MedPharm Benefits Overview

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.

Maintains the pharmaceutical Quality Management System across manufacturing operations. Responsibilities include validation and qualification review, deviation and OOS investigations, CAPA and change control oversight, batch record review and release, quality risk assessments, supplier quality, internal audits, regulatory inspection readiness, SOP management, and quality trend analysis. The role collaborates with manufacturing, engineering, supply chain, warehouse, and quality control teams to ensure GMP, client, and regulatory compliance.

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.