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 jnj.com.
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.
Job Function:
Supply Chain ManufacturingJob Sub Function:
Manufacturing AssemblyJob Category:
Business Enablement/SupportAll Job Posting Locations:
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 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 for Ethicon in Ciudad Juarez.
Purpose:
- Provide overall support for engineering activities.
- Provide support during validation activities and writing the documentation.
- Responsible for engineering purchases through different purchasing platforms
- Provide overall support for VMP activities.
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 of 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 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.
- Review all PLM System (Software solution used by Quality Systems to manage the document control process) validation documentation to Complete VMP Action Tasks.
- Update VMP logs with all applicable validation references, protocols, completion reports etc. that support the validated state of the validation components.
- Generate and provide quarterly change orders to create, release, and revise VMP Procedures and VMP Logs.
- Ensure all validation packages (group of a specific document class) involve the required documentation to support and assure the validated state of a validation component.
- Monitoring, tracking and assurance that the annual review activities are performed.
- Ensure Validation Baseline/Periodic Reviews are completed on time.
- Supports the VMP related documentation changes in compliance with Ethicon's Change management system.
- 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:
EDUCATION: A minimum of High School Diploma and Engineering Bachelor's Degree complete or in progress.
EXPERIENCE: 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.
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS*
- Bilingual English/Spanish (Preferred).
- Computer skills: Excel (including charts/graphs), Word, Internet Explorer.
- Experience in medical device manufacturing environment. (Preferred)
- Knowledge of 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 a cross-functional team to complete projects, knowledge in PE tools such as Kaizen
- Ability to solve basic problems using Fl 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.
Required Skills:
Preferred Skills:
Agile Manufacturing, Assembly Operations, Communication, Data Savvy, Execution Focus, Good Manufacturing Practices (GMP), Manufacturing Processes, Manufacturing Science and Technology (MSAT), Plant Operations, Predictive Analytics, Predictive Maintenance, Problem Solving, Process Oriented, Quality Auditing, Repair Management, Safety-Oriented, Technologically Savvy