Tarak Dave Email & Phone Number

Hoschton, Georgia, Us

Hunt Valley, Maryland, Us

Perform Method validation and method Transfer to execute protocol.Official Trainer and mentoring juniors on analytical skills.Investigate OOS results and write LIR.Plan schedule and generates reports for API release

Toronto, Ontario, Ca

Develop and validate analytical methods for drug substance, drug product and residual swabs (e.g. related compounds, assay, dissolution, residual solvents, impurities, etc.)Design and execute laboratory experiments and interpret analytical data. Perform routine analytical testing for new product development using instruments such as HPLC, GC, UPLC, Dissolution, Particle Size, and KF titrate. Prepare SOPs, method of analysis and design development, release and stability specification.Execute and Review method of analysis, Validation protocols, development report, and create change control as per SOP on timely manner..Method development on Tablet Processing Workstation (TPW)

Toronto, Ontario, Ca

Perform routine analytical tests of pharmaceutical raw materials, in-process samples, finished products, and stability samples include Assay, CU, BU, Degradation product, Dissolution ,Residual solvent, Prepare and determine laboratory investigations and write reports Troubleshoot laboratory equipment and methods. Responsible for the timely execution of lab analysis and related documentation.

Toronto, Ontario, Ca

Develop and validate analytical methods for drug substance, drug product and residual swabs

Toronto, Ontario, Ca

Develop dissolution tests methods on new product formulations and compare with brand product. Accountable for Method verification and validation of drug products dissolutionDocument and interprets all tests, calculations and observations and completes report summaries. Performs additional related duties, as assigned, in accordance with job responsibilities and necessary departmental objectives

Accountable for the analysis of raw materials, in-process samples, finished products and stability samples as per USP and In-house method ( e.g., Assay, RC, CU, BU, Dissolution, water content, residual solvent, wet chemistry). Actively participates in the development of QC Chemists (train, mentor, and guide).Initiate and investigate the Out-of-Specifications and Analytical Deviations of QC lab investigations.Experience in handling , troubleshooting and maintaining analytical instruments to include: HPLC, Dissolution, GC, IR, UV, AAS, DSC, TGA, Malvern particle size, etc. Ensure that products are being test strictly under cGMP conditions and disposition is taken on time as per the committed production plan for every month (C of A, ) and or procedural requirements. Prepare test solutions, compounds, and reagents for laboratory personnel. Legibly document the data and report the results associated with each analysis.Diligently follow written laboratory protocols, guidelines, procedures and methodsManage with quality multiple projects and tight timelines.

Basking Ridge, Nj, Us

Conduct testing of API, Finished Product, process validation , Fermentation ,cleaning validation samples, enzymes and antibiotics testing and stability samples using an advanced analytical techniques.Performs review of lab notebooks, analytical data, and analytical reports.Assists in preparing technical documentation including test reports, OOS and analytical test procedures.Develop antibiotics products using enzymes routes of reaction such as Amoxicillin, cefadroxil,, cephalexin, Ampicillin Perform Test for Purified Water and Waste water treatment samples ( TOC, COD, BOD)

Develop agrochemical products ( phosgenation method to Isocynates)Develop Chlorprofam Active intermediate pharmaceutical ingredients via Isocynate.Experience of Pilot batch scale up to plant commissioning of Isocynate, chlorprofam as an R&D feed back to set up commercial product.