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.
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.
B.Pharm, Pharm.D or equivalent with two years post-qualification experience in clinical project management and/or clinical trial/ study monitoring in a recognised organisation / institute
Graduate degree in Life Sciences / Biotechnology / Microbiology / Agricultural Sciences. At least one year experience in sample processing, staining, microscopy, general laboratory work including autoclaving, processing of glasswares, media preparation.
Graduate in Biological Sciences from a recognised University with two years experience from a recognized institution OR Masters degree M.Sc. Biotechnology in the Biological Sciences from a recognised university.