Fda Jobs
CPL Recruitment - County Mayo
, pharmacy, and biotechnology) Min 3 years relevant experience in Laboratory preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO, CMO, CDMO Industry Negotiable
from: cpljobs.com - 24 days ago
Electronic Engineer
Life Science Recruitment Ltd - Dublin
principles (e.g. ISO 9001 or ISO 13485) and/or FDA quality system regulation processes according to 21 CFR part 820 and EU MDR. Does this sound like your next career move? For more info forward 55000.0
from: irishjobs.ie - 19 days ago
Quality Operations Manager
Embecta - Dublin
Certification is a bonus). Knowledge of FDA requirements and experience managing FDA audits. Experience with process validation, sterilization, and clean room environments is advantageous. Strong interpersonal 12000.0
from: irishjobs.ie - 21 days ago
QA Validation
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 - 15 days ago
Quality Systems Technician
Smart Reactors Service Limited - Galway
13485/ 21 CRF Part 820 Experience 2+ years industry experience working in a regulated medical device/ manufacturing area. Good knowledge of FDA 21CFR820 and international regulatory requirements
from: irishjobs.ie - 18 days ago
Validation Engineer
Almac Group Ltd - Louth
by the EU and FDA. This involves being a local validation subject matter expert, supporting ongoing projects and initiatives, and occasionally traveling to other business sites, equipment vendor sites
from: irishjobs.ie - 15 days ago
Quality Director
Life Science Recruitment Ltd - Galway
Quality Management System (QMS) to ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable standards and regulations. Partner closely with Operations, R&D, Regulatory Affairs 100000.0
from: irishjobs.ie - 18 days ago
Quality Engineer II
Sigmar Recruitment - Galway
experience in medical device manufacturing. Familiarity with FDA and EU regulatory requirements, including QSR and ISO standards. Demonstrated ability to manage priorities, solve complex problems, and lead 70000.0
from: irishjobs.ie - 18 days ago
QA Validation Specialist
Cregg Group - Clare
and FDA regulations. Key Responsibilities: Preparation and Maintenance of the site validation plan. Maintenance and archiving of Validation/Qualification documentation. Follow up with other departments 75000.0
from: irishjobs.ie - 24 days ago
QA Director (CQV, Pharma, Data Centers)
Gertek Project Management - Republic of Ireland
construction. Ensure compliance with FDA regulations (cGMP), ISO standards (ISO 9001, ISO 27001), GAMP 5, and other relevant industry standards and regulations. Lead and manage the QA and CQV teams, including 12000.0
from: irishjobs.ie - 25 days ago
