Technical Lead – Digital Mental Health

Macedonian Human Resources Association

Technical Lead supporting the Digital Mental Health project team within the Health Quality and Access group. Contributing to the development of AI regulatory frameworks for mental health products.

Posted 7/7/2026part-timeLondon • 🇬🇧 United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in regulatory compliance for AI and medical devices, with a strong focus on stakeholder engagement and proactive service delivery. Possesses a solid foundation in scientific, engineering, or medical disciplines, ensuring attention to detail and effective monitoring of compliance activities.

Highest-signal resume keywords

Regulatory Affairs ExperienceMedical Device RegulationAI Compliance KnowledgeCustomer Service SkillsBachelor's Degree in Scientific Discipline

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory ComplianceQuality AssuranceMedical AffairsDigital Mental Health TechnologiesAttention to Detail

Soft Skills

Proactive ServiceFlexible AttitudeDiplomatic CommunicationInitiativeTeam Collaboration

Industry Keywords

AI Regulatory SandboxStakeholder EngagementSafety and SurveillanceClinical SettingCommercial SettingPolicy Setting

About the role

Key responsibilities & impact

Support the development and implementation of the DMHT AI regulatory sandbox
Assist senior colleagues in various compliance activities
Engage with internal and external stakeholders to ensure access to safe medical devices
Collaborate with the safety and surveillance team for compliance activity on digital mental health technologies

Requirements

What you’ll need

Proven customer service skills to deal confidently and diplomatically with external stakeholders and colleagues at all levels
Experience of a flexible and adaptable attitude towards work, providing a proactive service and the ability to use initiative, foresight, and have a willingness to go the ‘extra mile’ and excellent attention to detail
Regularly monitor your own and team’s work against milestones ensuring individual needs are considered when setting tasks
Previous experience in software, AI or medical device regulation, including in a clinical, commercial, academic or policy setting. This could include experience developed through previous roles in Regulatory Affairs, Quality Assurance or Medical Affairs
Bachelor’s degree of equivalent in a scientific, engineering or medical discipline

Benefits

Comp & perks

Flexible, hybrid way of working
Minimum of 8 days per month working on site
Internal move, temporary promotion, loans will be considered