About The Position

As a member of Stryker Corporation, you will support the design and testing of new products, ensuring that everything functions well and meets quality standards. Your role will involve identifying and preventing potential problems, particularly risks, defects, and inspection issues, while ensuring that the product can be manufactured efficiently and safely. You will also support validations, including process, tool, and equipment testing.

Requirements

  • University degree in engineering (or similar).
  • Experience in regulated industries, such as medical devices or pharmaceuticals.
  • Understanding of manufacturing processes and quality tools such as FMEA, CAPA, PPAP, validations, and inspections.
  • Knowledge of standards such as ISO 13485.
  • Advanced English communication skills.

Nice To Haves

  • Experience with Process Flow Mapping (PFM) or process risk assessment.
  • Experience with non-conformity management.

Responsibilities

  • Support the design and testing of new products.
  • Ensure that everything functions well and meets quality standards.
  • Identify and prevent potential problems, especially risks, defects, and inspection issues.
  • Ensure the product can be manufactured efficiently and safely.
  • Support validations, including process, tool, and equipment testing.
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