Cordis-posted 2 months ago
Miami Lakes, FL
Miscellaneous Manufacturing

When you join the team at Cordis, you become part of an inspiring mission to save lives, impacting millions of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart of innovation to transform cardiovascular care. At Cordis, we're teammates, not just employees. We embrace an empowered and one-team culture where teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients. If you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions, then Cordis is just the place for you. We are the people behind the people who keep saving lives.

  • Gathers, compiles files and reports documentation to QC/QA Manager/Supervisor
  • Compiles data records and statistical data, documents findings and interprets results
  • Inputs data and information into internal and external databases
  • Compiles and maintains quality requirements documentation and prepares records for record retention
  • Ensures that information on computer systems complies with actual records
  • Performs varied product inspections, components, incoming materials or new products, finished goods, by observing, measuring and recording data
  • Compares inspection results to defined requirements or specifications and documents differences found
  • Ensures proper documentation and disposition of defective product
  • Perform Release transactions of lots
  • Recommends adjustments to processes to correct standard problems
  • Reports rejects to proper department
  • Follows up on corrective actions being taken
  • Confers with other departments regarding quality standards
  • Participates in the establishment of future inspection procedures
  • Identifies workmanship defects and recommends corrective action
  • Assist in the documentation change control process
  • Follows all corporate policies and procedures
  • Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance
  • Performs other duties as may be assigned
  • High school diploma or general education degree (GED)
  • 4 or more years of related experience and/or training; or equivalent combination of education and experience
  • Experience in the medical device industry would be an additional asset
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