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:** Technology Product & Platform Management **Job Sub** **Function:** Business Systems Analysis **Job Category:** Scientific/Technology **All Job Posting Locations:** Ciudad 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 MES Business Administrator II to be in Cd. Juarez in plant Independencia.** **Purpose:** Works to achieve day-to-day objectives under close supervision with limited impact beyond the area of responsibility. Completes simple data analysis to support business solutions and meet reporting requirements. Applies functional business systems knowledge to determine solutions to business needs including identifying, analyzing and documenting requirements. Assists with developing, modifying, applying, and maintaining standards for systems quality operating methods, systems, and procedures. Compiles data for technical reports, technical memoranda, and other documents. Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team. This job is salaried. **You will be responsible for** **:** In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: • Leads engineering projects ensuring they are completed on schedule and within budget with no impact to quality or customer service. • Develops and executes detailed project plans using standard project management tools like Microsoft project, charter, Gantt chart and others. • Prepares/reviews capital & expense forecasts for assigned projects. Prepares capital authorization requests (aCAR). • Controls project costs by approving and monitoring expenditures, administrating supplier contracts. • Reports status on assigned projects in various formats to various organizational levels. • Manages the NC and CAPA process by documenting, investigating, root cause analysis, and implementing corrective actions for product non-conformances. • Ensures effective use of engineering and quality systems and adherence to quality system regulations (QSR). • Follows the design control process for all applicable projects. • Performs process validations on new, transferred, or modified processes for MES Implementation. • Confirms product performance by designing and conducting tests and performs process validation on new, transferred, or modified MES configuration. • Ensures compliance to the quality policy in all activities. • Maintains project integrity and reputation through compliance with state and federal regulations. Is responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. • Maintains safe and clean working environment by enforcing procedures, rules, and regulations. • Leads cross functional teams during investigations for MES Continues improvement. • Is responsible for supervising technicians in Manufacturing Engineering Systems. • Responsible for communicating business related issues or opportunities to next management level. • 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. • 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:** • Experience in a manufacturing environment and/ or medical device industry preferred. • A minimum of bachelor’s degree in an Engineering or Science discipline. • Strong proven experience on MES software administration (CAMSTAR, ERP, AQR). • Experience in CAMSTAR configuration (WF, BOP, E-procedure, Task list, UDCD, queries). • Strong experience on troubleshooting Personal Computers (PCs) and the different devices (drivers, controllers). • B.S Engineering Degree or Science Discipline. • Starter English Level is preferred. • Approximate experience, or equivalent knowledge and skills, necessary to satisfactorily perform the position responsibilities. • 2 to 4 years’ experience in manufacturing/design engineering. •Strong PC (Personal Computer (PC)) experience required. • Experience in project management and good documentation practices. • Experience in CAMSTAR Software configuration. • Position requires excellent communication skills plus the ability to function in a team-based manufacturing environment. • Bilingual: English/ Spanish. • Knowledge of information systems including but not limited to ERP, Quality Systems & Documentation Control Systems. • Desired/Preferred Qualifications. • Six Sigma or Lean certification as Green Belt or Black Belt is preferred. • Knowledge on equipment validation documents (IQ (Installation Qualification) or equivalent). • Knowledge on GxP (Good x Practice) software validation (SDCL methodology). • Medical device or pharmaceutical industry experience. • Experience with OPC servers and/or WinCC (Kepware/Omni server, etc.).