Found Description
MDx CRO is seeking a Senior Regulatory Affairs & Quality Assurance Specialist to oversee regulatory projects for medical device manufacturers. The position, suited for professionals with 3–5 years of experience, emphasizes ownership, client interaction, and problem-solving in a consulting environment.
The role involves leading multiple projects, maintaining compliance strategies, and supporting clients with QMS implementation.
This position is remote-friendly based in Spain, with opportunities for career progression and professional development.
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