Regulatory Affairs Specialist - UAE Submissions

AMICO Group; Dubai; On-site; AED 180,000 - 300,000; Full time

Job summary

A leading healthcare company in Dubai is seeking a Regulatory & Affairs Specialist (U.A.E National) to manage regulatory compliance and document submissions. Ideal candidates will have at least 2 years of experience in the Pharmaceutical or Medical device industry and must possess knowledge of regulatory affairs in the U.A.E. The role involves building relationships with regulatory agencies and developing strategies to ensure compliance. Join a diverse team committed to innovation and excellence.

Qualifications

• Minimum 2 years of work experience in a Pharmaceutical or Medical device industry in U.A.E.
• Must be a U.A.E National with the Family book.

Responsibilities

• Ensure all products comply with local and international regulations.
• Manage submission of regulatory documents to health authorities.
• Build relationships with regulatory agencies and stakeholders.
• Conduct risk assessments and develop mitigation strategies.
• Develop regulatory strategies aligning with business goals.
• Collaborate with quality assurance to ensure compliance.

Skills

Regulatory affairs knowledge

Excellent communication skills

Relationship management

Risk assessment

Education

Bachelor’s degree or equivalent

Master’s degree preferred

Job description

A leading healthcare company in Dubai is seeking a Regulatory & Affairs Specialist (U.A.E National) to manage regulatory compliance and document submissions. Ideal candidates will have at least 2 years of experience in the Pharmaceutical or Medical device industry and must possess knowledge of regulatory affairs in the U.A.E. The role involves building relationships with regulatory agencies and developing strategies to ensure compliance. Join a diverse team committed to innovation and excellence.