Medical Device Regulatory Affairs Jobs
Reg Affairs Manager - Remote role
Sigmar Recruitment - Dublin
of global regulatory frameworks Knowledge of MRP, DCP, CP Knowledge of medical devices highly desirable Excellent attention to detail and organisational skills Capable of working on own initiative and taking 100000.0
from: irishjobs.ie - 2 days ago
Clinical Affairs Specialist
Wallace Myers International - Galway
info see Skills: Clinical Affairs Clinical Trials Medical Device Regulatory affairs 60000.0
from: irishjobs.ie - 10 days ago
CPL Recruitment - Manchester
qualification (or equivalent experience) · Minimum 5 years’ experience in a GCP environment with demonstrable, working knowledge of GCP practices · Desirable: working knowledge of IVD or medical device Negotiable
from: cpljobs.com - 7 days ago
Regulatory Affairs Specialist 2
Cook Ireland Ltd - 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 - 9 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 - 10 days ago
Hollister Incorporated - F26 F3X5 Ballina, MY, IE
: Pharmaceutical and Medical Device Act (2014) Australia: Therapeutic Goods (Medical Devices) Regulations 2002 Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Exercise
from: Hollister Incorporated - 14 days ago
Director of Regulatory Affairs
Life Science Recruitment Ltd - Galway
Director of Regulatory Affairs Medical Device Start-Up Galway About the Company Our client is an ambitious, well-funded medical device start-up based in Galway, entering a critical phase 100000.0
from: irishjobs.ie - 10 days ago
Regulatory Affairs Specialist
Cregg Group - Clare
in the Medical Devices industry is required. Understanding of applicable guidelines and regulations, for example experience with ISO 10993 Experience with FDA regulatory requirements, European Medical Devices 65000.0
from: irishjobs.ie - 24 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 - More than 30 days ago
