Key Accountabilities:
- Become familiar with MoonLake's products, technical agreements, regulatory dossiers and subcontracted manufacturing supply chain
- Maintain awareness of international GMP compliance requirements for Investigational Medicinal Products, Biotech API and drug product manufacture including the GCP interface
- Become familiar with MoonLake's quality systems (contributing to their maintenance and ongoing improvement)
- Ensure GXP compliance of contractors for API manufacture and testing, taking responsibility for QA contact with CMO/CTO on set-up, deviations and change assessment and batch review
- Provide advice on GMP to client groups within MoonLake, providing necessary oversight to ensure compliance
- Become familiar with MoonLake's drug product manufacture and packed stock release procedures and ensure QPs are made aware of any compliance issues which could impact upon the safety of MoonLake's clinical products
- Provide QA support to validation activities at CMOs/CTOs
- Undertake other quality assurance duties as required
