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Regulatory Affairs Leader – Medical Devices/IVD (UAE)

Abbott

Dubai

On-site

AED 293,000 - 368,000

Full time

4 days ago
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Job summary

A global healthcare firm in Dubai is seeking a Regulatory Affairs Manager to coordinate regional regulatory activities for their Infectious Disease portfolio. The ideal candidate will have at least 8 years of experience in Regulatory Affairs with a solid understanding of medical device regulatory frameworks and excellent communication skills in English and Arabic. This role involves managing the regulatory submissions and serving as the regulatory liaison during product life cycles, and offers opportunities for professional growth within a supportive international company environment.

Benefits

International career development opportunities
Employee engagement initiatives
Diversity and inclusion programs

Qualifications

  • Minimum 8 years of experience in Regulatory Affairs in Medical Devices/IVDs.
  • Understanding of the medical device regulatory and IVD frameworks.
  • Good knowledge of the regional regulatory landscape.

Responsibilities

  • Coordinate and manage Regional Regulatory activities for the Infectious Disease portfolio.
  • Ensure the preparation and timely completion of submissions for in vitro diagnostic devices.
  • Serve as the regulatory liaison throughout the product lifecycle.

Skills

Regulatory strategy execution
Project management
Interpersonal skills
Communication skills in English and Arabic

Education

Bachelor's or Master's degree in a related field

Tools

Microsoft Excel
Microsoft PowerPoint
Microsoft Word
Job description
A global healthcare firm in Dubai is seeking a Regulatory Affairs Manager to coordinate regional regulatory activities for their Infectious Disease portfolio. The ideal candidate will have at least 8 years of experience in Regulatory Affairs with a solid understanding of medical device regulatory frameworks and excellent communication skills in English and Arabic. This role involves managing the regulatory submissions and serving as the regulatory liaison during product life cycles, and offers opportunities for professional growth within a supportive international company environment.
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