Educational Qualification: M.Pharm (Regulatory Affairs), M.Sc./M.Tech in biotechnology/biopharmaceutical technology/biological sciences/regulatory certification in regulatory affairs of biotech/biopharmaceutical products.
Experience Level: Entry-level position suitable for fresh graduates or those with minimal experience in the field.
This role is ideal for recent graduates eager to gain hands-on experience in regulatory affairs, specifically in cell and gene therapy. As a Trainee, you will play a supporting role to our regulatory affairs team in various key responsibilities, including:
– Assisting in the preparation of regulatory submissions for cell and gene therapy products.
– Mapping out regulatory requirements and guidelines for CAR-T products.
– Collaborating cross-functionally on projects at different stages of product development.
– Contributing to submission activities for product approval, coordinating with regulatory bodies.
Interested in this exciting opportunity? Share your profile with careers@immuneel.com
