Careers
Disciplines we work in
Regulatory affairs
Strategy, technical documentation and submissions across global markets.
Quality and quality engineering
QMS, audits, design controls, risk management and software quality.
Clinical and medical writing
Clinical and performance evaluation, literature reviews and PMCF.
Post-market and vigilance
Complaint handling, reportability, trending and periodic reports.
AI and software engineering
Building and validating our regulatory AI platforms.
Business development
Helping manufacturers find the right regulatory route and team.
How to apply. Send your CV and a short note on the role or discipline you are interested in to info@medoqi.tech, with "Careers" in the subject line.
Partnerships
Organisations we work alongside
Manufacturers often need more than one specialist provider. We coordinate with yours, and we are open to new partnerships that serve device and IVD manufacturers well.
- Contract research organisations and clinical sites
- Testing laboratories and sterilisation providers
- In-country representatives and distributors
- Technology and AI partners
- Industry associations, incubators and startup programmes