Cleaning Validation Analyst
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Our client, a leading pharmaceutical organization, is seeking a Cleaning Validation Analyst to manage the planning, execution, and reporting of validation studies. This role supports both operational and project teams by ensuring the effectiveness and compliance of cleaning processes for drug products.
Responsibilities
- Draft protocols and reports for cleaning validation and risk assessment studies.
- Schedule and execute routine cleaning qualification studies.
- Analyze results to ensure adherence to operational standards.
- Assist with the practical preparation and reporting of validation for planned product and process changes.
- Investigate quality issues and contribute to lifecycle management.
- Monitor cleaning processes proactively to ensure ongoing effectiveness and compliance.
Requirements
- Bachelor's degree in industrial pharmacy, bio-engineering, or a related engineering field.
- 1+ years of experience in Cleaning Validation within a GMP environment.
- You bring proficiency in technical writing and PC software applications.
- You have strong problem-solving abilities and an organized, accurate working style.
- You are fluent in Dutch and English.
Nice to Haves
- Willingness to work in a shift system.
- Experience with risk assessments and deviation management.
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