Maharashtra

This position will support and manage the regulatory activities associated with the Chemistry, Manufacturing and Controls for New Drug Applications across globe. Regulatory activities focus on filing activities/query responses/post approval changes as suggested across globe.

This position provides medical and scientific expertise for regulatory submissions and implies in-depth expertise within medical science, with primary goal of authoring clinical and non-clinical expert reports and summaries supporting new submissions of Generics, Innovative and Medis organizations in international markets

Analysis of Raw material, Stability and Finished product samples, must have hands on experience of instruments like, HPLC, GC, UV, KF, ICPMS & IR etc. QC investigation and QMS

Ph.D. in the area of Pharmaceutics/ Pharmaceutical Sciences/ Pharmacy/ Formulations/ Pharmaceutical Technology/ Industrial Pharmacy or equivalent. Ph.D. completed or Thesis submitted candidates can also apply.

M.Pharm can apply; Novel Pharmacotherapeutic interventions to reduce neuro-inflammation and improve cognitive outcomes in Brain Tumors, A preclinical in vitro-vivo study

Bachelor of Pharmacy. Independently drafting, negotiating, and finalizing new agreements, and amendments to existing agreements, as per Pharmacovigilance Agreement, PVA standard operating procedures.

Graduation mandatory. Science/Pharma Graduate preferred . Should have relevant Team Handling and Pharma experience

B.Pharmacy, M. Pharm, Bsc or MSc; Achieve timely submission of dossier/DMF and deficiency responses to regulatory authority by reviewing, collating, and compiling documents in order to ensure approvals for launch in stipulated time

Provide inputs to define the strategy and manage the execution of sourcing for the domestic business – this includes identifying molecules, building a perspective on the business case, identifying suppliers, handling negotiations, contract structuring, ensuring delivery and monitoring compliance