qc chemist ii resume example with 9+ years of experience

Jessica Claire
  • Montgomery Street, San Francisco, CA 94105 609 Johnson Ave., 49204, Tulsa, OK
  • H: (555) 432-1000
  • C:
  • Date of Birth:
  • India:
  • :
  • single:
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CAREER SUMMARY: I am aspired for securing an ideal position that will utilize all my relevant expertise and knowledge as an Analytical chemist. Professional Expertise Experienced in operating & trouble shooting a variety of analytical instruments. Knowledge of laboratory techniques in the preparation of solutions/reagents, analysis of in-process and finished products. Highly energetic, motivated, and committed to delivering top quality testing. Efficient and Productive in pharmaceutical test techniques like HPLC (Agilent & Waters), UV Spectroscopy (Perkin Elmer, Agilent), IC- Dionex (5000+), GC(Agilent 7890’s & 6890’s)with headspace. FTIR (with KBr pellet & ATR), Karl-Fischer titrator(Metrohm) Thin layer chromatography, Loss on drying, Particle size distribution(Malvern 2000& 3000)Osmometer(advance instrument)viscosity & density meter, colorimeter and wet chemistry as per USP/NF. Proficient in Empower3, QUMAS, Trackwise, UV ChemStation, Totalchrom Chromeleon, SAP. Knowledge of cGMP, GLP, GDP, SOP, FDA guidelines, OSHA Health & Safety guidelines. Experience in testing and handling of DEA substances. Computer skills include: MS Office, Database Entry, Internet / Email, C, C++ etc. Superb ability to work accurately and with sharp problem solving & minimal supervision. Strong ability to do repetitive work without losing concentration. Uncommon ability to work under pressure in a fast-paced environment. Create reports for different hypothetical studies and great attention to detail. Sound knowledge and understanding of instruction theory and practice. Excellent oral & written communications. Strong interpersonal and organizational skills.

Multi-talented Chemist tests inorganic and organic compounds with systematic and organized approach. Knowledgeable about analytical tests, documentation requirements and writing technical documents . Talented planner with strong attention to detail and more than 7 years of related experience.

  • UV spectroscopy
  • UPLC
  • GC-FID
  • HPLC
  • Microsoft - Excel, word, outlook, PowerPoint
  • MRP
  • C , C++
  • Quality Control
  • Receiving, inventory control
  • SOP
  • Specification
  • Validation
  • Detailed oriented
  • Analytical chemistry
  • Self motivated
  • Wet chemistry
  • Chemistry expertise
  • QA and QC processes
  • Organic chemistry
  • Physics and chemistry knowledge
  • Expert in chemistry
QC Chemist II, 04/2016 - 07/2020
Apex Systems Malvern, PA,
  • Analytical chemical testing as per in-house specification & methods including Content uniformity, Blend Uniformity, Identification test by TLC, Infrared spectroscopy & colorimeter, disintegration, Dissolution for IR & for ER using Distek autosampler, Bulk density, tapped density, Particle size analysis by Malvern& ATM sonic shifter, LOD by Computrac, friability, hardness, Osmolality, Assay, chemical purity Residual solvent analysis, Related compound analysis for the finished product.
  • Performed GMP drug product/substance release/stability testing using various techniques like Ultra Performance Liquid Chromatography (UPLC), Hi-Performance Liquid Chromatography (HPLC) with PDA, UV, RI, Conductivity detectors, Gas Chromatography(GC)by using headspace.
  • Performed testing for Inprocess samples, Hold time study samples as per process validation protocol.
  • Generate & maintain detailed records/ documents in compliance with SOPs.
  • Maintained laboratory with good housekeeping practices using 5s & in compliance with cGMP.
  • Provided general laboratory support such as testing for equipment cleaning verification.
  • Tested Quality Control Stability Samples as per in-house specifications & test requests.
  • Evaluated test results and decide on the acceptability of the samples based on the test results.
  • Performed supporting analysis for OOT, OOS & atypical results.
  • Initiated & wrote Laboratory Incident as per in-house SOP through track wise.
  • Well experienced in testing for solid doses like tablets, capsules, powder for oral solutions, oral suspension, topical powder, otic solution as per specifications.
  • Provided guidance to lab technicians & junior chemists for routine analysis.
  • Detected abnormality during the performance of a test by the hypothetical study.
  • Analyzed samples submitted for testing and reported results.
R & D Chemist, 12/2014 - 03/2016
Sherwin-Williams Kailua Kona, HI,
  • Provided Assistance in Analytical method development and validation for drug substances, drug products, and excipients; stability and release testing; testing to support pharmaceutical development efforts.
  • Sample analysis like Assay, Related compounds, Residual solvents analysis, dissolution, and water content for stability samples and Release samples & EB batches filed to FDA.
  • Assisted in supporting the response for FDA deficiency.
  • Worked on dissolution studies - dissolution profile by using USP I & II apparatuses, Bio dissolutions(USP apparatus III) Analyzed Hold time study samples as per protocol.
  • Executed analytical method validation (Accuracy, Linearity, Method precision, specificity, QL, Forced degradations) for different products as per validation protocol.
  • Provided required test results for pilot batches.
QC Chemist, 07/2013 - 11/2014
Adare Pharma Solutions Vandalia, OH,
  • Operated various technical laboratory instruments such as pH meter, Hardness tester, Friability tester, Karl Fisher auto-titrator, UV spectrometer, Disintegration tester, Dissolution apparatus.
  • Analytical testing of finished products by following cGMP & SOP.
  • Removal of samples from the lab after completion of testing through the proper system as per SOP.
  • Performed laboratory procedures in accordance with approved procedures and methods remained current with and complied fully with cGMP, SOP and test procedure Conducted calibration of the laboratory equipment like balance, PH meter, KFT, conductivity meter.
  • Conducted wet chemistry- physical testing as per USP/NF, EP.
  • Gained experience with cGMP compliance & laboratory regulatory.
  • Reviewed Documents for Quality Assurance during the process and before the batch release.
  • Analyzed finished & stability samples for Assay, Related compounds, dissolution using USP Apparatus I & II, water content LOD, Disintegration for stability samples.
Material coordinator, 01/2011 - 07/2013
Iconma, L.L.C. De Pere, WI,
  • Using the MRP system (Man Ex) verify all incoming materials from Receiving.
  • Completed kits (ready for production) will be staged in a secure staging area on the production floor.
  • If any discrepancy for any part found & identify the root cause for the discrepancy.
  • During production or testing the floor needs any replacement or missing parts, shortages shall be provided, and adjusting the MRP system.
  • Unused parts from return kits shall be verified & placed in the proper location in the stockroom.
Education and Training
Bachelor of Education: , Expected in 1999
MS University of Vadodara - , Gujarat
Status -
Master of Science: Organic Chemistry, Expected in 1997
MS University of Vadodara - , Gujarat
Status -
Bachelor: Science (Chemistry), Expected in 1995
MS University Vadodara - , Gujarat
Status -
Activities and Honors

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Resume Overview

School Attended

  • MS University of Vadodara
  • MS University of Vadodara
  • MS University Vadodara

Job Titles Held:

  • QC Chemist II
  • R & D Chemist
  • QC Chemist
  • Material coordinator


  • Bachelor of Education
  • Master of Science
  • Bachelor

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