Medical Device Jobs
Senior Regulatory Affairs Specialist
Stryker Ireland - Cork
, Europe and international medical device regulations required. Previous experience with Class II/III medical devices preferred. Previous experience drafting 510(k)s and EU submissions preferred. Experience 12000.0
from: irishjobs.ie - 17 days ago
Hollister Incorporated - F26 F3X5 Ballina, MY, IE
Management experience preferred Length of Experience 8+ years of relevant industry experience preferably in medical devices Specialized skills / Technical knowledge Innovative/Creative Thinker – must
from: Hollister Incorporated - More than 30 days ago
Quality Engineer
Life Science Recruitment Ltd - Galway
start up helping develop a product from its very early stages. Company: My client an early-stage medical device start-up company focused on the design and development of novel devices for the treatment 65000.0
from: irishjobs.ie - 18 days ago
Perrigo - D02 TY74 Dublin, IE
Broad expert knowledge of pharmaceutical, medical device, nutritional, API, and cosmetic manufacturing processes. Excellent communication skills (verbal, written, and presentation). Excellent analytical
from: Perrigo - More than 30 days ago
Medical Scientist
Bon Secours Health System - Dublin
that ensures compliance with relevant regulations including the Blood Directive 2002/98/EC and the Medical Devices Directives 93/42/EC and 98/79/EC, where applicable. Complete assigned actions, including those 12000.0
from: irishjobs.ie - 16 days ago
Environmental Health and Safety Officer
BMS Recruitment - Dublin
& Safety is required. Compliance background in medical device, manufacturing, chemicals, or pharma is advantageous. Accreditations in any of the following ISO's is a plus: . THE PACKAGE: Salary: €50,000 55000.0
from: irishjobs.ie - 18 days ago
Quality Director
Life Science Recruitment Ltd - Galway
Quality Director Medical Device Start-Up Galway About the Company Our client is a dynamic, well-funded medical device start-up based in Galway, poised for significant growth as it moves 100000.0
from: irishjobs.ie - 20 days ago
Validation Quality Engineer
Cpl Resources - Cork - Cork (+1 location)
Role Purpose To lead and execute validation activities for medical devices, ensuring full compliance with applicable regulatory standards and quality system requirements. Key Responsibilities Manage 80000.0
from: jobs.ie (+2 sources) - 17 days ago
Regulatory Scientist 2
Cook Ireland Ltd - 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 - 20 days ago
Clinical Affairs Specialist
Wallace Myers International - Galway
My client who are a growing Medical Device start-up company are seeking a Clinical Affairs Specialist to join their team and assist with the design, planning and execution of clinical trials. As part 60000.0
from: irishjobs.ie - 20 days ago
