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 https: //www.jnj.com

Job Function:

Quality

Job Sub Function:

Quality Assurance

Job Category:

Professional

All Job Posting Locations:

Ciudad Juarez, Mexico, MX905 Manuel Talamas Camandari 2849, Lote Bravo, Ciudad Juarez, Chihuahua

Job Description:

Assists in the management of Quality Systems issues through internal quality audits, testing, and intermediate quality checks in line with the organization’s Quality Assurance (QA) standards, international standards, and government regulations. Develops complex subject matter expertise on systems and standards to review results of quality audits and regulatory inspections, and provides support in developing corrective action plans. Surfaces the potential impact of identified risks from internal audits. Constructs processes that ensure effective deployment and monitoring of quality systems. Implements processes to collect internal data and feedback, leveraging dashboards and performance monitoring tools. Helps establish relationships with internal partners and regulatory agencies when appropriate to develop subject matter expertise on regulatory requirements. Coaches more junior colleagues in techniques, processes, and responsibilities.​ Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.

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

About Cardiovascular

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 Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at https: //www.jnj.com/medtech

We are searching for the best talent for SENIOR QUALITY ENGINEER to be in Ciudad Juarez, Mexico.

You will be responsible for:

• 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, and 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:

o Supervise and/or provide guidance to Inspectors and Technicians in Quality LCM, Quality Operation or Quality Assurance activities.

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 As an individual researcher, carries out assignments requiring the development of new or improved techniques or procedures.

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.

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

• Responsible for communicating business related issues or opportunities to next management level.

• Responsible for ensuring 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.

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

• Performs other duties assigned as needed

Requirements:

Education:

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

Experience and Skills:

Required:

• 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.