*Role Validation Engineer - Medical Devices* Duration: 9+ Months
Location: PA, CO, NY , FL Skill Tag Black Box Testing, CSV, ISO 13485 *Overall Responsibilities: * Project Quality Support in the CSV Equipment Legacy Review Project Quality Support in CSV Equipment Remediation Projects Tasks: v Cover the part of the GxP-Compliance in the project. v Creation of the Validation documentation for GxP relevant system elements. v Know and follow the guidelines regarding the code of conduct, ethics and compliance programs and other relevant regulations Extended Duties: v Planning, coordination, execution and reporting of activities related to the project Requirements: v Higher education (Engineer or similar) and background in IT v Experience in similar position or extended experience as executer required. v Knowledge of national and international regulations and standards v GAMP5, ISO 13485, ISO 62304, FDA QSR, 21 CFR, Part 820, Part 11 v CSV Experience in the area of Medical Devices Manufacturing v Team Player v Excellent Communication skills -- You received this message because you are subscribed to the Google Groups "REQSRESUMES" group. To unsubscribe from this group and stop receiving emails from it, send an email to reqsresumes+unsubscr...@googlegroups.com. To post to this group, send email to reqsresumes@googlegroups.com. Visit this group at http://groups.google.com/group/reqsresumes. For more options, visit https://groups.google.com/d/optout.
