My client, a global CRO company is recruiting for a Validation Engineer to join their team in South Dublin.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Writing, reviewing and executing validation documents. Liaising with the relevant Department Manager for the review of validations documents and prioritise validations projects. Liaise with the Validation Project Manager on validation projects. Project Manage the full lifecycle for validation projects including but not limited to; delivering on time and to specification ensuring the delivery of a quality validation project within the business. Responsible for developing, preparing the installation of and revising test validation procedures/protocols in accordance with appropriate regulatory agency validation requirements, corporate, internal company standards and current industry standards. Write or assist in writing of SOPs for Validation Projects. Participate in validation project meetings, workshops, training of staff and production of related documentation. Present validation system programmes at internal and external audits as required. Provide progress reporting and input into established project documentation.
- Education: **Science Qualification or Equivalent Experience: 2 Years work experience in a similar role within a pharmaceutical, medical device or CRO industry.
For a full Job Spec and to apply for this role please call Zoe on +353 1 2784671 or e-mail firstname.lastname@example.org
Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671