Overall Purpose: Validation engineer required for a medical device manufacturer in north Dublin. You will be responsible for validating key equipment, Systems and utilities. Essential Duties, Functions and Responsibilities: Responsible for leading and executing Validation strategies (Validation Plans, Validation Protocols, Validation Reports) for key site Equipment, Systems and Utilities, in line with current regulatory requirements, corporate policies and site procedures. Ensuring site Qualifications are executed in adherence with Site Validation Master Plan, Validation Plans & SOPs, and presenting executed Qualifications during internal and external audits. Ensuring that a continuous state of Validation is maintained for site Equipment, Systems and Utilities, including providing Validation input for site Change Controls. Responsible for executing site Periodic Review and Revalidation activities for Equipment, Systems and Utilities. Drafting and executing site Process Validation protocols. Maintains a contemporary understanding of cGMP regulations and guidance in relation to all aspects of qualification of process and equipment. Skills/Knowledge Required: Knowledge of medical device manufacturing an advantage. 3+ years experience. Bachelors Degree (or equivalent) in Science (Chemistry, Microbiology, or Pharmacy preferred) or Engineering (Chemical/Mechanical/Electrical. Salary and benefits. Competitive base salary. Healthcare. Bonus. Pension. Applicants should email their cv to firstname.lastname@example.org or call me on 01-9476227 for a confidential conversation. This job originally appeared on RecruitIreland.com.
6 days ago