Required skills
Languages: English
Job description
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.
Contact person
Marco Ferreira
P: [contact removed]
E: [contact removed]
- 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) - Central Switzerland
General information
Your qualifications
- Reference: 180546
- Start: 2027-01-04
- Duration: 12 Months ++
- Location: Central Switzerland
- Scope of work: full-time
- Languages: English
- 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.
- Remote: onsite
- Location: Central Switzerland, DE
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