Rebecca Jordan
About Rebecca Jordan
Rebecca Jordan is a Senior Manager/Principal Engineer in Sterility Assurance for Cell Therapy at Bristol Myers Squibb, with over a decade of experience in the pharmaceutical manufacturing industry.
Company
Rebecca Jordan is currently working at Bristol Myers Squibb, a global pharmaceutical company. She holds the position of Senior Manager/Principal Engineer - Sterility Assurance focused on Cell Therapy. Bristol Myers Squibb is known for its contributions to innovative medicines and therapies, and Jordan's role is crucial in maintaining sterility assurance for advanced cell therapy products.
Title
Rebecca Jordan serves as Senior Manager/Principal Engineer - Sterility Assurance - Cell Therapy at Bristol Myers Squibb. In her role, she ensures the sterility of cell therapy products, which is critical for patient safety and therapy efficacy. Her work includes designing contamination control programs and implementing sterility testing protocols.
Education and Expertise
Rebecca Jordan holds a Bachelor of Science (BS) in Biology/Biological Sciences, General, from Fitchburg State University. She has over a decade of experience in the pharmaceutical manufacturing industry, specializing in sterility assurance and contamination control for Advanced Therapy Medicinal Products (ATMPs). Her expertise includes bioburden, endotoxin, and sterility testing, as well as proficiency in rapid methods for these tests.
Work Experience
Rebecca Jordan has a diverse work history spanning multiple organizations. Prior to her current role, she served as a Sr. QC Specialist (Microbiology) at Bristol Myers Squibb for 11 months in 2020 in the Greater Seattle Area. She has also worked at Juno Therapeutics, Inc. as a Sr. Associate and Specialist, QC Microbiology from 2018 to 2020, and held positions at Alcami Corporation and Associates of Cape Cod, Inc. She began her career as a QC Analyst I (Microbiology) at Bristol-Myers Squibb in 2009.
Background and Skills
Rebecca Jordan's background includes substantial experience in pharmaceutical manufacturing, in both large and small organizations, start-ups, and CDMOs. She is adept at new equipment and product implementation, including Installation Qualification (IQ), Operational Qualification (OQ), method validation, and Environmental Monitoring Program Qualification (EMPQ). She is proficient in water purification systems (WFI) monitoring and contamination root cause analysis (RCA), and experienced in aseptic process simulation (media fill). Her skills include creating interactive training presentations and she is known for her resiliency and adaptability in fast-paced environments.