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.

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.

Lead client-facing CDMO programs by coordinating internal teams, managing schedules and budgets, mitigating risks, driving scope changes, and maintaining client records to ensure on-time, compliant delivery and high client satisfaction.

Lead all cGMP manufacturing operations for a CDMO site, ensuring safe, compliant, and efficient production. Develop manufacturing strategy, drive operational excellence, manage budgets and KPIs, partner cross-functionally (Quality, MS&T, Engineering, Supply Chain), support regulatory inspections, and build high-performing teams to meet client delivery, quality, and cost objectives.

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.

Provide strategic and operational leadership for Quality Control and Analytical Development labs. Implement cGMP methodologies, oversee analytical method development/validation and QC operations (in-process, release, stability, microbiology, environmental monitoring), manage CROs, ensure audit and regulatory inspection readiness, lead people and budgets, manage technology transfers, and support 24/7 manufacturing and cross-functional collaboration.

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.