CrawlJobs Logo
ElevenLabs Logo ElevenLabs · IT - Administration

Compliance Engineer - EU

United Kingdom, London · Job Posted May 16, 2026
Apply Position
Job Link Share

Job Description

ElevenLabs is at the frontier of AI — and with that comes a real obligation to meet the compliance demands of the world's most regulated industries. As a Compliance Engineer focused on the EU, you'll help us navigate one of the most complex and fast-moving regulatory environments in the world: GDPR, the EU AI Act, DORA, NIS2, HDS, and beyond. This isn't a checkbox role. You'll work closely with engineering, product, and legal teams to embed compliance into how we build — writing the technical documentation that earns enterprise trust, building tooling that makes staying compliant frictionless, and directly shaping our go-to-market story for regulated sectors like finance and telecommunications. You'll be the person who turns regulatory complexity into a competitive advantage for ElevenLabs in Europe.

Job Responsibility

  • Navigate EU regulatory environments including GDPR, EU AI Act, DORA, NIS2, HDS, and beyond
  • Work closely with engineering, product, and legal teams to embed compliance into how we build
  • Write technical documentation that earns enterprise trust
  • Build tooling that makes staying compliant frictionless
  • Shape go-to-market story for regulated sectors like finance and telecommunications

Requirements

  • Proven experience working with EU regulatory frameworks — GDPR, EU AI Act, DORA, NIS2, and/or HDS
  • Hands-on with ISO 27001, ISO 42001, or the broader ISO 27000 series — gap analysis, risk assessments, audit support
  • Able to produce clear, precise technical compliance documentation that stands up to enterprise scrutiny
  • Comfortable supporting enterprise sales — responding to security questionnaires, customer compliance queries, and regulated-sector procurement
  • Experience building or maintaining compliance-as-code tooling to automate monitoring and reduce manual overhead
  • Based in EU/EMEA and able to operate within European business timezones

Nice to have

  • Direct experience in regulated industries such as financial services or telecommunications
  • Familiarity with CIS benchmarks and risk documentation at scale
  • Scripting or engineering background that lets you go beyond documentation into automation

What we offer

  • Innovative culture
  • Growth paths
  • Learning & development through annual discretionary stipend
  • Social travel annual discretionary stipend
  • Annual company offsite
  • Co-working monthly stipend
ElevenLabs - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Compliance Engineer - EU

8 matching positions

Compliance Engineer

The Product Compliance Engineer will partner with global product developers and ...
Location
Location
United States , Needham
Salary
Salary:
72700.00 - 111400.00 USD / Year
sharkninja.com Logo
SharkNinja
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, Systems Engineering, Materials Engineering, Computer Science, or a related technical discipline
  • RAC certification a plus
  • Minimum 2–4 years of compliance or design-related experience with consumer, commercial, or medical electromechanical products
  • Working knowledge of medical device regulatory standards including: IEC 60601-1 and applicable collateral/particular standards (esp. IEC 60601-1-2 for EMC, IEC 60601-1-6 for usability, IEC 60601-1-11 for home healthcare environments)
  • ISO 14971 – Risk Management for Medical Devices
  • ISO 13485 – Quality Management Systems
  • IEC 62366-1 – Usability Engineering
  • IEC 62304 – Medical Device Software Lifecycle (where applicable)
  • ISO 10993 series – Biocompatibility Evaluation
  • 21 CFR Part 820 – FDA Quality System Regulation
Job Responsibility
Job Responsibility
  • Support the execution of certification activities and risk analysis for multiple new product development projects, including FDA-regulated medical devices and products subject to EU MDR 2017/745
  • Assist in preparing regulatory filings including FDA 510(k) submissions and Technical Files/Design Dossiers, and maintain Design History Files (DHF) in compliance with 21 CFR Part 820 Design Controls and ISO 13485 requirements
  • Support the establishment of project needs and deliverables for both product development teams and third-party regulatory partners, including Notified Bodies and FDA-accredited testing laboratories
  • Execute risk management activities in accordance with ISO 14971
  • Support usability engineering processes per IEC 62366-1
  • Evaluate project risk during the development process and support contingency planning
  • Participate in weekly reviews for all assigned projects
  • Assure that all activities related to product certification commence and execute as planned and on schedule
  • Support product development teams as a subject matter expert
  • Contribute to intradepartmental continuous improvement and special projects
What we offer
What we offer
  • Medical insurance
  • dental insurance
  • vision insurance
  • flexible spending accounts
  • health savings accounts (HSA) with company contribution
  • 401(k) retirement plan with matching
  • employee stock purchase program
  • life insurance
  • AD&D
  • short-term disability insurance
  • Fulltime
Read More
Arrow Right

