Quality Control Chemist Resume Samples

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Quality Control Chemists use chemistry lab skills to assess the quality of products made in a manufacturing unit. Common duties seen on a Quality Control Chemist resume sample are collecting samples for tests, checking if substances meet standards, preparing reports, operating specialized equipment, and ensuring safety at the workplace. The ideal candidate should showcase in his or her resume lab skills, attention to safety, an eye for details, effective communication, and teamwork. A Bachelor’s Degree in chemistry or a similar field is required for this position.

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1

Quality Control Chemist

Developed and improved formulas, processes, and analytical methods which helped increase efficiencies in batch time and attained substantial cost savings ($000s) due to reduction of errors.

  • Performed process improvement on analytical methods and procedures to streamline efforts and reduce preparation time.
  • Executed quality control to ensure specifications of the customer were always maintained.
  • Conducted out-of-specification investigations and recommend corrective actions.
  • Administered routine analyses of in-process materials, environmental samples, finished goods, and stability samples.
  • Calibrated, validated, and maintained laboratory equipment.
  • Developed and reviewed SOPs.
Candidate Info
2
years in
workforce
2
years
at this job
BS
Biochemistry
MA
Business Leadership, Marketing Research, Marketing
2

Quality Control Chemist

Provide productive and analytical data for routine samples to meet standard and non-routine samples to support continuous improvement activities.

  • Prepared and tested samples with established procedures using various analytical instruments (ICP, XRD, pH, ISP, Conductivity, Balance, and etc.) to keep manufacturing activity
  • Prepared and tested samples with developing procedures to support continuous improvement of product quality
  • Calibrated and maintained instruments in compliant working status which produced reliable data efficiently.
  • Worked at off shift schedule and overtime whenever needed which supported high volume manufacturing activities
  • Finished lean project and made recommendations on improving analytical procedures
  • Performed other duties as assigned
Candidate Info
12
years in
workforce
3
years
at this job
BS
Chemical Engineering
MS
Chemical Engineering
MS
Biosystems Engineering
3

Quality Control Chemist

Kelly Scientific Resources contractor hired to permanent employee

  • Independently performed testing for all areas of the lab: API, In-Process, Final Product, TSR's, Validations, Investigations, and Controlled Substances II & IV
  • Site SME for Flame AA and GFAA. Exclusively responsible for entire test load for 2 years before training 5 additional analysts to run testing
  • Worked with contracted specialist to design a comprehensive AA/GFAA training course, presentation, and technical qualification
  • Sole analyst on a five person team involved in a Tobramycin API Aluminum content investigation that eventually led to the discovery of a miscalculation on suppliers behalf resulting in contaminated product never reaching the market
  • Maintained professional customer relationship with AirGas and PerkinElmer to safely and optimally run and preserve instruments
Candidate Info
15
years in
workforce
6
years
at this job
BS
Chemistry
4

Cleaning Validation Quality Control Chemist

Performed cleaning validation using analytical techniques for testing and release of equipment

  • Communicated and orchestrated testing of manufacturing equipment to support production schedule
  • Performed method validation and Cleaning Validation Analytical Summary Report
  • Reviewed results for accuracy and resolved technical issues in consultation with management
  • Provided input on generated SOP's and methods
  • Actively participated in investigation process to find sources of error (root cause) and derived preventive/corrective actions
Candidate Info
9
years in
workforce
2
years
at this job
BS
Chemistry
MS
Chemistry
5

Quality Control Chemist

Analyzed the samples from R&D for purity and stability for further use of the in-process and finished pharmaceutical products

  • Analyzed the solvents obtained from production department of association companies for purity
  • Tested purity using chromatographic techniques and moisture content, density, loss on drying, titration using calibrated volumetric apparatus, Ph and melting point detection
  • Documented quality control reports for the sample with detailed summary of the experiments conducted for approval or rejection useful for further analysis
  • Assisted the supervisors with HPLC and GC for obtaining chromatograms to report percentage purity
Candidate Info
1
year in
workforce
1
year
at this job
BA
Bachelor of Arts
MA
Chemistry
Research Assistant
6

