"• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Proce...
To lead the Granulation department with respect to developing the second line. • To ensure the delivery of products as per the production target. • To ensure and monitoring yield, Wastage, WIP & operation expenses of Granulation area. • To ...
"• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Proce...
"• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Proce...
Principal task and Responsibilities: 1) Analytical Method Development by HPLC for all Project. 2) Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. 3) To mai...
- To prepare, review and submit dossiers for Life cycle management, and other submissions as required for EU region. - Preparation, review and submission of eCTD Renewal, variations, post marketing applications and other related activities....
"• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Proce...
"• To ensure compliance of cGMP requirements & Good Engineering Practices, other statutory laws, rules and regulations. • Planning of work and manpower on day to day basis. • Ensure efficient operation and maintenance of HVAC system. • To e...
"• To make a daily plan based on the monthly plan and share to the reporting managers. • To ensure the availability of lubricated blend, core tablets, coating materials and equipment before plan. • To distribute the operational activities a...
1. Readiness of facility for internal and external inspections. 2. Documents issuance and timely submission to QA. 3. Preparation of documents as per regulatory requirement like MMD, SOPs and other technical documents. 4. Environmental moni...
· 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...
"• Ensure the cGMP Compliance and schedule M compliance in production. • Ensure the proper utilization of men and machine of Granulation area. • Ensure the training of production staff and worker. • Ensure the development progress periodica...
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...
"• 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. • ...