www.jet3dscan.comAt Jet 3D scan we are innovative, passionate and determined to unveil the path of 3D arena with endless opportunities. We provide service in area of 3D scanning, Reverse Engineering, Product development, 3D Printing, Engineering solutions such as product inspections and much more that enable clients to achieve desired outcomes.

Quesada Burritos and Tacos

• Handle OTC and NHP – raw material, bulk products and finished products on daily basis• Manage test sample database – login sample, evaluate test level, assign testing and compile documents for release for in-house manufactured bulks, finished products, purchased bulks and raw materials • Manage manufacturer database to assign testing requirements for raw materials, purchased bulks and finished products to adhere GMP guidelines • Update manufacturer database to associate vendor and manufacturer information • Coordinate with contract testing laboratories to establish Quality Agreement and Non-disclosure agreement• Compile Health Canada license (DEL), lab certifications, precursor license, narcotic license to put in file for records • Participated in Health Canada audit as scribe and review documents prior to providing them to auditor• Organize and maintain batch records and QC raw material retain samples• Initiate, recommend and follow up of CCR (change control request), MCR (New material qualification), PNCR (non-conformance report) and SOR (deviation)• Effectively manage contract laboratory testing, QA review and release of OTC/NHP samples• Liaise OOS investigation and data integrity queries to contract testing laboratories• Managed analytical method transfer and verification project to contract testing laboratories • Handle stability sample for testing according to sample pull time point• Reduced backlog of test orders by streamlining test sample database

• Carry out bench scale batches to characterize and optimize process for 3 semisolid products (ointment, paste and cream) and two liquid products• Improved process by suggesting a different sequence of adding components• Completed batch records as per instructions• Developed a bench scale operation for experimental batches

• Prepared liquid dosage form to analyze turbidity of preparation • Performed quality control tests for liquid preparations and analyzed data for same

• Received hands-on training on in-process and finished products testing in a cGMP environment• Engaged in Analytical Method Development for the API Quality Analysis• Sampling of raw materials, in-process sampling and finished product • Completed documentation including data entry and laboratory log books• Hands on training K-F Titrator, UV/VIS Spectrophotometer, HPLC, GC, 1H NMR and 31 P NMREarned trainer’s recommendation as an Quality Control Analyst