Senior Manufacturing Quality Engineer in London

Senior Manufacturing Quality Engineer in London

London Full-Time 50000 - 65000 £ / year (est.) No working from home possible
Story Terrace Inc.

At a Glance

  • Tasks: Drive quality improvements in manufacturing for cutting-edge biosensing technology.
  • Company: Join SAVA, a pioneer in advanced health tech transforming patient care.
  • Benefits: Competitive salary, dynamic work environment, and opportunities for professional growth.
  • Other info: Collaborative culture with a focus on innovation and quality.
  • Why this job: Shape the future of medical devices and make a real impact on health.
  • Qualifications: 5+ years in manufacturing quality engineering and a degree in Engineering or Life Sciences.

The predicted salary is between 50000 - 65000 £ per year.

About SAVA

All the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real-time and affordable way.

The Role

We are hiring for a Senior Quality Engineer to join our Manufacturing team. This role will be central to identifying critical gaps in our manufacturing process and implementing solutions to address them. Quality isn’t just a department. It is how we aim to operate. We firmly believe that our product is only as good as the culture we build around quality. This role is the missing piece that will help mature our quality architecture and scale our processes. If you want to build something from the ground up that will directly shape how a novel medical device reaches patients, keep reading.

What You’ll Do

  • You’ll play a key role in in-process quality at Sava, sitting within the Manufacturing team. Your day will split between the production floor and cross-functional collaboration.
  • Embed within Manufacturing to build a hands‑on understanding of sensor design, materials, process steps and the failure modes that matter most.
  • Define and continuously refine inspection protocols across every manufacturing stage, with acceptance criteria that are clear, measurable and practical for a production environment.
  • Spot quality risks early and intervene before small problems become expensive ones.
  • Lead root cause analysis and CAPA focused on systemic fixes: process drift, material variability, yield loss.
  • Provide guidance to quality specialists on reviews, CAPAs, and NCEs.
  • Develop and track quality metrics and yield trends that feed directly into manufacturing decisions.
  • Keep us aligned with ISO 13485 and regulatory requirements without letting compliance slow us down.
  • Act as the quality bridge between Manufacturing and QA/RA, translating requirements into processes that make sense on the floor.
  • Be the person during audits who can answer the hard questions calmly and credibly.
  • Train and mentor Manufacturing QA Specialists and technicians.
  • Establish defect libraries and failure mode catalogues.

What We’re Looking For

  • Bachelor's degree in Engineering, Life Sciences, or a related field.
  • 5+ years in manufacturing quality engineering within medical devices or a similarly regulated environment.
  • Genuine floor experience. You've spent real time on production lines.
  • Strong grasp of process control, defect analysis, root cause investigation, and yield improvement.
  • Hands on experience designing or implementing inspection protocols or quality control frameworks in a manufacturing setting.
  • Working knowledge of ISO 13485 and what it actually takes to operate within a regulated manufacturing environment.
  • Equally comfortable designing a quality framework and troubleshooting a defect.
  • Someone who collaborates well across functions – with manufacturing engineers, process technicians, regulatory specialists, and production leads.

Bonus Points For

  • Experience working in clean room environments.
  • Background in wearable medical devices, biosensing, continuous glucose monitoring, or similar sensor technologies.
  • Experience in a startup or scale‑up where you built quality systems from the ground up.

Senior Manufacturing Quality Engineer in London employer: Story Terrace Inc.

At SAVA, we pride ourselves on being an innovative employer that fosters a culture of quality and collaboration. Our commitment to employee growth is evident through hands-on training and mentorship opportunities, allowing you to shape the future of medical technology in a supportive environment. Located in a dynamic setting, we offer a unique chance to work at the forefront of biosensing technology, where your contributions will directly impact patient care and health interactions.

Story Terrace Inc.

Contact Details:

Story Terrace Inc. Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Manufacturing Quality Engineer in London

Tip Number 1

Get to know the company inside out! Research SAVA's products and values so you can speak confidently about how your experience aligns with their mission. This shows genuine interest and helps you stand out.

Tip Number 2

Network like a pro! Connect with current employees on LinkedIn or attend industry events. Building relationships can give you insider info and even lead to referrals, which can be a game-changer in landing that interview.

Tip Number 3

Prepare for the interview by practising common questions related to quality engineering and manufacturing processes. Use the STAR method (Situation, Task, Action, Result) to structure your answers and showcase your problem-solving skills.

Tip Number 4

Don’t forget to follow up after your interview! A simple thank-you email reiterating your enthusiasm for the role can leave a lasting impression. Plus, it shows you’re proactive and genuinely interested in joining the team.

We think you need these skills to ace Senior Manufacturing Quality Engineer in London

Quality Engineering
Manufacturing Process Understanding
Inspection Protocol Development
Root Cause Analysis
CAPA (Corrective and Preventive Actions)
ISO 13485 Compliance
Defect Analysis

Some tips for your application 🫡

Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Senior Manufacturing Quality Engineer role. Highlight your hands-on experience in manufacturing quality engineering and any relevant projects you've worked on.

Craft a Compelling Cover Letter:Use your cover letter to tell us why you're passionate about quality in manufacturing, especially in the medical device sector. Share specific examples of how you've tackled quality challenges in the past and how you can contribute to our mission at SAVA.

Showcase Your Problem-Solving Skills:In your application, emphasise your ability to identify and solve quality issues. We want to see how you've led root cause analyses or implemented inspection protocols that made a real difference in your previous roles.

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you're keen to be part of the SAVA team!

How to prepare for a job interview at Story Terrace Inc.

Know Your Quality Standards

Familiarise yourself with ISO 13485 and other relevant quality standards before the interview. Be ready to discuss how you've applied these standards in your previous roles, especially in manufacturing environments.

Showcase Your Hands-On Experience

Prepare examples that highlight your real-time experience on production lines. Discuss specific instances where you identified quality risks and implemented solutions, demonstrating your proactive approach to quality engineering.

Be Ready for Technical Questions

Expect questions about defect analysis and root cause investigation. Brush up on your knowledge of inspection protocols and be prepared to explain how you've designed or improved these processes in past roles.

Emphasise Collaboration Skills

Since this role involves cross-functional collaboration, think of examples where you've successfully worked with manufacturing engineers, regulatory specialists, or production leads. Highlight your ability to translate complex requirements into practical solutions on the floor.