Qualified Person (QP )
MedPharm LtdEngland, United Kingdom
Posted November 28, 2025
Contract / Temporary
About the Company
MedPharm Ltd is a leading CDMO specializing in the development and manufacturing of topical and transepithelial therapies. With over two decades of experience, they offer comprehensive services including formulation development, clinical trial supply manufacture, and high-potency capabilities. MedPharm stands out by combining cutting-edge research with deep regulatory expertise to deliver tailored solutions that ensure patient success worldwide.
Job Description
This position is a contract/consultancy role as a Qualified Person (QP) providing QP certification, compliance oversight, and expert GMP support on an as-needed basis. The QP is responsible for ensuring compliance with EU GMP, UK Human Medicines Regulations, and clinical trial protocol requirements.
Requirements
- Batch certification and release
- Quality oversight
- Importation and QP declaration
- Audits and compliance
- Technical leadership
- Training and mentoring
- Continuous improvement
