Job Description

We are looking for a Drug Regulatory Affairs Specialist with a minimum of 4 years of experience and strong exposure to providing dossiers for exports. The ideal candidate will manage regulatory submissions, ensure compliance with international standards, and support the export of pharmaceutical products.

Key Responsibilities:

• Prepare and submit regulatory dossiers for pharmaceutical exports.
• Ensure compliance with international regulatory requirements and guidelines.
• Liaise with regulatory authorities for approvals and documentation.
• Review and update dossiers as per regulatory changes.
• Coordinate with cross-functional teams to ensure timely and accurate submission.

Skills & Qualifications:

• Minimum 4 years of experience in Drug Regulatory Affairs, with a focus on exports.
• Strong knowledge of regulatory guidelines and dossier preparation for export markets.
• Excellent communication and organizational skills.
• Ability to work independently and handle multiple submissions.

Education:

• Bachelor’s degree in Pharmacy, Life Sciences, or a related field.

Skills Required

• Recruitment Coordination Experience
• Strong leadership and problem-solving skills