A holistic objective of dispensing health through a portfolio of injectable products across various therapeutic segments and delivery systems, has helped us expand to seven manufacturing facilities in India, with a capacity of approximately 750 million units. These include four facilities with 22 production lines for finished formulations and three Active Pharmaceutical Ingredient (API) facilities. Our products are produced at world-class manufacturing facilities and conform to global compliance, regulatory and quality specifications.
Vacancy Details
Date: 7th September, 2022
Time: 9.00 AM – 10.00 AM
Venue: GLAND PHARMA LIMITED BLOCK – C PHASE – I, VSEZ, DUVVADA, Visakhapatnam, Andhra Pradesh, India
Roles and Responsibilities
1.Review of Executed BPCR cross verifying with log books.
2. Preparation and Review of Master BPCRs.
3. Review of production log books.
4. Monitoring personnel hygiene in production entry.
5. Coordinate with QA regarding BPCR review and compliance.
6. Cross check of BPCR.
7. Complies of review points from QA.
8. Receiving BPCRs from QA.
9. Initiation of Error Ratifications in the BPCRs if any.
10.Implementation of standard operating procedures.
11.Continuous training of workmen for cGMP compliance.
12.Reporting all deviations to Production In charge.
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