Jobs at MedPharm

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.

Lead and oversee formulation development studies: prepare and amend study plans, protocols, reports and updates; communicate progress and deviations to Project Management and stakeholders; review study data with scientists; perform literature review and maintain subject-matter knowledge.

Lead and provide scientific and regulatory oversight for preclinical in vitro studies (IVRT, IVPT, research biology). Draft study plans, review reports, ensure protocol compliance and data integrity, liaise with sponsors, contribute to SOPs, and support process improvements and training.

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.

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.