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Johria Shaukat

Johria Shaukat

Willing to relocate: Anywhere

Talent
AllentownMember since July 13, 2026
HPLCUPLCICP-MSMass spectrometerLIMSSAPGMP complianceFDA regulationsALCOA+ principleCAPA reportsQuality controlBatch recordsSOPsInternal auditsQuality systemsGLP
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HPLCUPLCICP-MSMass spectrometerLIMS

About

Performed analytical testing of 503B pharmaceutical products using HPLC/UPLC and ICP-MS. Executed testing according to validation methods, SOPs, GMP, and GLP requirements. Executed instrument setup, calibration, system suitability testing, and routine maintenance to ensure reliable analytical performance.

Experience

QC Chemist - CAPS Pharmacy ( B. Braun) - Allentown, PA

(2025-03 - 2025-06)

  • Performed analytical testing of 503B pharmaceutical products using HPLC/UPLC and ICP-MS.
  • Executed testing according to validation methods, SOPs, GMP, and GLP requirements.
  • Executed instrument setup, calibration, system suitability testing, and routine maintenance to ensure reliable analytical performance.
  • Processed, reviewed, and interpreted chromatographic data using laboratory software and maintained accurate analytical records in LIMS.
  • Supported method verification, validation, and analytical troubleshooting while collaborating with Manufacturing, QA, and Quality teams.
  • Maintained GMP-compliant laboratory operations, including reagent labeling, instrument logbooks, and laboratory startups.

Formulations Chemist - OraSure Technologies - Bethlehem, PA

(2022-01 - 2024-12)

  • Prepared formulations according to Batch Production Records (BPRs), SOPs, and Work Instructions.
  • Performed raw material evaluation, formulation preparation, and in-process testing to ensure product quality.
  • Performed qualitative and quantitative analysis using HPLC/UPLC and UV-vis spectometry following approved test methods, SOPs, GMP, GLP, and GDP requirements.
  • Evaluated chromatograms for peak integrity, retention time consistency, baseline quality, and compliance with system suitability requirements.
  • Authored and revised batch records, laboratory documentation, and technical reports.
  • Worked closely with Analytical Development, Manufacturing, and Quality teams to achieve project objectives.
  • Assisted with laboratory investigations, troubleshooting formulation issues, and implementing process improvements.
  • Participated in safety training and maintained compliance with laboratory safety procedures.

Quality Analyst - AmeriSci New York - New York, NY

(2019-02 - 2021-09)

  • Conducted quality testing and reviewed analytical documentation for GMP compliance.
  • Prepared technical reports and documented laboratory results according to standard operating procedures.
  • Assisted FDA inspections and internal quality audits.
  • Investigated quality issues and supported corrective and preventive actions (CAPA).
  • Collaborated with laboratory personnel to improve quality systems and operational efficiency.

Education

Bachelor's degree - Biology/Chemistry - City College CUNY (2016-09 - 2018-05)

Skills

Willing to relocate: Anywhere

Reviews

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