Regulatory Affairs Specialist

İş Təsviri

SCANDENS

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: Hökmeli village, Absheron district, 15 km from the Baku-Shamakhy highway.
About the Vacancy:

Position Type: Full-time
Candidates who meet the requirements are kindly requested to send their CVs to the e-mail address, 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.