in engineering, Life Sciences, Chemistry, or a related field. 7–8 years of hands-on experience in instrument validation in regulated...
Responsibilities: Support client site with computer-related systems validation activities. Work in a GMP environment in lifecycle documentation development, protocol execution and leading project efforts for computerized systems includin...
Responsibilities: Validation documentation Authoring (validation plans, user requirements specifications, risk assessment, IQ-OQ-PQ protocols, trace matrix and summary reports). Experience in validating GMP Lab systems and Equipment. Re...