3-4

Candidate should have experience in the field of Analytical Research and Development Involved in Analytical Method development & validations, Stability analysis, Regular analysis activities.

Routine Analysis, Dissolutions, handling of HPLC /GC/ ICP-MS / AMT Activities. Should have thorough understanding of instruments Spraytec, SprayView, Cascad impactor, HPLC and Various detection systems like GC and UV.

B.Pharm/ M.Sc; Analytical QA activities mainly to review and maintain GLP in QC review of analytical report of RM,IP,FP and stabilty data.

B. Pharma/ B. Sc/ M. Sc; Knowledge of STP/SOP, BMR/BPR, hold time study, Product Transfer, process validation, protocol preparation

Handling of QMS activities like Deviation, Incident, Investigation, CCP, Protocol Preparation, Risk Assessment etc.

Hiring potential candidate for multiple positions based our Ahmedabad Facility.

B.Pharmacy or M.Pharmacy, 02 to 05 Years in Pharmaceutical Formulation - OSD - Tablets Manufacturing facility

Pre-formulation studies lab formulation development trials of solid oral. Literature survey, to design strategy for the formulation of the projects

Collaboration with R&D and other stakeholders to enable timely filing and review of documents for EU, UK, CA, AUS for solid oral and topical dosage forms RA strategy in collaboration with partners with focus on cost implications. RA grid planning for extension projects and execution in plant