40 Fda Jobs in Dunboyne
-
QA Validation PSC Biotech Ltd - Dunboyne, Ireland regulations and all other applicable governing regulations. The Quality Assurance Validation Specialist will fulfill the educational requirements for this role and have the necessary experience within an FDA 3 days ago
-
CQV Engineer Formulation New CPL Recruitment - Dublin practices, company policies and EU & FDA regulations. Responsible for ensuring that all non GMP equipment, are tested in compliance with project related standards from a commissioning perspective. Deviation Negotiable 4 days ago
-
Planner - Pharma - Dublin North Cpl Resources - Science & Engineering - Dublin environment. Experience with ERP systems (e.g., SAP, Oracle, JD Edwards). Familiarity with GMP, FDA, and regulatory requirements in pharma manufacturing. Excellent organizational and time management skills 55000.0 8 days ago
-
Director, Regulatory Labeling Regeneron Ireland DAC - Dublin completion of complex labeling projects. Expert knowledge of FDA, EMA, and international labeling regulations, ICH guidelines, and CIOMS core labeling guidelines. Ability to assimilate clinical and scientific 12000.0 2 days ago
- Forum: Start a Discussion Join
-
CQV Equipment Engineer Life Science Consultants (LSC) - Dublin . Responsible for ensuring Utilities are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations. Responsible for ensuring that all non GMP equipment Utilities are tested 100000.0 8 days ago
-
QC Instrumentation Analyst Cpl Resources - Dublin of laboratory GMPs, FDA regulations, and their application to API manufacturing Ability to prepare for and participate in Regulatory and Customer audits Experience in Equipment Validation and change control 4 days ago
-
CQV Engineer New CPL Recruitment - Dublin documentation/electronic records for equipment and utilities assigned. Responsible for ensuring Utilities are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations Negotiable 8 days ago
-
Senior Analytical Chemist Cpl Resources - TEG - Dublin , receptive to new ideas. Knowledge of FDA and European GMP requirements, particularly pertaining to laboratory operations. Other Benefits include: Excellent opportunities for career enhancement and personal 65000.0 5 days ago
-
Regional Demand Planner New CPL Recruitment - Dublin (ex-Tableau, Excel) • Understanding and exposure to current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) or other regulatory industries • Basic operational understanding Negotiable 3 days ago
-
Product Development Engineer Medical Devices New CPL Recruitment - Dublin , with a strong understanding of design controls and regulatory requirements (e.g., FDA, ISO 13485). · Hands-on experience in product design, prototyping, and testing, including both hardware and software Negotiable 12 days ago
Top locations