Evaluate change control requests and assess their impact on product stability. Review laboratory test results (CoAs), investigate OOS/OOT findings, and prepare non¬conformity reports.
B.Pharm and / or M.Pharm from a recognized institution. Minimum 2 years of relevant experience in Clinical Trials, Clinical Research, Clinical Trial Pharmacy Management, and/or Clinical Trial Data Management.
MSc. in Chemistry / Analytical Sciences / Bio-chemistry / Biotechnology or M.Pharm. To carry out scientific work on instrumental analysis and tobacco protocol development.
M.Sc./M.Tech. in Life Sciences/Biotechnology/Molecular Biology/Biochemistry/ Bioinformatics/Genomics / Pharmacy or any other related subject, and National level SRF eligibility test such as NET, GATE, etc. qualified with 2 years of research experience.
Preference will be given for Nursing Graduates/ PGs, Pharm D, MPharm (Pharmacology/Pharmacy Practice) with some experience in clinical research, Other Life Sciences PG degrees with clinical research experience
M.Pharm / M.S (Pharm) in Pharmacology / Biotechnology. Selected candidate with Pharmacology/Biotechnology qualification will have to perform in- vitro enzyme & adipocyte cell-based bio-assays, In-vivo, toxicological and pharmacokinetic studies
M.Sc. / M.Tech. in Life Sciences / Agricultural Microbiology / Biochemistry / Biotechnology / Bioengineering / Molecular Biology / Bioinformatics / structural biology/ Genomics / Pharmacy or any other related subject, with two- years of research experience in R& D in industrial / academic / scientific institutions.