Job Description
Position: Manufacturing Inspector Location: On-site, Oxford, UK Global, innovative medical device company dedicated to improving patient outcomes and saving lives. Our company specializes in advancing technology in Medical Devices and is committed to making a global impact. They are expanding operations and seeking a motivated
Manufacturing Inspector
to join our team. Position Overview The Manufacturing Inspector will play a key role in supporting daily manufacturing activities and conducting product release testing for medical devices. The role involves performing and documenting in-process inspections and a variety of technical tests on assemblies, sub-assemblies, and finished products. This position offers the opportunity to contribute to impactful work in a fast-paced environment. It is a flexible, on-site role based at our facility in Oxford, UK. Key Responsibilities Ensuring adherence to Good Document Practice (GDP) and Good Manufacturing Practice (GMP) standards by inspecting subassemblies and final products against established release criteria. Carrying out and recording inspections during production, along with performing technical evaluations on assemblies, sub-assemblies, and completed devices. Contributing to initiatives aimed at achieving measurable improvements in performance. Assisting with the resolution of non-conformance issues, investigations, and exceptions related to manufacturing processes or products. Conducting routine inspections of manufacturing areas, including General Area Line Assessments (GALA) checks. Identifying and analyzing trends from GALA assessments, non-conformance reports, and final batch release reviews. Reviewing and maintaining the accuracy and relevance of work instructions, SOPs, and test specifications, and implementing updates when needed. Serving as a Subject Matter Expert (SME) in assigned areas, supporting regulatory audits such as those conducted by BSI or FDA. Taking on additional duties as reasonably requested by the Manager of Outbound Quality. Skills and Experience A thorough knowledge of GDP and GMP requirements. Proven experience in drafting and updating standard operating procedures, work instructions, and specifications. The ability to interpret technical drawings and apply inspection criteria effectively. Hands-on experience in manufacturing processes within the medical device industry or Pharma industry. Proficiency in using basic measurement tools such as calipers, jigs, and gauges.
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Position: Manufacturing Inspector Location: On-site, Oxford, UK Global, innovative medical device company dedicated to improving patient outcomes and saving lives. Our company specializes in advancing technology in Medical Devices and is committed to making a global impact. They are expanding operations and seeking a motivated
Manufacturing Inspector
to join our team. Position Overview The Manufacturing Inspector will play a key role in supporting daily manufacturing activities and conducting product release testing for medical devices. The role involves performing and documenting in-process inspections and a variety of technical tests on assemblies, sub-assemblies, and finished products. This position offers the opportunity to contribute to impactful work in a fast-paced environment. It is a flexible, on-site role based at our facility in Oxford, UK. Key Responsibilities Ensuring adherence to Good Document Practice (GDP) and Good Manufacturing Practice (GMP) standards by inspecting subassemblies and final products against established release criteria. Carrying out and recording inspections during production, along with performing technical evaluations on assemblies, sub-assemblies, and completed devices. Contributing to initiatives aimed at achieving measurable improvements in performance. Assisting with the resolution of non-conformance issues, investigations, and exceptions related to manufacturing processes or products. Conducting routine inspections of manufacturing areas, including General Area Line Assessments (GALA) checks. Identifying and analyzing trends from GALA assessments, non-conformance reports, and final batch release reviews. Reviewing and maintaining the accuracy and relevance of work instructions, SOPs, and test specifications, and implementing updates when needed. Serving as a Subject Matter Expert (SME) in assigned areas, supporting regulatory audits such as those conducted by BSI or FDA. Taking on additional duties as reasonably requested by the Manager of Outbound Quality. Skills and Experience A thorough knowledge of GDP and GMP requirements. Proven experience in drafting and updating standard operating procedures, work instructions, and specifications. The ability to interpret technical drawings and apply inspection criteria effectively. Hands-on experience in manufacturing processes within the medical device industry or Pharma industry. Proficiency in using basic measurement tools such as calipers, jigs, and gauges.
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