Principal Engineering Clerk

**Job Function**:
Supply Chain Manufacturing
**Job Sub Function**:
Manufacturing Assembly
**Job Category**:
Business Enablement/Support
**All Job Posting Locations**:
Ciudad Juarez, Chihuahua, Mexico

**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.

**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.

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

**Purpose**:
Helps ensure the completion of key tasks for the support function of the Manufacturing Assembly area to ensure accuracy, timeliness, and quality of deliverables.
Implements set up, operation, maintainence, and troubleshooting techniques based on best practices in the industry and fosters a safe working environment.
Moves, packs, and sorts raw materials or finished goods, ensuring quality and efficiency as materials move along the assembly line.
Evaluates staff competency with specialized machinery/equipment in order to develop staff and undertake new projects.
Helps coordinate delegation and scheduling of routine and maintenance tasks.
Demonstrates Johnson & Johnson’s Leadership Imperatives and Credo.

**You will be responsible for**:

- 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.

**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