19 Oct
Indo Professionals
Great Britain
Senior Regulatory Specialist – Freelance
Our client is looking for a freelance Senior Regulatory Specialist for a full-time contract focused on global medical device registrations.
Location:
Remote
Position:
Senior Regulatory Specialist/Manager.
Focused on product registrations of Class IIa/IIb medical device products, globally.
Please apply today or contact [email protected] / 07929235128
Job role:
In addition, as an extended member of the development project team, the successful RA Specialist will have input into regulatory plans for new products.
Full role responsibilities include:
- Monitoring & analysing regulatory changes and implementing strategies for meeting new and changed requirements
- Liaison with internal and external stakeholders, providing training and support to ensure that regulatory requirements are met
- Preparing and submitting pre- and post-market reports to regulators and local representatives
- Planning and performing clinical evaluations of the company’s medical devices
- Maintaining Technical Documentation and ensuring that the company’s compliance with applicable standards, regulations and guidance is documented
- Acting as a lead auditor of internal functions and external suppliers
- Line manager/supervision for the Regulatory Affairs Coordinator
The ideal applicant:
Our client is looking for a Senior RA Specialist or Manager with thorough experience of medical device product registrations including via distributors.
Indo Professionals is a specialist Med-Tech focused recruitment company supporting hires for medical device & IVD organisations within regulatory, quality, and clinical research. Please contact us today to discuss your next career challenge.
▶️ Regulatory Specialist - Contract
🖊️ Indo Professionals
📍 Great Britain