1 of 1 Permanent ISO 13485 Jobs in Merseyside

contribute to the success of a leading medical device company, we want to hear from you! Key Responsibilities: Assist in maintaining compliance with certifications and regulatory approvals such as ISO 27001, ISO 9001, ISO 13485, UKCA, CE, and FDA 510(k). Support the update and maintenance of QMS and ISMS documentation. Help coordinate and conduct … inclusive work environment. The Person Degree or equivalent qualification in Life Sciences, Quality Management, or a related field. 2+ years of relevant experience is preferred. A basic understanding of ISO standards or medical device regulations is desirable. Excellent organisational skills with strong attention to detail. Clear written and verbal communication abilities. A commitment to following procedures and maintaining accurate More ❯