Sign up to unlock the estimation.Sign up to unlock the estimation~£45,000 - £60,000per annum· Meev estimate
Posted 5 days ago
Description
Role Overview Quality Engineer responsible for ensuring medical devices meet stringent quality and regulatory standards within a growing therapeutics company.
Key Responsibilities
Implement and maintain Quality Management Systems compliant with ISO 13485
Manage non-conformances, CAPAs, and root cause investigations
Conduct internal and supplier audits
Support design control activities from concept through post-market surveillance
Ensure regulatory compliance for UKCA and CE marking submissions
Requirements
Experience in medical device quality engineering
Knowledge of ISO 13485, FDA QSR, and MDR
Strong problem-solving and documentation skills
Amber Therapeutics is an equal opportunity employer committed to diversity and inclusion.
Amber Therapeutics
Developing adaptive neuromodulation therapy to treat mixed urinary incontinence in women
DidcotMedical Devices11 - 50
Amber Therapeutics
Medical Devices
Join a multidisciplinary team developing breakthrough therapies that restore physiological function for millions of underserved women. Work at the forefront of intelligent neuromodulation technology backed by compelling clinical evidence.
Click to learn more
Amber Therapeutics
Medical Devices
Join a multidisciplinary team developing breakthrough therapies that restore physiological function for millions of underserved women. Work at the forefront of intelligent neuromodulation technology backed by compelling clinical evidence.