R&D

To design and implement integrated strategies, linking appropriate chromatography and mass spectrometry tools, to perform a qualitative and quantitative assessment of product related variants and impurities.

Analytical Method development & Validation. Routine Analysis. IPQA, QMS, Analytical QA, R&D Complances

M.Pharm with 15 to 20 years of experience in Formulation development of sterile, non-sterile Dosage forms as per guidelines of US, EU, Canada, Brazil and ROW market. Literature search, Pre - formulation and compatibility studies,formulation & development as per QbD, Scale-up and Technology transfer.

M.Pharm in Pharmaceutics, Pharmacology, Pharmaceutical Biotechnology and preferably GPAT qualified.

Master Degree or PG Diploma in Life Sciences or Biomedical Sciences or Pharmacy or Public Health or Clinical Research.  at least 4 years of demonstrated experience in clinical trial monitoring or clinical site management experience.

Doctoral Degree in Science from a recognised university or equivalent in stem cell biology, developmental biology, pharmacology, and or maternal or child health.

The candidate must have a M.S, M.Pharm, degree in Medicinal chemistry, Natural Products, Pharmaceutical Analysis from a PCI, AICTE, UGC, NAAC recognized, accredited University, Central Autonomous Institutes with 60% marks or above.

M.D Pharmacology M.V.Sc. Pharmacology M.Pharma, M.Sc. Medicinal Plants with specialization in Pharmacology from a recognized University Institution. Post Graduate degree in the Chemistry from a recognized University, Institution.

A Masters M.Pharm or M.Sc. or M.Tech. or M.E. or Bachelors B.Tech or B.E. or B.Pharm. An understanding of the Process Development and Industrial perspective of Biotherapeutics/ Biosimilars. Basic understanding of analytical techniques, statistical analysis, data management and analysis.