Novartis Careers

Summary This position is responsible for the direction and oversight of the analytical projects. He/she supports analytical investigations, validation, remediation, transfer and implementation of analytical methods. He/she works cross-functionally with QC, MS&T (Manufacturing Sciences and Technology), Manufacturing, Supply Chain and the Novartis networks to ensure the success of assigned projects. …

Summary This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia. About the Role Major accountabilities: Sample storage and management -Analytical testing/documentation of drug product / finished product / …

Summary This role support/provide quality oversight in ensuring a smooth manufacturing operation, new product launches/transfer in a compliant/timely manner, drug substance batch review/release are in full gmp compliance to regulatory standards and ensures quality strategy/continuous improvement are driven in alignment to site objective/s. About the Role Key Responsibilities: Ensure all …

Summary In line with overall product strategy, the Medical Lead is responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design & organise clinical studies, building educational dialogue with KOLs and regulatory stakeholders About the Role Major accountabilities: Ensure …

Summary As Equipment Specialist , you will be responsible to produce pharmaceutical products by executing assigned activities according to production schedule in compliance with the relevant GMP, work, operating, environmental and safety instructions and guidelines. About the Role Key Responsibilities: Execution of all assigned manufacturing activities according to production schedule …

Summary This role support/provide quality oversight in ensuring a smooth manufacturing operation, new product launches/transfer in a compliant/timely manner, drug substance batch review/release are in full gmp compliance to regulatory standards and ensures quality strategy/continuous improvement are executed in alignment to site objective/s. About the Role Key Responsibilities: Ensure all …