Overview
Regulatory Affairs Jobs in Doha, Qatar at Premium Solutions Consultancy
Premium Solutions Consultancy is seeking a highly skilled and motivated Regulatory Affairs professional to join our team. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our client projects. You will work closely with cross-functional teams to prepare and submit regulatory applications, maintain product registrations, and monitor regulatory changes.
Responsibilities
Prepare and submit regulatory applications, including product registrations and notifications
Coordinate with internal and external stakeholders to collect necessary documentation and information
Maintain up-to-date knowledge of relevant regulations and guidelines
Monitor and communicate changes in regulatory requirements that may impact our clients
Conduct regulatory assessments for new products and ensure compliance throughout the product lifecycle
Participate in regulatory agency inspections and audits
Collaborate with cross-functional teams to develop regulatory strategies and plans
Review and provide input on labeling and promotional materials to ensure compliance
Requirements
Bachelor’s degree in a scientific or healthcare-related field
Minimum of 3 years of experience in regulatory affairs in the pharmaceutical, medical device, or biotechnology industry
Strong knowledge of local and international regulatory requirements and guidelines
Excellent communication and project management skills
Experience in preparing and submitting regulatory applications
Attention to detail and strong analytical skills
Ability to work independently and in a team environment
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Title: Regulatory Affairs
Company: Premium Solutions Consultancy
Location: Doha, Qatar
Category: Healthcare (Healthcare Compliance, Healthcare Administration)
