Job Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 jnj.com

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:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Assembly

Job Category:

Business Enablement/Support

All Job Posting Locations:

Juarez, Chihuahua, Mexico

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re 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 https://www.jnj.com/medtech

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

We are searching for the best talent for Principal Engineer Clerk to be in Ciudad Juarez.

Under supervision of the engineering manager and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Support validation project and process improvements projects.
• Follows compliance and EHS policies and guidelines.
• Performing and documenting activities for IQ, OQ and PQ.
• Supports creating production documentation and providing input into new product BOMs, routings, and DMR.
• Support raw material and supplier qualifications.
• Supports closure of NCRs, CAPAS, audit observations, ergonomics and safety related action items.
• Supports critical engineering tasks in other departments as assigned.
• Uses project management tools and methodologies to deliver projects on-time, on-budget, and on-scope.
• Serves as the engineering approver for process development studies and validation documentation when authorized.
• Performs complex assignments designed to continue the development of professional work knowledge and abilities requiring advanced application of standard engineering techniques, procedures and criteria in carrying out engineering tasks.
• Performs assignments that have complex objectives and require the investigation of multiple variables.
• Performs work which involves complex conventional types of plans, investigations, surveys, structures, or equipment with highly complex features for which there may be no precedents.
• Support the Design of experiments and capability studies, develops process specifications, and designs and procures process tooling.
• Analyzes new processes and equipment with the intent of achieving continuous improvement of present methods.
• Communicates and monitors process and material quality targets.
• Measures performance to targets and implements remedial actions as instructed.
• Develops process documentation and training materials for new processes, materials, and equipment.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed
• Supports the revision of documentation through Adaptive, including VMP tasks.

Qualifications / Requirements:

• A minimum of High School Diploma and Engineering Bachelor’s Degree complete or in progress.
• From 6 to 8 years of experience in related fields. Or currently pursuing an Engineering Bachelor’s Degree with half of School credits completion or
  recently completed.
• Bilingual English/Spanish (Preferred).
• Computer skills: Excel (including charts/graphs), Word, Internet Explorer.
• Experience in medical device manufacturing environment. (Preferred)
• Knowledge of medical product and process design concepts such development, materials, standardization science and basic statistics. (Preferred)
• Knowledge of word processing, spreadsheet analysis, presentation graphics, some engineering analysis and some statistical software (Minitab preferred).
• Analytical thinking to provide and lead product inquiry investigations.
• Ability to work in a cross-functional team to complete projects, knowledge in PE tools such as Kaizen
• Ability to solve basic problems using FI methodologies such as Five Whys, 5Ms, and others.

Required Skills:

Preferred Skills:

Agile Manufacturing, Assembly Operations, Communication, Data Savvy, Execution Focus, Good Manufacturing Practices (GMP), Manufacturing Processes, Manufacturing Science and Technology (MSAT), Plant Operations, Predictive Analytics, Predictive Maintenance, Problem Solving, Process Oriented, Quality Auditing, Repair Management, Safety-Oriented, Technologically Savvy