Finished Goods Quality Control Analyst
About the Role
ATCO Laboratories is seeking a meticulous Finished Goods (FG) Analyst in Karachi to conduct pharmaceutical product testing, verify batch releases, and ensure compliance with DRAP, cGMP, and ISO 17025 standards.
Key Responsibilities
- Perform chemical and physical analysis of semi-finished, finished pharmaceutical products, and stability samples
- Operate and calibrate laboratory instrumentation including HPLC, UV-Vis spectrophotometers, and dissolution apparatus
- Standardize volumetric solutions, indicator reagents, and maintain primary reference standards per USP/BP compendia
- Document analytical test data, prepare Certificate of Analysis (COA), and report Out-of-Specification (OOS) results
- Ensure adherence to good laboratory practices (GLP), DRAP regulations, ISO/IEC 17025, and laboratory safety protocols
Qualifications & Skills
Basic Requirements
- B.Sc. / M.Sc. in Chemistry, Applied Chemistry, or Pharm-D from an accredited university
- 1 to 2 years of quality control laboratory experience in a reputable pharmaceutical manufacturing plant
- Hands-on experience in HPLC analysis, wet chemistry testing, and dissolution testing of solid dosage forms
- Familiarity with cGMP, DRAP guidelines, and pharmacopoeial analytical methodologies
- High precision, analytical thinking, and disciplined record-keeping abilities
Preferred Qualifications
- Experience with Waters Empower or Chromeleon chromatography data systems
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About ATCO Laboratories
ATCO Laboratories Limited is one of Pakistan's leading pharmaceutical companies, manufacturing and exporting high-quality life-saving medicines and healthcare formulations.
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