Scientist I, Formulation Development
6 months ago
Responsibilities:
Design, execute, and interpret cryoformulation and fill/finish development experiments in collaboration with other team members, utilizing fundamental cryobiology and first principles. Evaluate and integrate cutting-edge technologies into the cellular therapy cryopreservation process. Identify meaningful process parameters ( ranges and impact on quality attributes) while applying suitable analytics for enhanced efficiency and effectiveness. Perform technology transfer of the cryopreservation process to cGMP-compliant manufacturing facilities within the company or to CDMO partners. Prepare experimental proposals, standard operating procedures,technical protocols, and reports while interacting in a cross-functional environment. Analyze and document experimental data in electronic laboratory notebooks in a timely and accurate manner in accordance with the company quality management system. Prepare and present scientific data in internal and external forums. Train and supervise staff members in supporting cryopreservation-related activities.
Minimum Requirements:
or MSc. degree in a Biological Science, such as Biochemistry, Immunology, Molecular Biology, or similar MSc. 9+/ PhD 0-2 years of experience, preferably in an industry setting Hands on expertise in developing cryopreservation processes and broad knowledge in cryobiology are required. Understanding and experience of molecular techniques such as cell imaging, flow cytometry, or qPCR and ddPCR is required. Experience with data processing and statistical analysis software toolsis required. Practical knowledge of experimental design (, DoE) is desired. Ability to plan experiments and independently execute complex tasks. Strong English written and verbal communications skills. Proficiency in technical scientific writing. Ability to work in a fast-changing environment. Collaborative team player.-
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