Explore 75 Remote Iso 13485 Jobs
Join Neko Health as a Senior Regulatory Affairs Engineer to ensure compliance of medical devices with global standards.
T.B
Twist Bioscience
The Project Manager will coordinate and manage library projects at Twist Bioscience, focusing on customer communication and project execution.
Join RQM+ as an ISO 13485 Lead Auditor, supporting internal audits for clients in the U.S. on a contract basis.
Medtrans
Medtrans
The Validation Engineer will coordinate and execute the validation of processes, ensuring compliance with quality and regulatory standards.
Y.D.O
468y D3 Oncology
The Regulatory Affairs and Quality Assurance Engineer ensures compliance and quality in medical device product development.
Join CellCarta as a Senior Manager to lead supplier quality and quality management systems in a remote role.
Join iRhythm as a Quality Systems Engineer - CAPA, focusing on compliance and quality improvement in healthcare.
The Quality & Regulatory Manager will oversee the Quality Management System for medical devices, ensuring compliance with regulations and managing audits.
The Technical Manager QMS will lead training and compliance processes for medical device auditors.
D.M
DEU Medtronic
Lead Quality Assurance and Regulatory Affairs activities in India for Medtronic, ensuring compliance with medical device regulations.
The QA/RA Project Manager is responsible for leading quality assurance and regulatory activities in medical device software development.
Aeon is seeking a part-time Quality Manager to establish a Quality Management System in a remote setting.
Mendaera
Mendaera
Lead and scale remote technical support for a next-generation robotic medical device platform.
Jobgether
Jobgether
Lead data privacy initiatives and ensure compliance with GDPR in a dynamic environment.
Elvie
Elvie
Join Elvie as a Design Engineer to innovate and deliver groundbreaking products that empower women.