Consultant, Qualification and Validation, Biotech
Genève, Geneva, Switzerland
Full Time
2 weeks ago
No Sponsorship
Key skills
Communication
About this role
Role Overview
- Participate in equipment qualification/validation activities
- Support quality teams in evaluating deviations, CAPAs, and change controls
- Draft qualification and validation protocols and reports (facilities, utilities, laboratories, CSV)
- Perform initial and periodic qualification/validation
- Review protocols/reports and documentation from the validation department
- Approve closure of exception records identified during execution of qualification and validation protocols
- Contribute to the site's continuous improvement
Requirements
- Minimum 6 years' experience in the pharmaceutical/biotechnology industry
- Good knowledge of cGMP standards and Good Documentation Practices
- Very good command of French and English (spoken and written)
- Excellent communication skills and ability to collaborate constructively
- Strong analytical and synthesis skills
- Autonomous, meticulous, well-organized, and able to adapt quickly
Benefits
- Technical and personal support during each assignment
- Strong career management and follow-up
- Training to develop professional skills
- Access to dedicated events
- Dynamic team