- GMP production of crucial enzymes through bacterial fermentation in a bench-top scale bioreactor, including sample preparation and SDS-PAGE analysis of product conformity.- Upstream and downstream oligonucleotide production using Mermade and AKTA synthesizer including reagent preparation, synthesis, and subsequent characterization and purification of product. - Process development, data analysis, and troubleshooting for increased product yields in enzyme production. - GMP documentation reviewing, editing, and creation.

- AGC Biologics is an international CDMO responsible for manufacturing of GMP regulated active pharmaceutical ingredients. - Large scale (3,000L) mammalian cell culture in up to ISO 5 cleanrooms.- Stainless steel and single-use systems.- Operation and maintenance of sensitive analytical equipment.

- Aspire Health Science is an FDA registered, cGMP compliant cellular therapy research and manufacturing laboratory.- Extensive experience in manufacturing tissue-based cellular therapies in an ISO-6 cleanroom, BSL-2 environment according to standard operating protocols.- Production of cellular therapies for FDA and Health Canada approved clinical trials.- Responsible for authoring and optimizing new production operation protocols.- As inventory manager, responsible for tracking and ordering supplies under cGMP guidelines.- One of three authors in writing a production batch record for a cellular therapy accepted by the FDA as an Investigational New Drug (IND) for the treatment of COVID-19 induced pneumonia. - Gained experience in protein purification, ELISA, flow cytometry, reagent preparation, cell culture maintenance, troubleshooting lab equipment, and other laboratory skills.

-Built and maintained business relationships with 15 grocery chain locations generating over $5 million in yearly sales.-Through sales tactics and reliable service, achieved a 4% increase in yearly sales despite a shrinking market.

-Wrote stability reports for stability studies on novel drugs for submission to the FDA. -More than doubled the amount of stability reports completed by my predecessor.-Facilitated communication between different departments for the gathering of relevant data for accurate completion of these reports.-Shadowed laboratory scientists in the regenerative therapy and small-molecule drug development labs.