Compliance Engineer - Product Development

The Compliance Engineer will work with product engineering teams to ensure all r...
Location
Location
Ireland; Canada , Dublin; Halifax
Salary
Salary:
Not provided
resmed.com Logo
ResMed
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 2+ years of experience navigating technical products through audits like MDR, SOC2, MDSAP, HDS, or any other regulatory framework
  • Proficiency in report writing, analysis, and compliance procedures
  • Thorough understanding of regulatory frameworks
  • Solid technical knowledge and understanding of product/process design
  • An understanding of Software Development Lifecycle
Job Responsibility
Job Responsibility
  • Lead critical design control activities including Safety risk analysis
  • Security risk analysis
  • Requirements traceability
  • Design review
  • SOUP/CSV management
  • Represent the team in audits, including medical device audits such as MDSAP and EU MDR and security audits such as HITRUST, SOC, and ISO 27001
  • Perform gap analyses to new and upcoming compliance standards and regulations
  • Make improvements to Resmed's Quality Management System procedures
  • Provide input on product regulatory strategy and be involved in communication with regulators and notified bodies
What we offer
What we offer
  • A supportive environment that focuses on people development and best practices
  • Opportunity to design, influence, and be innovative
  • Work with global teams and share new ideas
  • Be supported both inside and outside of the work environment
  • The opportunity to build something meaningful and seeing a direct impact on people's lives
  • Fulltime
Read More
Arrow Right

Regulatory Compliance Engineer

This role has been designed as ‘’Onsite’ with an expectation that you will prima...
Location
Location
United States , Roseville
Salary
Salary:
89400.00 - 206500.00 USD / Year
https://www.hpe.com/ Logo
Hewlett Packard Enterprise
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Must have 5-10 years of Regulatory compliance experience
  • Have a Bachelor’s or Master’s degree in electrical engineering
  • 5-10 years of industry experience
  • Expert knowledge in EMI/EMC, Safety and Telecom standards/requirements for ITE/Telecom products
  • Proven track record managing global product certifications across development teams, test labs, suppliers, manufacturing, and OEM/ODM partners
  • Solid experience in acquiring global regulatory compliance approvals for new and released products
  • Experience working with Safety Agencies (UL, CSA, TUV) engineers early in the design phase to identify design constraints to achieve safety certification without surprises after the design freeze
  • Experience working with the relevant EMC Labs and various countries regulatory body such as FCC, IEC, CCC, EAC, KCC, Brazil Anatel, Taiwan BSMI, India TEC, EU etc…
  • Proven track record with performing or supporting the design and testing required to obtain Safety, EMC, Telecom, and similar certifications
  • Communicate regulatory strategy, testing required, approval schedule, estimated cost, key risks and concerns to the NPI program team
Job Responsibility
Job Responsibility
  • Leads the project team on internal and outsourced product development projects to design reliable, cost effective and high-quality EMC and safety compliance solutions for moderately to complex Networking products
  • Collaborates and communicates with management, internal, and outsourced development partners regarding design status, project progress, and issue resolution regarding regulatory compliance
  • Represents the electrical hardware team on all aspects of Global regulatory requirements in the product design phase
  • Provides regulatory compliance support to engineering development projects and existing product changes throughout the product life cycle
  • Interfaces with cross-functional teams consisting of engineering, operations, manufacturing, sourcing, quality, service, and marketing to assure ongoing products are compliant to global regulations
  • Solve complex Safety, EMC, Telecom test issues and challenges, including debugging/troubleshooting to recommend resolution
What we offer
What we offer
  • Health & Wellbeing
  • Personal & Professional Development
  • Unconditional Inclusion
  • Fulltime
Read More
Arrow Right

QA Engineer – Security, Compliance & Automation

We are looking for a QA Engineer specializing in security, compliance, and autom...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
Codvo AI
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 5+ years of experience in QA or Test Automation for enterprise applications
  • Strong knowledge of C#, .NET, Angular, or Java-based testing frameworks
  • Experience with Selenium, Playwright, Postman, JMeter, or Robot Framework
  • Hands-on experience with SAST/SCA tools (SonarQube, Snyk, Checkmarx, or similar)
  • Familiarity with secure SDLC, OWASP Top 10, and DevSecOps pipelines
  • Working knowledge of compliance frameworks (CRA, SOC 2, ISO 27001)
  • Strong analytical, debugging, and documentation skills
Job Responsibility
Job Responsibility
  • Design and implement automated test frameworks for secure SDLC validation (unit, integration, functional, and regression)
  • Conduct compliance-driven testing aligned with EU CRA, NIS2, and ISO 27001
  • Build and maintain security and compliance test suites in CI/CD pipelines (e.g., GitHub Actions, Jenkins, Azure DevOps)
  • Execute vulnerability validation, SBOM verification, and dependency testing using SCA/SAST/DAST tools
  • Collaborate with developers to triage and validate remediation fixes for security and compliance findings
  • Generate audit-ready QA documentation for regulatory assessments
  • Support performance, reliability, and failover testing in security-critical systems
  • Fulltime
Read More
Arrow Right
New

