Jobs at MedPharm

Performs analytical testing of pharmaceutical compounds, drug substances, and drug products using HPLC and GC. Supports formulation development, stability studies, drug product release, analytical method development and validation, forced degradation, solubility, compatibility, and stability experiments. Documents results according to GLP, data integrity, SOPs, and quality requirements while collaborating with R&D, QC, QA, project management, and external partners.

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.

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.