Job Description
Job Title: Manufacturing Inspector
Job Type: Permanent
Location: Oxford, UK
A world-leading medical technology company developing innovative solutions is 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 organization 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:
1. Performing and documenting in-process inspection and testing and a number of technical tests on assemblies, sub-assemblies, and finished products.
2. Maintaining Good Document Practice/Good Manufacturing Practice (GDP/GMP) compliance within the manufacturing QC areas through inspection of subassemblies and finished products against related release specifications.
3. Supporting initiatives to deliver measurable performance improvements.
4. Supporting completion of area-related NC, investigations, and exception documents for non-conforming products and processes related to manufacturing.
5. Performing weekly/monthly checks of the manufacturing areas – GALA (General Area Line Assessments) walks.
6. Performing statistical trending analysis of GALA walk rounds/NC raised during manufacturing or final batch release and Service Centre.
7. Ensuring that all work instructions, SOPs, and test specs that make up part of the BOM/DHR files are current and correct and implementing improvements where applicable.
8. Acting as Subject Matter Expert for the area of expertise by maintaining knowledge of the relevant procedures and specifications related to current job specification, including participating in and supporting external audits (e.g., Notified Body, FDA, etc.).
9. Supporting and completing any other work-related tasks set by their manager.
Skills and Experience:
1. Bachelor’s degree within an engineering discipline or equivalent.
2. 5 years of experience working in Manufacturing Quality for medical devices.
3. Working knowledge of GDP/GMP requirements.
4. Strong ability to create and write SOPs and work instructions/specifications.
5. Understanding of inspection criteria and use of drawings/specifications.
6. Experience working in manufacturing for medical devices.
7. Knowledge of SAP (desirable).
8. Knowledge of Master Control or other eQMS.
9. Understanding of using basic measurement tools (e.g., calipers, jigs, and gauges).
Please reach out to emily.james@skillsalliance.com or call 02033765104 for further details.
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