Medical Device Reporting Specialist (Manufacturing)
Medical Device Reporting Specialist
As one of the world´s leading manufacturers of cardio- and endovascular medical devices, BIOTRONIK is headquartered in Berlin, Germany, and represented in over 100 countries by its global workforce. The work of our committed, highly specialized, exceptionally skilled employees results in crucial advancements in the world of cardiology and changes the lives of patients every day.
BIOTRONIK is looking to add a Medical Device Reporting Specialist to our Regulatory team. The Medical Device Reporting Specialist is responsible for executing activities associated with medical device complaints, including complaint processing, investigation, and reporting to FDA (when applicable). The Medical Device Specialist receives both implantable and non-implantable medical devices, and processes and reports them according to company procedures and FDA regulations. Position is also responsible for corresponding with field representatives, customers, the manufacturer and the FDA to ensure compliance with applicable regulations.
Preferred Education and Experience
Are you interested? Please apply online through our application management system! We are looking forward to welcoming you.
Location: Lake Oswego, OR | Working hours: Full-time | Type of contract: Undefined
Apply now under: www.biotronik.com/careers
Job ID: 47261 | Contact: Amanda Willott
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law.