Performed key QC tasks in a rapidly changing contract manufacturing FDA EMEA certified cGMP biopharmaceutical company requiring rapid client assay transfer and implementation for simultaneous clients. Responsible for multiple projects in GMP laboratories.Performed all aspects of Quality Control including writing SOPs, excursion investigations, in-process and environmental testing, new equipment installation validation and training, client assay tech transfer and qualification, cleaning validation design and execution, contract testing lab coordination (sample shipping, data management,), technician training and supervision.Negotiated consumables and equipment cost reductions saving the company $150,000+.Key in planning and execution of large-scale validations requiring precise manpower and equipment scheduling allowing project to meet stringent time-line goals.

Managed fermentation and production QC of all fungal products. Research and development of new fungal products. Established and implemented key company functions. Streamlined and reduced cost of QC procedures by reducing analysis times and replacing costly raw materials and time-consuming operations with more efficient procedures. Quality Control and Compliance.Maintenance and preservation of stock cultures.Developed new product formulations expanding product markets.Created a rapid response customer support system by the design and administration of a $10K technical product database and establishing a customer service/ technical support department. Daily maintenance of 100+ customer accounts. Corporate support for field sales staff.Developed new filing systems, order tracking and electronic forms.Tracked and maintained product inventories of US warehouses. Negotiated purchases of raw materials and $100K sales of products.Assumed concurrent responsibility for multiple critical functions including QC, R&D, sales and customer support, production, graphics design, shipping & receiving, HazMat classification allowing Thermo Trilogy Corp. to meet it's financial, production and sales goals during the company's start-up.

Designed and ran bench and scale up of highly hazardous chemical reactions. Performed GC, HPLC and other analytical tests on lab and pilot scale samplesIsolation and screening of potential mycoherbicides and pesticides.Took over in-vivo and in-vitro QC program after unplanned loss of personnel assuring uninterrupted production schedule. Assisted in formulations and process development of fungal and phytochemical products that resulted in several new marketable products creating greater product portfolio value.