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SCANDENS

Səhiyyə

Regulatory Affairs Specialist

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Regulatory Affairs Specialist

  • Deadline 8 Noyabr 2025
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Müraciət üçün aşağıdakı email ünvanı köçürmək lazımdır.

Key Responsibilities:

  • Assist in the development and execution of regulatory strategies for domestic and international markets
  • Ensure product compliance with regulatory bodies such as the FDA, EMA, and others
  • Prepare, review, and maintain regulatory documentation and filings
  • Communicate with regulatory agencies to expedite approvals
  • Monitor changes in regulations and advise internal teams accordingly
  • Support risk assessments and mitigation plans for compliance issues

Skills and Qualifications:

  • Bachelor’s degree in pharmacy, Chemistry, Engineering, or a related scientific field
  • 2–3 years of experience in regulatory affairs (preferably in pharma, biotech, or medical devices)
  • Strong understanding of regulatory guidelines (FDA, ISO, etc.)
  • Excellent written and verbal communication skills
  • Familiarity with documentation, product registration, and dossier preparation

Benefits:

  • Shuttle bus
  • Lunch
  • Pasha Insurance
  • Pasha Life (Endowment insurance)

Working Conditions:

  • Working Hours: 5 days a week, from 09:00 to 18:00.
  • Workplace: Hokmali village, Absheron district, 15 km from the Baku-Shamakhi highway.

About the Vacancy:

  • Position Type: Full-time

Candidates who meet the requirements are kindly requested to send their CVs to the email address in the Apply for job button, indicating the position title (Regulatory Affairs Specialist) in the subject line.

Note: Applications from candidates who do not meet the job requirements, do not follow the above-mentioned instructions, or apply after the specified deadline will not be considered.

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