CQV Engineer

Are you a skilled and experienced Engineer looking for your next career step within Commissioning Qualification Validation?

Proclinical is seeking a CQV Engineer to support validation tasks related to equipment and facilities. This role involves coordinating equipment installation, drafting and executing IQ/OQ/PQ protocols, and documenting results in compliance with cGMP standards. This temporary contract position is based in Visp, Switzerland.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport..

Responsibilities:

• Coordinate and execute validation activities for facilities, utilities, and processes.
• Prepare and execute IQ/OQ/PQ protocols for equipment, systems, and utilities.
• Document validation activities thoroughly and accurately.
• Identify efficiencies in the validation program and apply industry regulatory changes.
• Perform Quality Systems activities including document management, change control, and CAPA's.
• Write and revise procedures related to engineering activities.
• Support the engineering team in validation, requalification, and maintenance programs.
• Perform other duties as assigned.

Key Skills and Requirements:

• Bachelor's Degree in Science or Technical field.
• Proficiency in German is mandatory; English is advantageous.
• Excellent technical writing and communication skills.
• Strong organizational and time management abilities.
• Ability to work effectively across departments.

If you are having difficulty in applying or if you have any questions, please contact Emile De Beer at [email protected].

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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