MES OT Lead

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

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Johnson & Johnson is recruiting for a MES OT Lead to join our team in Irving TX.

About MedTech

Fueled by innovation at the intersection of biology and technology were 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 MES and OT Lead is a technical expert on different MES software and related technology capable of providing support and/or troubleshooting skills to solve problems to the different business units through the implementation of new/update MES configuration. Must be able to lead different projects related to MES (schedule plan forecast resource and manage all the technical activities aiming at ensuring project accuracy and quality from conception to completion).

Key Responsibilities:

• Lead engineering projects ensuring that projects are completed on schedule and within budget with no impact to quality or customer service.

• Develop and execute detailed project plans using standard project management tools (Microsoft project charter Gantt chart etc.).

• Prepare/review capital & expense forecasts for assigned projects. Prepare capital authorization requests (CAR).

• Controls project costs by approving and monitoring expenditures; administering contractor contracts.

• Report status on assigned projects in various formats to various organizational levels.

• Manage the NC and CAPA process by documenting investigating root cause analysis and implementing corrective actions for product non-conformances.

• Ensure effective use of engineering and quality systems and adherence to quality system regulations (QSR).

• Perform 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.

• Ensure compliance to the quality policy in all activities.

• Maintains safe and clean working environment by enforcing procedures rules and regulations.

• Lead cross functional teams during investigations for MES Continues improvement.

• Responsible for supervising technicians in Manufacturing Technician MES.

• 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.

Experience and Education:

• 4-7 Years of Experience

• Experience in a manufacturing environment and/ or medical device industry preferred.

• A minimum of Bachelors degree in an Engineering or Science discipline.

• Strong proven experience on MES software administration (Camstar JDE SAP Kepware Wonderware).Experience in Camstar configuration (WF BOP E-procedure Task list UDCD queries etc.)

• Strong experience on troubleshooting Personal Computers (PCs) and the different devices (drivers controllers)

Required Qualifications

• Strong 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.

• Knowledge of information systems including but not limited to JDE Quality Systems & Documentation Control Systems.

Preferred Qualifications

• Six Sigma or Lean certification as Green Belt or Black Belt is preferred.

• Knowledge on equipment validation documents (SOR SRS CSV IQ or equivalent).

• Knowledge on GxP software validation (SDCL methodology).

• Medical device or pharmaceutical industry experience

• Experience with middleware software (Kepware/Wonderware etc.)

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please contact us via or contact AskGS to be directed to your accommodation resource.

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