Terry Mc Clelland
About Terry Mc Clelland
Terry Mc Clelland is a Principal Scientist at Bristol Myers Squibb in Phoenix, Arizona, with extensive experience in compliance and validation leadership within biological production facilities.
Company: Bristol Myers Squibb
Terry Mc Clelland is currently employed as a Principal Scientist at Bristol Myers Squibb, located in the Phoenix, Arizona Area. Bristol Myers Squibb is renowned in the pharmaceutical industry for developing and delivering innovative medicines that help patients prevail over serious diseases.
Title: Principal Scientist
As a Principal Scientist, Terry Mc Clelland is responsible for spearheading scientific research and development programs. His role involves guiding technical processes, ensuring compliance with industry standards, and managing various scientific projects to support the company's objectives.
Previous Work at Celgene
In 2015, Terry Mc Clelland served as a Principal Scientist in Technical Services at Celgene in Phoenix, AZ. Although this tenure lasted only one month, it added to his extensive experience in the pharmaceutical and biotechnology sectors.
Previous Role: Director, Validation Technical Services at ImClone Systems
Terry Mc Clelland worked at ImClone Systems as the Director of Validation Technical Services from 2004 to 2007. During his three-year tenure in Branchburg, NJ, he directed validation projects and oversaw validation technical services crucial for the company’s compliance and operational efficiency.
Education and Expertise
Terry Mc Clelland holds a BS in Biology from Victoria University of Wellington, where he also pursued Honors Level studies. His academic background laid the groundwork for his expertise in quality assurance team leadership, validation project management, and aseptic production. He has notable proficiency in cleaning validation, aseptic process simulations, and computer system validation.
Skills in Compliance and Validation Leadership
With over 15 years of experience, Terry Mc Clelland is adept at managing compliance and validation leadership within biological production facilities. His skills include providing metrics-based guidance to manage risk in production and QC testing, resolving investigations using problem-solving tools, and implementing CAPA. His knowledge extends to promoting manufacturing alignment with U.S. and EU regulations.