To perform In-process Quality Assurance for the process / products being manufactured and packed in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of the products being manufactured and Packed in Main Pharma Blo...
"• Ensure efficient operation and maintenance of Utility (Boiler, chilling plant, Air compressor, cooling tower and N2 System). • To ensure strict compliance of cGMP requirements & Good Engineering Practice requirements besides other statut...
Follow cGMP and GLP PRACTICES. • To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed / implemented properly. • To follow safety Procedure in QC department. • To ...
Responsible for all activities related to raw material and packaging material of main pharma QC at Dholka plant. • To ensure current good laboratory compliances and ensuring all SOPs related to quality control laboratory are prepared and re...
- Compilation, review and submission of eCTD dossiers, renewal applications, variations, site transfer projects, post marketing applications and any other relevant submissions for UK/EU/AU/NZ/CA regions. - Preparation of deficiencies respon...
- To develop chemical process which is having least hazardous chemicals and cost effective process of API in lab and the technology to be transferred at plant scale. - To check the proof of concept of selected synthetic route. - To develop ...
· To ensure Registration dossier submission of products in different Africa countries (Region I) as per agreed timeline. · To ensure Renewal of registered product prior to validity expiration of Africa countries (Region I). · To Review Regi...
· To ensure Registration dossier submission of products in different Africa countries (Region I) as per agreed timeline. · To ensure Renewal of registered product prior to validity expiration of Africa countries (Region I). · To Review Regi...