As part of our growth in Switzerland, we are looking for a process Validation and equipment Qualification consultant to be involved in our development in the pharmaceutical industry.
Your main tasks and responsibilities are:
- Defining the Qualification and Validation approach;
- Establishing procedures for qualification and validation in accordance with international standards (GMP, FDA);
- Writing qualification/validation documents;
- Coordinating and executing qualification and validation tests.
An Engineering degree and a first experience in the same area of expertise is required.
The successful candidate is autonomous and holds good written and oral skills in english.