QUALIFICATIONS

• University degree in Pharmacy, Chemistry, Biology, Medicine, or a related scientific discipline.
• 2–5 years of professional experience in Regulatory Affairs, Government Relations, or External Affairs within the pharmaceutical industry.
• In-depth understanding of local and international (EU) regulatory frameworks and submission procedures.
• Ability to engage effectively and professionally with external stakeholders and regulatory authorities.
• Strong analytical, organizational and communication skills.
• Excellent command of written and spoken Azerbaijani and Russian; good command of English (both written and spoken).
• Computer literacy and good knowledge of MS Office tools.

JOB DESCRIPTION

• Reviewing registration files and all related product documentation, ensuring compliance with local regulatory requirements.
• Preparing application forms and other documents for registration, re-registration, and variation submissions. Ensuring that all documentation, samples, and other required materials are provided to the relevant authorities.
• Tracking regulatory documentation flow and progress reporting.
• Monitoring and analyzing changes in legislation and regulatory requirements.
• Maintaining effective communication with government institutions and relevant regulatory bodies.

Please send your resume to the e-mail address in the Apply for job button with reference “Regulatory & External Affairs Specialist” in the email subject line.