QC GC Analyst

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QC GC Analyst

work outline icon5 - 7 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Concord Biotech Ltd

time outline iconAhmedabad, Gujarat, India

Posted on 03-09-2025

1 Vacancy

Description

  • Perform Analytical Testing: Conduct routine and non-routine analysis on raw materials, in-process samples, and finished products using gas chromatography (GC) to ensure they meet specifications.
  • Operate and Maintain Instruments: Operate, calibrate, and perform routine maintenance and troubleshooting on GC and GC-MS (Gas Chromatography-Mass Spectrometry) instruments to ensure proper function and data accuracy.
  • Adhere to SOPs and Regulations: Follow all Standard Operating Procedures (SOPs) and strictly comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
  • Document Results: Meticulously record all test data, observations, and results in lab notebooks or a Laboratory Information Management System (LIMS) to ensure traceability and data integrity.
  • Investigate Non-Conformances: Conduct thorough investigations into any Out-of-Specification (OOS) or Out-of-Trend (OOT) results, identifying root causes and recommending corrective actions.
  • Review Data: Perform peer review and approval of analytical data to ensure accuracy, completeness, and compliance with all quality standards before a product is released.

 

Category

Pharmaceuticals

Functional Area

Pharma Quality Control (QC)

Preferred Education

MSc (Master of Science)BSc (Bachelor of Science)BPharm (Bachelor Of Pharmacy)

Key Skills

Attention to DetailCommunicationTeam WorkProblem Solving

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