Regulatory Affairs Specialist – Medical Devices & IVD
mid
Posted 1mo ago · via Teamtailor
About this role
We are seeking a detail-oriented and organized Regulatory Affairs Specialist to support the registration, maintenance, and regulatory compliance of Medical Devices and In Vitro Diagnostic (IVD) products in Saudi Arabia. Key Responsibilities Prepare, review, and follow up on SFDA/MDMA registration, renewal, and update applications. Review technical and regulatory documentation to ensure compliance with SFDA requirements. Prepare and submit regulatory files, and follow up on SFDA comments, inquiries, and requests for additional information. Coordinate with manufacturers and suppliers to obtain missing, updated, or revised regulatory documents. Support medical device and IVD product classification and regulatory assessments.…
Read the full description on Seamless Specialized Services's site →
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
We compare your skills against the role requirements.
2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in a specific location. We weight your proximity and willingness to relocate.
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Free · no card · written explanation included