Senior Manufacturing System Engineer
- Location
- Belfast City District, Northern Ireland, United Kingdom
review, user access management and continuous improvement. Develop, maintain and improve manufacturing software systems, electronic records, reporting tools and digital workflows in compliance with GMP, FDA, ISO 13485, 21 CFR Part 11 and applicable regulatory requirements. Lead Computer System Validation (CSV) activities, including the development and execution of Validation Plans … Basic SQL knowledge and ability to create database queries. Knowledge and experience with Power Bi, Power Apps, Power Automate is desired. Good knowledge of GMP/FDA regulatory requirements and current Health and Safety Regulations legislation. Proven Project Management skills through the delivery of business-critical projects. ...