Johnson & Johnson Careers

Staff Supplier Quality Engineer

Le Locle, Switzerland
Quality (Eng)


Job Description

Requisition ID: 1805690435W

"Caring for the world… one person at a time” … inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable Credo


DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world. DePuy Synthes Companies offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, more agile and better equipped to meet the needs of today’s evolving health care environment. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.

For our site in Neuchatel / Lo Locle we are currently looking for a:

Staff Supplier Quality Engineer

your responsibilities:

  • Provide overall quality assurance leadership in the management of select contract manufacturing sites engaged in the production of Johnson and Johnson products. 
  • Provide complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes. 
  • Utilize multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), and international organization for standardization (ISO). 
  • Report on contract manufacturer performance metrics. 
  • Handle complex technical issues for manufacturing processes that are to be transferred to satellite facilities




Qualifications

  • A minimum of a Bachelor's degree is required, preferably in an Engineering, Life Science, or related discipline. 
  • A minimum of 6 years of experience in a highly regulated industry. 
  • Experience in the Medical Device industry and/or Pharmaceutical industry is required. 
  • FDA and ISO regulations knowledge is required, with FDA CFR Part 820 and ISO 13485 knowledge required.  
  • Auditing background.  
  • Blueprint literacy including GD&T is preferred. 
  • Experience in root cause analysis. 
  • Experience or knowledge with machining manufacturing processes and injection molding an asset. 
  • Six Sigma, Lean, or ASQ Certification and trainings. 

This position will require up to 25% travel with occasional international



If you feel attracted by this challenge and want to be part of a successful and growing organization, then please send us your online application (CV, Motivation Letter, Working References etc.) by clicking here.

 
Please click on DePuy Synthes and Johnson & Johnson if you want to learn more about our business and check our new career channel on YouTube  www.youtube.com/user/CareersAtJNJ to understand our working culture


Primary Location
Switzerland-Neuchâtel-Le Locle-
Organization
Medos International Sarl (7898)
Job Function
Quality (Eng)
Requisition ID
1805690435W