Prepares all protocols and reports for validation work. Coordinates all validation activities by constant communication with affected departments and personnel; oversees and reviews validation area processes and procedures. May require a bachelor's degree. Typically reports to a manager or head of a unit/department. Gains exposure to some of the complex tasks within the job function. Occasionally directed in several aspects of the work. Typically requires 2 to 4 years of related experience.
Create an Alert for Validation Engineer II Jobs
Create a Job Alert
Get notified when new Validation Engineer II jobs are posted
Job Details. Job Location. BMSC - Coppell, TX. Position Type. Full Time. Salary Range. Undisclosed. Validation Engineer II. Position Summary. The. Validation Engineer II prepares validation documents and executes them against a project timeline. This position trains other teams on documentation and validation practices, and must have a good knowledge of manufacturing processes, cleaning processes, test methods, and/or equipment. This position l...
Validation Engineer II is a full-time specialty, technical, professional position. A Validation Engineer II is responsible for reviewing engineering design documentation, developing testing methodologies, authoring commissioning, qualification, and validation testing protocols, performing (executing) field testing, and authoring final reports for completed testing. Position Basic Qualifications. Masters of Science degree in Chemical engineering a...
Job Summary. The Validation Engineer II is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes. Essential Functions. Design, review and execute validation document activities such as Factory acceptance test (FAT), Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) for equipment /utilit...
Position Description. The CQV Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. These people are responsible for protocol writing and execution (field verification), and development of summary reports at client sites. Other responsibilities include planning / coordinating work and directing small teams in document development and / or execution. Requirement...