SENIOR QUALITY ENGINEER

8286-Cordis De Mexico Legal Entity; Ciudad Juárez; Presencial; MXN 600.000 - 900.000; Jornada completa

Descripción de la vacante

Johnson & Johnson MedTech seeks a seasoned Quality Engineer to participate in new product teams, lead verification tests, and support design validation. You will ensure compliance with FDA, ISO 13485, MDR, and QSR standards while driving continuous improvement and mentoring junior staff.

Required: 4–6 years in quality, manufacturing or R&D within regulated environments; ASQ/Six Sigma knowledge and GD&T experience preferred; Bachelor’s degree in a related field; Master’s degree desired.

Formación

• Bachelor’s degree in a related field is required.
• Master’s degree in a related field is preferred.
• ASQ certification, Six Sigma knowledge and/or Process Excellence tools desirable.
• Knowledge of GD&T is desirable.
• Strong understanding of GMP and QSR requirements for medical devices.

Responsabilidades

• Plan, develop, coordinate, and direct medium-sized engineering projects or multiple small projects.
• Drive development of new or refined techniques and procedures.
• Contribute to development of new equipment, materials, processes, products, and methods.
• Assess feasibility and soundness of proposed tests when data is insufficient.
• Ensure adherence to design control requirements and design validation protocols.
• Lead systemic CAPA initiatives and support supplier quality as needed.
• Mentor junior staff and supervise Inspectors/ Technicians in QA activities.
• Coordinate planning to ensure product acceptance and regulatory readiness.

Conocimientos

Analytical Reasoning

Coaching

Customer Centricity

Data Savvy

Document Management

Financial Competence

ASQ Certification

GAMP

Lean

Process Improvements

Quality Control Testing

Quality Standards

Quality Systems Documentation

Quality Validation

STEM Application

Supervision

Supply Planning

Technologically Savvy

Educación

Bachelor’s degree in related field

Master’s degree preferred

Herramientas

ASQ Certification Tools

Descripción del empleo

Job Function

Quality Job Sub Function: Quality Assurance Job Category: Professional All Job Posting Locations: Ciudad Juarez, Chihuahua, Mexico, Ciudad Juarez, 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 https://www.jnj.com/medtech

Purpose

Participate in new product/process teams to develop quality-engineered systems and products, lead and support design verification tests, process validations, quality processes to ensure compliance with the company’s Quality System policies and procedures and applicable external requirements and standards, including FDA, ISO 13485, CMDCAS, PMDA and other worldwide regulatory agencies, Johnson & Johnson Environmental, Health & Safety Practices, and other applicable standards as pertains to medical devices. Drive quality assurance activities intended to ensure effective product quality processes are in place and executed throughout lifecycle of product. May receive technical guidance on complex problems, but independently determines and develops approaches and solutions. Shares technical expertise with others and helps develop junior level engineers.

Qualifications / Requirements

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: Primary responsibilities include working in Quality Engineering and with other functional groups in support of new product/process development, quality operations or quality assurance. Utilizing Quality Engineering tools/processes in development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle. Leading efforts with quality improvement opportunities as appropriate to legacy products, continuous improvement, and customer satisfaction. Develop and establish effective quality control and support associated risk management plans. Write, review and/or approve process and product validation protocols and reports, equipment qualifications, engineering change orders. Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE). Determine sterility, biological and packaging test requirements utilizing appropriate industry or agency standards for new products. Ensure that development activities follow design control requirements, product is tested per applicable standards, European Essential Requirements are met per the MDR, and product is properly transferred to manufacturing. Provide all planning necessary to ensure effective product acceptance. This includes, but is not limited to: Part qualifications Specification development Sampling plans Support vendor audits as technical lead as needed and support Supplier Quality as Quality representative as appropriate. Initiate and investigate Corrective and Preventative Actions (CAPA) as appropriate. Assist in complaint analysis as appropriate. Assist Regulatory Affairs in developing submissions for process changes, inspection changes, and new processes/devices as necessary. Participate in design reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes.

Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate work. Consults with supervisor and provide guidance as needed concerning unusual problems and developments. Responsible for one or more of the following as needed: Supervise and/or provide guidance to Inspectors and Technicians in Quality LCM, Quality Operation or Quality Assurance activities.

Project Management Responsibilities

• o In a supervisory capacity, plans, develops, coordinates, and directs a medium-sized engineering project or a number of small projects with varying levels of complexity.


• o Work is expected to result in the development of new or improved techniques or procedures.


• o Work is expected to result in the development of new or refined equipment, materials, processes, products, and/or methods.


• o Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment, when necessary, data are insufficient or confirmation by testing is advisable.

Additional responsibilities

• o Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.


• o 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.


• o Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.


• o Performs other duties assigned as needed.

You will be responsible for: Bachelor’s degree in a related field, along with a minimum of 4–6 years of quality, manufacturing, or research and development experience in a medical device or other regulated industry is required. Master’s degree is preferred. American Society for Quality (ASQ) certification, Six Sigma experience, and/or knowledge of Process Excellence tools is desirable. Knowledge of GD&T (Geometric Dimensioning and Tolerancing) is desirable. Ability to develop and implement Quality standards. Thorough knowledge of Quality and operations systems and processes, including GMP and QSR requirements for medical devices. Thorough knowledge of leading-edge Quality Engineering, design control, and verification and validation (V&V) tools and methodologies. Ability to apply project management skills to ensure fulfillment of new product development requirements. Demonstrated auditing and problem-solving skills. Understanding of Six Sigma and Business Excellence tools and methodologies. Lean manufacturing experience desirable. Ability to train and mentor a diverse array of employees on quality topics. Good understanding of theoretical and practical fundamentals and experimental engineering techniques.

Required Skills

Analytical Reasoning, Coaching, Customer Centricity, Data Savvy, Document Management, Financial Competence, Good Automated Manufacturing Practice (GAMP), Lean Supply Chain Management, Process Improvements, Quality Control Testing, Quality Services, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy

Preferred Skills

Analytical Reasoning, Coaching, Customer Centricity, Data Savvy, Document Management, Financial Competence, Good Automated Manufacturing Practice (GAMP), Lean Supply Chain Management, Process Improvements, Quality Control Testing, Quality Services, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy

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 https://www.jnj.com/.

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