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 ...
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 ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
0.50 LPA TO 5.00 LPA
Prepare, modify, and maintain engineering drawings using AutoCAD.
Develop GA drawings, P&IDs, equipment layouts, piping layouts, and fabrication drawings.
Support plant expansion, modification, and new project activities by preparing design documents.
Coordinate with Production, Maintenance, Utility, and Project teams to understand design requirements.
Conduct site visits for measurements, design verification, and drawing updates.
Review vendor ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 8.00 LPA
Key Responsibilities:
Prepare, compile, and review regulatory submissions (CTD/eCTD formats) for product registrations, renewals, and variations as per regional and international guidelines.
Ensure timely submission and follow-up of applications with regulatory authorities.
Maintain up-to-date knowledge of changes in drug regulatory environments and communicate impacts to relevant departments.
Coordinate with cross-functional teams (R&D, QA, QC, ...