Process Engineer Ii

hace 2 semanas

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 **PROCESS EGINEER II** to be in **Salvarcar.**

**JOB SUMMARY**

Identifies and develops internal areas of opportunities through the DMAIIC methodology and tools of Excellency in processes with the purpose of reducing the manufacturing cost of the products and continue with the culture of continuous improvement and follows up in quality and regulatory requirements comprehended in the business strategy

**DUTIES & RESPONSIBILITIES**

Under (e.g. limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

- Must know and follow the policies and procedures of the company in which he/she works at, related to work activities of his area of responsibility, as well as ensuring that his/her subordinates know and follow the policies of the company and the procedures related to their work activities and area of responsibility.
- Completes the trainings in the area of responsibility within the assigned period of time. The training is required for the changes and implementations of existing policies and procedures, new functions, etc. Completes the retraining in areas such as safety and environment.
- Follows all the safety policies of the company and safety precautions within the work area. Promotes safety to all the associates that enter the work area.
- Responsible for the leadership and execution of projects focused on the reduction of the variation originated by process and/or product design that influences positively in the metrics of the business, strategic directions and financial results.
- Maintains updated work plans for projects through the year such as design changes in the products that are base of the business (extension in product lines), process changes and cost improvement projects.
- Identifies and executes cost improvement projects to support the manufacturing supply chain goals and/or of the suppliers.
- Directs technical projects in his/her manufacturing site and/or with suppliers, in order to improve

the capacity process, maintenance, instruments assembly capacity and the performance of the

produced instruments.
- Provides technical support for the approval and validation of the changes and improvements in

the processes within his/her manufacturing site and/or with the supplier.
- Provides technical support for the resolution of Quality problems of the components.
- Potentially coordinates supervision activities in MEST technical areas (Manufacturing

Engineering Science and Technology) (RMI/CAD/BOM).
- Maintains the continuity of the supply chain qualifying and validating the tools through the

approval procedures of the components.
- Ensures the closing of non-conformities of the component problems, besides their timely

correction and the approval of control plans within his area or of the suppliers.
- Other specific functions of the position are:
Has the responsibility of multiple components and/or manufacturing processes with moderate complexity in the development / revision of a product.
- Responsible for communicating business related issues or opportunities to next management level
- 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**:
**EXPERIENCE AND EDUCATION**
- Engineering
- Masters or Doctorate in Science or Engineering, preferably.
- Bilingual (English-Spanish), preferably

Trained to have technicians under his charge.

2 to 4 years of experience in a product development and/or manufacturing environment, or equivalent experience. Experience in the medical product industry is preferable.

**REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS**
- To possess abilities in group dynamics, ability to work multifunctionally and obtain collaboration among multiple functional groups.
- Effective communication skills, written, spoken and in presentation.
- Ability to manage projects, lead teams in different places performing projects.
- Technical competences, preferably
- Tool design
- Product/process risk assessmen

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