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  • Job title:

    Sr. Associate QA/Validation Engineer

  • Sector:

    Medical Devices, Biotechnology

  • Job ref:


  • Start Date:


Location: Breda
Duration: 1 year  (extension is possible)
Language: English
Industry: Biotechnology
Start date: 1-11-2022 

The Company
Our client is the leader in the field of biotechnology, deeply value-based in science and innovation to transform new ideas and discoveries into medicines for patients with serious illnesses.

Role Description
As a Sr. Associate QA/Validation Engineer you will be responsible for the validation of equipment, automation and information systems for the Quality Risk Management.

- Review and approve validation documentation

-Perform process, equipment and IS validation
-Manage ABR’s device responsibilities and ensure alignment with GMP regulations
-Perform final review of technical change control.

-MBO or Bachelor’s degree in Life Sciences or process technology related field

-3 years of experience of working in a pharmaceutical or medical devices environment
-Knowledge of GMP, IS validation and computer compliance
-Preferred experience with CAPAs and Change Control

Are you ready to the next step in your career? Do not hesitate to apply below.