Senior Regulatory Affairs & Quality Assurance Specialist | MedTech

Location: Spain, Portugal and UK (Remote)

Employment type: Full-time

Role Summary

We are looking for an experienced and proactive Regulatory Affairs & Quality Assurance professional to join our growing consulting team.

As a Senior Regulatory Affairs & Quality Assurance Specialist , you will lead regulatory and quality projects for medical device manufacturers, helping clients navigate complex regulatory requirements and implement robust quality systems that enable successful market access.

You will work directly with international clients, leading multiple projects simultaneously while collaborating with multidisciplinary experts across regulatory affairs, quality assurance, clinical research, and medical writing.

This role is ideal for professionals with