Vacancy - Regulatory Engineer

The Role:

CLIN-r+ now has an exciting opportunity for a contractor Regulatory Engineer to join our team.
Do you have experience in MedTech validations? Are you a engineer with exposure in compiling validation plans or validation protocols? Have you been part of teams maintaining or developing medical devices as a manufacturer or contract manufacturer? Do you desire working from home and setting your own hours? Then we want to speak to you.

The role is fully remote so the ideal candidate must have mastered remote
working and have a home office set up that can deal with reviewing multiple documents.
The role initially requires a minimum of 10 hours a week availability and as the contractor masters our workflow more hours can be allocated as you need.

This role will be in the Regulatory Affairs team primarily supporting interesting MedTech and Invitro Diagnostic transitions to EU MDR/IVDR. You’ll work with subject matter experts and consultants with documentation, but will also be an important part of the wider team and there is potential for further development.

Please state your availability on your application

 

Essential Skills & Experience:

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Key Responsibilities:

No agency applications please.