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Recently posted jobs
Biotech • Pharmaceutical
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.
Biotech • Pharmaceutical
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.
Biotech • Pharmaceutical
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.
Biotech • Pharmaceutical
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.
Biotech • Pharmaceutical
Manage and maintain Smartsheet timelines and resources across projects, oversee procurement, logistics, and warehouse operations at Stirrup Creek, support Smartsheet administration and reporting, resolve resource conflicts, and produce management reports and KPIs.
Biotech • Pharmaceutical
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.
Biotech • Pharmaceutical
Lead and execute client programs across CDMO services, serve as primary client liaison, manage project timelines, budgets, risks, and change orders, maintain project records in Salesforce/Smartsheet, mentor junior PMs, and drive process improvements to ensure on-time, compliant delivery.
Biotech • Pharmaceutical
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.



