Design Quality Engineer I - MedTech Impact & Growth

Brighter Signals; West Chester (Chester County); On-site; USD 90,000 - 120,000; Full time

Job summary

Johnson & Johnson's DePuy Synthes quality group seeks a Design Quality Engineer to support orthopaedic implant development and lifecycle management. You will collaborate with R&D, Regulatory, Manufacturing, and Quality to ensure performance, safety, and regulatory compliance across Trauma and CMF products.

The role emphasizes design reviews, verification/validation testing, risk management, supplier qualification, and maintaining the Quality System.

Qualifications

• B.S. in Engineering or technical science required.
• Minimum 1 year in GMP or ISO regulated industry.
• Fluent English language required.

Responsibilities

• Support Design Quality Engineering for Trauma, CMF, and related businesses.
• Lead product realization planning and conduct design reviews.
• Support design verification/validation including mechanical testing.
• Apply statistical methods and design excellence tools.
• Assist risk management planning and reporting.
• Collaborate with suppliers on qualification and transfer to manufacturing.
• Drive lifecycle management including design changes and cost improvements.
• Maintain the Quality System elements (CAPA, complaints, post-market surveillance).
• Communicate across Quality, R&D, Regulatory, Manufacturing, and Marketing.

Skills

MS Office

English fluent

Education

B.S. in Engineering or technical science

Job description

Johnson & Johnson's DePuy Synthes quality group seeks a Design Quality Engineer to support orthopaedic implant development and lifecycle management. You will collaborate with R&D, Regulatory, Manufacturing, and Quality to ensure performance, safety, and regulatory compliance across Trauma and CMF products.

The role emphasizes design reviews, verification/validation testing, risk management, supplier qualification, and maintaining the Quality System.