PDA is updating Technical Report 56 on Phase-Appropriate GMPs and Quality Systems. We are seeking individuals with expertise in this area, and specifically those with expertise in phase-appropriate GMPs and Quality Systems for the development of advanced therapies/cell & gene therapies, vaccines, and products undergoing accelerated approval processes.
Note: This is a "Members Only" opportunity.
Please send your CV to [email protected]. For additional information or questions, do contact [email protected].
- Project Management
- Technical Writing/Editing
- Process Engineering
- Quality & Compliance
- ATMP/Gene and Cell Therapy