GxP Qualification & Validation Specialist (m/f/d)

Project overview

For a long-term project with our client we are looking for an experienced GxP Validation Specialist to support qualification and validation activities in a regulated environment.

Responsibilities

Interested?

Interested? We look forward to receiving your detailed CV in electronic form.

Your Contact:

Marco Ferreira

*@*.ch

*

• Perform qualification and validation activities in a GxP-regulated environment.
• Qualify production equipment, cold storage facilities, warehouses and utility systems.
• Plan, execute and document IQ, OQ and PQ testing activities.
• Prepare and maintain validation plans, test protocols, traceability matrices (RTMs) and final reports.
• Ensure compliance with GMP regulations, SOPs and applicable quality standards.

Project details

GxP Qualification & Validation Specialist (m/f/d)

General information

Reference:180546

Central Switzerland

04.01.2027

Volume:full-time

12 Months ++

Languages:English

Your Skills

• Strong experience in qualification and validation within GxP/GMP-regulated environments.
• Hands-on experience with Kneat for electronic validation documentation (mandatory).
• Solid knowledge of IQ, OQ and PQ processes and associated documentation.
• Experience in pharmaceutical equipment, facility or utility system validation.
• Fluent English; experience with Veeva is an advantage.
• Start: 2027-01
• Duration: 12 Monate
• Remote: onsite
• Location: Central Switzerland, Schweiz, CH
• Languages: English