Senior Manufacturing Validation Engineer
Terumo Aortic, East Freeland, Renfrewshire
Senior Manufacturing Validation Engineer
Salary not available. View on company website.
Terumo Aortic, East Freeland, Renfrewshire
- Full time
- Permanent
- Onsite working
Posted 1 week ago, 4 Oct | Get your application in now before you miss out!
Closing date: Closing date not specified
Job ref: 8faa37e3b5ef4f8eb8dda10f319496dd
Location ref: East Freeland, Renfrewshire
Full Job Description
Terumo Aortic are currently recruiting for a Senior Manufacturing Validation Engineer to join our team. The successful candidate will be responsible for ensuring equipment and processes are validated to the regulated standards.The main responsibilities are;Plan validation activities to ensure customer and business needs are met in alignment with the overall project plans and objectivesExperience in authoring, executing and reporting IQ/OQ/PQ and Test Method Validations of Manufacturing Equipment and Processes to meet regulatory requirementsAids other Validation Engineers with correct approach for Validation activitiesPrepares and issues Validation Master Plans and revalidation schedules, summary reports and other required documentation for a validation exerciseDesignee for Engineering Leader - Validations, as and when requiredOrganize and execute validation activities in order to provide an effective validation serviceProvide validation expertise to ensure that all operations are carried
out in compliance with regulatory and company requirementsProvide validation support and advice to other areas of the business as and when requiredProvide specialist knowledge on process, equipment issues within the sitePromote effective working relationships and ensure they are maintained through the validation working partySupport a continuous improvement culture within the businessAddress site validation gaps via generation and completion of Validation Master Plans and schedulesMaintain site validation status according to regulatory requirementsIdentify resource requirements and rate limiting steps within Validation Master Plan complianceSupport the provisions of quality data/reports/charts for the manufacturing groupGenerate relevant required documentation in support of regulatory updates and filingsPerform any other duties/tasks/projects as require by managementAssume other responsibilities from time-to-time in order to support plant's strategic plan and personal career
plansResponsible for archiving and storage of all completed and approved validation documentsQualifications & Experience;Degree qualified with validation experience from within a scientific regulated environmentA good working knowledge of appropriate standards and regulationsExperience in direct investigation/troubleshooting of validation problemsExperience in authoring, executing and reporting IQ/OQ/PQ and Test Method ValidationsExcellent statistical knowledge (DOE, capability studies, Gauge R&R, sample size definition, etc)Experience in the areas of qualification, analytical methods, lab equipment qualification, computer system validation, and re-qualification #J-18808-Ljbffr