Fda Jobs
CPL Recruitment - County Mayo
regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry. · Experience in project management is desireable · BSc/M.Sc. in a relevant science discipline (e.g. cell € 45000
from: cpljobs.com - 23 days ago
CPL Recruitment - County Mayo
2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry. Experience in project management Negotiable
from: cpljobs.com - 23 days ago
Global Head of Regulatory Affairs, Pharmaceuticals
The Panel Group - Dublin
and challenges in key markets. Provide strategic guidance on regulatory pathways and requirements for diverse international regions (e.g., FDA, EU, Canada, ROW, APAC, LATAM). Oversee the preparation and submission
from: irishjobs.ie - 16 days ago
Documentation Controller
doTERRA Global Limited - Cork
FDA and other regulations and cGMP requirements including data integrity required. Knowledge of SAP preferred Knowledge of Master Control preferred Benefits: Private Health insurance for employee 50000.0
from: irishjobs.ie (+1 source) - 18 days ago
Clinical Affairs Specialist
Wallace Myers International - Galway
and regulatory authorities such as the FDA and Competent Authorities. Liaise with external vendors such as CROs, core labs, and biostatisticians. Liaise with study coordinators and investigational site personnel 60000.0
from: irishjobs.ie - 18 days ago
QA Compliance Specialist
Gertek Project Management - Sligo
for accuracy and compliance. Total commitment to quality and maintaining high standards. Demonstrates integrity, strong work ethic, and supports compliance with cGMP and HPRA/FDA regulations and company policies 12000.0
from: irishjobs.ie - 16 days ago
Quality Engineer II- Medical Device Start-up
Wallace Myers International - Galway
engineering, life science or related field. 3-5 years experience at a quality assurance role in the medical device sector essential, preferably in a FDA/MDR regulated environment. Quality certification and lead 60000.0
from: irishjobs.ie - 17 days ago
CPL Recruitment - Dublin
is a distinct advantage. · Experience in life science sector, GMP solutions deployment and validation and FDA's regulations for electronic documentation (FDA 21 CFR Part-11) will be a distinct advantage Negotiable
from: cpljobs.com - 23 days ago
Quality Technician
Total Talent Solutions - Westmeath
environment (medical device, FDA, or ISO 13485 preferred) Proficiency in MS Office (Excel, Word, PowerPoint, etc.) Knowledge of quality and statistical tools (e.g., Pareto analysis, trend analysis) Familiarity 45000.0
from: irishjobs.ie (+1 source) - 22 days ago
Senior Manufacturing Engineer
Sigmar Recruitment - Galway
, and quality issues. Lead validation efforts develop protocols, execute tests, analyze data. Support CAPAs, audits, and compliance with ISO 13485 and FDA standards. Develop SOPs, work instructions, and training 75000.0
from: irishjobs.ie - 22 days ago
