Fda Jobs

Life Science Recruitment Ltd - Galway
, and market expansion activities. Manage all regulatory submissions (CE marking, FDA 510(k)/PMA, and other global submissions) and ensure alignment with commercial and operational timelines. Serve 100000.0
from: irishjobs.ie - 17 days ago

Regeneron Ireland DAC - Limerick
maintenance and calibration functions Working closely with Operations, Systems Support, and Quality functions to ensure Regulatory Compliance (FDA, HPRA, EPA, NIST) and ensuring prompt customer service Applying 12000.0
from: irishjobs.ie (+1 source) - 11 days ago

WuXi Biologics Ireland Limited - Louth
for the company; expected to be a point of contact for project coordination, including email and client meetings. Ability to support regulatory inspections from FDA, EMA, etc. and cGMP audits from clients, as well 50000.0
from: irishjobs.ie - 13 days ago

Gertek Project Management - Sligo
and overall facility operations. Compliance and Standards: Ensure all utility systems comply with GMP, FDA, and EHS regulations. Collaborate with QA and validation teams to meet documentation and qualification 12000.0
from: irishjobs.ie - 15 days ago

Claran Consultants Ltd - Dublin
strategies Ensure all CQV activities are conducted in compliance with GMP, FDA, EMA, and other applicable regulatory standards. Support the qualification of analytical instruments in accordance with regulatory
from: irishjobs.ie - 14 days ago

WuXi Biologics Ireland Limited - Louth
. Knowledge/Experience: At least 10 years relevant work experience in BioPharma industry, preferably Validation, Quality or MSAT roles. Must be familiar with EMA & FDA regulations; ICH and WHO guidelines 100000.0
from: irishjobs.ie - 8 days ago

Sigmar Recruitment - Galway
into compliance with the current US FDA QMSR. Working in the QA Dept, and directed by the QA/RA Manager, the successful candidate will drive day to day responsibility for the change and development of current 55000.0
from: irishjobs.ie - 22 days ago

Cook Ireland Ltd - Limerick
in implementing regulatory requirements in accordance with ISO13485, MDD 93/42/EEC, EU Medical Device Regulation 2017/745 and FDA 21CFR Part 820 as required and other jurisdictions as required. Knowledge 12000.0
from: irishjobs.ie - 17 days ago

PM Group - Limerick
, and validation of electrical and instrumentation systems, ensuring compliance with GMP and FDA regulations Provide technical support for existing equipment, identifying and resolving electrical and instrumentation 12000.0
from: irishjobs.ie - 21 days ago
CPL Recruitment - County Mayo
preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO, CMO, CDMO Industry. Analytical techniques (HPLC, GC, MS and similar) experience essential. Experience Negotiable
from: cpljobs.com - 21 days ago