Job Description:

Key Responsibilities:
Perform analysis and testing of Raw Materials (RM), Packaging Materials (PM), in-process samples, finished products, and stability samples as per pharmacopoeia standards.
Operate, calibrate, and maintain analytical instruments such as HPLC, GC, UV, IR, Dissolution Apparatus, etc.
Ensure timely release of materials/products with accurate and complete documentation.
Maintain records, calibration logs, data integrity, and adherence to SOPs.
Follow cGMP, GLP, and regulatory compliance in the QC laboratory.
Handle OOS / OOT results, deviations, lab incidents, and prepare required reports.
Prepare and review STPs, COA, specifications, and test reports.
Coordinate with QA, Production, and Warehouse teams to ensure smooth operations and timely batch release.




Support internal and external audits such as WHO / USFDA / MHRA / etc.

Desired Profile / Criteria / Skills :

Requirements:
B.Sc./M.Sc. Chemistry or B.Pharm/M.Pharm.
Hands-on experience in RM/PM analysis (3–6 years).
Knowledge of pharma guidelines (IP, BP, USP).
Strong documentation and compliance skills.
Gujarati-speaking preferred.
QC: 1 year (Preferred)

Offered Advantages / Facilities :

Why Join Us?
Exposure to regulated pharma workplace.
Skilled growth in a leading formulation company.
Supportive work culture with career stability.

📌 Qc Chemist Executive Amreli (India)
🏢 Pramukh Staffing
📍 India