Validation Engineer

CPL

Westmeath

A medical device company in the mid lands is looking for a Validation Engineer to join their team. Overview: The successful candidate will form part of an established Quality team and report to the Head of Quality. They will be responsible for Validation Projects including: Coordinate and execute process validations including preparation of protocols, data analysis and reports. Work with vendors and other stakeholders to deliver equipment installs and Tech transfers on time and in line with budget constraints. Ensure software validations for equipment and systems are completed in line with industry standards. Ensure regulatory compliance with European and US validation requirements. Support the day the day activities of the cross functional project team. Support design and installation of ancillary equipment. Support Qualification of equipment from FAT through to PQ. Drafting and releasing of process and equipment documentation. Criteria: - Degree in Engineering/ Science or Quality. - Minimum 3 years’ experience in a Validation role within a similar manufacturing organization. - Knowledge of Medical Device Manufacturing & GMP environment would be an advantage. - Lean Tools - Good Analytical Skill and Problem Solving. - Capable of working in a fast paced environment. Interested candidates please contact Rebecca Meaney on +35391507509 or email your CV to rebecca.meaney@cpl.ie. This job originally appeared on RecruitIreland.com.

2493 days ago