Neo Prism Solutions LLC has openings for the position Regulatory Quality Engineer with Master’s degree in Regulatory Affairs, Computer Science, Technology, any Analytical Science or related and 2 yrs of exp. in reviewing, evaluating, archiving, maintaining the regulatory documents and submissions. Review, approval for product labeling, advertising and promotion. Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents. Provide technical review of data or reports that will be incorporated into regulatory submissions. Review Tests for various systems in Medical Device environment adhering to FDA guidelines. Prepare project schedules and implement protocols for validation. Develop test strategies for validation products.
Work location is Schaumburg, IL with required travel to client locations throughout the USA. Please mail resumes to 917 N Plum Grove Rd., Suite C, Schaumburg, IL 60173 (or) e-mail: firstname.lastname@example.org
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