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

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.

Enclosed the project details:

GxP Qualification & Validation Specialist (m/f/d) - Central Switzerland

General information

• Reference:
• Start: -4
• Duration: 12 Months ++
• Location: Central Switzerland
• Scope of work: full-time
• Languages: English

Your qualifications

• 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.

Your tasks

• 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.

Contact person

Marco Ferreira

P:

E: