.Business Area:**Location**:Ciudad Juárez, MXCountry:Employment type:**A global job with an impact**In the job as Automatization Engineer, you will have the chance to provide support to the organization, impact product development and your own daily tasks and responsibilities. You will experience a very varied working day in a dynamic organization. You will work closely with your local and international colleagues from Denmark and Asia, but also in the US.**DUTIES & RESPONSIBILITIES**:The Automatization Engineer must be the expert on different automated equipment and control systems functions and needs in the medical manufacturing environment, capable of assessing, anticipate and provide support and/or troubleshooting skills to solve problems related to automation and control elements of the manufacturing equipment. Must be able as needed to direct and lead different projects related to automated equipment.- Capabilities to work with projects, manage changes, find machinery, implement, and validate new machinery.- Experience in PLC- Experience project management of machine constructions- Must be able to work under pressure and obtain good results individually and as a team.- Manufacturing Experience in the Medical Industry is desirable- Industrial, mechanical, or plastic engineering degree- Lead project teams to increase productivity, reduce scrap, implement lean manufacturing, improve system availability, safety, and product quality. The ability to recognize opportunities and appropriately prioritize projects based on potential improvement and risk is imperative.- Perform root cause investigations for the CAPA process. Report findings to cross functional team, propose and implement corrective actions and verify corrective action effectiveness.- Develop SOPs for equipment operation, part inspection, equipment change-over, and preventive maintenance activities that are current and accurate.- Write Capital Appropriations for new equipment required to support Manufacturing. Create justification for approval of investments. Work with vendors to provide quotes and identify system specifications. Coordinate project timelines to meet manufacturing requirements.- Write, Review, and Execute PVP, IQ, OQ, PQ, FMEA, and RA documents and summaries. Familiarity with cGMPs, ISO, and other Medical Device Industry regulations and specifications.- Support manufacturing by diagnosing system or process failures and working with Maintenance and/or the Tool Room personnel to implement system fixes.- Coordinate engineering expertise to identify and implement safety improvements consistent with OSHA standards.- Collaborate with manufacturing to study, evaluate and improve equipment and processes utilizing data driven analysis, DOE and any other applicable methods