Process Engineer Ii 2nd Shift

hace 3 semanas

Norte, México Johnson & Johnson A tiempo completo

**Job Function**:Supply Chain Engineering**Job Sub**Function**:Process Engineering**Job Category**:Scientific/Technology**All Job Posting Locations**:MX301 - Circuito Interior Norte - BWIFueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.**We are searching for the best talent for Process Engineer II 2nd shift to be in Juarez City.****You will be responsible for**:- 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**Qualifications / Requirements**:- 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- Bachelor's degree- 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 assessment- Cleaning validation- Equipment design and automatization- Interplant transfers

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