Ingeniero de Procesos II (3er turno)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .

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:

Job Sub Function:

Job Category:

All Job Posting Locations:

Job Description:

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions 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 are searching for the best talent for Process Engineer II to be in Juarez Salvarcar Plant.

Purpose: Adds value through the knowledge of process engineering; provides support to the stabilization and to the life cycle of projects for continuous improvement from the identification to the execution and closing in terms of cost quality efficiency and time cycle. Quick response to operations in: technical resolutions change of direction manufacturing scalability process development/operations product and material replacement. Can complete projects in his/her work area or with suppliers in order to provide an interrupted flow of components for the assembly operations that has the established requirements of instruments quality cost and delivery times.

You will be responsible for:

Under limited supervision 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.
• 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:

• 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.
• 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 o Product/process risk assessment
• Cleaning validation o Equipment design and automatization o Interplant transfers
• Test methods development and validation o Lean and Six Sigma skills o Process validation
• Design validation and verification
• Operations direction o Process technical writing o Regulations knowledge o Plastic injection molding

Technical skills preferably:

• Plastic processing o Mechanical and electrical skills
• Process characterization
• Geometric Dimensions and Tolerances (GD&T)
• FEA (Finite Element Analysis)
• Knowledge of polymers
• Chemical processing o Electrical electronic and PLC
• DFMA (Manufacturing and Assembly Design)
• Development of the assembly and equipment process
• Calibrators development and metrology
• PLC (troubleshooting)
• Knowledge of operations products and processes of the company preferably.
• Knowledge of the Quality system of the company.
• Knowledge of GMP/ISO preferably
• Computing skills.
• Efficiency in word processing programs spreadsheets presentations and data base applications.
• Statistical analysis software
• Engineering applications software (FEA CAD etc.) when required

Required Skills:

Preferred Skills: