Masters in Life Sciences / Pharmaceutical Sciences/ Biochemistry/Biotechnology/ Molecular Biology. Research Experience in In - vitro Cell Culture, Cell based Assays and techniques like RT-PCR, Western blotting, Flow Cytometry etc.
BPharm /MBBS /Integrated BS-MS /MSc /BE /B. Tech or equivalent degree in Engineering Technology or equivalent degree, with 55% marks and passing of valid NET/GATE score/test.
This initiative is designed to empower and inspire talented female students pursuing STEM disciplines by providing them with opportunities to gain hands-on experience, along with scholarship and valuable mentorship.
Postgraduate degree in Life Sciences / Biology or an associated field, possesses National Eligibility Tests- CSIR UGC NET including Lectureship and GATE certificate or qualified National Level examination conducted by Central Government departments/agencies /institutions
M.Sc./B. Tech in Biotechnology, Microbiology, Biochemical Engineering, Biochemistry, Molecular Biology, Life Sciences or equivalent. with NET/GATE or equivalent.
B.Sc. and M.Sc. in Biotechnology with a good academic record. The candidate MUST have undertaken a 6-month training during his / her Masters degree in a research laboratory where they have had HANDS-ON TRAINING in the above-mentioned techniques.
M.Sc. in Biological Sciences, Microbiology, Biotechnology, Biochemistry, Food Sciences from a recognized University with 60% marks. and 3 years of research experience in working with microbiology, Biotechnology lab, with proven experience in Scientific publications and other Scientific activities
Candidate should be capable of operating Analytical instruments such as HPLC, GC,Dissolution Appratus, UV, IR, KF etc. should be aware and capable of Qualitative, Quantitative, Sample, Wet, Routine analysis of drug substances, intermediates, finished products, raw materials etc.
Supports to the Laboratory functions to handle Investigations, Deviation Management, Specifications ,test methods, method validations equipment qualifications ,internal audits and escalations if any.
Responsible for post approval submissions to Europe, Australia, New Zealand and Canada market. To provide Regulatory inputs during inspections by Regulatory authorities and Customer as and when required.