Quality Systems Manager

Skin Analytics; London; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading health tech company is seeking a Quality Systems Manager to enhance quality and information security systems for medical devices. You will ensure compliance with global regulations while leading audit preparations and integrating AI standards into operations. Join a passionate team to revolutionize healthcare with innovative AI solutions.

Benefits

Competitive salary

Share options package

Private healthcare

25 days annual leave plus bank holidays

Enhanced parental leave

Training budget

Social activities including company offsite

Qualifications

• Minimum 5 years of hands-on QMS management experience in medical devices.
• Strong expertise in ISO 13485, EU MDR, and FDA QSR.
• Experience in leading significant management system changes.

Responsibilities

• Oversee and develop medical device Quality Management System and Information Security Management System.
• Lead audit preparation and certification efforts.
• Act as liaison for certification bodies during audits.

Skills

Analytical skills

Problem-solving

Leadership

Education

Bachelor’s or Master’s degree in Engineering, Life Sciences, Regulatory Affairs, Quality Management

Tools

ISO 13485

ISO 27001

Job description

About Skin Analytics
Skin Analytics is an award-winning, health tech company that works with dermatology teams to deploy world-leading skin cancer pathways using AI as a medical device, DERM.

Following our recent £15M series B funding round and regulatory milestones, we're ready to scale internationally, making history for AI in healthcare and the future of dermatology.

We're proud to epitomise AI for good - with a Class III CE mark, DERM is the only AI as a medical device approved to make clinical decisions autonomously in the cancer space, as well as being the first company to receive a NICE recommendation for use across the NHS.*

DERM is deployed at more than 25 NHS organisations where we're supporting dermatology teams to build sustainable services that enable patients to gain quicker access to skin cancer diagnosis. If that's not enough, we also collaborate with some of the largest health insurers to reach patients in their own homes.

We are a team of passionate people on a mission to build a future where no one dies from skin cancer.

London based - Hybrid (3 days a week in the office)

The role
The Quality Systems Manager ensures the effectiveness of our quality and information security systems, supporting compliance with global medical device regulations. They lead audit preparation, certification efforts, and continuous system improvements. This role also supports the integration of AI-specific quality standards into our operations. You'll be at the forefront of a cutting-edge AI product that's revolutionising medical diagnostics and transforming patient care.

Key Responsibilities

• Oversee and develop our medical device Quality Management System (QMS) and Information Security Management System (ISMS), ensuring compliance with ISO 13485, MDSAP, US FDA QSR, EU MDR and ISO 27001.
• Implement and secure certification for an Artificial Intelligence Management System in line with ISO 42001 and/or equivalent CENELEC standard(s).
• Act as primary liaison for certification bodies and regulatory authorities during external audits and inspections.
• Oversee the drafting and updating of QMS, ISMS procedures, work instructions and forms; ensure effective document control and distribution.
• Oversee CAPA and complaint investigations for our medical devices and ensure that activities are initiated, planned, executed and closed within defined timelines.
• Analyse trends from quality management system data, coordinate internal audits, recommend systemic improvements, and report to management on QMS & ISMS effectiveness.

• Lead our quality training program and mentor cross-functional teams on quality best practices and compliance principles.

• Bachelor’s or Master’s degree in Engineering, Life Sciences, Regulatory Affairs, Quality Management, or related field.

• Minimum 5 years of hands-on QMS management experience in medical devices, preferably with AI/Software as a Medical Device (SaMD) products.
• Demonstrable expertise in ISO 13485, EU MDR and FDA QSR (21 CFR 820) quality system requirements.
• Proven track record supporting external audits (notified body, FDA inspections).
• Experience leading significant management system changes and improvements.
• Strong analytical and problem-solving skills, with ability to find pragmatic and creative solutions.
• Certification as a Lead Auditor (ISO 13485) and/or Certified Quality Auditor (CQA) is a plus.

• Competitive salary
• Share options package - all our employees have ownership in the company
• Private healthcare
• 25 days annual leave (+ company shut down in August + bank holidays)
• Enhanced parental leave - includes adoption & foster
• Training budget
• Besides weekly catch-ups, monthly meetings to talk about you, your ambitions and make plans
• Lots of fun social activities including company offsite!

The Real Stuff

Skin Analytics embraces and is committed to diversity and equal opportunities. We are dedicated to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.


Skin Analytics manufactures medical devices and complies with ISO standards 13485 and 27001. As part of your employment, you will be assigned Quality Management System (QMS) and Information Security Management System (ISMS). We require that our employees agree to complete their assigned training and diligently follow all company quality management and information security processes.

*The National Institute for Health and Care Excellence has recommended DERM for use within the NHS until May 2028, while further evidence is gathered