Johnson & Johnson Careers

Staff Engineer, External Manufacturing & Supplier Quality

Jacksonville, Florida
Regulatory Compliance


Job Description

Requisition ID: 4869190830

Johnson & Johnson Vision, part of Johnson & Johnson’s Family of Companies, is seeking a Staff External Manufacturing (EM) & Supplier Quality Engineer located in Jacksonville, FL.  


At Johnson & Johnson Vision, we have a bold ambition: to change the trajectory of eye health. That’s why, through our operating companies, we’ve developed solutions for every stage of life—to help people see better, connect better and live better. We partner with eye care professionals to provide some of the world’s leading products and technologies to address refractive error, cataracts, dry eye, and beyond. We are committed to using our reach and size for good, and strive to put quality eye care within reach of everyone, everywhere. Visit us at www.jjvision.com. Follow @JNJVision on Twitter and Johnson & Johnson Vision on LinkedIn.


As part of a broader Quality team at the site, this Staff EM & Supplier Quality Engineer provides overall quality assurance leadership in the management and qualification of suppliers and/or external manufacturers (EMs).  This role provides the opportunity to work with many internal functions including Procurement, Material and Supplier Engineering, R&D Materials, Quality Assurance including Laboratory and Document Control.  Also, the role has external interactions with Suppliers, EMs, and other J&J supplier quality groups including working internationally.


The Staff EM & Supplier Quality Engineer will establish and maintain quality assurance programs, procedures and controls, ensuring that performance metrics of both the supplier quality systems and suppliers are continually measured to drive improvement initiatives. This position aids in the identification and to eliminate supply chain risks via internal and supplier partnerships.  This Quality professional leads/participates in supplier/EM engagements to assess technical competency and general compliance to requirements.  Key areas of focus within supplier management are performance monitoring/reporting, compliance to J&J standards and stream line processes. Key areas of support provided to team members include; risk management/communication, defect resolution, process capability/process improvement, and quality assurance general support.


The position may require up to 30% domestic or international travel. 



Qualifications

Requirements:

  • Bachelors of Arts (BA) or Bachelors of Science (BS) degree preferably in an engineering, science or technical field. 
  • Minimum of 7 years of experience as a professional in a regulated industry.
  • Working knowledge of Word, Power Point and Excel with competency in moderately complex functions for data analysis and trending.

 

Preferences:

  • Medical Device experience
  • Demonstrated basic understanding of the Medical Device Quality Systems, emphases on purchasing controls.
  • Experience in the Pharmaceutical industry or Chemical, Packaging, or Plastics industry is an asset.
  • FDA and ISO regulations knowledge. 21 CFR 820; 21 CFR 210/211; ISO 13485; ISO 9001; Canadian CMDCAS; Japanese PAL; Anvisa Australian TGA.

 

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

 



Primary Location
United States-Florida-Jacksonville-
Organization
Johnson & Johnson Vision Care, Inc. (6094)
Job Function
Regulatory Compliance
Requisition ID
4869190830