
1001 - 5000 employees
🏭 Manufacturing
🏥 Healthcare
🧬 Biotechnology
Manufacturing • Healthcare • Biotechnology
LivaNova is a global medical technology company built on nearly five decades of experience and a relentless commitment to improve the lives of patients around the world. With a focus on medical devices, neuromodulation, and cardiac surgery, LivaNova offers advanced technologies and breakthrough treatments that provide meaningful solutions for patients, healthcare professionals, and healthcare systems. Headquartered in London and active in over 100 countries, LivaNova emphasizes bringing both clinical and economic value to its customers, being recognized as a market leader in cardiopulmonary and neuromodulation solutions.
🔥 0 minutes ago
🇨🇴 Colombia – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
🔧 QA Engineer (Quality Assurance)
👻 Ghost score 10%
Where this job comes from
Posted on LivaNova's careers page, not through a job board
First seen by Remote Rocketship 0 minutes ago

1001 - 5000 employees
🏭 Manufacturing
🏥 Healthcare
🧬 Biotechnology
Manufacturing • Healthcare • Biotechnology
LivaNova is a global medical technology company built on nearly five decades of experience and a relentless commitment to improve the lives of patients around the world. With a focus on medical devices, neuromodulation, and cardiac surgery, LivaNova offers advanced technologies and breakthrough treatments that provide meaningful solutions for patients, healthcare professionals, and healthcare systems. Headquartered in London and active in over 100 countries, LivaNova emphasizes bringing both clinical and economic value to its customers, being recognized as a market leader in cardiopulmonary and neuromodulation solutions.
• Support Customer Quality activities for Neuromodulation therapies, including complaint handling, investigations, regulatory reporting, and technical support. • Receive customer feedback and provide technical troubleshooting to resolve customer issues. • Initiate and investigate product complaints, including root cause analysis. • Prepare and submit medical device vigilance and regulatory reports to applicable regulatory authorities. • Maintain accurate complaint files, quality records, and supporting documentation. • Identify potential product or quality trends and escalate findings for further evaluation. • Collaborate with Quality, Regulatory Affairs, R&D, Clinical, and other teams to support compliance and continuous improvement.
• Bachelor’s degree in Engineering. • Strong written and verbal communication skills in English. • Strong analytical and problem-solving skills. • Collaborative mindset with a willingness to learn, develop, and work within international teams. • Interest in healthcare, medical technology, quality, or regulated industries. • Proficiency in Microsoft Office, including Excel, Word, and PowerPoint. • Internship, academic project, or previous exposure to engineering, quality, healthcare, medical devices, pharmaceutical, or another regulated industry is desirable.
• Purpose-driven work focused on improving patient outcomes worldwide. • Global exposure and the opportunity to collaborate with international teams. • Structured learning, mentorship, and career development opportunities. • A culture that values innovation, quality, collaboration, and continuous improvement. • Exposure to advanced medical technologies and a highly regulated global environment. • Competitive base salary. • Supportive, inclusive, and collaborative environment.
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🇨🇴 Colombia – Remote
💰 Private Equity Round on 2012-03
⏰ Full Time
🟠 Senior
🔧 QA Engineer (Quality Assurance)