Posted:14 hours ago|
Platform:
On-site
Full Time
1. To prepare and revise the existing BMR, BPR as per in house Standard and latest guidelines.
2. To Prepare S.O.P of each procedure and Make sure that the S.O.P is being followed.
3. To Coordinate with Q.C and production department and minimize the Batch to Batch variation, Deviation and work towards the improvement of the quality of products.
4. To review all Documents like BMR, BPR, SOP, COA, PROTOCOLS and make sure that all the relevant documents are being followed.
5. To coordinate with all departments, extract the desired output.
6. To review the label content and different parameters and guidelines of regulatory authority while assessing the content.
7. Stay up to date with emerging trends and development in the relevant field and identify opportunities for Process development.
8. To Stay up to date with new guidelines of the ministry of Ayush and FDCA.
9. To review current products of the organization and work continuously towards the improvement in quality of products.
10. Must have high knowledge of all documentation relevant to the pharmaceutical industry.
Job Types: Full-time, Permanent
Pay: ₹20,000.00 - ₹27,000.00 per month
Benefits:
Work Location: In person
Speak with the employer
+91 7383637388
Eximburg International Pvt.Ltd.
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