Medical Device Regulatory Affairs Jobs

Real - Cork

in obtaining and retaining country-specific regulatory registrations worldwide MDSAP Implementation: Manage the implementation of the Medical Device Single Audit Program within the organization Regulatory £60.43 - £64.74/hour

from: CV-library.ie - 7 days ago

Cook Medical - Limerick

Overview The Regulatory Affairs Specialist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices 12000.0

from: irishjobs.ie - 11 days ago

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 - 10 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 - 10 days ago

Cook Medical - Limerick

medical devices. In addition, the Regulatory Affairs Specialist will perform activities associated with PMS, including Post Market Clinical Follow-Up (PMCF), and Clinical Evaluation Plans and Reports (CEPs 12000.0

from: irishjobs.ie - 14 days ago

CPL Recruitment - Edinburgh

The role is a full-time, permanent position working 37.5 hours per week. An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department Negotiable

from: cpljobs.com - 13 days ago

Cook Medical - Limerick

with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets and providing regulatory affairs input for the functional areas. Reporting to: Principal Regulatory 12000.0

from: irishjobs.ie - 22 days ago

Cregg Group - Clare

with FDA regulatory requirements, European Medical Devices Regulation (EU MDR), Regulation (EU) 2017/745 and international regulatory agency requirements. Ability to effectively manage multiple projects 65000.0

from: irishjobs.ie - 23 days ago

Catalyx - Cork

within regulated industries (pharmaceutical, biotech, medical devices, etc.). Experience with FDA 21 CFR Part 11, GAMP 5, and other regulatory guidelines. Skills: Strong knowledge of validation principles

from: my.hirehive.io - 27 days ago