Location
Remote, kingdom of spain, Spain
Posted
July 19, 2026
Job Description
Join Roche as an International Regulatory Affairs Professional to drive regulatory solutions for global IVD/MD instruments and software. Bring your expertise in regulatory strategy, compliance, and cross‑functional collaboration to impact patient care worldwide.
Key Responsibilities
Lead and support regulatory strategies for global IVD/MD instrument and software submissions.
Ensure compliance with international regulatory requirements and standards.
Collaborate with cross‑functional teams (R&D, Quality, Clinical) to drive regulatory initiatives.
Provide regulatory guidance to support product development and lifecycle management.
Stay abreast of evolving regulatory trends and implement best practices.
Requirements
Bachelor’s Degree in Life Sciences, Regulatory Affairs, or related field.
5 to 7 years of experience in Regulatory Affairs (Regulatory, R&D, Quality, and/or Clinical), preferably in healthcare regulatory affairs.
In‑depth knowl...
Key Responsibilities
Lead and support regulatory strategies for global IVD/MD instrument and software submissions.
Ensure compliance with international regulatory requirements and standards.
Collaborate with cross‑functional teams (R&D, Quality, Clinical) to drive regulatory initiatives.
Provide regulatory guidance to support product development and lifecycle management.
Stay abreast of evolving regulatory trends and implement best practices.
Requirements
Bachelor’s Degree in Life Sciences, Regulatory Affairs, or related field.
5 to 7 years of experience in Regulatory Affairs (Regulatory, R&D, Quality, and/or Clinical), preferably in healthcare regulatory affairs.
In‑depth knowl...