Troy Bartron Email & Phone Number

Boston, Massachusetts, United States

Waltham, Massachusetts, United States

Norristown, Pennsylvania, United States

-Project management of USP & EU GMP Clinical Trial 1 / 2 small molecule dosage form development and production-Client facing with tele-conferences, timeline design and discussion, and direct oversight / observation during experiments or GMP processes-In-house team coordination of various projects and resources (personnel, equipment, rooms)-Multiple dynamic and shifting process train development and oversight including dispensing, spray drying (Buchi / Mobile Minor scales), granulation (wet / dry, various scales), blending, compression (rotary & hand press), encapsulation (manual & automatic), capsule banding, tablet / capsule coating (various systems), multiparticulates (beads), multiparticulate coating (various systems), topicals production and dispensing (gels/creams), nasal swab production, and packaging (bottles/caps, foil bags, peelable pouches, bulk)-Characterization of in-process and finished products per USP or EU Protocols -GMP Batch Record Draft / Execution / Review / Approval & GLP experimental design and execution-GMP SOP Draft / Review / Approval & Subsequent Hands-On Training Design and Execution-Oversight and management of technicians during GMP processes or development experiments-GMP IQ/OQ/EQ Validation Drafting / Execution / Review for pharma equipment-PM Draft / Design / Execution / Review for pharma equipment-Repair and Calibration Coordination (In-House and Vendor) for pharma equipment-Equipment Logbook Upkeep and Management of On-Hold System for GMP Cleaning Verification-Raw Material Vendor Sourcing / Approval / PO / Invoice Coordination -Shipping coordination of in-process and finished products-Stability Study Draft / Review for Engineering or Clinical Trial Materials -Coordination of sampling and testing with analytical department and review of analytical data for next step decision making-Lab notebook upkeep & Reports-Proficiency with Microsoft Word, Excel, Powerpoint, Project, Visio, Teams, WebEX and Zoom

Norristown, Pennsylvania, United States

-Project management of USP & EU GMP Clinical Trial 1 / 2 small molecule dosage form development and production-Client facing with tele-conferences, timeline design and discussion, and direct oversight / observation during experiments or GMP processes-Multiple dynamic and shifting process train development and oversight including dispensing, spray drying (Buchi / Mobile Minor scales), granulation (wet / dry, various scales), blending, compression (rotary & hand press), encapsulation (manual & automatic), capsule banding, tablet / capsule coating (various systems), multiparticulates (beads), multiparticulate coating (various systems), topicals production and dispensing (gels/creams), nasal swab production, and packaging (bottles/caps, foil bags, peelable pouches, bulk)-Characterization of in-process and finished products per USP or EU Protocols -GMP Batch Record Draft / Execution / Review / Approval & GLP experimental design and execution-GMP SOP Draft / Review / Approval & Subsequent Hands-On Training Design and Execution-GMP IQ/OQ/EQ Validation Drafting / Execution / Review for pharmaceutical equipment-PM Draft / Design / Execution / Review for pharmaceutical equipment-Repair and Calibration Coordination (In-House and Vendor) for pharmaceutical equipment-Raw Material Vendor Sourcing / Approval / PO / Invoice Coordination -Shipping coordination of in-process and finished products-Stability Study Draft / Review for Engineering or Clinical Trial Materials -Coordination of sampling and testing with analytical department and review of analytical data for next step decision making-Lab notebook upkeep & Reports-Proficiency with Microsoft Word, Excel, Powerpoint, Project, Visio, Teams, WebEX and Zoom

Norristown, Pennsylvania, United States

-Execute GMP Batch Records for Cleaning, Dispensing, Manufacturing, and Packaging across various process trains and equipment related to solid oral dosage form production for USP & EU Clinical 1 / 2 Trials-Draft, Design, and Execution of GLP and Development Experiments for GMP under supervision-Characterization of In-Process and Finished Products per USP Testing-Execute PM for various pieces of pharmaceutical equipment or instrumentation-Assist Scientists and Project Managers during teleconferences providing first hand observations and data presentation-Direct client oversight during GMP or developmental processes-Small scale management of experiments including raw material acquisition, room and equipment upkeep, logbook upkeep, etc.

Hillsborough, Nj

-Organic Synthesis, Optimization, and Purification, and Characterization – γ-glutamyl-ρ-nitroaniline (HCl Salt), Phosphonazo III, ο-aminophenyl phosphate, glucose-1,6-phosphate, PEPK, γ-glutamyl-3-carboxy-4-nitroanilide, 1-methoxyphenazine-Enzymatic Substrate Syntheses and Purification and Characterization – AcNAD, SNAD, Glucose-1-Phosphate, Glucose–6-Phosphate-Enzyme Purification and Characterization – PPO, PFK, PGM, LDH, MDH-Various culturing of yeast and bacterial strains for research based around enzyme purification and metabolite synthesesBlood Test Kit Development (Enzymatic Assays) / Stability Studies-Quality Control of manufactured materials via various testing methods (HPLC - UV/VIS Spectrophotometry - KF Titrations - TLC - Enzymatic Assay - Optical Rotation)o Supervision of Assistant Scientists working on separate projects-Cleaning and Maintenance of Labware and Equipment-Lab Notebook Upkeep-Proficiency with Microsoft Word, Excel, Powerpoint etc.