Principal Mechanical Design Technician(Fixed-Term 6 Months)

J&J Family of Companies; Ciudad Juárez; Presencial; MXN 480.000 - 720.000; Jornada completa

Descripción de la vacante

Johnson & Johnson MedTech is seeking a Manufacturing Engineering Clerk Principal to support engineering activities in a surgery-focused environment. You will participate in validation activities, write documentation, and manage NCR investigations to ensure GMP and ISO compliance across manufacturing processes.

The role emphasizes cross-functional collaboration, data-driven problem solving, and continuous improvement using Kaizen principles within a fast-paced medical device setting.

Formación

• From 6 to 8 years of experience in related fields.
• Engineering Bachelor's Degree in progress or recently completed.
• Bilingual English/Spanish preferred.
• Experience in medical device manufacturing environment preferred.
• Knowledge of statistics and data analysis concepts.

Responsabilidades

• Perform NCR lifecycle documentation and investigation using statistical concepts.
• Provide technical support to identify causes of non-conformances and process failures.
• Lead investigations including origination, bounding, product control and documentation.
• Support validation activities, execution of protocols, studies and documentation.
• Write engineering documentation (protocols, procedures, reports).
• Update and ensure compliance of VMP-related documentation and change management.

Conocimientos

NCR investigations

Validation

Documentation

Quality systems

Statistical thinking

Cross-functional teamwork

Kaizen knowledge

GMP knowledge

Educación

Engineering Bachelor's Degree

Pursuing degree (half credits)

Herramientas

Minitab

Excel

Descripción del empleo

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where 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 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

Job Description:

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 Surgery

Fueled by innovation at the intersection of biology and technology, we're 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 that's 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 world's 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: Engineering Clerk Principal

Purpose:

• Provide overall support for engineering activities.
• Provide support during validation activities and writing the documentation.
• Responsible for engineering purchases through different purchasing platforms
• Provide overall support for VMP activities.

You will be responsible for:

• Perform NCR lifecycle documentation and investigation, using statistical concepts.
• Provides technical support to identify the causes of non-conformances and process failures and to implement corrections thus assuring process performance and compliance against Ethicon's QSR, GMP and ISO requirements for the manufacturing process.
• Performs non-conformance investigations including NCR origination, bounding, product control, failure
• investigation, correction, and documentation with the non-conformance system.
• Support engineers in performing validation activities, execution of protocols, engineering studies and documentation.
• Help Write engineering documentation (protocols, procedures, special instructions, reports, etc.).
• Supports the documentation changes in compliance with Ethicon's Change management system.
• Engineering support in the completion of projects mainly focused on quality improvements, cost/scrap reduction, increased capacity and New Products.
• Conduct robust investigations. Analyzes data and recommends actions for process, equipment and system improvement.
• Review all PLM System (Software solution used by Quality Systems to manage the document control process) validation documentation to Complete VMP Action Tasks.
• Update VMP logs with all applicable validation references, protocols, completion reports etc. that support the validated state of the validation components.
• Generate and provide quarterly change orders to create, release, and revise VMP Procedures and VMP Logs.
• Ensure all validation packages (group of a specific document class) involve the required documentation to support and assure the validated state of a validation component.
• Monitoring, tracking and assurance that the annual review activities are performed.
• Ensure Validation Baseline/Periodic Reviews are completed on time.
• Supports the VMP related documentation changes in compliance with Ethicon's Change management system.

Qualifications / Requirements:

• 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 that 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.#LI-Onsite

Required 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

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