At a Glance
- Tasks: Manage technical documentation and oversee software validation for medical devices.
- Company: Doccla, a forward-thinking MedTech company with a focus on ethics and innovation.
- Benefits: Flexible remote work, inclusive culture, and opportunities for professional growth.
- Other info: Hybrid role with office locations in London and abroad.
- Why this job: Join a team that values integrity and make a difference in healthcare technology.
- Qualifications: 3-6 years in Medical Device QA with knowledge of risk management and software validation.
The predicted salary is between 50000 - 60000 £ per year.
Doccla is seeking a RAQA Specialist to maintain delivery continuity during active Technical Documentation review cycles.
You will manage technical nonconformities and oversee software validation planning to ensure compliance with regulatory standards.
The ideal candidate will have 3–6 years’ experience in Medical Device QA alongside a strong understanding of risk management and software validation processes.
This hybrid role offers flexibility with office locations in London and abroad.
Doccla values ethics, innovation, and integrity, promoting an inclusive workspace for all candidates.
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We think you need these skills to ace MedTech RA/QA Specialist — Software Validation (Remote) in London
Technical Documentation Review
Software Validation
Regulatory Compliance
Risk Management
Medical Device Quality Assurance
Nonconformity Management
Analytical Skills
