Principal Engineering Clerk

hace 2 meses

Ciudad Juárez Chih, México Johnson & Johnson A tiempo completo

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.

We are searching for the best talent for PRINCIPAL ENGINEERING CLERK (TEMPORARY 6 MONTHS) to be in Juarez, Chih., 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:
Responsibilities may include, but are not limited to:

- 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

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