Validation Engineer

DescriptionTeam Horizon is seeking a Validation Engineer on a permanent basis for our client’s manufacturing facility in the North West.Why you should apply:You will get the opportunity to coordinate, implement and actively participate in the site Validation Program and general Technical Operations activitiesWhat you will be doing:Coordination / direction and active participation in the validation of site Facility, equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.Generation/maintenance/execution of the Site Validation Master Plan, Project Validation Plans and schedulesGeneration of validation protocols and final reports to cGMP standards.Generation of validation investigations and implementation of corrective actions.Creation, review and approval of various quality documents and test data.Management of validation exception events and change control processes.Maintenance and tracking of validation equipment, if applicable.Performing cross training within the team and training of new team members.Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.Communicating with peers and management regarding activities in the area, including elevation of events or concerns.What you need to apply:Qualification and/or degree in engineering or scientific discipline. 3 years plus validation experience in pharmaceutical, diagnostics or medical device industry 3 years plus of knowledge of cGMP and regulatory requirements relating to pharmaceutical, diagnostics or medical device industry. Strong communication (written and oral), presentation and troubleshooting skills required. Effective interpersonal and organizational skills