Responsibilities: Independently design, plan, organize and perform scientific experiments for the preparation and timely delivery of biologic drug products (DP), processes and procedures.
Independently design, plan, organize and perform specific analytical tests related to the experiments as well as for related stability studies.
Document raw data from the scientific experiments including all conducted analytical tests as well as evaluation, interpretation, and reporting of all results of the scientific experiments together with the project responsible (Functional Lead).
Interpret results including drawing relevant conclusions and deliver respective work packages to meet agreed objectives & timelines in the project team. Ensure and drive information exchange in DP sub-team.
Be a core member of the Drug Product development sub-team, representing scientific and technical excellence and potentially be a member of the CMC team ad-hoc if required.
Participate in function-specific project sub-team meetings and discussions based on the project status.
If required, support the compilation of scientific protocols/reports and lab procedures based on existing templates as well as contribute to compilation of SOPs.
Take over responsibility for specific tools/equipment and utilize special tools/equipment or specialized facilities as an expert.
Schedule and perform maintenance and qualification of tools/instruments/equipment as needed.
Develop new methods or optimize existing laboratory methods/processes as well as contribute to development and implementation of new technologies.
Minimum Requirements: PhD in Chemical Engineering, Biochemical Engineering, Pharmaceutical Technology, or equivalent.
Well-founded experience in biotech/pharma industry with emphasis on biologics drug product formulation and process development, manufacturing, scale-up, and technology transfer.
Experience in protein analytics, lyophilization, and primary packaging development for biologics.
Experience in BLA/MAA submission is an advantage.
Hands-on experience in drug product formulation development and analytics for biologics including control for each unit operation, including mixing, filtration, and fill finish, experience in lyophilization and primary packaging development for biologics is an advantage.
Proficient in English – spoken and written, and basic or proficient knowledge in German as local language is an advantage.
Strong skill in MS Office tools (Word, Excel, PowerPoint, TEAMS) as well as Data & Digital savviness.
Highly structured and organized working style.
Proven track record for working independently in development laboratory environment including basic knowledge on GLP and HSE requirements for development laboratories.
Good understanding of data integrity requirements in development environment.
#J-18808-Ljbffr