowledge of spoken and written English

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Requirements

  • Must have at least 5 years’ experience in ISO 13485 and IEC 62304
  • Must have software knowledge in Medical Devices
  • 5 years’ experience in the field of design, quality, quality management, quality assurance or in another regulated industry in compliance with regulation
  • 3 years’ experience in risk management, ideally in medical technology
  • Knowledge of the project management tools
  • Very good knowledge of spoken and written English

Responsibilities

  • Maintain the QMS in accordance with certification standards and ensure its evolution
  • Lead quality improvements projects
  • Provide the necessary support to the controllers in order to guarantee the relevance of the Quality decisions with regards to the requirements of the products
  • Implementing product development requirements
  • Support in the creation of test methods
  • Monitoring of compliance with processes and standard

Skills

IEC 62304ISO 13485

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