Job Description:-

1. In-Process Monitoring: Oversee and Monitor in-process quality checks during production to ensure compliance with GMP and SOPs.

2. Documentation: Maintain accurate and timely documentation of in-process checks, deviation, and corrective actions.

3. Batch Record Review: Review batch manufacturing records for completeness and accuracy before release.

4. Deviation Management: Investigate and document deviations, implementing, correcting and preventive actions (CAPA).

5. Training: Train production staff on quality standards, procedures, and regulatory requirements.

6. Audits: Assist in internal and external audits, ensuring readiness and compliance.

7. Continuous Improvement:



Identity areas for improvement in the IPQA processes and implement changes to enhance quality.

We are Looking for:-

- Robust understanding of GMP, in- process quality assurance practices and regulatory requirements.
- Excellent attention to details, analytical and problem- solving skills. Proficient in MS Office and quality management software.
- Minimum of 3-5 years of experience in IPQA within the pharmaceutical industry, preferably in API manufacturing.

Skills: api manufacturing , Ipqa, Pharmaceutics, Quality Assurance

Experience: 1.00-4.00 Years

📌 QA Executive (Kolkata)
🏢 Apeejay Stya Group
📍 Kolkata