**Johnson & Johnson Medical Devices Companies**At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered.In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products, solutions and help people live longer, healthier lives. And you can be part of it too within Ethicon Endo Surgery.**Job Summary**:Completes engineering projects by organizing and controlling project elements and is responsible for all engineering and technical disciplines that projects involve. The project engineer will schedule, plan, forecast, resource and manage all the technical activities aiming at assuring project accuracy and quality from conception to completion.Coordinate phases of work with outside vendors.Write and execute validation documents aligned with GDP's.Perform data gathering and data analysis**Education**:B.S Engineering Degree or Science Discipline.**Job Experience**:2 to 4 years experience in manufacturing/design engineering.**Ideal Requirements**:Bilingual: English / Spanish preferred.Six Sigma Green or Black Certification and/or other project management methodology is preferredAble to read and understand engineering drawings and translate product drawings into process informationExperience with manual and automation assembly equipment and/or processesExcellent organizational and communication skills (written and oral, fluent in English) plus the ability to function/lead in a team-based manufacturing environment.Experience in Bill of Material (BOM) structures.Understanding of Lean Manufacturing and lean principles with an ability to promote and drive continuous improvement.Understanding of design and production costs to include waste, downtime, scrap and re-workUnderstanding of calibration concepts and Measurement systems.Understanding of International customs procedures.Experience with the essential requirements of the Medical Device Directive (MDD), ISO 13485, FDA design controls or similar regulatory environment in design control and process validationExperience on medical device (Class II or Class III) projects.Experience utilizing enterprise resource planning (ERP) tools.**Location**: This position is located in Ciudad Juarez. Expected travel for either domestic and international is 20%**Type of contract**: Temporary 24 monthsTipo de puesto: Tiempo completo, Por obra o tiempo determinadoSalario: $27,600.00 - $27,601.00 al mesHorario:- Turno de 8 horasPrestaciones:- Vales de despensaIdioma:- Inglés (Obligatorio)Disponibilidad para viajar:- 25 % (Obligatorio)