Senior Plant Engineer

At Argenta, we’re more than a company — we’re a global team, dedicated to health...
Location
Location
United States , Shawnee
Salary
Salary:
Not provided
argentaglobal.com Logo
Argenta
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 5+ years working experience in cGMP environment
  • Knowledge in Pharmaceutical regulations
  • Bachelors degree in engineering discipline
  • Pharmaceutical background prefer sterile manufacturing experience with knowledge in pharmaceutical regulations
Job Responsibility
Job Responsibility
  • Makes independent decisions within defined areas of responsibility
  • Serves as a consultant to management within a specified areas/discipline
  • Advance technical project proposals to senior management, following through successful completion
  • Influences commitment of resources at divisional / departmental level
  • Continuously improve and support existing production equipment to support the efficient operation of the Argenta production facility
  • Manage capital projects, develop and track budgets
  • Interface with internal and external resources to facilitate the transfer of process knowledge to the manufacturing environment
  • Ensure that all Engineering activities within the area of responsibility adhere to all applicable engineering standards, codes, cGMP’s, FDA and EU guidelines, safety and environmental procedures
  • Reviews and approves standard operating procedures describing validation principles and activities
  • Participate with completing risk analyses for qualifications and validations with participation of Quality, Production and MEU
  • Fulltime
Read More
Arrow Right
New

Sr Principal Engineer - Software Quality

This is where new knowledge is discovered. Baxter’s Research and Development tea...
Location
Location
United Kingdom , Gloucester
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor of Science or Bachelor of Engineering in Software Engineering, Computer Science, Electrical, Biomedical, or related discipline required
  • Master’s degree or PhD preferred with 10+ years of progressive experience in software quality engineering, including regulated medical device software and/or digital health platforms
  • Strong expertise in: ISO 13485 Quality Management Systems
  • EU MDR (Regulation (EU) 2017/745) and software implications
  • Software lifecycle standards (e.g., IEC 62304, IEC 82304 where applicable)
  • FDA software and quality system expectations
  • Proven ability to integrate Agile development practices with regulatory compliance, including traceability, documentation, and change management
  • Broad understanding of: Software architecture and system integration
  • Cloud-based systems, cybersecurity, and data privacy considerations
  • Software risk management, including hazard analysis and vulnerability management
Job Responsibility
Job Responsibility
  • Lead and govern activities that ensure alignment with Baxter’s Product Lifecycle Management (PDLM) and Change Control Management (CCM) processes and compliance with design controls and quality system regulations
  • Translate Agile software development practices into compliant frameworks that meet Baxter, ISO 13485 and EU MDR expectations, including traceability, documentation, verification, and validation
  • Ensure effective implementation of software design controls, including: Software requirements and architecture, Risk management (software hazard analysis, cybersecurity risk), Verification and validation strategies (manual, automated, CI/CD pipelines), Configuration and change management
  • Lead integration of Quality Management System (QMS) processes into software development workflows, including: CAPA and nonconformance handling, Complaint handling and feedback loops into Agile backlogs, Audit readiness and inspection support
  • Ensure compliance with EU MDR requirements, including: Support for technical documentation and software lifecycle evidence, Alignment of software changes with regulatory impact assessments, Post-market surveillance inputs (e.g., trending, signal detection)
  • Apply advanced quality and engineering tools including root cause analysis, reliability engineering, and data analytics to improve software quality and system performance
  • Oversee development of technical documentation supporting: Design history files (DHF) / technical files, Software lifecycle documentation (per IEC 62304 where applicable), Risk management files, Verification and validation reports, Regulatory submissions
  • Serve as subject matter expert for software quality, cybersecurity, and lifecycle management, providing guidance across teams and influencing enterprise-wide standards
  • Collaborate closely with Quality, Regulatory Affairs, R&D (software and systems), Product Management, Cybersecurity, Clinical, and Manufacturing teams to ensure software products are safe, effective, secure, and compliant
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right
New

