The Technology & Innovation department strives to transform Global Drug Substance Development (GDSD) operations by exploring and evaluating cutting-edge technologies with agility and efficiency. Our mission is to create a diverse project portfolio that ranges from quick wins to visionary advancements and shine a light on future trends and empower our teams to embrace every challenge as an opportunity for growth.Key ResponsibilitiesThis position is
The Technology & Innovation department strives to transform Global Drug Substance Development (GDSD) operations by exploring and evaluating cutting-edge technologies with agility and efficiency. Our mission is to create a diverse project portfolio that ranges from quick wins to visionary advancements and shine a light on future trends and empower our teams to embrace every challenge as an opportunity for growth.Key ResponsibilitiesThis position is
In this role your responsibilities will include:Perform routine testing techniques such as the following, with a high degree of reliability, efficiency and accuracy:HPLC/UPLC chromatography-based methodsCapillary electrophoresis based methodsSpectrophotometry based methodsProcess related impurities testing based on ELISA, ddPCROD and TOC Test.Compendials methodsDeliver data treatment and analytical reports of high quality.Contribute to the writing of SOPs
In this role your responsibilities will include:Perform routine testing techniques such as the following, with a high degree of reliability, efficiency and accuracy:HPLC/UPLC chromatography-based methodsCapillary electrophoresis based methodsSpectrophotometry based methodsProcess related impurities testing based on ELISA, ddPCROD and TOC Test.Compendials methodsDeliver data treatment and analytical reports of high quality.Contribute to the writing of SOPs
Key Accountabilities Coordinate and ensure the preparation and maintenance of documentation (e.g., SOP/WI, protocols/reports) within your area of expertise.Support the scaling-up from 200L to 2000L of suitable purification processes for manufacturing operations (Pre-clinical and Clinical).Assist your manager in coordinating activities within your scope of responsibility.Produce large-scale NBEs for pre-clinical or clinical
Key Accountabilities Coordinate and ensure the preparation and maintenance of documentation (e.g., SOP/WI, protocols/reports) within your area of expertise.Support the scaling-up from 200L to 2000L of suitable purification processes for manufacturing operations (Pre-clinical and Clinical).Assist your manager in coordinating activities within your scope of responsibility.Produce large-scale NBEs for pre-clinical or clinical
As part of the Global Drug Substance Development department, you will join a team of motivated scientists dedicated to develop and optimize process for production of new biological therapeutics. The successful candidate will play a key role in designing and operating experimental studies to evaluate robotic screening processes in the development of monoclonal antibodies (mAbs). Key Responsibilities: Design and execute experimental studies to assess
As part of the Global Drug Substance Development department, you will join a team of motivated scientists dedicated to develop and optimize process for production of new biological therapeutics. The successful candidate will play a key role in designing and operating experimental studies to evaluate robotic screening processes in the development of monoclonal antibodies (mAbs). Key Responsibilities: Design and execute experimental studies to assess