The QA Executive (Entry-Level) will support the Quality Assurance department in ensuring compliance with cGMP, regulatory guidelines, and internal quality standards. The role includes documentation review, shop-floor compliance monitoring, and assisting in quality systems activities.
Key Responsibilities1. Documentation & Records Management
Review Batch Manufacturing Records (BMR/BPR) for accuracy and completeness.
Issue and control SOPs, logbooks, and other controlled documents.
Maintain documentation as per GDP (Good Documentation Practices).
2. GMP Compliance
Monitor production and packaging areas for compliance with cGMP.
Provide line clearance for manufacturing and packing activities.
Report any non-conformance or deviations observed on the shop floor.
3. In-Process Quality Checks
Perform in-process checks such as weight, hardness, pH, dissolution, etc. (as applicable).
Record results and escalate abnormalities to seniors.
4. Quality Systems Support
Assist in handling Deviations, Change Controls, CAPA, and Incident reports.
Support internal audits and regulatory inspections.
5. Training & Continuous Improvement
Attend departmental and GMP training sessions.
Participate in quality improvement initiatives and cross-functional interactions.
Required Skills
Basic knowledge of cGMP, GLP, and GDP.
Understanding of pharmaceutical manufacturing or packaging processes.
Good communication and documentation skills.
Ability to identify issues and maintain accuracy.
Willingness to learn and adapt.
Job Types: Full-time, Permanent
Pay: ₹15,000.00 - ₹20,000.00 per month
Benefits:
Food provided
Health insurance
* Provident Fund
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