QC Validation Scientist
QC Validation Scientist
Location: Geneva Area
Workload: 100%
Start Date: ASAP
Contract Duration: Until 31.08.2027
In this role, you'll lead analytical and validation activities to ensure compliance with pharmaceutical quality standards.
Ideal for an experienced scientist with a strong background in raw material analysis, process validation, and regulatory documentation.
Key Responsibilities
- Conduct risk analysis and assessments of raw materials
- Verify and evaluate pharmacopoeial methods across various standards
- Lead analytical method and cleaning validation activities
- Prepare and review transfer/validation protocols and reports
- Provide accurate analytical data aligned with SOPs and regulatory requirements
- Implement and maintain quality systems within the laboratory
- Manage deviations, change controls, CAPAs, and complex technical issues
- Plan and execute full product transfer activities from raw materials to finished products
- Provide technical support to lab technicians and critically assess transferred methods
- Drive continuous improvement initiatives and support strategic lab projects
Your Profile
- Master's degree in Chemistry or equivalent
- Minimum 4 years of experience in pharmaceutical QC/validation
- Strong expertise in raw materials and chemical analysis (e.g., HPLC)
- Fluent in French; English at B2 level or higher
- Proficient in SAP, LIMS, and Empower
- Autonomous, proactive, and quality-focused
For further information, please apply with your CV.
Please note: Only candidates with the right to work in Switzerland can be considered (e.g., EU citizens or holders of a valid Swiss work permit).
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