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

Westhouse Group; Nidwalden; On-site; CHF 120,000 - 150,000; Full time

Job summary

Westhouse Group seeks an experienced GxP Validation Specialist for a long-term project in Central Switzerland. The role focuses on qualification and validation activities in a GMP-regulated setting, with hands-on Kneat documentation and IQ/OQ/PQ execution.

Fluency in English is required; knowledge of Veeva is a plus. The contract is full-time with potential extension, based in Central Switzerland.

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.

Responsibilities

• 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.

Skills

GxP Validation

Kneat

IQ/OQ/PQ

Equipment validation

English

Tools

Kneat

Veeva

Job description

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: 180546
• Start: 2027-01-4
• 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: [phone]

E: [e-mail]