Medical Device Regulatory Affairs Jobs in County Dublin

Ocumetra - Dublin

Engineering, Life Sciences, Quality Management) Minimum 2–4 years of experience in regulatory affairs, preferably with medical device software or digital health products Familiarity with ISO 13485, ISO/IEC

from: my.hirehive.io - 20 days ago

CPL Recruitment - Dublin

standards within the medical device industry. Reporting to: VP of Global Operations Key responsibilities · Program Management: Lead and manage multiple programs that span the lifecycle of medical Negotiable

from: cpljobs.com - 20 days ago