Stephanie Maulit ( Hafner)
About Stephanie Maulit ( Hafner)
Stephanie Maulit (Hafner) is the Manager of CAR T Site Supply Chain Program Management (Compliance Programs) at Bristol Myers Squibb in Summit, New Jersey.
Current Position at Bristol Myers Squibb
Stephanie Maulit (Hafner) is currently serving as the Manager for CAR T Site Supply Chain Program Management (Compliance Programs) at Bristol Myers Squibb. Based in Summit, New Jersey, she started this role in March 2021. Her responsibilities include ensuring compliance within the supply chain operations of CAR T therapy sites, which is crucial for maintaining regulatory standards in the biopharmaceutical industry.
Previous Roles at Bristol Myers Squibb
Prior to her current role, Stephanie Maulit (Hafner) worked as a Consultant at Bristol Myers Squibb from 2020 to 2021. During her 10-month tenure in Summit, New Jersey, she provided expertise in compliance and operational efficiency within the supply chain programs. This role was instrumental in paving the way for her current managerial position.
Experience at Roche Molecular Systems
Stephanie Maulit (Hafner) has an extensive background in molecular biology and pharmaceutical manufacturing, underscored by her 12 years at Roche Molecular Systems. From 2007 to 2019, she worked as a Senior Scientist, gaining significant experience in oligo purification and other specialized molecular biology techniques. Her role involved maintaining compliance through stringent good manufacturing practices (cGMP) and good documentation practices (GDP).
Educational Background in Biotechnology and Molecular Biology
Stephanie Maulit (Hafner) holds a Master of Science (M.S.) degree in Biotechnology from William Paterson University of New Jersey, which she earned from 2009 to 2011. She also has a Bachelor's degree in Molecular Biology from Montclair State University, completed between 2003 and 2007. Her academic background laid the foundation for her expertise in molecular biology and biotechnology.
Specialized Skills and Expertise
Stephanie Maulit (Hafner) is proficient in oligo purification, an advanced technique in molecular biology. She also possesses strong skills in good manufacturing practices (cGMP) and good documentation practices (GDP), essential for ensuring compliance in the pharmaceutical industry. Additionally, she has expertise in document drafting, change control, and validation, all of which are critical for maintaining regulatory standards in manufacturing operations. Furthermore, her supervisory experience in manufacturing operations highlights her leadership and management capabilities.