Experienced Supplier Quality Engineer, Orthopedics

Johnson & Johnson Innovative Medicine

Grecia, Costa Rica
**
Supplier qualification and performance management
Supplier corrective actions and continuous improvement
Mitigate supply risk
** Johnson & Johnson Innovative Medicine is seeking an Experienced Supplier Quality Engineer for their Orthopedics division in Grecia, Costa Rica. The role involves ensuring quality and compliance of materials and processes in a highly regulated environment, focusing on supplier qualification, corrective actions, and continuous improvement. **

Job Summary

  • The Source Quality Engineer is responsible for ensuring the quality, compliance, and continuity of materials, components, and outsourced manufacturing/processes that support medical device products.
  • This role leads to supplier qualification and performance management activities, drives supplier corrective actions and continuous improvement, and partners cross-functionally to mitigate supply risk and support product launches and lifecycle changes in a regulated environment and according to internal procedures.
  • You will be responsible for technical leadership in establishing quality expectations at the supplier, to include process changes in partnership with Source Quality and New Product Development (NPD) Teams.

Matching Summary

Match Score: 75

** Johnson & Johnson Innovative Medicine is seeking an Experienced Supplier Quality Engineer for their Orthopedics division in Grecia, Costa Rica. The role involves ensuring quality and compliance of materials and processes in a highly regulated environment, focusing on supplier qualification, corrective actions, and continuous improvement. **

Skills & Requirements

Must-have

  • Supplier qualification and performance management
  • Supplier corrective actions and continuous improvement
  • Mitigate supply risk
  • Quality engineering leadership
  • Supplier auditing and compliance assessment
  • Investigate product issues

Nice-to-have

  • Drive reliability and foster culture of quality
  • Technologically savvy
  • Persistence and tenacity
  • Cross-functional collaboration

Key Requirements

  • 2 to 4 years’ experience in a highly regulated industry
  • University Bachelor’ degree in science, engineering, or related field
  • Strong knowledge of GMP/GDP, FDA/ISO regulations
  • Demonstrated experience managing supplier nonconformance, CAPA, and change control
  • Direct experience performing supplier audits
  • Demonstrated problem-solving skills with root-cause analysis

Work Rights

Not specified

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