Cordis-posted 22 days ago
Full-time • Mid Level
Miami Lakes, FL
1,001-5,000 employees

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.

  • Lead and manage projects to improve existing manufacturing processes, implement new technologies, and support new product introductions.
  • Develop, document, and implement new or improved manufacturing procedures and work instructions.
  • Plan, write, and execute process and equipment validation protocols (IQ/OQ/PQ).
  • Investigate and disposition Non-Conformance Reports (NCRs) and Corrective and Preventive Actions (CAPAs).
  • Design and perform experiments, including Design of Experiments (DOE), to characterize, optimize, and improve process performance.
  • Provide technical guidance, mentorship, and leadership to junior engineers and technicians.
  • May supervise one or more engineers or technicians as required.
  • Collaborate daily with assemblers, production supervisors, engineers, and management to ensure process efficiency and compliance.
  • Partner with suppliers and external resources to develop, qualify, and implement new processes or equipment.
  • Work closely with R&D and Manufacturing teams to interpret design intent and translate it into robust, scalable production processes.
  • Foster clear, effective communication across all project and operational stakeholders.
  • Identify and communicate business-related issues, risks, or opportunities to management in a timely manner.
  • Ensure compliance with all Company Health, Safety, and Environmental (HSE) policies, and verify that necessary resources and equipment are available and in good condition.
  • Maintain compliance with all applicable Federal, State, local, and Company regulations, including Quality System and regulatory requirements for relevant markets.
  • Perform other related duties and responsibilities as assigned.
  • Bachelor’s degree in Mechanical, Biomedical, Electrical or related Engineering discipline with minimum of 5 years of relevant experience, preferably in a medical device environment.
  • Proven track record working within ISO 13485 and FDA-regulated environments.
  • Experience with risk management (ISO 14971), design controls, and documentation practices.
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