May 2024

MBBS, BDS, BAMS, BHMS OR Graduation in Science, B.Pharm, Life Science, Biotech, Zoology, Botany, etc. PG Diploma in Clinical Research is desirable.

Establishment of Bioinformatics and Computational Biology for Woman and Child Health funded by Department of Biotechnology. Doctoral Degree in Science or Master’s degree in Engineering or Technology from a recognized University or equivalent

B.Pharm / M.Pharm; Preparation of responses to clarification requests received from Canadian authorities. Communicate with external suppliers for the preparation of packaging components and ensure technical feasibility.

Expertise in Molecular Biology, Cell Biology, Structural biology, Immunology. The candidate should also be familiar with studying Protein- small molecule interaction, Tissue culture techniques, animal handling, enzymatic assays, Immune phenotyping.

B.Pharm / M.Pharm; Manager / Sr. Manager OSD Manufacturing, Team Leader OSD Manufacturing; Manager / Sr. Manager Liquid Syrup Manufacturing

As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide.

Perform all the labelling update activities and tracking in systems for record maintenance with respect to New Product Development NPD label creation and Product Life Cycle Management PLCM update for products in USA and Canada market

Assist in submission of product documents to regulatory authorities in accordance with country specific regulatory requirements to ensure approvals and market launch in stipulated time and support in handling post-approval changes, maintenance, and updation of documents during the products life-cycle. Achieve timely submission of dossier/DMF and deficiency responses to regulatory authority by collation, and compiling documents in order to ensure approvals for launch in stipulated time