Handheld Device Reporting - 22+ job offers

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

A company is looking for a Global MDR Submissions Analyst III. Key Responsibilities Review and resolve complex medical device complaints, ensuring appropriate documentation and compliance with regulatory requirements Coordinate complaint-related tasks with cross-functional teams and prepare submissi

Intuitive

A global medical device company is seeking a Post Market Clinical Follow up Specialist to lead and execute PMCF strategies. The successful candidate will manage cross-functional teams, ensuring compliance with regulatory requirements. This role requires a strong background in clinical research and t

A healthcare technology company is seeking an Embedded Tester for software integration testing without design or development responsibilities. This role involves understanding complex C and C++ designs, performing requirement analysis, and developing software integration test plans for handheld medi

Intuitive

A global medical device company is seeking a Post Market Clinical Follow up Specialist to lead and execute PMCF strategies. The successful candidate will manage cross-functional teams, ensuring compliance with regulatory requirements. This role requires a strong background in clinical research and t

Orkin

Overview Join the Best in Pests℠ – Build Your Future with Orkin! Are you looking for a hands-on career—not just a job? Do you have experience in construction, roofing, or home improvement, and want to use your skills to build a stable career in a recession-resistant industry? At Orkin, we protect wh