- Bristol Myers Squibb (Devens, MA)
- …utilities and maintaining equipment systems in a qualified / validated state a cco r ding to established policies and pr o cedures. The i ndividual participates in ... proj e cts an d ongoing wor k activities of medium to high...Executes and/or Leads installation, commissioning activities of area specific process equipment, validation of SIP/CIP processes, qualification of environmental… more
- Bristol Myers Squibb (Seattle, WA)
- …going through critical lifecycle changes, eg, vector changes, drug product process changes, new manufacturing sites and suites establishment. This individual will ... with subject matter expert representatives from key functions, including analytical, process , manufacturing, quality, regulatory, etc., and key matrix leaders from… more
- Bristol Myers Squibb (Bothell, WA)
- …shields, lab coats, full body gowns, hairnets, gloves, and hearing protection. + May be r equire d to work in and around laboratories and controlled, enclosed, ... of cGMP regulations and Regulatory Agency requirements applicable to biologics and cell therapy manufacturing. + Demonstrated experience building...restricted areas, includ ing clean rooms. + May be r equire d to carry and/or lift… more
- MetroHealth (Cleveland, OH)
- …with laboratory equipment. Ability to prepare, review and execute GMP documents. Experience in scale-up/ process R & D and technical transfer. Knowledge of ... of laboratory and cell therapy experience and prior experience working with biologics , the FDA, and other regulatory bodies. Extensive knowledge of lab, service… more