This offer is part of the Job Marketplace of the Health Sector Talent event, which will take place in person at the Employment Fair on October 15th from 3:30 PM to 6:30 PM, organized by Barcelona Activa in collaboration with the Health Hub Barcelona.
Role Description:
Provide support to the regulatory department in managing technical documentation, ensuring compliance, and assisting with product registration processes.
Key Responsibilities:
Review and prepare regulatory documentation.
Assist in national and international registration processes.
Monitor regulatory updates and legislative changes.
Collaborate with quality assurance and pharmacovigilance teams.
Required Education:
Master's degree in Regulatory Affairs, Health Law, or related fields.
Undergraduate background in Pharmacy, Chemistry, Biotechnology, or Biomedical Sciences.
Knowledge of EMA, AEMPS, FDA regulations is highly valued.
