Executive - Quality Assurance

Actively Reviewing

Centrient Pharmaceuticals

Rupnagar Full-Time 2–4 yrs exp Posted 1 month ago · Apply by Jul 18, 2026

Job Description

To ensure that the Products provided to the market are tested as per Customer specifications and in compliance with applicable pharmacopoeias as well cGMP/GLP/ICH/USFDA /ISO guidelines.

Key Responsibilities:

To participate in vendor qualification activities
To participate in Internal/External audit activities
To ensure compliance as per applicable regulatory requirement
Release/rejection of finished products, intermediates & raw material as per approval specification
Creation & release of Certificate of analysis
Issuance and review of Batch production records
QC analytical data review
Handling sales return, recalls and compilation of APR data
To coordinate investigation of market complaints/deviation/OOS/OOT
Log books management for various activities
To ensure that sampling of all Finished products are done as per defined procedure and proper record is being kept compliance to cGMP practice
To ensure compliance to all SHE guidelines and to ensure safe working
Conducting monthly safety audit and ensuring the closures of observations
Reporting of Near misses/Incidents
Ensuring that all SHE related guidelines/rules are followed while doing any activity to achieve the goal of SAFE place to work
Clearance of safety work permits to ensure execution of activities in safe manner
To release the Batches of Intermediates and Finish goods in SAP

Requirements

Post-Graduation in Chemistry having knowledge of cGMP & GLP guidelines, ICH/ USFDA guidelines
Knowledge of documentation related to quality and regulatory guidelines
Minimum 9 years of experience in Pharmaceutical industry and extensive Quality Assurance experience in API manufacturing industry