We are looking for an experienced Compliance Engineer to join a exciting medical device organisation and support regulatory compliance across the full product lifecycle.
This medical device Compliance Engineer opportunity would suit someone with strong technical documentation experience who enjoys working across Quality, Engineering, NPD and Manufacturing within a highly regulated environment.
The Role
As Compliance Engineer, you will be responsible for creating, reviewing and maintaining regulatory and technical documentation to ensure products remain compliant and audit-ready.
Key Compliance Engineer responsibilities will include:
Authoring and maintaining Technical Files, Design Dossiers and regulatory documentation.
Supporting EU MDR and UK regulatory compliance activities.
Preparing technical reports, declarations and compliance records.
Supporting regulatory submissions, registrations and market access activities.
Reviewing documentation for accuracy, completeness and regulatory compliance.
Managing documentation updates following design, process or regulatory changes.
Supporting risk management and design control documentation.
Assisting with Notified Body, Competent Authority and external audit requirements.
Monitoring changes to regulations, standards and guidance.
Supporting post-market compliance and regulatory change assessments.
Contributing to continuous improvement of Quality and Regulatory processes.
About You
The successful Compliance Engineer will ideally have:
Experience within medical devices (ISO13485), pharmaceuticals or another regulated life sciences environment.
Strong experience creating and maintaining controlled technical documentation.
Knowledge of EU MDR 2017/745, ISO 13485 and ISO14971
Understanding of design control, risk management and technical documentation requirements.
Experience supporting regulatory submissions or Technical File activities.
Excellent technical writing and attention to detail.
Strong organisational and cross-functional communication skills.
The Compliance Engineer will work closely with Quality, Engineering, Product Development and Manufacturing teams, providing compliance input into both existing products and new product development.
This Compliance Engineer position offers the opportunity to take ownership of meaningful compliance activities while developing broader exposure across regulatory submissions, product lifecycle management and international medical device requirements.
If you are a medical device Compliance Engineer looking for a technically varied role within a regulated medical device environment, apply to discuss the opportunity in more detail.
