Matthew Randolph Email & Phone Number

Horseheads, Ny, Us

Horseheads, Ny, Us

St Petersburg, Florida, Us

I have taken responsibility for large parts of the validation infrastructure across my region, managing the a small validation engineering group across three locations across the North East United States region.In addition to primary responsibility for the management of the validation and process monitoring program within my manufacturing facility, I supervise the execution of the validation and process monitoring programs for my region.As Jabil Healthcare continues to develop its own, unique quality system, I have taken the primary role in developing the validation program. This task has fallen to me as one of the most experienced validation engineers in the company, and almost certainly the most passionate about developing a robust, flexible program. My responsibilities include review of all equipment and process validation documentation and guiding performers through the validation process. I manage the regional CSV program, as well as acting as the first point of contact for corporate software validation for the region. I develop and maintain the Site Validation Master plan. This includes the development of site-specific and regional criteria and methods, in order to maintain consistency in program implementation.

St Petersburg, Florida, Us

Continuing my role after the transition of Johnson and Johnson's medical device manufacturing to Jabil Healthcare, I was responsible for the management of the validation and process monitoring program within my manufacturing facility, while also representing and leading my region in the development of validation procedures used across the Jabil franchise.My responsibilities include review of all equipment and process validation documentation, and guiding performers through the validation process. This includes the development of site-specific criteria and methods, in order to maintain consistency in program implementation. On a global level, I am one of a select group responsible for development of the validation program being implemented across the entire Johnson and Johnson medical device franchise. This includes frequent discussion on and review of current procedures, in order to ensure compliance across a wide array of process and equipment types. In addition, I provide guides and techniques to smaller groups to ensure quality at all organization levels.

Raynham, Ma, Us

I am responsible for the management of the validation and process monitoring program within my manufacturing facility, while also representing and leading my region in the development of validation procedures used across the full Johnson and Johnson Medical Device franchise.My responsibilities include review of all equipment and process validation documentation, and guiding performers through the validation process. This includes the development of site-specific criteria and methods, in order to maintain consistency in program implementation. On a global level, I am one of a select group responsible for development of the validation program being implemented across the entire Johnson and Johnson medical device franchise. This includes frequent discussion on and review of current procedures, in order to ensure compliance across a wide array of process and equipment types. In addition, I provide guides and techniques to smaller groups to ensure quality at all organization levels.

Raynham, Ma, Us

Oklahoma City, Ok, Us

Performing a large variety of tasks to bring into and keep equipment suitable for use in GMP facilities. This includes the design and performance of equipment and software qualification protocols, development of equipment and validation SOPs, management and training of new employees, and the selection and purchasing of process equipment.In this position, I have troubleshot, validated and gained experience with a wide array of devices, including bioreactors, autoclaves, building automation systems, air filtration systems, biological safety cabinets, centrifuges, homogenizers, chillers, all manner of cold chain storage, pumps, and other assorted equipment.

Norman, Oklahoma, Us

Designed and tested experiments to reduce the immunogenicity of targeted cancer therapy proteins through PEGylation. Work included literature research, experimental design, weekly research presentation, SDS-PAGE, size exclusion chromatography, protein production, and various other assays for testing concentrations, binding strength, and protein activity.