1 Opening(s)
15.0 Year(s) To 25.0 Year(s)
15.00 LPA TO 20.00 LPA
To review and implement a Quality Management System for cGMP compliance at the Production (Injectable) plant.
To prepare, Review and Approve BMR, BPR and related documents.
Handling of Caliber QAMS, DMS, Nichelon 5 CMS, Dynamic, Schedule and Track and trace Serialization & aggregation.
Giving the required training also Responsible for Media fill and ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
Key Responsibilities:
Conduct routine microbiological testing (water, environment, raw materials, in-process & finished products).
Perform environmental monitoring of cleanrooms, utilities, and aseptic areas.
Support media fill, sterility testing, endotoxin testing, and microbial limits testing.
Ensure compliance with cGMP, SOPs, and regulatory guidelines (USFDA, EU, WHO, etc.).
Review and document microbiological data, deviations, and OOS/OOT investigations.
Participate ...
30 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 7.00 LPA
Responsible for Checking & distribution of approved artwork.
Responsible for colour approval of the shade card.
Responsible for the Allocation & Verification of the Pharma code.
Responsible for the Allocation & Verification of GTIN numbers as per GS1 guidelines.
Artwork management as per the product brief.
To verify artwork as per the Labelling Act.
To review ...
5 Opening(s)
0 To 2.0 Year(s)
0.50 LPA TO 3.00 LPA
Key Responsibilities:
Support operation and maintenance of production and utility equipment (e.g., granulators, blenders, tablet compression, coating machines).
Assist in monitoring equipment performance and documenting key parameters.
Follow Standard Operating Procedures (SOPs) and Good Engineering Practices (GEP).
Participate in preventive and breakdown maintenance of machinery and utility systems.
Ensure timely documentation of maintenance activities and ...