Freelance regulatory consultant / specialist

Barrington James are exited to post a fantastic opportunity for one of our close clients. This company is a small Medical Device Manufacturer in Belgium. They are backed by some serious investors the industry and are looking for future support within their Regulatory Affairs team. This opportunity is prefect for someone who is ambitious, independent and wants to play a key role in working on the most innovative projects.

Key Responsibilities

• Prepare documentation for regulatory submissions (both drug products and medical devices)
• Update Technical Documentation
• Act as PRRC for Technical Documentation (depending on qualifications and training)
• Assess the regulatory impact of change controls.
• Perform gap assessments as a result from new standards/guidelines/regulations specific to products and markets
• Act as process owner for assigned processes
• Update the tracking systems within the Regulatory department
• Maintain quality related files and records ensuring traceability in accordance with the appropriate procedures
• Act as a team member to represent regulatory affairs on assigned product and project teams
• Support written and verbal communication with customers and regulatory bodies

This truly is an exiting opportunity for someone to join an ambitious company who are continuing to impress the market with their ground-breaking studies.

The opportunity has understandably been incredibly popular. We encourage all interested candidates to apply immediately as it is likely that recruitment will close prematurely.

By clicking \"apply\" you will be sending your CV to Charlie at Barrington James. Charlie is an senior RA/QA Recruitment specialist and will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself.