Expert- Science and Technology (Oral solids formulation development)

You will be responsible for designing, planning, performing, interpreting, and reporting the results of scientific experiments to prepare and deliver drug substances, drug products, and processes within a multifunctional project team led by a Project Leader. You will manage technical laboratory and plant activities. As a part of the Management Track, you will lead a team in developing pharmaceutical, biological, or cell-gene therapies in a small manufacturing plant environment. You will execute the functional strategy, drive operational excellence in line with TRD vision and strategy, and ensure full portfolio support in alignment with GDD, Sandoz, NTO, and NIBR plans. In the role of an Associate Scientist, you will design, plan, perform, interpret, and report scientific experiments for the development and timely delivery of drug products within a project team. Additionally, you will manage technical lab and plant activities. As a Scientist, you will be responsible for designing, planning, performing, and interpreting scientific experiments for the development and timely delivery of drug products. You will lead and manage project activities, support team members, contribute to overall strategies and goals. In the position of a Senior Scientist, you will design, plan, perform, document, and interpret scientific experiments and GMP testing or pilot plant processes for generic products. You will maintain equipment, manage operational aspects in the lab or plant, and ensure timely delivery. Key Responsibilities: - Meet quality, quantity, and timeline goals in all projects while aligning with the overall drug development process. - Plan, organize, perform, and document scientific experiments in collaboration with project teams under minimal guidance. - Provide efficient processes for specialized facilities and manufacturing operations. - Document raw data, evaluate results, propose next experiments, and optimize methods and workflows. - Generate lab procedures, reports, instructions, and SOPs, and transfer procedures to production. - Communicate problems, conduct safety searches, manage chemicals, and collaborate with team members. - Evaluate new equipment, contribute to maintenance, and ensure adherence to quality and compliance standards. - Support resource planning, quality mindset, and training compliance. - Adhere to HSE rules and guidelines, contribute to increasing efficiency, and provide measurable contributions to projects. Minimum Requirements: - B. Pharm /M. Pharm with 3-8 years of relevant experience. - Experience in safe handling of chemicals and equipment, working in interdisciplinary teams, and knowledge of SOPs and GMP regulations. - Proficiency in scientific/technical areas, laboratory tools, software, and communication skills. Join Novartis to be part of a community dedicated to helping people with diseases and their families. Collaborate, support, and inspire breakthroughs that change patients" lives. Ready to create a brighter future together ,