Senior Quality Assurance Specialist for Medical Devices

5 days ago


Glostrup, Glostrup Kommune, Denmark Agilent Technologies, Inc. Full time
Job Description

We are seeking a Senior Quality Assurance Specialist to join our team at Agilent Technologies, Inc.

This role will be responsible for ensuring compliance with internal and external requirements during design and development of new products, especially with regards to design control.

The ideal candidate will have a Master's degree in biotechnology, engineering, or a related field and +4 years of experience in the development of In Vitro Diagnostics (IVD), Medical Devices, and/or Pharmaceuticals.

The salary for this position is approximately $85,000 - $110,000 per year, depending on location and experience.

About the Role
  • Provide guidance on design control activities to identify innovative and efficient solutions for various quality topics.
  • Conduct reviews and approvals of design control documents, design changes, nonconformances, CAPAs.
  • Drive quality initiatives to support continuous improvements of our processes.
Requirements
  • Master's degree in biotechnology, engineering, or a related field.
  • +4 years of experience in IVD, Medical Devices, and/or Pharmaceuticals.
  • Proficient in Quality System Standards (ISO13485, FDA CFR21 Part 820, MDSAP) and IVD/Medical Devices legislation in EU and USA.
  • Business oriented and a desire to work in a dynamic and adaptable environment.
Benefits
  • An inspiring and social environment with around 40 skilled colleagues in the QA department.
  • A great opportunity for you to make a significant impact and develop your skills in a world-class company that takes pride in developing new innovative solutions.
  • Agilent offers core global benefits to all staff, including life insurance, pension, healthcare, physiotherapy, and more.


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