Regulatory Affairs, Senior Supervisor

Job Title: Global Regulatory Affairs, Senior Supervisor Strategic Responsibilities: • Regulatory Compliance: Assist in ensuring compliance with pharmaceutical regulations and standards. • Submission Support: Support the preparation and submission of regulatory documents. • Documentation Management: Maintain accurate and up-to-date regulatory documentation. • Cross-functional Collaboration: Collaborate with other departments to address regulatory concerns. • Industry Knowledge: Stay updated on changing regulatory requirements and industry guidelines. • Regulatory Strategy: Contribute to the development of regulatory strategies for product launches. Functional Responsibilities: • Regulatory Submissions: Assist in preparing and submitting dossiers for product registrations and approvals. • Product Compliance: Ensure product compliance with local and international regulations. • Regulatory Guidance: Provide regulatory guidance and support to cross-functional teams. • Audits and Inspections: Assist in preparing for and managing regulatory audits and inspections. • Labeling and Packaging: Ensure regulatory compliance in product labeling and packaging. • Documentation Maintenance: Organize and maintain regulatory documents and records. Competencies: • Transparency. • Communication is Key. • Ownership & Accountability. • Collaboration & Team Unity. • Employee Development & Training. • Innovation & Creativity. Experience: Required • Minimum of 6 years in Regional and Global Pharmaceutical Regulatory Affairs. Qualifications: Required Master’s Degree Professional - Certificate in relevant field . Language: French English Arabic