MedPharm Benefits Overview

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.

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.

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.