MedPharm Benefits Overview

Perform calibration, preventative and corrective maintenance, testing, troubleshooting, and repair of laboratory and GMP manufacturing instrumentation. Maintain logs and CMMS records, write OOTs and deviations, support IQ/OQ/PQ activities, coordinate with validations, quality, R&D and contractors, and ensure instrumentation fitness and compliance across GMP and non-GMP sites.

Develop and validate GMP-compliant analytical methods (HPLC/GC) to support formulation development. Perform stability and forced degradation studies, troubleshoot instruments, author validation and technical reports, mentor junior scientists, and collaborate with QC/QA and formulation teams while maintaining GMP lab practices.

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.