Pharma Jobs

Identification of clinical and immunological subtypes and exploring the role of type I interferon and adaptive immunity in Juvenile Dermafomvositis; Previous experience on cell culture, flowcytometry, molccular characterization of genetic variants and genotype-phenotype correlation.

Experience in analysis of Solid Oral - FP, In-process or Stability samples. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation, Transfer Solid Oral. Experience of GC, ICPMS and or LCMS operation.

Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose

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

The incumbent would be responsible for conducting PT activities as per ISO 17043:2023 and Instrumental, Chemical, Physical analysis in agri, food & allied products, water etc.

Targeting riboswitches with synthetic small molecules for development of anti-tubercular drugs. experience in operation of equipment to aid in chemical synthesis, purification and interpretation of spectral data obtained for techniques like NMR, MS, IR, and HPLC etc. M.Sc. in Chemistry, Organic Chemistry, Pharmaceutical Chemistry, Medicinal Chemistry

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India.

Candidate should have experience in Oral formulations Solid and liquid for Handling of APQR, IPQA activity and Process Validation. Candidate should have experience in regulatory plant with hand on experience in Raw Material and Packing Material in formulation unit.