Lisa De Candia
About Lisa De Candia
Lisa De Candia is a Sr. Manager at Bristol Myers Squibb, specializing in Global Quality Systems and QMS Document Management. She has extensive experience in the pharmaceutical industry, with a background in quality assurance and compliance.
Current Position at Bristol Myers Squibb
Lisa De Candia holds the position of Sr. Manager, Global Quality Systems - QMS Document Management at Bristol Myers Squibb. Based in Summit, New Jersey, she is responsible for overseeing the quality management systems (QMS) document management within the company. Her role focuses on maintaining and improving the standards of quality management to ensure compliance and efficiency in the organization's pharmaceutical operations.
Previous Experience at Bristol Myers Squibb
Before taking on her current role, Lisa De Candia worked as the Manager of Global GMP/GDP Compliance at Bristol Myers Squibb. During her 10-month tenure from 2019 to 2020, she contributed significantly to the company's adherence to good manufacturing and distribution practices (GMP/GDP), enforcing high standards and regulatory compliance in pharmaceutical manufacturing and distribution.
Work History at Celgene
From 2014 to 2019, Lisa De Candia worked at Celgene in Berkeley Heights, New Jersey, focusing on Global Quality Operations Systems - Product Complaints. During her five-year stint, she handled quality operations and addressed product complaints, aiming to ensure that Celgene's products met stringent quality standards and regulatory requirements.
Early Career in Pharmaceutical Industry
Lisa De Candia's career in the pharmaceutical industry began at Hoffmann-La Roche, where she worked as a Lab Technician from 1996 to 2002. She then served as an Investigations Specialist at Actavis from 2002 to 2009. Following that, she spent five years at Halo Pharmaceuticals as Sr. Supervisor, Quality Assurance before joining Celgene and later Bristol Myers Squibb.
Educational Background at Thomas Edison State University
Lisa De Candia pursued her academic studies at Thomas Edison State University, earning an associate degree. Her education has provided her with a strong foundation in the principles and practices of quality management systems, which she has applied throughout her extensive career in the pharmaceutical industry.