In this role, the Commissioning Qualification Validation (CQV) Engineer will be responsible for a range of tasks related to the validation of equipment and facilities within the pharmaceutical industry. This position involves coordinating equipment installation, drafting and executing validation protocols, and ensuring compliance with current Good Manufacturing Practices (cGMP). The CQV Engineer will play a crucial role in maintaining the integrity of validation processes and documentation.
Project Duration: Approx. 9 Months
Starting Date: ASAP
Place of Work: Visp