"Regulatory Affairs Specialist" Jobs in Saudi Arabia
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Johnson and Johnson · Saudi Arabia
Responsible for regulatory product submissions, compliance, and support for medical devices in Saudi Arabia, requiring analytical reasoning and communication skills.
Skills
1 weeks ago
ApplyRegulatory Affairs Specialist | Johnson & Johnson MedTech | Riyadh - KSA
Johnsons and Johnsons · Riyadh
Johnson & Johnson MedTech seeks a Regulatory Affairs Specialist to manage medical device product registrations and submissions for the Saudi Arabia market. Responsibilities include preparing registration files, supportin
Skills
1 weeks ago
ApplyRegulatory Affairs Specialist | Johnson & Johnson MedTech | Riyadh - KSA
Johnson & Johnson MedTech · Riyadh
Johnson & Johnson MedTech seeks a Regulatory Affairs Specialist in Riyadh to manage medical device product registrations and submissions with the SFDA. Requires a Bachelor's degree in Biomedical Engineering or Sciences a
Skills
1 weeks ago
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NAOS (Bioderma - Institut Esthederm - Etat Pur) · Jeddah
Saudi National only Education/Degree: Bachelor of Pharmacy Background: 2 to 4 years in regulatory,Technical skills: Microsoft Office, good knowledge in Excel & Word. Languages: Arabic (is a must) + Fluent in English PROD
Skills
1 months ago
ApplyRegulatory Affairs Specialist KSA
Galderma · Riyadh
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum
Skills
2 months ago
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Galderma · Riyadh
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum
Skills
2 months ago
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MSD · الرياض
Job Description Responsible for supporting the preparation, submission, and maintenance of marketing authorizations for assigned products, under the supervision of the Country Lead / Associate Director Regulatory Affairs
Skills
2 months ago
ApplyRegulatory Affairs Specialist I
Masimo · Riyadh
Masimo seeks a Regulatory Affairs Specialist I to manage international filings and registrations in the META Region. The role requires 3+ years of experience in international medical device Regulatory Affairs, knowledge
Skills
2 months ago
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Masimo · Riyadh
Duties & Responsibilities: • Process and maintain international filings/registrations in the assigned countries within the META Region. • Generate and maintain product and process compliance checklists for the assigned c
Skills
2 months ago
ApplyRegulatory Affairs Specialist I
Masimo · الرياض
Duties & Responsibilities: Process and maintain international filings/registrations in the assigned countries within the META Region. Generate and maintain product and process compliance checklists for the assigned cou
Skills
2 months ago
ApplyRegulatory Affairs Specialist
Bevatel · Riyadh
Company: Bevatel Location: Riyadh, Saudi Arabia Employment Type: Full-Time (Saudi National) Experience Level: 2–5 Years I. Role Summary Bevatel is seeking a highly motivated Regulatory Affairs Specialist to manage our in
Skills
2 months ago
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Bevatel · Riyadh
Company: Bevatel Location: Riyadh, Saudi Arabia Employment Type: Full-Time (Saudi National) Experience Level: 2–5 Years I. Role Summary Bevatel is seeking a highly motivated Regulatory Affairs Specialist to manage our
Skills
2 months ago
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GSK · Riyadh
Site Name: Saudi Arabia - Riyadh Posted Date: Apr 8 2026 GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and de
Skills
2 months ago
ApplyRegulatory Affairs Specialist | Johnson & Johnson MedTech | Riyadh - KSA
Johnson & Johnson · الرياض
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less in
Skills
2 months ago
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GlaxoSmithKline · Riyadh
Prepare and submit SFDA applications, maintain product licenses, and support regulatory projects with strong organizational and communication skills required.
Skills
3 months ago
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