Sobre

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function: Supply Chain Manufacturing Job Sub Function: Manufacturing Assembly Job Category: Business Enablement/Support All Job Posting Locations: Juarez, Chihuahua, Mexico Job Description: About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech About Surgery Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent for Engineering Clerk I to be in Cd. Juarez, in plant Independencia. Purpose: Provide overall support for engineering activities. Provide support during validation activities and writing the documentation. Responsible for engineering purchases through different purchasing platforms Provide overall support for VMP activities. You will be responsible for: Perform NCR lifecycle documentation and investigation, using statistical concepts. Provides technical support to identify the causes of non-conformances and process failures and to implement corrections thus assuring process performance and compliance against Ethicon’s QSR, GMP and ISO requirements for the manufacturing process. Performs non-conformance investigations including NCR origination, bounding, product control, failure investigation, correction, and documentation with the non-conformance system. Support engineers in performing validation activities, execution of protocols, engineering studies and documentation. Help Write engineering documentation (protocols, procedures, special instructions, reports, etc.) Supports the documentation changes in compliance with Ethicon’s Change management system. Engineering support in the completion of projects mainly focused on quality improvements, cost/scrap reduction, increased capacity and New Products. Conduct robust investigations. Analyzes data and recommends actions for process, equipment and system improvement. Review all PLM System (Software solution used by Quality Systems to manage the document control process) validation documentation to Complete VMP Action Tasks. Update VMP logs with all applicable validation references, protocols, completion reports etc. that support the validated state of the validation components. Generate and provide quarterly change orders to create, release, and revise VMP Procedures and VMP Logs. Ensure all validation packages (group of a specific document class) involve the required documentation to support and assure the validated state of a validation component. Monitoring, tracking and assurance that the annual review activities are performed. Ensure Validation Baseline/Periodic Reviews are completed on time. Supports the VMP related documentation changes in compliance with Ethicon’s Change management system. Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable. For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable o Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures Performs other duties assigned as needed Qualifications / Requirements: A minimum of High School Diploma or equivalent is required From 0 to 2 years of experience in related fields. Bilingual English/Spanish (Preferred). Computer skills: Excel (including charts/graphs), Word, Internet Explorer. Experience in medical device manufacturing environment. (Preferred) Knowledge of medical product and process design concepts such development, materials, standardization science and basic statistics. (Preferred) Knowledge of word processing, spreadsheet analysis, presentation graphics, some engineering analysis and some statistical software (Minitab preferred). Analytical thinking to provide and lead product inquiry investigations. Ability to work in a cross-functional team to complete projects, knowledge in PE tools such as Kaizen  Ability to solve basic problems using FI methodologies such as Five Whys, 5Ms, and others. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. 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