April 2024

MSc Pharmacy, Pharmacology. Engineering of Long-lasting Breast Hydrogel Implants for Cancer Immunochemotherapy

A multi-OMICS Approach to Decipher the Stress Signaling Network in Rhodiola imbricate Edgew. Post Graduate Degree in Basic Sciences or Graduate/ Post Graduate Degree in Professional Courses

The research intern will perform cloning, and over expression of proteins along with bioinformatic analysis. The preference will be given to candidates who have background knowledge in at least two of the following areas: Molecular Biology, Protein biochemistry, Structural Biology, and Bioinformatics

M.Sc or M.Pharm. Coordinate with all concerned department to ensure timelines and compliance to regulatory or sponsor requirements for preparation, compilation and delivery of reports. Electronically generate, review study documents and submission of study reports in CTD/eCTD format as per regulatory requirements.

The incumbent would need to build a strong New Product Portfolio and its management and delivery in a time bound manner for India Business of Sun. Works closely with the Business/Marketing, Business Development, R&D, Manufacturing, Regulatory, IP, Market Research, SFE, CEO Office, Commercial, Medical, Clinical Research, CQA, Finance, PMO, New Product Launch, Network Strategy, Packaging development teams etc.

To develop approaches for Downstream processes, designing and managing multiple process development projects; to take up new technology initiatives within the downstream development group. To draft primary documents for functional deliverables.

As a CDC Trial Manager is the main accountable person in making sure that deliverables are met as per project timelines, within budget and complying with Protocol, country regulatory requirements, Helsinki Declaration, GCP, Good Clinical Practice, and NN SOPs Standard Operating Procedures. bachelor degree in life science, pharmacy, or nursing qualification or equivalent.

Provides critical support and coordination in the review of safety and regulatory publishing documents, ensuring timely and accurate processing upon receipt. Plays a key role in maintaining document quality by tracking safety and regulatory publishing data, ensuring seamless uploading into internal and/or external electronic trial master files.