Job Title: Manufacturing Inspector Job Type: Permanent Location: Oxford, UK A world-leading medical technology company developing innovative solutions are seeking a motivated Manufacturing Inspector to join the team as part of its global expansion. This is an opportunity to work in an innovative, fast-paced global medical device organisation committed to improving patient outcomes. The position of Manufacturing Inspector is responsible for supporting the day to day activities within manufacturing and performing product release testing of medical devices.
Responsibilities: responsible for performing and documenting in process inspection and testing and a number of technical tests on assemblies and sub-assemblies and finished product Maintaining Good Document Practice/Good Manufacturing Practice (GDP/GMP) compliance within the manufacturing QC areas through inspection of subassemblies/finished products against related release specifications. Performing and documenting in process inspection and testing and a number of technical tests on assemblies and sub-assemblies and finished product. Supporting initiatives to deliver measurable performance improvements. Supporting completion of area related NC, Investigations and exception documents for product and processes that are non-conforming related to manufacturing. Performing weekly/monthly checks of the manufacturing areas – GALA (General Area Line Assessments) walks. Performing statistical trending analysis of GALA walk rounds/ NC raised during manufacturing or final batch release and Service Centre. Ensuring that all work instructions, SOP`s and test specs that make up part of the BOM/DHR files are current and correct and implement improvements where applicable. Act as Subject Matter Expert for area of expertise by maintaining knowledge of the relevant procedures and specifications related to current job specification. To include participating in and supporting external audits e.g Notified Body, FDA etc. Supporting and completing any other work-related tasks set by their manager. Skills and Experience
Bachelor's degree within an engineering disciple or equivalent 5 years experience of working in Manufacturing Quality for medical device Working knowledge of GDP/GMP requirements Strong abilty to create and write SOPs and work instructions/specifications Understanding of inspection criteria, use of drawings/specifications. Worked in manufacturing for medical devices. Knowledge of SAP (Desirable) Knowledge of Master Control or other eQMS Understanding of using basic measurement tools (e.g. calipers/jigs and Gauges) Please reach out to or call 02033765104 for further details.