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QAV Engineer

  1. Frankfurt
  1. Contract
  1. Compliance / Quality Assurance
Date Posted02 Mar 2020
I am working with a Global Medical Device Manufacturer based in Germany.

The successful organization develops manufactures and markets products that simplify, automate and innovate biomedical testing.

The award-winning business is currently looking for a QAV Engineer to join their existing team on a Contract basis.

Reporting to the QA Manager the successful QAV Engineer will have experience working within a GMP environment holding responsibility for process validation and equipment qualification.


Responsibilities & Experience:
  • Validation of the master plan and associated procedures
  • Planning and implementation of qualification, preparation and approval of the related documents
  • Ensuring GMP-compliant documentation; creating and training of quality-related procedures and processes
  • Planning and monitoring of validation projects and qualification projects and their implementation
  • Fluent German and English
  • Strong analytical and communication skills and understanding of complex relationships
  • Knowledge in dry chemistry is a bonus
  • Ideally will have knowledge of ISO 13485, and 21 CFR 820

If you would like to discuss this opportunity in more detail, please submit your profile and I will be in touch at my earliest convenience.

The candidate must have the rights to work in the location stated in the job advert.

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