Quality Control Chemist II

Analyzed pharmaceutical component chemicals, in-process materials, finished products, and stability products for active ingredients, degradants, and preservatives in support of Alcon's quality program which is FDA and EPA regulated

  • Performed quantitative and/or qualitative tests using HPLC, GC Headspace, Karl Fischer, Hiac, Microtrac, and UV-Vis spectrometry instrumentation via existing procedures
  • Interpreted and evaluated data, spectra, and chromatograms in terms of accuracy and precision in compliance with internal SOP's and reported on deviations from specified requirements
  • Carried out re-tests and troubleshooting when necessary with controls in order to establish accurate results
  • Performed method transfers and validations from other Novartis companies
  • Recorded test data, calculated statistical information, and reviewed and approved co-workers test data
Candidate Info
18
years in
workforce
5
years
at this job
BS
Chemistry
7

Quality Control Chemist

Conducted laboratory testing in FDA regulated environment in accordance with GMP.

  • Set up laboratory equipment and instrumentation for required tests.
  • Performed troubleshooting, repairs and calibration of laboratory equipment.
  • Performed analyses using USP/NF monographs.
  • Conducted drug purity assays using HPLC, UV/VIS and IR spectrometry, and wet chemistry.
  • Documented all laboratory testing and activities in accordance with GMP documentation practices.
  • Collaborated with members of other departments in order to collect, organize and report data for Statistical Process Control studies.
  • Created detailed reports and graphs using Microsoft Word and Excel.
Candidate Info
5
years in
workforce
4
years
at this job
AAS
Chemical Technology
BS
Industrial Technology Concentration Bioprocess Manufacturing
8

Quality Control Chemist II

Supported the quality control stability group in generating GMP data on stability samples including intermediates, drug substance, and drug products including UV/Vis, SDS-PAGE, Densitometry, and both a cuvette and 96-well potency analysis as needed.

  • Assisted in the transfer, qualification and validation of any GMP required test methods.
  • Reviewed and approved GMP data generated by QC analysts for accuracy and completeness.
  • Operated/Troubleshot LS 55 Luminescence Spectrometer and Spectramax instrumentation to determine potency on intermediates, drug substance, and drug products.
Candidate Info
6
years in
workforce
7
months
at this job
BS
Biomedical Engineering
JD
Law, Public Health Law
9

Quality Control Chemist

To quantitatively analyze biological samples for the determination of active compounds and their metabolites from pharmacokinetic studies by LC/LC/MS/MS

  • To quantitatively analyze manufactured drug product samples to determine the levels of various active components by LC/LC/MS/MS in a GMP environment
  • To review data produced by coworkers and laboratory notebooks to meet and maintain quality control standards
  • To design templates for data calculation following analysis of GLP and GMP samples
  • Utilized and maintained API 4000, API 4000 QTrap and API 5000 instruments performing basic maintenance and method development as well as routine analysis of samples
Candidate Info
17
years in
workforce
1
year
at this job
BS
Chemistry
MS
Biomedical Basic Sciences
10

Quality Control Chemist

Performed testing on raw material, in-process, and finished products according to STM and United States Pharmacopeial (USP) in a GMP and GLP environment.

  • Examples of tests performed: Assay, Impurity, Dissolution, Hardness, LOD, Residue on Ignition, Heavy Metals, Particle Size, IR, etc..
  • Maintained and calibrated laboratory instruments (ex: HPLC, Dissolution Tester, UV, GC, etc.)
  • Wrote & executed IQ/OQ/PQ to retrospectively qualify laboratory instruments (ex: Oven, Hardness Tester, Friabilator, Stability Chamber).
  • Performed method validation, method verification, method transfer.
  • Managed Stability Program with Filemaker software, wrote summary report for all commercial products upon completion of stability study.
Candidate Info
6
years in
workforce
2
years
at this job
BS
Bachelor of Science

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