This permanent role, reporting into the site Quality Manager, is part of the Quality & Validation team and will help to embed equipment and services into client sites.
This is a 360 role where you will build strong working relationships with the Cork site manufacturing team, as well as pharmaceutical clients.
A number of customers are based overseas so you will get an opportunity to travel and deliver projects at client sites (up to 30% of your time) A bit more about the role: Preparation of validation documents (FAT / IQ & OQ protocols) Execution of FAT, SAT, IQ, OQ, CD and PQ activities according to established protocols Project team member actively involved in delivering projects and involved in customer design meetings / URS reviews Design Qualification (Traceability Matrix) of projects Draft and revise testing SOPs and quality documentation Performing risk assessments for equipment Supporting regulatory audits and inspections Role requirements: Technical / Scientific qualification with at least 18 months experience in a Validation or Quality role with exposure to Validation principles.
Quality focused with knowledge and understanding of scientific rationale and cGMP quality systems Proven problem solving skills Excellent interpersonal skills and the ability to communicate well, both verbally and written Familiarity with automation validation concepts and principles Open to travelling internationally Experience in interpreting P&ID diagrams and electrical drawings is highly desirable If you would like to find out more about this role please click the 'Apply Now' button below or reach out to Kellie on .
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
Skills: Validation Project support Document writing Customer focus Process flow