Experienced Supplier Quality Engineer, Orthopedics

Johnson & Johnson MedTech

Grecia, Costa Rica
Onsite
Supplier qualification and performance management
Supplier corrective actions and continuous improvement
Mitigate supply risk
Johnson & Johnson MedTech is seeking an Experienced Supplier Quality Engineer for their Orthopedic division in Grecia, Costa Rica. The role involves ensuring quality compliance and managing supplier performance within a highly regulated environment, while the company emphasizes innovation and inclusivity in healthcare solutions

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: 85

Johnson & Johnson MedTech is seeking an Experienced Supplier Quality Engineer for their Orthopedic division in Grecia, Costa Rica. The role involves ensuring quality compliance and managing supplier performance within a highly regulated environment, while the company emphasizes innovation and inclusivity in healthcare solutions.

Skills & Requirements

Must-have

  • Supplier qualification and performance management
  • Supplier corrective actions and continuous improvement
  • Mitigate supply risk
  • Regulated environment quality engineering
  • Supplier audits and compliance assessment

Nice-to-have

  • Drive reliability and foster culture of quality
  • Technologically savvy
  • Persistence and tenacity

Key Requirements

  • 2 to 4 years’ experience in a highly regulated industry
  • 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
  • University Bachelor’ degree in science, engineering, or related field

Work Rights

Not specified

Tailored Resume

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