IPQA

1. Conduct in-process inspections (IPIs) to ensure compliance with GMP, SOPs, and regulatory requirements.

2. Monitor production processes, including manufacturing, packaging, and labeling.

3. Verify batch documentation, including batch records, labels, and packaging materials.

4. Perform line clearance, room clearance, and equipment clearance.

5. Conduct regular audits of production areas, equipment, and processes.

6. Investigate and address deviations, discrepancies, and non-conformities.

7. Collaborate with production and quality control teams to resolve issues.

8. Review and approve batch records, SOPs, and other documentation.

9. Participate in internal audits, customer audits, and regulatory inspections.

10. Implement corrective and preventive actions (CAPAs) to improve processes.

**Skills:]

1. Good documentation practices (GDP)

2. GMP regulations (FDA, EU, etc.)

3. Quality management systems (QMS)

4. Auditing and inspection techniques

5. Root cause analysis (RCA) and CAPA implementation

6. Microsoft Office and document management systems

Job Types: Full-time, Fresher

Benefits:

• Provident Fund

Experience:

• total work: 1 year (Preferred)

Work Location: In person