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.

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Job Function:

Supply Chain Engineering

Job Sub Function:

Quality Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Jacksonville, Florida, United States of America

Job Description:

Johnson and Johnson Visioncare is recruiting for a Staff Engineer, External Manufacturing and Supplier Quality located in Jacksonville, Florida.

About Vision

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 on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.

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

Lead the pursuit of excellence across a global supplier and external manufacturing network by driving quality, compliance, and continuous improvement. This role partners closely with suppliers, technical teams, and business partners to ensure robust quality systems, mitigate supply chain risks, and deliver high-performing products that meet customer and regulatory expectations. Through supplier engagement, operational leadership, data-driven decision making, and problem-solving expertise, the position plays a critical role in strengthening supplier performance, advancing process capability, and safeguarding product quality across the value chain.

Key Responsibilities:

• Lead supplier and external manufacturer qualification, oversight, and performance management.
• Drive quality, compliance, and continuous improvement across the supply network.
• Develop, maintain, and enhance supplier quality systems, processes, and metrics.
• Conduct supplier assessments, audits, and technical reviews to verify capability and compliance and identify improvements.
• Identify, assess, and mitigate supply chain quality risks.
• Monitor supplier performance and implement improvement initiatives to enhance quality and reliability.
• Lead investigation and resolution of supplier nonconformance supplier-related issues.
• Partner internally and externally to lead and implement supplier related changes with minimal impact to the business
• Use data and performance metrics to support informed decision-making and operational excellence.
• Strengthen process capability, efficiency, and quality at suppliers to minimize risk and improve performance.
• Provide technical leadership, coaching, and quality support to internal collaborators and supplier partners in the execution of supplier quality and purchasing processes and controls
• Champion compliance with J&J quality standards, regulatory requirements, and industry best practices.

Qualifications

Education:

• Bachelor of Arts (BA), Bachelor of Science (BS) or equivalent degree is required.

Experience and Skills:

Required:

• 4-6 years of related experience is required.
• Demonstrates a foundational understanding of medical device quality systems, with an emphasis on purchasing controls.
• Proficiency in Microsoft Word, PowerPoint, and Excel, including moderately complex functions for data analysis and trend identification.
• Professional experience in a regulated industry is required; medical device experience is preferred.

Preferred:

• Experience in the Medical Device industry.
• Experience in the Pharmaceutical industry or Chemical, Packaging, or Plastics industry.
• FDA and ISO regulations knowledge. 21 CFR 820; 21 CFR 210/211; ISO 13485; ISO 9001; Canadian CMDCAS; Japanese PAL; Anvisa Australian TGA.

Other:

• Up to 30% travel may be required.
• Full-time position with standard weekday business hours.

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.

 

 

Required Skills:

 

 

Preferred Skills:

Coaching, Consistency, Controls Compliance, Critical Thinking, Data Savvy, Engineering, Financial Competence, Good Automated Manufacturing Practice (GAMP), ISO 9001, Lean Supply Chain Management, Leverages Information, Process Improvements, Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy