Role & responsibilities
Conduct routine and non-routine High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC) analysis to evaluate product quality.
Operate and calibrate laboratory instruments as per standard operating procedures (SOPs).
Analyze raw materials, intermediates, and finished products to ensure compliance with established specifications.
Conduct stability studies and evaluate results for ongoing product quality assessment.
Prepare, review, and update Standard Operating Procedures (SOPs) as per regulatory requirements.
Ensure proper documentation for audits, internal reviews, and regulatory inspections.
Follow cGMP, ICH, and regulatory guidelines applicable to the pharmaceutical API industry.

Preferred candidate profile
M.Sc. in Organic Chemistry / Analytical Chemistry or M.Pharm.
2 to 5 years of experience in Quality Control (QC) within the API industry.
Hands-on experience with HPLC, GC, and other analytical techniques.

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