Draft technical documents such as SOPs, proposals, presentations, batch records, protocols, reports, deviations, investigations, and regulatory submission documents, and maintain high-quality laboratory documentation in line with regulatory guidance and site SOPs. This includes literature search, pre-formulation, excipient selection, formulation design, hands-on laboratory development, troubleshooting, process scale-up and optimization, exhibit and clinical batch manufacture, technology transfer, process validation, and commercial launch.