Perform and review analysis of Raw Materials, Finished Products, In-Process Samples, and Stability Samples.
Operate and troubleshoot analytical instruments such as HPLC, GC, UV, IR, Dissolution, and other laboratory equipment.
Review analytical data, test reports, and laboratory documentation.
Ensure compliance with cGMP, GLP, SOPs, STPs, and regulatory requirements.
Investigate OOS, OOT, deviations, and laboratory incidents.
Prepare and review analytical reports, specifications, and protocols.
Coordinate with QA, Production, and other departments for quality-related activities.
Support method validation, method transfer, calibration, and stability studies.
Participate in internal audits, customer audits, and regulatory inspections.





Qualification
B.Pharm / M.Pharm / M.Sc (Chemistry) or equivalent.

Experience
Minimum 5 years of experience in Quality Control within a pharmaceutical manufacturing company.

Skills:
Hands-on experience with HPLC, GC, UV, IR, and Dissolution.
Knowledge of cGMP, GLP, Data Integrity (ALCOA+), and regulatory requirements.
Documentation review and investigation handling.
Solid analytical, communication, and team management skills.

Pay: ₹200,000.00 - ₹400,000.00 per year

Work Location: In person

📌 Senior Executive Qc Wada (MIDC)
🏢 US Pharma (I)
📍 MIDC