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 Manufacturing
Job Sub Function:
Manufacturing Assembly
Job Category:
Business Enablement/Support
All Job Posting Locations:
Ciudad Juarez, Chihuahua, Mexico
Job Description:
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 Principal Engineering Clerk
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:
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
Perform NCR lifecycle documentation and investigation, using statistical concepts.
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.
Performs non-conformance investigations including NCR origination, bounding, product control, failure investigation, correction, and documentation with the non-conformance system.
Support engineers in performing validation activities, execution of protocols, engineering studies and documentation.
Help to Write engineering documentation (protocols, procedures, special instructions, reports, etc.)
Supports the documentation changes in compliance with Ethicon’s Change management system.
Engineering support in the completion of projects mainly focused on quality improvements, cost/scrap reduction, increased capacity and New Products.
Conduct robust investigations. Analyzes data and recommends actions for process, equipment and system improvement.
Ensure compliance to the quality policy in all activities.
Ensure safe working conditions and practices in the department as well as providing support on the plan safety requirements.
Enable proactive approach for process performance and customer satisfaction driving appropriate actions across all levels of the organization.
Acts in accordance with safety regulations and procedures.
Supports internal and external audits and inspections.
Submit purchase requisitions for Engineering department.
Support Project Spending Management.
Other responsibilities may be assigned and not all responsibilities listed may be assigned.
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
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
