Teams at MedPharm

Provide QA support for IMP manufacturing and Quality Management Systems to ensure GMP/GCP/GLP compliance. Manage QMS records (deviations, CAPAs, change controls), review and approve controlled documents in eQMS, perform QA oversight of manufacturing and laboratory activities, support audits/inspections, supplier qualification, data integrity, training, archiving, and continuous improvement across cross-functional teams.

Lead and oversee formulation development studies: prepare and amend study plans, protocols, reports and updates; communicate progress and deviations to Project Management and stakeholders; review study data with scientists; perform literature review and maintain subject-matter knowledge.

Perform analytical testing (HPLC, GC) to support pharmaceutical R&D, including method development, validation per ICH/FDA, data analysis in Empower, GLP-compliant documentation, cross-team collaboration, lab maintenance, and adherence to health and safety/COSHH requirements.