Senior Engineer

**"Johnson & Johnson companies are equal opportunity employers"**At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity.Diversity & 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 Next Move Could Mean Our Next Breakthrough.**COMPANY**: Ethicon WCR**SENIOR ENGINEER - FIXED TERM POSITION (24 months)**The Senior Engineer completes engineering projects by organizing and controlling project elements and is responsible for all Engineering and technical disciplines that projects involve. The project engineer will schedule, plan, forecast, resource and manage all the technical activities aiming at assuring project accuracy and quality from conception to completion.**DUTIES & RESPONSABILITIES**:Under limited supervision, and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:- Complete technical projects with suppliers to improve supplier process capacity, supplier process capability, supplier process maintainability, instrument assembly capability, and instrument out put performance- Determine tooling and spare requirements to maintain component supply- Provide technical support for the approval/ validation of changes/ improvements in supplier processes.- Other responsibilities may be assigned and not all responsibilities listed may be assigned.- Creates validation documentation and any other documentation required to support validations.**Qualifications**EDUCATION AND EXPERIENCE**- B.S. Engineering Degree or Science discipline.- (4-6) years related experience, or equivalent knowledge and skills.- Proven experience in Medical Devices industry.**REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS****Required**:- Knowledge on process validation (OQ, PQ, Process Confirmation).- Knowledge on equipment validation (SOR, SRS, CSV, IQ or equivalent).- Able to read and understand engineering drawings.- Technical process writing.- Hands on experience with manual and automation assembly equipment and/or processes.- Experience managing new equipment introduction as following up with vendors, follow up on the project milestones, etc.- Position requires excellent organizational and communication skills (written and oral, fluent in English) plus the ability to function/lead in a team-based manufacturing environment.- Strong analytical, problem solving, and communications skills.- Experience in project management,- Regulatory knowledge.- Understanding of customer expectations and deliverables with an awareness of the impact of failure/cost of poor quality.- Experience on Good Documentation Practices.- Language Skills: Bilingual (Spanish & English).**Preferred**:- Experience with design of experiments and statistical process control- Experience on programming under different architectures and different levels (low and/or high level).- Statistical analysis software such as Minitab.- Other skills may be required and not all skills listed may be utilized.**Other**:- English proficiency.- Able to cross to El Paso to visit vendors.**LOCATION**: Juarez (Mexico)**Primary Location**Mexico-Chihuahua-Juarez- **Organization**E.E.S., S.A. de C.V. Mexico (8283)**Job Function**Engineering**Requisition ID**W