Beata Corral

- Manage all aspects of Cadwell’s Regulatory and Quality Assurance system including direct management of the QA / Regulatory team - Develop and maintain quality requirements and standards for the development of medical products, from incoming inspection of supplier material to final inspection of products - Implementation of ISO standard requirements including ISO 9001, ISO 17025, and ISO 13045, as well as FDA QSR Standard and European Medical Device Directive

- Develop and edit technical documents and procedures as part of the implementation of maintenance processes and procedures across Mission Support Alliance facilities - Ensure compliance with the requirements of the US Department of Energy (DOE), mission support contract, and MSA quality assurance program

- Prepare new laboratory for the process of ISO certification and establish a new QC system - Draft, prepare, and create necessary SOPs, forms, and other pertinent documents

- Serve as a board member and webmaster / editor for this international organization - Translate documents, help prepare newsletter, and organize social, cultural, and educational programs for the expatriated community

(Specialization: Usage of Energy/Illumination)