* Developed a clinical assistant to help clinicians navigate Long COVID / ME / CFS diagnosis and treatment with a rapid turnaround* Translate customer requirements into tangible projects* Compile financials, assist with operations* Assist with fundraising* Set up CICD pipelines* Configured Kubernetes clusters

Serves as a point of contact for LIMS and scientific computing software needs for the organizationSpearheads the purchase of COTS LIMS (Laboratory Information Management Systems) platforms for multiple shared facility service labsDetermines and clarifies LIMS user requirements for multiple laboratory cores. Ensures that the needs of a diversity of stakeholders are fairly consideredBuilds, and tests prototypes of software solutionsPrioritizes multiple projects and drives them toward completionPlans and implements DevOps for complex projectsEnsures strong security of applications

Executed successful LIMS and eBR implementationsBuilt and managed highly available and fault tolerant AWS cloud infrastructurePropelled tech transfer from lab scale to production

Executed the development and implementation of multiple electronic batch record systems (eBR systems) as well as multiple LIMS and ELN systems supporting global operationsDrove tech transfer by translating lab scale documentation to GMP production SOPsCollaborated with and provided guidance to process development staff and production technicians to arrive at user requirement and functional specificationsTrained and consulted with the staff at Contract Research Organizations on the operation implemented systemsProvided general GMP training and operation support

Reviewing GMP documents form Contract Manufacturing Organizations (CMOs) and Contract Research Organizations (CROs)Overseeing contract manufacturer activities such as technology transfer, protocol development, and GMP production of APIs and finished products Troubleshooting manufacturing problemsDeveloping international regulatory filings

Developed and validated analytical methods using GC-FID, HPLC-UV/Vis, Karl Fischer, and other techniques to test the identity and purity of small molecule APIs, excipients, in-process materials, and finished productsLiaised between clients’ management, internal management, and technical staffTranslated analytical project objectives into a schedule of actions and coordinated the allocation of equipment, supplies, and staff to complete projects quickly and accurately Developed Operational Qualification (OQ) and Performance Qualification (PQ) protocolsProvided troubleshooting and guidance for junior scientists and interns by devising appropriate solutions to problems, researching literature, and collaborating with peersDeveloped sample extraction procedures to compensate for incompatibility between materials tested and USP methodsSought out novel techniques scientific journals and industry publicationsMaintained an inventory of reagents; Made purchase orders as necessaryTrained junior scientists to perform laboratory proceduresEnsured proper QC and Good Laboratory Practices were adhered toWrote and revised Standard Operating Procedures (SOPs)

Developed analytical methods:Method development with GC, HPLC, UV/VIS, Karl Fischer and other instrumentationReported and presented results to other departmentsResearched options to troubleshoot formulation problems