Associate MDR/Vigilance Specialist

We anticipate the application window for this opening will close on - 10 Jan 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life At Medtronic...

Identify and document appropriate complaint categories to assure trend accuracy within the complaint database. Writes investigation summaries based on technical product analysis information provided Ensures record documentation is maintained in a con Associate, Specialist, Manufacturing, Healthcare

Job Summary:Medtronic, plc is seeking a highly skilled Associate MDR/Vigilance Specialist to join our team. This role plays a critical part in ensuring the accuracy of complaint data within our database. The successful candidate will analyze technical product information and document trends to maintain high-quality records.About the Role:This position...

Must Have: 1. Experience supporting, coordinating and / or leading projects 2. Remediation experience (DHF, Regulatory compliance, e.g., EU MDR, UKCA) 3. Experience in development of new or existing medical devices 4. Knowledge of industry standards (ISO 13485) and regulations, specifically EU MDR and UKCA Nice to Have: Approving Design Control Documentation...

Quality Engineer I W2 Only No C2C Hybrid (3 onsite per week) ~North Haven Top 3 technical skills that are required for the role: ~Remediation experience (DHF, Regulatory compliance, e.g., EU MDR, UKCA) ~Experience in development of new or existing medical devices ~Knowledge of industry standards (ISO 13485) and regulations, specifically EU MDR and UKCA ...

Must Have: 1. Experience supporting, coordinating and / or leading projects 2. Remediation experience (DHF, Regulatory compliance, e.g., EU MDR, UKCA) 3. Experience in development of new or existing medical devices 4. Knowledge of industry standards (ISO 13485) and regulations, specifically EU MDR and UKCA 1. Investigation and root cause analysis skills 2....

Role: Regulatory Affairs AssociateLocation: Abbott Park, IL 60064Key Responsibilities:Assist in the preparation, review, and submission of regulatory documents for new and existing medical devices.Support the regulatory team in ensuring compliance with U.S. FDA regulations, EU MDR, and other international regulatory standards.Monitor and track the regulatory...

Role: Regulatory Affairs AssociateLocation: Abbott Park, IL 60064Key Responsibilities:Assist in the preparation, review, and submission of regulatory documents for new and existing medical devices.Support the regulatory team in ensuring compliance with U.S. FDA regulations, EU MDR, and other international regulatory standards.Monitor and track the regulatory...

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