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Click here or scroll down to respond to this candidateCandidate's Name
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CO: PHONE NUMBER AVAILABLE- EMAIL AVAILABLEOBJECTIVE : Looking For a challenging position in the Pharmaceutical industry with strong background in formulation analytical research and development. EDUCATION :Uka Tarsadia University, Bardoli, Gujarat, India 2013-2015 Master of Science (Pharmaceutical chemistry), 8.50 CGPA Veer Narmad South Gujarat University, Surat, Gujarat, India 2009-2012 Bachelor of Science (Biotechnology)US Equivalent Master and bachelors degree and Certification, Evaluated from WORLD EDUCATION SERVICES (WES)NJDOH Jan_2023-currentMedical technologist:Receiving area: Receiving mailers, scanning the mails, mails in envelope. check the specimens with quality, birth date, sample date, sample time, birth weight, cutoff date should not >14 days of samples submission date, unsaturation for initials also works on repeats, apply 1st and 2nd barcode and separate the top copy. punch the specimens for initial, unsaturation and repeats. daily tally, count the kits, work on tray keys, make a space for the kit, filling the kits, Filling IEM-3, make a box for kit and give accession number of start to end, year and month, box number on the box. Daily and weekly maintenances of punching machines, clean the machines, Weekly flush the eye wash, clean bench space Data entry for a top copyMS LAB: Record the temperature for trines freeze, humidity of lab, take nitrogen and argon reading, refill wash solvent and flow solvent. punching retest if needed, take out EWS, controls, reverse pipette training, place transfer plate and punching plate on their location, punching controls and CDCS. Make EWS, IS standard, wash the cone. print the barcodes for diet management, work on diet management-check birth date, quality, >14 days of unsaturation specimen, gender, make a call if needed rinse the pipette before using it and open the file which are going to use for transferring the samples. create, import, and print a worksheet by the instrument, check the repeats if anything is missing while punching. daily maintenance of instruments such as jack, Phryne, and Simon CMIC CMO USA Corporation Jun 2021-dec 2022CHEMIST: Perform test such as disintegration, average tablet weight, appearance, conductivity testing, ROI, TOC, TOC M9, IR by lab solution, UV by 800 Beckman coulter, environmental monitoring, dissolution, data trading for water & EM, retain sample management. Performed Instruments Calibration and Performance Verification on Analytical Balance & Ph meter. Preparing Media and standards. Collecting water sample for micro testing.Austar Pharma Jan 2021- Jun 2021(contract)LAB TECHNICIAN: Perform Test Such as T.O.C. (Total Organic Carbon), water Testing, Dissolution, KF Titration, IR, Bulk & Tap Density, Ph Meter and Sieve analysis. Perform conductivity testing for water. Performed Instruments Calibration and Performance Verification on Analytical Balance & Ph meter. Preparing Media and standards. Prepare Purchase order for laboratory chemicals. Followed Good Documentation Practices and Good Laboratory Practice for all above testing. General QA Standard Work, Included In routine QC work including Batch Release.Cromak Research Inc, Somerset, NJ March 2020- Jan 2021 (Contract, Part Time) Chemist Analysis of Pharmaceutical products, Raw Materials By USP, NF & In-House test Method Using HPLC, (EMPOWER), GC, TLC, UV, IR And Wet Chemical Technique. Conduct Dissolution Testing OF Solid Dosage Forms. Calibrate & Maintain Laboratory Equipment, ensure compliance with CGMP and perform troubleshooting. Execution of Test Method Development and Method validations by utilizing USP<1225> to Established Performance and Limitations. Review Batch Records and Other applicable Documents and enter result in LIMS data on timely Manner.Jan 2019 to Dec 2019 on Maternity LeaveRELEVANT EXPERIENCE:Raritan pharmaceutical, East Brunswick, NJ July 2017 -2018 November Quality Assurance Performing in-process quality assurance checks for tablets, capsule, and liquid orals. Issuing line clearance at every step of batch manufacturing. Maintaining and updating the Batch Manufacturing Records. Documentation of logbooks, calibration records, temperature, and humidity records. Identify, rectify and report errors in a timely manner. Train and educate new fellow technicians on relevant procedures. Proficient with laboratory Standard Operating Procedures, Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP). Ability to work cross-functionally in a team environment as well as independently as required Manage multiple projects. Physical Evaluation of drug products such as but not limited to : Torque test, Leakage, Fill Weight etc. In Process inspection of drug products during filling and packaging Operation for correct product strength, Lot, Expiration date etc. Collecting and testing cleaning samples and assisting with cleaning validation Verify the raw materials/incoming components are in the right status in JDE and physical location. Perform shop floor QA Activities.Dunkin Donuts, East Windsor, NJ August 2015-july 2017 Accepting payments from customers and made changes as necessary. Cleaning and preparing various foods for cooking and serving. Checking the quality and quantity of the received products. Storing clean equipments and utensils. Helping co-worker.Macleods Pharmaceuticals Ltd, Daman, IndiaAnalytical Chemist Jan 2015 - May 2015 Conducted GC, Dissolution, Conductivity, Potentiometric, KF Titrations, and UV analysis on finished products. Conduct routine operation of raw material, in-process material and finished products according to approved SOPs using analytical techniques. Performed Wet Chemistry analysis including Titrations and pH, color and moisture testing. Hands on Experience with basic lab instrumentation skills like Viscometer, pH Meter. SKILLS:Computer Skills: Proficient with the use of Microsoft Word, Excel, PowerPoint, |
