It is located in *SPRING HOUSE, PA.* *Duties:* Prepares and executes all protocols and reports for validation work. May coordinate all validation activities by constant communication with related departments and personnel; oversees and reviews validation area processes and procedures. May require a bachelor's/master's degree in engineering and 2-5 years of experience in the field or in a related area. Familiar with standard concepts, practices, and procedures within a particular field. Three (3) years experience.
In this position, consultant will be supporting the GMP/QSR validation for Analytical Research and Development laboratory instrument computer systems and the validation of infrastructure applications. *Responsibilities include: ** Managing the validation of laboratory instruments and computer systems * Corporate validation and QA policy * Supervising the validation * Maintaining the validated states of instruments and equipment for preclinical and clinical lab, formulation lab, and translation medicine lab, including HPLC, plate reader, UV/VIS spectrophotometer, LC/MS etc.. --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "US_IT.Groups" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [email protected] For more options, visit this group at http://groups.google.co.in/group/us_itgroups?hl=en -~----------~----~----~----~------~----~------~--~---
