Rebranding Quality Engineer

Job description

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).