Executing chemical reactions in mg to gm scale and to synthesize required quantities of molecules/compounds as per client specifications using efficient route and techniques.
Responsible for the ordering and tracking of specific regulatory requirements such as registration samples, Certificates of Pharmaceutical Product, Legal documentation e.g. Letters of Authorisation, Powers of Attorney, Translations of regulatory documentation
PhD Degree in Life Sciences from a recognised university or equivalent. Research requiring cell biology techniques including culturing routine cell lines, maintenance of stocks and transfection.
Prior experience in stem cell culture or genome editing would be an advantage but is not mandatory. Enthusiasm to learn, attention to detail and excellent organizational skills are important. The candidate should be able to work both independently and also be able to collaborate with others.
M.Sc. or M. Tech in Bioinformatics, Computational Biology, Computer Science with NET/ SLET and PhD in Bioinformatics with experience in Computational Biology, Omics Technology and coding is preferred.
Responsible for release of the product by ensuring review of relevant audit trial of Manufacturing. Strong knowledge of cGMP, ICH guidelines, FDA regulations, and other relevant standards for biologics manufacturing.