Analista De Validação De Reprocessamento

Philips UK

Varginha, , Brazil
**
Develop and validate reprocessing methods
Iso 17664 series compliance
Material compatibility testing
** Philips UK is seeking a Reprocessing Validation Analyst in Varginha, Brazil, who will be responsible for ensuring the biological safety and performance of patient monitoring products through reprocessing validation and material compatibility testing. The ideal candidate should have a background in engineering or microbiology, with experience in reprocessing verification and validation, and strong communication skills. **

Job Summary

  • Ensure the biological safety and performance of Philips Hospital Patient Monitoring products by leading product reprocessing validation and material compatibility testing.
  • Assess and manage the impact of manufacturing, supplier, and material changes on patient-monitoring medical devices and accessories.
  • Collaborate and clearly communicate with internal and external stakeholders to ensure proper planning and execution of reprocessing validation and material compatibility testing.

Matching Summary

Match Score: 75

** Philips UK is seeking a Reprocessing Validation Analyst in Varginha, Brazil, who will be responsible for ensuring the biological safety and performance of patient monitoring products through reprocessing validation and material compatibility testing. The ideal candidate should have a background in engineering or microbiology, with experience in reprocessing verification and validation, and strong communication skills. **

Skills & Requirements

Must-have

  • Develop and validate reprocessing methods
  • ISO 17664 Series compliance
  • Material compatibility testing
  • Risk assessments for reprocessing efficacy
  • Global regulatory requirements (ISO, FDA, EU MDR)

Nice-to-have

  • Experience with Contract Resource Organizations
  • Detailed understanding of product development
  • Proficiency in statistics

Key Requirements

  • Bachelor's degree in Material Engineering, Chemical Engineering, Chemistry, Mechanical Engineering, Microbiology, or Biomedical Engineering
  • Minimum 2 years of experience in reprocessing verification & validation
  • Working understanding of global medical device regulations
  • Effective project management and communication skills
  • Ability to travel approximately 10%

Work Rights

Not specified

Tailored Resume

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