CQV Engineer

Updated: April 15, 2024 05:11 PM GMT

Panda

Visp

For my client – a globally renowned biotech CDMO in Visp, Switzerland – I am looking for a CQV Engineer to join an innovative and dynamic team!

Job description

As a Commissioning Qualification Validation engineer, you will be responsible for carrying out a variety of tasks crucial to equipment and facility validation. This role involves coordinating the installation of equipment, drafting IQ/OQ/PQ protocols, executing the IQ/OQ/PQ tests, and documenting the results according to cGMP requirements.

Main activities:
• Preparation of validation documents
• Execution of IQ/OQ and PQ for equipment, systems, and utilities
• Compilation of detailed reports on validation activities
• Continuous evaluation of validation program efficiency and implementation of enhancements
• Staying updated on regulatory changes impacting equipment/facility validation
• Engaging in Quality Systems activities including Document Management, Change Control, Non-Conformities, and CAPA’s
• Crafting and refining... More Detail