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Regeneron Pharmaceuticals에서 B.S./M.S. 학위 취득자중 경력직 (Sr. Associate Scientist) 채용합니다. 아래의 Job posting을 참조하시고 많은 지원을 바랍니다. 지원은 링크를 통해서 하시고 (Sr. Associate Scientist - Formulation Process Development, Tarrytown, New York, United States of America | Regeneron Careers), mintai.hwang@regeneron.com으로 별도 이메일 부탁드립니다.

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Regeneron's Formulation Development Group (FDG) Process Development Team is seeking a Sr. Associate Scientist to support drug product process development studies for biologics (e.g. monoclonal antibody) and gene-based (e.g. viral delivery such as AAV) modalities. The candidate will work closely with FDG leads and scientists to ensure seamless technology transfer to various manufacturing sites and to provide technical support towards GMP manufacturing, validation campaigns, and post-launch activities.

A Typical Day In The Role Might Look Like:

• Plan, optimize, design, and execute drug product process development studies to ensure robust characterization of different unit operations (freeze/thaw, lyophilization, mixing, filtration, filling, etc.).
• Assist in developing small-scale models to effectively mimic manufacturing unit operations and support technology transfer to manufacturing teams.
• Work closely with FDG leads/scientists to ensure seamless progression of multiple late-stage process-related activities.
• Prepare, review, and edit technical reports.
• Bring in new ideas from literature and present work at group, department, and cross-functional meetings.
• Demonstrate strong and proactive problem-solving skills via critical thinking and effective communication.
• Manage process development equipment installation, operation, maintenance, calibration, and repairs.

This Job Might Be For You If You Have:

• The ability to work effectively independently as well as within a team environment.
• Capacity to multitask and quickly adapt to changes in priorities, as needed.
• Strong initiative and drive to complete challenging tasks and learn new technologies.

This position requires a BS degree in Biomedical or Chemical Engineering, Pharmaceutical Sciences, or related field with at least 6+ years of relevant industry experience or a MS degree with 3-6+ years of relevant industry experience. Experience with drug product development and characterization (formulation and process). Hands-on experience with analytical instruments used for biologics and gene-based therapeutics including HPLC-based chromatographic techniques (icIEF, SEC, IEX), biophysical methods (DLS, DSC, and UV-Vis), particle characterization methods (MFI and HIAC) required and vector quantification methods (ddPCR, ELLA) preferred. Basic understanding of common protein degradation pathways. Experience with statistical software is a plus (JMP).