Qc Executive

Department: Quality Control

Location: Tehsil Inodra, Kangra (HP). Near by Pathankot

Reporting to: QC Manager / Head Quality Department

Key Responsibilities:

• Conduct routine testing of raw materials, in-process materials, and finished products as per approved specifications and standard test procedures (STPs).
• Perform chemical and instrumental analysis using HPLC, UV, IR, GC, KF, etc.
• Maintain accurate and up-to-date laboratory records, worksheets, and logbooks.
• Ensure timely calibration and maintenance of laboratory instruments and equipment.
• Review and follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Assist in method development and method validation activities as required
• Conduct stability testing and prepare stability summary reports.
• Ensure compliance with company SOPs, quality standards, and regulatory requirements (such as USFDA, MHRA, WHO, etc.).
• Participate in internal and external audits and implement corrective and preventive actions (CAPA).
• Manage sampling, labeling, and storage of test samples as per SOPs.
• Handle out-of-specification (OOS), out-of-trend (OOT), and deviations according to quality procedures.
• Coordinate with production, QA, warehouse, and other departments for quality-related issues.
• Monitor environmental conditions of the lab as per the standard protocol.

Desired Candidate Profile:

• Education: B.Pharm / M.Pharm / B.Sc / M.Sc Chemistry or related field
• Experience: 2–10 years in QC role within a pharmaceutical formulation plant

• Skills Required:

• Proficient in operating analytical instruments (HPLC, GC, etc.)

• Knowledge of GMP, GLP, ICH guidelines
• Strong documentation and communication skills
• Attention to detail and ability to work under pressure
• Good analytical and problem-solving skills