Related skills
documentation gmp quality systems capa cgmp📋 Description
- Review and approve non-conformances and CAPAs for QA Operations.
- Review GMP docs: procedures, work instructions, protocols and reports.
- Provide quality support to production plants.
- Ensure Change Controls are processed on time and in compliance.
- Participate in QA check rounds.
- Establish and maintain relationships with Business and Quality partners.
🎯 Requirements
- Master's degree in chemistry/pharmaceutical sciences/bioengineering.
- Experience in chemical/pharma supply chain or QA; release responsibility a plus.
- Experience with non-conformance handling.
- Knowledge of pharma development, qualification, validation, manufacturing, packaging, labeling and release.
- Fluent in English and Dutch.
- In-depth cGMP knowledge domestic and international and ICH guidelines.
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