Empleo QA supervisor oscor inc.
Ensure the proper functioning of quality assurance established for manufacturing processes, meeting the minimum criteria of the rules and policies governing the manufacturing processes of medical devices.
Coordinate inspections of incoming raw materials in the shortest time possible so that it can be used in the process of manufacturing
Coordinate human resources required for the necessary inspections are conducted to ensure quality and compliance with specifications during the manufacturing process
Document the inspections and incidents and deviations that arise during the manufacturing process
Coordinate and monitor environmental, microbiology and water testing that are made in production areas
Validation and approval of the documentation generated in the manufacturing and transfer of new products processes
Participate in the validation process of new product
Conduct ongoing internal audits and participate in external audit processes
Adaptability and flexibility to work in a constant changing environment. Analysis of data and information for decision making. Analysis of process flow. Ability to team work and leadership. Knowledge of statistical process controls. Knowledge of standards and quality regulations established for the medical industry and manufacturing of medical devices. Dynamic and proactive. Focus on continuous improvement and quality. Effective communication skills in oral and written English and Spanish. MS Office. Details Oriented. Results oriented. Sense of urgency. Trouble solving.
Nivel académico de Grado, Postgrado, Máster
2 o más años de experiencia
Inglés: dominio del idioma (nativo ó 2do. idioma)
Requiere residencia actual en República Dominicana
Currículum con foto
35 a 45 años de edad (Preferible)
Tipo de contrato
Medical Devices Manufacturing
Área de trabajo
1. Colocar en el asunto del correo: QA Supervisor
2. Send an English resume to
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