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For your reference, we have included the original job posting below.
Principal Scientist
Job Number:
38341577
Company Name:
Amgen
Job Location:
West Greenwich, RI US
Job Categories:
Engineering & Architecture Science & Biotech
Principal Scientist
Serve as process sciences leader and subject matter expert in the development and characterization of mammalian cell culture processes for clinical- and commercial-stage manufacture of biopharmaceuticals.
Manage and supervise a diverse team of process scientists and associates, including performance management, goal setting, overcoming obstacles and delivering results within project timelines.
Provide strong leadership of cross-functional teams to resolve complex problems while meeting quality, schedule, communication and cost objectives.
Evaluate and develop new technologies for incorporation into processes, equipment and operations.
Provide technical investigation support and proactively address process and raw material risks to ensure supply.
Build and maintain effective collaborations with diverse partner organizations across the Amgen network and with external suppliers.
Infrequent domestic and international travel may be required.
Basic Qualifications Doctorate degree and 2 years of directly related experience OR Master's degree and 6 years of directly related experience OR Bachelor's degree and 8 years of directly related experience OR Associate's degree and 10 years of directly related experience OR High school diploma / GED and 12 years of directly related experience
Preferred Qualifications Advanced degree in Life Sciences or Chemical Engineering
Knowledge and understanding of cell biology, protein expression, cell culture, media development and small-scale bioreactor operations
Fundamental expertise and experience in development and characterization of mammalian cell culture processes
Experience in technology transfer and scale-up for cell culture and harvest processes
Demonstrated skills in building high-performing teams and cross-functional partnerships and in leading matrix teams to advance complex projects to completion
Knowledge and understanding of regulatory and cGMP requirements, including successful preparation and defense of CMC regulatory submissions and support of regulatory inspections
Excellent communication and technical writing skills
