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QA Validation Specialist

Company Description

In the context of an increase in the activity, one of the world’s leading companies in the medical devices market specialized in manufacturing biomedical products is looking for a QA Validation Engineer, in the Canton of Vaud.

Join a fast-growing company in the Medical Devices sector and bring your career one step higher! 

Job Description

As a QA Validation Engineer, you are in charge of Qualification/Validation activities for existing processes (planning, execution and test documentation) and for projects (QA documentation).

Your main responsibilities:

  • Enforce current Quality procedures
  • Conduct Qualification and Validation reviews according to GMP standards
  • Participate in Risk Analysis analyses of equipment and processes.

In some cases, you might be called to replace colleagues in their tasks:

  • Perform equipment qualification tests, BFU’s, CSV and periodic revalidations of sterilization, room qualification.


To lead this project, we are looking for a profile with:

  • Master’s Degree in engineering, pharmaceutical, biotechnology or medical device field
  • Minimum 2+ years of experience in medical device field, with a previous experience in Quality Assurance and Qualification / Validation activities.
  • Knowledge of regulatory requirements for Medical Devices (ISO 13485, QSR 21CFR part 820)
  • Excellent communication skills
  • Problem-solving oriented
  • Fluent English (spoken and written) and French (spoken and written)

One More Thing

You will have the opportunity to enjoy a permanent contract, a free week of holidays per year, free parking and an attractive salary depending on your experience.

Do you identify yourself with this description? Apply now or contact me directly!