Description
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 ManufacturingJob Sub Function:
Production Equipment Repair & MaintenanceJob Category:
Business Enablement/SupportAll Job Posting Locations:
Ciudad Juarez, Chihuahua, MexicoJob 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 Cardiovascular
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 Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
We are searching for the best talent for MES SPECIALIST II to be in Cd Juarez.
Purpose:
Completes tasks for the support function of the Production Equipment Repair & Maintenance unit, and follows administrative processes ensure accuracy, timeliness, and quality of deliverables.
Helps administer the technical implementation, modification and ongoing analysis of the quality, safety and efficiency of discrete production of unit-based items assembled from component parts.
Helps interpret key data points collaborating with Manufacturing Engineers to develop Repair and Maintenance schematics for the rollout of new and improved repair and maintenance processes, tools and equipment.
Checks regular status on operational control standards and testing equipment to assess conformance with engineering specifications, including test apparatus of raw materials, parts, components, finished items and packaging.
Demonstrates Johnson & Johnson’s Leadership Imperatives and Credo.
You will be responsible for:
• Representee of MES team to change request owner
• Supports shopfloor control team based on business impact
• Performs change intake process and understands requirements
• Performs change/impact assessments for MESDC
• Maintains and improves MES SOP’s
• Maps new processes or processes undergoing change
• Writes ECO’s, documents NR’s OBS, AP
• Takes voice of the customer and proposes internally how to improve processes
• Performs training and supports new hire introduction
• Participates in the administration and configuration of MES and connected systems.
• Coordinate and deliver training to MES users.
Provides support in the development, testing, validation, and implementation of configurations of
such systems.
• Provides support in the process of deploying the MES system to production, in aspects such as
documentation, training of production personnel and problem solving in the same area.
• Provides sustaining support to the MES and connected systems
• Participates in the modification and maintenance of guidelines and procedures related to the
areas of responsibility.
• Participates in the discussion of conceptual bases for the design and development of new
configurations of manufacturing systems.
• Responsible for monitoring Interfaces related to the MES system.
• Participates in QA non-conformities and Observations.
• Collaborates in CAPA actions related to the MES system.
• Responsible for communicating business-related issues or opportunities to the next
administrative level
• Responsible for ensuring that subordinates follow all of the Company's guidelines related to
Health, Safety and Environmental practices and that all necessary resources to do so are
available and in good condition.'
• Responsible for communicating business related issues or opportunities to next management
level
• 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:
• Studies in Technical Career or equivalent applicable to the area: Mechanical; Electrical;
Electromechanical; Electronic; Information Technology; Industrial or system preferably.
• Knowledge and Skills to successfully develop the responsibilities of the position.
• Experience in conducting system integration test, user acceptance test and production rollout
preferably
• Experience in user problem understanding, requirements gathering, analysis, design and
solution proposal preferably
• Extensive knowledge in computational packages.
• Excellent verbal and written communication skills including the ability to write technical
documentation and communicate technical information to non-technical audiences.
• Ability to read and understand technical documentation associated with the specific discipline.
• Advanced Language level: Spanish/English.
• Knowledge of GMP's (Good Manufacturing Practices) / ISO (Preferably)
• Knowledge in process and SDLC validation activities (Preferably)
Knowledge of FDA regulations 21-CFR part 820 and Part 11 (Preferably).
• Knowledge of SQL DB (Preferably)
• Knowledge of programming tools (Python, Microsoft Apps, etc.) (Preferably)
• Knowledge in CAMSTAR (Preferably).
• Knowledge of JDE, CMMS, cPDM, Windchill, SAP (Preferably)
• Knowledge in Engineering Changes ECOs. (Preferably)
• Experience in medical industry (Preferably)
