To ensure consistent product quality through rigorous testing, documentation, and regulatory compliance.
Key Responsibilities:
Perform analysis of raw materials, in-process, and finished products (UV, HPLC, GC, IR)
Maintain and calibrate instruments
Prepare analytical reports, COAs, and logbooks
Ensure GMP, GLP, and regulatory compliance
Conduct stability studies and support method validation
Handle deviations, OOS, and CAPA
Coordinate with QA/Production for batch release
Maintain audit-ready documentation
Uphold lab safety and hygiene
Qualifications & Skills:
B.Pharm / M.Sc / B.Sc in Chemistry or Pharma Sciences
Valid Manufacturing Chemist License (Form 25/28)
Hands-on with analytical instruments and documentation
Knowledge of ICH, IP/BP/USP standards
Strong attention to detail and audit readiness
Communication in English and Hindi
Preferred Attributes:
Experience in tablet/capsule/injectable QC
Exposure to audits and data integrity
Quality-focused and disciplined
Job Type: Full-time
Pay: ₹25,000.00 - ₹30,000.00 per month
Benefits:
Health insurance
Work Location: In person
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