Job Description / Responsibility
• To prepare product dossier for export as per different country`s registration guideline requirement.
• To perform Annual Product Review (APR) of Ophthalmic & Injectable products.
• To counter check, change over clearance of sterile product.
• To perform sampling and In-process check (IPC) during manufacturing of sterile products.
• To compile updated GMP guideline requirements and to arrange training accordingly.
• To compile & review batch documents prior to product release.

Job Nature
Full-time

Educational Requirements
The incumbent should be M.Pharm from any reputed University.

Experience Requirements
1 to 2 year(s)

Additional Job Requirements
• Age At most 30 year(s)
• Preference will be given to the candidates having 1 -2 years work experience in any reputed pharmaceutical company specially in sterile products.
• Well conversant with MS office applications.
• Excellent communication skill in English.

Send your CV to hrd@generalpharma.com