Senior Supplier Quality Engineer

Johnson & Johnson; Ciudad Juárez; Híbrido; MXN 500,000 - 700,000; Jornada completa

Descripción de la vacante

A leading healthcare company is seeking a Senior Supplier Quality Engineer to support quality engineering activities in new product development and manufacturing. This role requires a Bachelor's degree in Engineering and 2-4 years of experience. The candidate should possess strong communication and regulatory compliance knowledge, focusing on quality assurance in medical devices. The position may require up to 25% travel and offers a hybrid work model.

Formación

• 2-4 years of related work experience.
• Knowledge of GMP, MDD, and 510K regulations.
• Proficiency in personal computer applications.

Responsabilidades

• Lead quality engineering activities for product life cycle.
• Ensure compliance with FDA and ISO quality systems.
• Drive continuous improvement and customer satisfaction.

Conocimientos

Communication skills

Regulatory compliance knowledge

Analytical thinking

Project management

Problem-solving

Organizational skills

Educación

Bachelor's degree in Engineering

Descripción del empleo

Overview

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: Supply Chain Engineering

Job Sub Function: Quality Engineering

Job Category: Scientific/Technology

All Job Posting Locations: Ciudad Juarez, Chihuahua, Mexico

Job Description:

Ethicon Endo-Surgery is recruiting for a Senior Supplier Quality Engineer. The preferred location is Cincinnati, OH. However, the position can also be in Juarez, Mexico or Guaynabo, Puerto Rico.

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

The position of Supplier Quality Engineer is responsible for support and leadership of Quality Engineering activities in New Product Development and ongoing manufacturing – including resolution of non-conformances (root cause & corrective action), CAPA, Quality System and process improvement activities.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

United States - Requisition Number: R-034778

Mexico – Requisition Number: R-035545

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Responsibilities

• Provide leadership in design & implementation of world-class quality Engineering to support entire product life cycle with focus on quality engineering activities such as reliability, root cause/corrective action risk management, analytics/statistical techniques, requirements management, verification & validation, and design control across the lifecycle of the products.
• Drive correction, corrective action, prevention, detection of defects at the earliest phase of product design, continuous improvement & customer satisfaction.
• Provide leadership and technical expertise to ensure conformance to ISO, FDA (Food & Drug Administration) & MDD (Medical Devices Directive) based quality systems.
• Provide review and approvals for the release of new products ensuring quality requirements are met.
• Provide leadership & support to J&J process excellence initiatives including Six-Sigma, design excellence & lean thinking.
• Direct development & consistent application of quality policies & procedures in product design & development, secondary development, manufacturing, external manufacturers & suppliers.
• Responsible for following and administering safety.
• Compliance with safety policies and procedures.
• Follow J&J and EES Records Management Policies for Convenience Information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and third-party vendor if applicable.
• Other responsibilities may be assigned and not all responsibilities listed may be assigned.
• 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.

Qualifications

Education:

• A Bachelor or equivalent degree in Engineering or applicable sciences is required. Other Bachelor/Master degrees acceptable with applicable work experience in a regulated industry. Electrical Engineering Degree preferred.

Experience and Skills

Required:

• 2-4 years of related work experience
• Regulatory compliance knowledge: GMP, MDD (Medical Devices Directive), 510K (Pre-market approval), and Government, trade association, industry & medical publications
• Strong communication skills (written and verbal)
• Negotiation and influencing skills
• Effective assertiveness and quality assurance
• Analytical and creative thinking abilities
• Project management skills to handle multiple initiatives concurrently
• Problem-solving and prioritization capabilities
• Strong organizational skills and ability to synthesize information from diverse sources
• Rapid comprehension of complex concepts
• Continuous research and ongoing learning of industry trends and regulatory requirements
• Proficiency in personal computer applications

Preferred:

• Experience working with medical device external manufacturers for Capital Equipment and/or PCBA assembly and production

Other:

• English proficiency (written and verbal) is required
• This position may require up to 25% travel
• Preferred certifications: CQA, CQE, CRE, Six Sigma GB or BB

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.

We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers. Internal employees contact AskGS to be directed to your accommodation resource.

#LI-Hybrid