Rebranding Quality Engineer Our client, a global leader in the medical device industry, is undergoing an exciting brand transformation. As part of this journey, they are seeking a Rebranding Quality Engineer to help ensure their new brand identity is fully supported by world-class quality standards. This role offers a unique opportunity to combine hands-on quality engineering with strategic influence, embedding quality excellence into every stage of the rebrand process. Key Responsibilities Act as the voice of quality during a major brand transition, ensuring processes, documentation, and systems align with the refreshed identity. Lead process improvement and cost optimisation projects using statistical tools such as DOE, sampling plans, and root cause analysis. Own and guide change controls, risk assessments, and process validations linked to rebrand-driven changes. Manage CAPAs, non-conformances, SCARs, and supplier quality activities to maintain product and process integrity. Conduct internal and supplier audits and support ISO/FDA regulatory inspections. Oversee updates to manufacturing, packaging, and labelling processes to reflect the new brand identity while ensuring full compliance. Develop and track KPIs to measure quality performance during and after the rebrand. Maintain CGMP and EHS standards throughout the transition. Skills & Experience Required Degree in Engineering, Science, or a related discipline. Minimum 3 years' experience in a regulated manufacturing environment, preferably medical devices or FDA/ISO 13485-certified industries. Strong working knowledge of quality tools (FMEA, DOE, root cause analysis, statistical analysis). Excellent attention to detail with proven problem-solving ability. Strong communication skills, with the ability to explain technical concepts to non-technical audiences. Proficient in MS Office applications (Excel, Word, PowerPoint).