Risk Manager
Salary/Rate:€60,000 - €70,000 DOE
Job type:Perm
Town/City:Bielefeld
Country:Germany
Business Sectors:Quality
Job ref:24690
Post Date:07. 11. 2023
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About the Role
Risk Manager
Location: Minden, North Rhine-Westphalia, Germany
Salary: Circa €60,000 - €70,000 DOE
Overview:
Our Client are committed to revolutionizing cardio-vascular patient treatment with cutting-edge Class III devices and software solutions. They foster a culture of collaboration, creativity, and a deep-seated commitment to harnessing the latest technology to transform the healthcare landscape. Their diverse team, consisting of software developers, engineers, and healthcare professionals, excels in creating state-of-the-art medical devices and software.
Benefits:
• A job with bright opportunities: at our company, everything revolves around the development and safety of medical devices for both patients and users
• Embrace teamwork: Open communication, mutual support, and respectful collaboration are integral to our daily work
• Flat hierarchies
• Modern working environment
• Flexible working hours and
• Remote work options
• Dedicated onboarding and ongoing investment in your professional and personal development
• A secure working environment with great people and exciting challenges
Tasks:
• Communication with notified body, competent authority
• Reliable handling of current standards (MDR 2017/745, ISO 14971)
• Perform risk assessment by analyzing current risks and identifying potential risks
• Collaborate with internal and external auditors in conducting policy and compliance audits
• Provide support and training to staff to build risk awareness amongst your team members
• Maintain records of insurance policies and claims
• Negotiate all modifications to Quality Assurance Agreement
Your Profile:
• Completed scientific or technical studies
• Several years of experience in the development of medical devices, ideally coupled with practical medical experience for class III devices
• Good technical understanding of systems, and experience in the areas of risk management and safety analyses (FMEA, FTA, PHA)
• Analytical, systematic way of working, strong communication skills and willingness to take responsibility
• Clear communication internally as well as to external partners, customers and notified bodies
• Confident German and English (spoken/written)
To apply or for more information please contact Luke via email on: luke.fines@adaptivelifescience.com
#LI-Hybrid #LI-LF1
Location: Minden, North Rhine-Westphalia, Germany
Salary: Circa €60,000 - €70,000 DOE
Overview:
Our Client are committed to revolutionizing cardio-vascular patient treatment with cutting-edge Class III devices and software solutions. They foster a culture of collaboration, creativity, and a deep-seated commitment to harnessing the latest technology to transform the healthcare landscape. Their diverse team, consisting of software developers, engineers, and healthcare professionals, excels in creating state-of-the-art medical devices and software.
Benefits:
• A job with bright opportunities: at our company, everything revolves around the development and safety of medical devices for both patients and users
• Embrace teamwork: Open communication, mutual support, and respectful collaboration are integral to our daily work
• Flat hierarchies
• Modern working environment
• Flexible working hours and
• Remote work options
• Dedicated onboarding and ongoing investment in your professional and personal development
• A secure working environment with great people and exciting challenges
Tasks:
• Communication with notified body, competent authority
• Reliable handling of current standards (MDR 2017/745, ISO 14971)
• Perform risk assessment by analyzing current risks and identifying potential risks
• Collaborate with internal and external auditors in conducting policy and compliance audits
• Provide support and training to staff to build risk awareness amongst your team members
• Maintain records of insurance policies and claims
• Negotiate all modifications to Quality Assurance Agreement
Your Profile:
• Completed scientific or technical studies
• Several years of experience in the development of medical devices, ideally coupled with practical medical experience for class III devices
• Good technical understanding of systems, and experience in the areas of risk management and safety analyses (FMEA, FTA, PHA)
• Analytical, systematic way of working, strong communication skills and willingness to take responsibility
• Clear communication internally as well as to external partners, customers and notified bodies
• Confident German and English (spoken/written)
To apply or for more information please contact Luke via email on: luke.fines@adaptivelifescience.com
#LI-Hybrid #LI-LF1