Depot Fleet EV Charging Engineer

This is a brilliant opportunity for someone who really enjoys getting hands-on w...
Location
Location
United Kingdom , London
Salary
Salary:
55000.00 - 58000.00 GBP / Year
pod-point.com Logo
Pod Point
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Hands-on EV Charging Expertise - Strong experience troubleshooting AC and DC charging infrastructure, with a deep understanding of EV ecosystems
  • OCPP Knowledge - Solid understanding of OCPP protocols, with the ability to analyse and interpret protocol messages
  • End-to-End Technical Understanding - Experience across full charging solutions including chargers, hubs, routers, and onsite networking, including data and message flows
  • OEM and Hardware Troubleshooting - Proven ability to use OEM tools and manuals to configure, manage, and resolve device issues
  • Networking Capability - Strong skills in configuring, managing, and troubleshooting local networks, routers, and load management systems
  • Electrical Qualifications - Qualified electrician, with knowledge of single and three-phase systems, voltage levels, and earthing setups across UK, EU, and US standards
  • Technical Support Experience - At least 3 years’ experience in technical support or managed services within EV, energy, or similar technical environments
  • Customer-Focused Mindset - Experience working in customer support environments, with excellent communication skills and a confident telephone manner
  • Problem Solving and Ownership - Strong analytical skills, with the ability to prioritise effectively and drive issues through to resolution
  • Health and Safety Awareness - Good understanding of health, safety, and environmental legislation, with the ability to promote safe working practices
Job Responsibility
Job Responsibility
  • Deliver Tier 2 Technical Support - you’ll resolve complex incidents, service requests, and problems, identifying trends and driving improvements across the estate
  • Monitor and Respond to System Alerts - you’ll proactively monitor multiple platforms to detect emerging issues, bottlenecks, and risks, taking swift action to prevent disruption
  • Own Customer Escalations - you’ll take full ownership of escalations through to resolution, ensuring customer expectations are exceeded at every stage
  • Collaborate Across Teams - you’ll work closely with Tier 3 software teams to identify bugs, and partner with third-party vendors and OEMs during major incidents and new service implementations
  • Manage OEM Escalations - you’ll drive complex issues through to resolution with charger manufacturers and external partners
  • Support Commissioning and Change Activity - you’ll contribute to onboarding new sites and complete out-of-hours activities, including upgrades, maintenance, and testing
  • Document and Enable Others - you’ll produce and maintain technical documentation, processes, and training materials, enabling Tier 1 teams to deliver effectively
  • Maintain Service Excellence - you’ll ensure KPIs, SLAs, and OLAs are consistently met, while upholding EO’s values, ethics, and customer-first approach
  • Drive Continuous Improvement - you’ll identify recurring issues, trends, and opportunities across the estate, using data and insights to drive improvements in system performance, stability, and customer experience
  • On Call Service Contribution - As part of a 24x7x365 support model, you will contribute to on call engineering coverage. On call engineers provide significant advantages where equipment uptime and operational continuity are critical. This Covers: Technical Support & Maintenance - respond promptly to faults and breakdowns
What we offer
What we offer
  • Access for you and up to 5 family/friends to the 'UnMind' wellbeing platform
  • Podpoint Charger
  • Discounted energy tariff (Pod Power or EDF Employee Programme)
  • Flexible hybrid working model
  • Work abroad for up to 20 days per year
  • Family & friend discount scheme
  • 25 days holiday (plus Bank Holidays)
  • Very generous parental and family leave
  • Pension scheme with a 4.5% matched contribution
  • Eyecare scheme
  • Fulltime
Read More
Arrow Right
New

Sr Principal Engineer - Software Quality

This is where your work makes a difference. At Baxter, we believe every person—r...
Location
Location
United Kingdom , Gloucester
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor of Science or Bachelor of Engineering in Software Engineering, Computer Science, Electrical, Biomedical, or related discipline required
  • Master's degree or PhD preferred with 10+ years of progressive experience in software quality engineering, including regulated medical device software and/or digital health platforms
  • Strong expertise in: ISO 13485 Quality Management Systems
  • EU MDR (Regulation (EU) 2017/745) and software implications
  • Software lifecycle standards (e.g., IEC 62304, IEC 82304 where applicable)
  • FDA software and quality system expectations
  • Proven ability to integrate Agile development practices with regulatory compliance, including traceability, documentation, and change management
  • Broad understanding of: Software architecture and system integration
  • Cloud-based systems, cybersecurity, and data privacy considerations
  • Software risk management, including hazard analysis and vulnerability management
Job Responsibility
Job Responsibility
  • Lead and govern activities that ensure alignment with Baxter's Product Lifecycle Management (PDLM) and Change Control Management (CCM) processes and compliance with design controls and quality system regulations
  • Translate Agile software development practices into compliant frameworks that meet Baxter, ISO 13485 and EU MDR expectations, including traceability, documentation, verification, and validation
  • Ensure effective implementation of software design controls, including: Software requirements and architecture
  • Risk management (software hazard analysis, cybersecurity risk)
  • Verification and validation strategies (manual, automated, CI/CD pipelines)
  • Configuration and change management
  • Lead integration of Quality Management System (QMS) processes into software development workflows, including: CAPA and nonconformance handling
  • Complaint handling and feedback loops into Agile backlogs
  • Audit readiness and inspection support
  • Ensure compliance with EU MDR requirements, including: Support for technical documentation and software lifecycle evidence
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right