Verify the accuracy of transcribed data by cross-referencing with original sources and ensure an accurate presentation of data in the report. Ensure that all transcribed data complies with internal quality standards and external regulatory requirements.
QA Specialist will serve as QA technical subject matter expert for CSV process, such as MES, KNEAT, DCS, including but not limited to GMP enterprise systems, manufacturing systems and computerized equipment, laboratory systems and computerized equipment and validation software tools.
HPLC Analyst, Operation of HPLC, Troubleshooting, Analysis of all In-process, Intermediates, RM, PM, Finish Product, Stability samples and other analytical samples of lab. Operation of GC, IR, UV, KF, Auto titrator, SOR and Wet Lab analysis.
M.Sc Chemistry from a recognized University, Institute.
Sound knowledge of marker analysis by HPTLC and HPLC. Method development and validation by HPTLC and HPLC
Skills of drafting, editing of scientific documents/ articles, technical reports etc.
M.Pharm / MSc. in Analytical Chemistry / Organic Chemistry; Execute the Isolation projects. Carry out the isolation, purification of known and unknown impurities, compounds by preparative HPLC and characterization of molecules using various analytical techniques. Involve in project acceptance.
M.Pharm or M.Sc Chemistry, Analytical Chemistry, Medicinal Plants, Phytochemistry from a recognized University, Institute. engagement of project staff in the programme Management Unit of Regional Raw Drug Repository of Trans Ganga Plain Region
First class M.Sc in Biological Sciences, Biotechnology, Pharmaceutical Sciences, Chemistry. Applicant must be qualified in any one of the following tests CSIR, UGC, ICMR including Lectureship Assistant Professorship OR GATE. National Level examination DST, DBT, MoE, ICMR, IIT etc.