Tarak Dave

Tarak Dave Email and Phone Number

Quality Control Supervisor @ Aavis Pharmaceuticals
Tarak Dave's Location
Hoschton, Georgia, United States, United States
Tarak Dave's Contact Details

Tarak Dave personal email

n/a
About Tarak Dave

Introducing myself highly skilled, organized and motivated QA/QC/R&D professional with progressive experience in Pharmaceutical, Health care, Biotech and agrochemicals industries with extensive experience in analytical techniques, instrumentation and documentation focusing on generics, branded generics product development, Antibiotic, Enzymes and QC Release. Expertise in Chromatography, Spectroscopy, organic synthesis reactions, wet Chemistry. Focus on time management and problem solving ability. Excellent analytical skills combined with well-developed communication and multitasking skills. Able to accept challenges and consistently met tight deadlines manage with quality multiple projects, working independently as well as cooperatively in a team. Strengths include interpersonal, organizational and problem solving skills. Proven track record of improving quality systems, teamwork skills and ensuring productivity targets are met. Technical proficiency in HPLC, GC, IR, Particle Size Analyser, Auto Clave, Empower, Chemstation and LIMS software.

Tarak Dave's Current Company Details
Aavis Pharmaceuticals

Aavis Pharmaceuticals

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Quality Control Supervisor
Tarak Dave Work Experience Details
  • Aavis Pharmaceuticals
    Quality Control Laboratory Supervisor
    Aavis Pharmaceuticals Nov 2022 - Present
    Hoschton, Georgia, Us
  • Modavar Pharmaceuticals Llc
    Sr Analytical Chemist
    Modavar Pharmaceuticals Llc Jul 2020 - Nov 2022
  • Granules Pharma Inc
    Sr Qc Chemist
    Granules Pharma Inc Apr 2019 - Jul 2020
  • Pii (Pharmaceutics International, Inc.).
    Sr Chemist
    Pii (Pharmaceutics International, Inc.). Oct 2017 - Apr 2019
    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
  • Apotex Inc.
    Analytical Method Development And Lab Automation Chemist
    Apotex Inc. Jul 2016 - Oct 2017
    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)
  • Apotex Inc.
    R&D Chemist -Product Evaluation & Product Optimization
    Apotex Inc. Jun 2013 - Jul 2016
    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.
  • Apotex Inc.
    Ad & Cleaning Validation
    Apotex Inc. Jul 2011 - Jun 2013
    Toronto, Ontario, Ca
    Develop and validate analytical methods for drug substance, drug product and residual swabs
  • Apotex Inc.
    Dissolution Development Chemist
    Apotex Inc. Jul 2010 - Jul 2011
    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
  • Cobalt Pharmaceuticals ( Allergan Group Of Company )
    Sr Qc Chemist
    Cobalt Pharmaceuticals ( Allergan Group Of Company ) Oct 2003 - Jul 2010
    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.
  • Torrent Pharma Inc.
    Api Analytical Chemist
    Torrent Pharma Inc. Sep 1997 - Jun 2002
    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)
  • United Phosphorous Limited
    Research Chemist (Organic Synthesis)
    United Phosphorous Limited Oct 1994 - Sep 1997
    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.
  • Consolidated Petrotech Inc
    Trainee Chemist
    Consolidated Petrotech Inc Sep 1993 - Aug 1994

Tarak Dave Skills

Hplc Dissolution Lims Cleaning Validation Gas Chromatography R&d Analytical Chemistry Gmp Glp Uv Ir Quality Control Laboratory Wet Chemistry Titration Sop Change Control Uv/vis Validation Lc Ms Chemstation Formulation Chromatography Pharmaceutics Chemistry Karl Fisher Ir Spectroscopy Empower Usp Ftir Spectrophotometry Raw Materials Regulatory Affairs Quality System Method Development Gc Fid Tpw3 Automation Particle Size Analysis Trackwise Capa V&v Tlc Technology Transfer Organic Synthesis Fda 21 Cfr Part 11 Gxp Anda Dissolution Method Development Updating Uplc Ms Operations

Tarak Dave Education Details

  • Ms University
    Ms University
    Organic Chemistry

Frequently Asked Questions about Tarak Dave

What company does Tarak Dave work for?

Tarak Dave works for Aavis Pharmaceuticals

What is Tarak Dave's role at the current company?

Tarak Dave's current role is Quality Control Supervisor.

What is Tarak Dave's email address?

Tarak Dave's email address is ta****@****o.co.in

What schools did Tarak Dave attend?

Tarak Dave attended Ms University.

What skills is Tarak Dave known for?

Tarak Dave has skills like Hplc, Dissolution, Lims, Cleaning Validation, Gas Chromatography, R&d, Analytical Chemistry, Gmp, Glp, Uv, Ir, Quality Control.

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