Johria Shaukat
Willing to relocate: Anywhere
Talent
AllentownMember since July 13, 2026
HPLCUPLCICP-MSMass spectrometerLIMSSAPGMP complianceFDA regulationsALCOA+ principleCAPA reportsQuality controlBatch recordsSOPsInternal auditsQuality systemsGLP
·
Hire this person
Send a job offer directly to this candidate
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