Staff Product Lifecycle Engineer (Medical Devices | Bilingual)
Job Summary
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:
R&D Product DevelopmentJob Sub Function:
Biomedical EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Ciudad Juarez Chihuahua MexicoJob Description:
About MedTech
Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at Surgery
Fueled by innovation at the intersection of biology and technology were 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 thats 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 worlds most prevalent conditions such as obesity cardiovascular disease and cancer. Patients are waiting.
Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for Staff Product Lifecycle Engineer (Medical Devices Bilingual)
Purpose:
The Staff Lifecycle Engineer serves as a technical leader responsible for driving product lifecycle initiatives design changes and continuous product improvements for medical devices. This role leads cross-functional projects focused on product quality manufacturability validation statistical analysis cost improvement and supply continuity while ensuring compliance with quality and regulatory requirements.
The position requires strong expertise in Product Engineering Six Sigma Methodologies problem solving design change management CAPA/NCR execution supplier collaboration and medical device manufacturing. The Engineer will partner closely with Quality Manufacturing Supply Chain and Engineering teams influencing technical decisions and driving project execution to deliver sustainable business results.
You will be responsible for:
In accordance with all applicable federal state and local laws/regulations and Corporate Johnson & Johnson procedures and guidelines this position:
Must know & follow EES policies & procedures related to work activities performed in areas of responsibility & assure that direct reports know & follow EES policies & procedures related to work activities performed in area of responsibility.
Complete training in area of responsibility within allowed time period. Training is required for changes and implementation of existing policies and procedures for new assignments etc. Complete required re-training in areas such as safety and environmental.
Follow all company safety policies and other safety precautions within work area. Promote safety to all associates that enter work area.
Responsible for the execution of projects focused on reducing design related product variation that positively influence the companys business metrics strategic directions & financial results.
Responsible for assuring projects are well scoped remain focused follow the PE process and that timely progress is being made towards completion. Use the Project Management Mastery principles to identify risks issues and scope changes in assigned project execution.
Maintain active project plans for significant projects throughout the year such as design changes and cost improvement projects. Conduct regular reviews as necessary with the team and management as well as drive adherence to the schedule.
Identify plan and execute cost improvement projects in support of supply chain objectives.
Sustain supply chain continuity by qualifying and validating supplier tooling as per component approval procedures.
Ensures closure to component non-conformance issues with timely corrective action submission and approval of suppliers control plans.
Manages assigned NCRS and CAPAS completes actions by due dates and provides periodic updates to management.
Follow established Design Variability Roadmap (DMAIIC process) in the execution of projects.
Act as Development Engineer for component or equipment change coordination development and validation new product stabilization as assigned.
Responsible for maintaining alignment and communication between stakeholders.
Manage project spending to meet objectives within forecasted budget.
Maintain technical expertise and familiarity with engineering statistical and predictive computer-based tools
Responsible for communicating business related issues or opportunities to next management level
Responsible for following all Company guidelines related to Health Safety and Environmental practices as applicable
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
Level of Responsibility:
May serve as a lead Operations engineer on a development/revision of a product of significant complexity or contribute significant unique expertise across multiple product lines to systematically reduce design-induced variation in our products creating sustainable improvements. Is viewed by the organization as a role model in demonstrating the behaviors outlined in the Standards of Leadership. Is an authority in a specific technical field exercising considerable latitude in determining technical objectives of assignments. Work is generally expected to result in the development of new or refined equipment materials processes products and/or technical methods
Qualifications / Requirements:
Bachelors Degree in Engineering or equivalent.
6-8 years of related engineering experience.
Strong knowledge and skills to successfully perform the responsibilities of the position.
Advanced English proficiency (written and spoken); Spanish preferred.
Proven ability to work cross-functionally and collaborate with multiple functional groups.
Strong verbal written presentation and communication skills.
Strong project management skills with the ability to lead diverse teams and execute projects across multiple locations.
Technical leadership and ability to influence stakeholders without direct authority.
Experience managing multiple projects and priorities simultaneously.
Manufacturing & Product Engineering Experience
Experience with Plastic Injection Molding Metal Injection Molding (MIM) Metal Stamping and Forming Machining Casting and/or Electronic PCBAs.
Design Quality & Continuous Improvement
Knowledge and experience with Design for Manufacturing & Assembly (DFMA) Design for Six Sigma Process Six Sigma Design of Experiments (DOE) Problem Solving Methodologies Risk Analysis (DFMEA PFMEA AFMEA) Statistical Analysis (SPC GR&R ANOVA Regression Analysis Capability Analysis) Geometric Dimensioning & Tolerancing (GD&T) Tooling Methodologies Assembly Process and Equipment Development Metrology and Gage Development and General Design Engineering Principles.
Product Lifecycle & Validation
Experience with Product Design and Development Design Change Management Product Lifecycle Management CAPA and NCR Management Supplier Collaboration and Technical Support Manufacturing Transfers Installation Qualification (IQ) Operational Qualification (OQ) and Performance Qualification (PQ).
Technical Tools
Experience using Statistical Analysis Software CAD/Solid Modeling Software FEA (Finite Element Analysis) Tolerance Stack-up Analysis and Microsoft Office applications including Excel Word and PowerPoint.
Preferred Experience
Medical Device Manufacturing.
Quality Systems and Regulatory Environments.
Supplier Qualification and Validation Activities.
Key Competencies
- Technical Leadership Project Execution Design Change Management Problem Solving Cross-functional Collaboration Stakeholder Influence Decision Making Continuous Improvement Portfolio Management and Strong Business and Technical Communication.
Required Skills:
Preferred Skills:
Bioinformatics Biological Engineering Biostatistics Coaching Critical Thinking Design of Experiments (DOE) Healthcare Trends Industry Analysis Innovation Medicines and Device Development and Regulation Product Development Relationship Building Research and Development Researching SAP Product Lifecycle Management Standard Scientific Processes and Procedures Technologically SavvyRequired Experience:
Staff IC
About Company
About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more