M.Pharm

In this role, the Senior Scientist-I will work on isolation, purification of known and unknown impurities, compounds by preparative HPLC and characterization of molecules using various analytical technique. Prepare, execute, and complete IQ/OQ/PQ of new instruments. Indent the required glass ware, chemicals, and columns for the ARD projects.

Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies

Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system.

The recruited candidate will perform majority of experiments proposed in the study, which includes preparation and characterization of nanoparticles, in vitro and in vivo safety and efficacy analysis etc. The Project Research Scientist-I will also take care of consumables ordering, storage and maintenance. The candidates with M.Sc., qualification shall enrol for Ph.D programme.

Provide technical inputs on review of CMC data for Central CDSCO and State dossiers related to new products under development Liaison with other departments such as l&D, Quality, Supply chain, Project Management, etc to deliver high quality dossiers, in accordance with business priorities

Graduate of minimum three years duration in pharmacy with three years experience in pharmacy OR Post graduate degree in Pharmacy. Neonatal and or Pediatric Nursing experience, Working Knowledge of Data Entry in the computers Experience in drug preparation in clinical research study preferably involving children or neonates.

Membrane preparation and characterization. Prior experience of working in research laboratory, industry desired. Direct Sea Water Electrolysis by electrolyte engineering & by coupling electrolyser directly with FO module.

Establish a Drug Metabolomics Laboratory for North Eastern States. Master degree in Pharmaceutical or Natural Science with first class.

Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry.