Madhya Pradesh

Postgraduate degree in Chemistry or M.Pharm. with Pharmaceutical Chemistry; JRF on coterminus basis for IMR Collaborative Project of Regional Ayurveda Research Institute

M.Sc. or equivalent / B.Tech in Biological Sciences Biotechnology/ Microbiology/ Pharmacology/ Toxicology/ Immunology; Defence Research and Development Establishment, DRDE, Gwalior a premier institute of Defence Research and Development Organisation

Well versed with Analytical methods validation/Method transfer/Cleaning validation, Handling HPLC, GC, DR and other instruments, Reviewing analytical data. Preparation of Validation protocols and reports.

Minimum 2 years' experience in analysis of FG/RM/Stability/ PM samples using various QC instruments (LCMS/HPLC/GC/Dissolution, Malvern 3000 etc). Exposure to LIMS preferred.

Responsible for reviewing batch manufacturing, monitoring process steps, and reviewing documentation. Additionally, support in handling deviations, change control, and CAPA management, internal and external audits to maintain compliance.

M.Sc. in Life Sciences, Biotechnology, Molecular Biology, Microbiology, Pharmacology, Toxicology, Immunology; Defence Research and Development Establishment

BPharm, M.Sc, M.Tech. Degree or equivalent in streams like Biotechnology, Biochemistry, Microbiology, Life Sciences. Indian Institute of Technology Indore

Candidate should be proficient in GLP. HPLC. GC, Instrumentation. Chemical Analysis, Raw Material Analysis, FG Analysis, UV. FTIR. In-Process Sample Analysis, and Stability Sample Analysis.

M.Pharm, B.Pharm, M.Sc ; Exposure to method validation, method transfer on various QC instruments LCMS, HPLC, GC, Dissolution, Malvern 3000 etc. Familiarity with protocol, report preparation.