Providing support services to the pharmaceutical, nutraceutical, and catalyst industries including instrumentation, calibration, equipment maintenance, product development services, compaction research, process consulting, and training.

• Executed Product Development batch protocols for all processes, sampling, and internal sample testing required.• SME for Bilayer Nova development scale tablet press and DirectorPro software.• Developed Protocol for performing compression profiles and performed analysis of resulting data. • Integral part of OQ/PQ and initial operational success of Collette 150L High Shear Granulator.• Responsible for introduction, initial testing, and reporting of Multi-tip tooling for Tablet Presses.• Assisted Formulators with troubleshooting formulations from a mechanical/functional perspective.

Responsible for all duties associated with the manufacturing of final dosage forms of pharmaceuticals for R&D, Clinical Trials, Production Scale-up and Commercial Sale in a cGMP facility. Processes included: • Dispensing of API & excipients, Milling, Blending, Twin-screw Wet Granulation, Roller Compaction, Near-Infrared Spectroscopy, Particle size analysis• Tablet Compression, Dry powder encapsulation, Automated weight inspection of tablets and capsules, Coating of compressed tablets, and Optical Inspection for defects• Responsible for cleaning, assembly, disassembly, preventative maintenance, and calibration of required equipment