Responsibilities: Lead computer system validation projects related to authoring and executing specifications and validation documentation for enterprise computer systems. Author validation protocols ensuring that the technology solutions...
Roles & Responsibilities: 2-5 years of experience in a Quality Engineering or similar role within an FDA regulated industry preferably medical device and diagnostics that includes experience with CAPA and auditing processes. Participate ...
Roles & Responsibilities: 8 yrs of experience on clinical trial data analysis using SAS. Preferably in UNIX environment Familiar with UNIX command and environment. Deep knowledge on CDISC Standards and solid ADaM programming experience. ...