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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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

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

We are searching for the best talent for Engineering Clerk Principal to be in Cd. Juarez, in plant Independencia.

Purpose:

• Provide overall support to engineering activities.
• Provide support during validation activities and writing the documentation.
• Responsible for engineering purchases through different purchasing platforms

You will be responsible for:

o Perform NCR lifecycle documentation and investigation, using statistical concepts.
o Provides technical support to identify the causes for 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.
o Performs non-conformance investigations including NCR origination, bounding, product control, failure
investigation, correction, and documentation with the non-conformance system.
o Support engineers in performing validation activities, execution of protocols, engineering studies and
documentation.
o Help to Write engineering documentation (protocols, procedures, special instructions, reports, etc.)
o Supports the documentation changes in compliance with Ethicon’s Change management system.
o Engineering support in the completion of projects mainly focused on quality improvements, cost/scrap
reduction, increased capacity and New Products.
o Conduct robust investigations. Analyzes data and recommends actions for process, equipment and system
improvement.
o Ensure compliance to the quality policy in all activities.
o Ensure safe working conditions and practices in the department as well as providing support on the plan
safety requirements.
o Enable proactive approach for process performance and customer satisfaction driving appropriate actions
across all levels of the organization.
o Acts in accordance with safety regulations and procedures.
o Supports internal and external audits and inspections.
o Submit purchase requisitions for Engineering department.
o Support Project Spending Management.
o Other responsibilities may be assigned and not all responsibilities listed may be assigned.
o Responsible for communicating business related issues or opportunities to next management level
o Responsible for following all Company guidelines related to Health, Safety and Environmental practices as
applicable.
o 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.
o Performs other duties assigned as needed.

Qualifications / Requirements:

• A minimum of High School Diploma and Engineering Bachelor’s Degree complete or in progress.
• From 6 to 8 years of experience in related fields. Or currently pursuing an Engineering Bachelor’s Degree with half of School credits completion or recently completed.
• Bilingual English/Spanish (Preferred).
• Computer skills: Excel (including charts/graphs), Word, Internet Explorer.
• Experience in medical device manufacturing environment. (Preferred)
• Knowledge on 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 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.
• Self-motivated
• Strong communication and interpersonal skills.
• Requires good networking.
• Entails significant interaction with technical peers and manufacturing associates.
• Self-motivated and capable of completing job duties with limited supervision