Junior Executive-QC (FP+IP)

Job Description:

Responsibilities

•  In-Process (IP) Analysis
• Perform real-time sampling and testing at granulation, compression, coating, and encapsulation stages.
• Conduct tests such as Weight Variation, Thickness, Hardness, Friability, Disintegration, LOD / Moisture content, Bulk and Tap density,.
• Ensure timely and accurate recording of results in BMRs / BPRs.
• Communicate and escalate any OOS, OOT, or deviations promptly.
• Maintain and calibrate IP testing equipment.
•  Finished Product (FP) Analysis
• Analyze finished dosage forms (tablets, capsules) before release.
• Perform tests including Assay, Related Substances (HPLC, UV), Dissolution, Uniformity of Dosage Units.
• Conduct physical parameter tests — Hardness, Friability, Disintegration, Weight Variation.
• Document all analysis in analytical worksheets and generate COAs.
• Ensure all analysis is as per approved SOPs and pharmacopoeia / in-house specifications.
• Handle and troubleshoot analytical instruments.

Qualification & Expeirnece

• B.Sc / M.Sc / B.Pharm
• Experience
• 1 – 3 years (OSD experience preferred).