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Senior Design Quality Engineer

Where

Cardiff

Type

Permanent

Salary

Annual

Halian is seeking a highly skilledSenior Design Quality Engineerto join a leading global medical device business based in Kent. This is a fantastic opportunity to contribute to the development of life-saving technologies while ensuring compliance with international quality and regulatory standards.

Key Responsibilities
  • Lead quality assurance activities across product development and manufacturing.
  • Ensure compliance with ISO 13485, ISO 14971, 21 CFR Part 820, and other relevant standards.
  • Act as the Quality Core Team Member, embedding quality into every stage of product design and realisation.
  • Apply advanced quality tools including risk management, design controls, verification and validation, CAPA, and statistical analysis.
  • Support regulatory compliance efforts, including audit readiness and responses to global regulatory bodies.
  • Develop and maintain product risk management files in accordance with ISO 14971.
  • Collaborate with cross-functional teams to manage product changes, participate in design reviews, and support design transfers.
  • Monitor global product data to identify trends, risks, and opportunities for improvement.
  • Provide guidance on resolving on-market product issues and escalate critical concerns to senior leadership.
  • Contribute to special projects and continuous improvement initiatives.
Skills & Experience
  • Strong understanding of Quality Management Systems and their integration with risk management, CAPA, complaints, and document control.
  • In-depth knowledge of medical device regulations and standards.
  • Proven ability to conduct complex investigations and apply systems thinking across hardware, software, and consumables.
  • Analytical mindset with the ability to interpret data and identify patterns leading to actionable insights.
  • Effective collaboration with engineering and manufacturing teams.
Qualifications
  • Bachelors degree in Engineering (Electrical, Mechanical, Biomedical, Software) or a related field.
  • Minimum 7 years of experience in R&D or Quality within the medical device industry.
  • ASQ Certified Quality Engineer (CQE) certification required or must be obtained within one year.

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