Analyze genomic and clinical datasets to assist in patient stratification and predictive modeling. Assist in creating documentation, presentations, and technical reports summarizing insights and results.
Perform chemical and physical analysis of raw materials, in-process samples, and finished products. Operate analytical instruments like HPLC, GC, UV Spectrophotometer, FTIR, Dissolution apparatus, etc. Conduct stability studies and routine sampling/testing as per SOPs.
UNDERSTAND DESIGN, SETUP, AND EXECUTION OF IN VIVO PHARMACOLOGY MODELS FOR EXPERIMENTS ASSOCIATED WITH GROSS IMMUNOLOGY, SOLID TUMORS, AND HEME-ONCOLOGY
TCS combines tech expertise and business intelligence to catalyze change and deliver results. Our mission is to help customers achieve their business objectives by providing innovative, best-in-class consulting, IT solutions and services and to make it a joy for all stakeholders to work with us. Clinical Data, Regulatory, Clinical Operations, Pharmacovigilance; Should be open to work In shifts
Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines
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.
Hands-on experience with HPLC, GC, UV-Visible Spectroscopy and Dissolution tester. Proficient in Empower-3 software.
Strong analytical and problem- solving skills.
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