UNDERSTAND DESIGN, SETUP, AND EXECUTION OF IN VIVO PHARMACOLOGY MODELS FOR EXPERIMENTS ASSOCIATED WITH GROSS IMMUNOLOGY, SOLID TUMORS, AND HEME-ONCOLOGY
BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.
As part of our team, you'll be responsible for a diverse range of tasks within the drug discovery process. In this role, you will have ample opportunities to collaborate with our dynamic team, providing scientific expertise and strategic leadership.
As Technical Leader, define, organize, plan and lead the projects that are technically complex and cross functional in nature at a global front. Broad understanding of the overall product and therapy along with deep technical expertise in one or more fields related to drugs and medical devices
The Senior Specialist, Expert License Management prepare dossiers and execute actions that support the license security and product compliance on the markets, and that meet companys and health authorities requirements. Encounter the challenges to enable representatives from all major disciplines involved to reach agreement on the license management strategy and approach.
Expertise in different types of purification techniques. Sound knowledge of different column chemistry used in HPLC. Responsible for troubleshooting of instruments and their calibration
Ensure that Bulk Viral Antigen production adheres to GMP standards on the shop floor, including line clearance, dispensing, and preparation processes. Examining and approving batch records, standard operating procedures, project plans, customer verification, and APS documents.
Handling equipment like HPLC, UPLC, GC dissolution tester, UV, Vis spectrophotometer, IR, KF titrator etc Trouble shoot in existing methods and support regular and stability analysis, Excipient analysis for formulation development