Rebranding Quality Engineer

Totaltalent; Ireland; On-site; EUR 50,000 - 70,000; Full time

Job summary

A global medical device company in Ireland is seeking a Rebranding Quality Engineer to ensure quality is embedded in their brand transformation. This full-time position requires a strong background in quality assurance, with at least 3 years of experience in regulated manufacturing, preferably in medical devices. The role involves leading process improvements, managing quality activities, and conducting audits in compliance with industry standards.

Qualifications

• Minimum 3 years of experience in a regulated manufacturing environment, preferably medical devices or FDA/ISO 13485-certified industries.

Responsibilities

• Act as the voice of quality during a major brand transition.
• Lead process improvement and cost optimisation projects.
• Manage CAPAs, non-conformances, SCARs, and supplier quality activities.
• Conduct internal and supplier audits and support ISO/FDA regulatory inspections.

Skills

Quality tools (FMEA, DOE, root cause analysis)

Problem-solving ability

Communication skills

Attention to detail

MS Office (Excel, Word, PowerPoint)

Education

Degree in Engineering, Science, or related discipline

Job description

Overview

Join to apply for the Rebranding Quality Engineer role at Total Talent

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).

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Civil Engineering