vacancies

Responsible for operation and cleaning of Automatic visual inspection machine and labelling machine for DP. Preparation, review and execution of Study protocol / SOPs / QRM / Study report / QRM report in the drug product facility.

Experience in execution of lab scale manufacturing, reverse engineering, analytical know-how, plant level manufacturing activities; scale-up and exhibit batches based on quality principles QbD, QTPP, CQA, CMA, CPP, RA, FMEA.

Experiences in HPLC/ GC/ IR/ UV/ Dissolution/ Polarimeter/ Potentiometric titrations/ KF/ PSD by Malvern. Awareness on current Data Integrity requirements & cGMP requirements. Stability studies

BPharm / MBBS /Integrated BS- MS/MSc/BE/B.Tech or equivalent degree, with 55% marks and passing of NET/GATE test. 

B.Pharm or 10+2 with Science stream (PCB) and Approved Diploma in Pharmacy.

1st class Masters degree in Microbiology, Biochemistry or life science from a recognized university with minimum five years research experience / training in the relevant subject.

B.Pharmacy or 10 plus 2 with Science stream PCB and Approved Diploma in Pharmacy. Min 03 years exp.

PhD in relevant field with experience in Electrochemical systems / Bioelectrochemical systems/ Algal Biorefinery / Constructed wetlands

The candidate requires to have submitted a doctoral dissertation. The candidate requires to be familiar with murine genetic models and with models of lung injury- repair.