Fda Jobs

Catalyx - Cork

Possesses a strong knowledge of FDA cGMP standards and regulatory guidance documents. Able to work independently. Demonstrates attention to detail and accuracy. Why Join Catalyx? At Catalyx we understand

from: my.hirehive.io - 2 days ago

Cpl Resources - 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

from: irishjobs.ie (+1 source) - 26 days ago

Cregg Group - Galway

of the investigation and timely closure of CAPA and NCRs External audits: lead the company in regulatory agency quality management system audits including FDA and Notified Body Key Requirements: Bachelor Degree 85000.0

from: irishjobs.ie - 5 days ago

Catalyx - Cork

with regulatory standards such as GxP, FDA 21 CFR Part 11, and EMA guidelines Prepare validation summaries, deviation reports, and corrective/preventive action (CAPA) plans. Skills and Experience: Bachelor’s degree

from: my.hirehive.io - 7 days ago

Stryker Ireland - Cork

, prioritize, multitask and organize a multi-disciplinary team(s) to successfully achieve project deliverables. Has applied knowledge of FDA & International medical device regulations. Ability to lead, motivate 12000.0

from: irishjobs.ie - 3 days ago

Stryker Ireland - Cork

. Has applied knowledge of FDA & International medical device regulations. Ability to lead, motivate, and influence a cross-functional team on moderate complexity projects that do not report directly 12000.0

from: irishjobs.ie - 5 days ago

CPL Recruitment

and external (HPRA/FDA etc.) Act as the primary point of contact for audit discussions relating to sample management. • Build and foster strong relationships within the biologics quality and global quality Negotiable

from: cpljobs.com - 9 days ago

LGC Limited - Tipperary

environment for medical devices Basic knowledge of FDA 21CFR820, ISO13485, IVDD98/79/EC, IVDR EU/2017/746 and international regulatory requirements Excellent communication skills and attention to detail 12000.0

from: irishjobs.ie - 7 days ago

Sanmina - Cork

JOB TITLE: Validation Quality Engineer DEPARTMENT: Quality Department REPORTING TO: Validation Quality Lead About Sanmina Fermoy Our Fermoy, Ireland, facility is FDA registered and certified to ISO 12000.0

from: irishjobs.ie - 5 days ago

CPL Recruitment - Dublin

chemistry. • Ability to work to tight timelines in a high-pressured environment. • Good Troubleshooting skills. • Openness to change, receptive to new ideas. • Knowledge of FDA and European GMP requirements Negotiable

from: cpljobs.com (+2 sources) - 20 days ago