Regulatory Affairs Expert
3 days ago
This is an excellent opportunity for someone who is passionate about quality and regulatory affairs to join a leading company in the medical device industry. As a QA/RA specialist, you will be responsible for ensuring compliance with regulatory requirements, including MDR and ISO 13485, and will have the opportunity to work on a wide range of projects, from developing and implementing quality management systems to collaborating with cross-functional teams to deliver high-quality products.
About UsRadiobotics is a leading company in the field of medical devices, dedicated to solving the global need for radiologists while ensuring every patient receives expert-level care. Our vision is to augment routine X-rays of the musculoskeletal system, enabling non-specialists to report imaging and facilitate safe and effective handling outside the hospital.
Key BenefitsDynamic and supportive work environment.
Opportunities for professional growth and development.
Chance to make a meaningful impact in the medical device industry.
We are committed to providing our employees with the support and resources they need to succeed in their roles and achieve their career goals.
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