Principal Task: 1) Routine analysis for GC-MS; ICP-MS; HPLC; DSC; TGA; PSD; XRD 2) Maintaining cGLP environment in laboratory. 3) Perform development; validation; calibration and release related activities. 4) Prepare and maintain various d...
Principal task: 1) To developed Analytical Method Development, Routine analysis and Validation, by GC & GCMS. 2) To take care of CSBU projects of Analytical Method Development and Validation, Method Transfer and Regulatory Queries by GCMS, ...
Responsibility • Process development and optimization before scale-up activities, Lab demonstration & scale up of optimized process. • Process development report, Investigation report, TT report, solvent recovery report preparation. • Impur...
To ensure timely completion of Project Procurement /Capex requirements activities in accordance to the given Budget, get maximum savings/ value for money/Investments and long lasing solutions by sourcing, Negotiations, Approvals and order p...
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 ...
"• To ensure operation and maintenance of Electrical network (HT & LT) of plant as well as planning, designing ordering & execution of brown field electrical project. • Ensure compliance to cGMP requirements & Good Engineering Practice requ...
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...
"• To meet agreed production targets with due compliance to regulatory norms. • To ensure proper utilization and productivity of manpower and machines. • To ensure all records/documents of department are maintained in compliance to regulato...
- 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...
Responsibility - Lab demonstration & scale up of new DMF and NDMF molecules, Process Optimization before Scale-up activities, Execution of Kilo Lab batches & technology transfer activity. Principal Tasks and Responsibilities: - Understandin...
- Analytical method development as per ICH guideline for OSD and injectable dosage form - Perform analytical method validation / verification as per the protocol. - To perform routine and stability sample analysis. - Analytical method trans...
as per shift schedule prepared by respective supervisor or Manager. • Labelling & weighing activity performed as predefined...