Tim Campbell

Tim Campbell

Car T Manufacturing Manager, Training And Compliance @ Bristol Myers Squibb

About Tim Campbell

Tim Campbell is the CAR-T Manufacturing Manager, Training and Compliance at Bristol Myers Squibb in Warren, New Jersey, with over 20 years of experience in the pharmaceutical industry, focusing on quality assurance and compliance.

Title

Tim Campbell currently holds the position of CAR-T Manufacturing Manager, Training and Compliance at Bristol Myers Squibb. He is based in Warren, New Jersey, United States.

Education and Expertise

Tim Campbell studied Business at Rockland Community College for one year from 1994 to 1995. Although the specific degree or certification achieved was not specified, his extensive expertise in the pharmaceutical industry spans over 20 years, particularly focusing on quality assurance, compliance, and document control management.

Background in Pharmaceutical Industry

Tim Campbell began his career in the pharmaceutical industry in 2000 at Wyeth Pharmaceuticals, where he worked as a Manufacture Supervisor for seven years. His career trajectory includes roles such as Sr. QA Associate II/Document Control Manager at Pfizer Pharmaceuticals (2008-2016), Team Lead Quality Assurance at Halo Pharmaceutical, Inc. (2016-2018), and QA Manager Compliance Training at Cambrex (2018-2020).

Experience in CAR-T Cell Therapy Manufacturing

Tim Campbell has been involved in CAR-T cell therapy manufacturing since joining Bristol Myers Squibb in 2020. In his current role, he manages training and compliance for CAR-T manufacturing, highlighting his specialization in advanced cell therapies and biopharmaceuticals.

Roles in Quality Assurance and Compliance

Throughout his career, Tim Campbell has held several managerial positions focused on quality assurance and compliance. At Pfizer Pharmaceuticals, he served as Sr. QA Associate II/Document Control Manager, where he managed document control for eight years. His subsequent roles at Halo Pharmaceutical, Inc., Cambrex, and Bristol Myers Squibb also emphasized his expertise in maintaining high standards of quality and compliance in the pharmaceutical manufacturing process.

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