Senior Design Quality Engineer

Senior Design Quality Engineer

Bournemouth Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead quality assurance for life-saving medical devices and ensure compliance with global standards.
  • Company: Join a top-tier global medical device company based in Kent, making a real impact.
  • Benefits: Enjoy competitive pay, career growth opportunities, and a chance to work on innovative technologies.
  • Why this job: Be part of a mission-driven team that values quality and innovation in healthcare.
  • Qualifications: Requires a degree in Engineering and 7+ years in medical device R&D or Quality.
  • Other info: ASQ Certified Quality Engineer certification is needed within one year of joining.

The predicted salary is between 48000 - 72000 £ per year.

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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Senior Design Quality Engineer employer: Halian Technology Limited

Halian is an exceptional employer, offering a dynamic work environment in Kent where innovation meets compliance in the medical device sector. Employees benefit from a culture of collaboration and continuous improvement, with ample opportunities for professional growth and development in a field that directly impacts lives. Join us to be part of a team that values quality and integrity while working on life-saving technologies.
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Contact Detail:

Halian Technology Limited Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Design Quality Engineer

✨Tip Number 1

Network with professionals in the medical device industry, especially those who have experience in quality assurance. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in quality management.

✨Tip Number 2

Familiarise yourself with the specific ISO standards mentioned in the job description, such as ISO 13485 and ISO 14971. Consider joining online forums or groups where these topics are discussed to deepen your understanding and show your commitment to compliance.

✨Tip Number 3

Prepare to discuss your experience with advanced quality tools during interviews. Be ready to provide examples of how you've applied risk management, design controls, and statistical analysis in previous roles, as this will demonstrate your hands-on expertise.

✨Tip Number 4

Research the company’s recent projects and initiatives in the medical device sector. Being knowledgeable about their products and challenges will help you tailor your conversations and show that you're genuinely interested in contributing to their mission.

We think you need these skills to ace Senior Design Quality Engineer

Quality Management Systems
ISO 13485
ISO 14971
21 CFR Part 820
Risk Management
Design Controls
Verification and Validation
Corrective and Preventive Actions (CAPA)
Statistical Analysis
Regulatory Compliance
Audit Readiness
Cross-Functional Collaboration
Data Interpretation
Problem-Solving Skills
Systems Thinking
Continuous Improvement

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in quality assurance and medical device regulations. Emphasise your familiarity with ISO standards and any specific projects that demonstrate your skills in risk management and compliance.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the medical device industry and your understanding of quality management systems. Mention specific achievements that align with the responsibilities listed in the job description, such as leading quality assurance activities or collaborating with cross-functional teams.

Highlight Relevant Certifications: Clearly state your ASQ Certified Quality Engineer (CQE) certification status in your application. If you are in the process of obtaining it, mention your timeline to completion, as this is a key requirement for the role.

Showcase Analytical Skills: Provide examples in your application that demonstrate your analytical mindset. Discuss how you've used data interpretation to identify trends or improve processes in previous roles, particularly in relation to product quality and compliance.

How to prepare for a job interview at Halian Technology Limited

✨Know Your Standards

Familiarise yourself with ISO 13485, ISO 14971, and 21 CFR Part 820. Be prepared to discuss how you've applied these standards in your previous roles, as this will demonstrate your expertise and understanding of regulatory compliance.

✨Showcase Your Analytical Skills

Prepare examples that highlight your analytical mindset. Discuss specific instances where you interpreted data to identify trends or risks, and how those insights led to actionable improvements in product quality.

✨Emphasise Collaboration

Since the role involves working with cross-functional teams, be ready to share experiences where you successfully collaborated with engineering and manufacturing teams. Highlight how you contributed to design reviews or managed product changes.

✨Prepare for Scenario Questions

Expect scenario-based questions that assess your problem-solving skills. Think of situations where you resolved on-market product issues or led quality assurance activities, and be ready to explain your thought process and outcomes.

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