Karnataka

Candidate should have knowledge of theoretical working principle of KF auto titrator, dissolution, spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC 

Masters degree in Life sciences or Biotechnology; Experience in 2D cell culture, stem cell science, and 3D cell culture techniques. Experience in scientific writing.

M.Pharm. / M.S. Pharm. / M.Tech Pharm / Ph.D / Postdoc. Development of Novel Activation Modulated pH Triggered controlled release Gastroretentive in situ gelling system for oral delivery of iron, In vivo evaluation in human subjects.

Knowledge of ASU drug standardization and analytical techniques. Handling analytical instruments like HPTLC, HPLC, etc. Drafting of scientific documents/ research articles/ technical reports etc., Working knowledge of computer applications. Master of Science M.Sc. in Chemistry/Analytical Chemistry or Master of Pharmaceutical Sciences M.Pharma

B.Pharmacy from a recognized institute. Approved Diploma in Pharmacy from an Institute recognized by the Pharmacy council of India and registered as pharmacist under the Pharmacy Art 1948.

Dual functional COX-2 inhibiting and antimicrobial NSAID-peptidomimetic conjugates as novel therapy to tackle septic infections. Ph.D, MD, MS, MDS or equivalent degree OR three years of research, teaching, design and development after MVSc, M.Pharm, M.E, M.Tech with at least tree research papers in high impact Journals. Candidates having research experience in organic synthesis, peptide synthesis, purification and characterization will be preferred.

Bachelor of Pharmacy B.Pharma degree with at least 02 years of experience in AYUSH Hospitals, Clinics. In case B.Pharma candidate is not available, Diploma in Pharmacy D.Pharma candidates with at least 02 years of experience will be considered. Should have computer knowledge.

M.Sc in Plant Biotechnology, Biochemistry, Botany, with Three Years Research Experience OR Doctoral Degree in Biotechnology, Biochemistry, Botany. Experience of working in plant tissue culture and transformation, molecular biology techniques and plant genome editing.

The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.