Lavipharm

Officer, Regulatory Affairs – Lifecycle Management

Lavipharm

full-time

Posted on:

Location Type: Hybrid

Location: Paiania • Greece

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About the role

  • Execute routine regulatory activities: renewals, variations, CTD/Module 1 preparation
  • Monitor and manage timelines for MA variations, post-authorization activities and renewal applications
  • Prepare and submit import/export applications for medicinal products
  • Review and update packaging materials and artworks in line with current guidelines
  • Maintain regulatory databases and departmental filing systems

Requirements

  • BSc in Pharmacy, Chemistry, Biology or a related field
  • 1–2 years of experience in a Regulatory Affairs role within the pharmaceutical industry
  • Familiarity with EU regulatory legislation and eCTD submission processes
  • Excellent command of the Greek and English language (written and spoken)
  • Very good computer literacy
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
regulatory activitiesCTD preparationimport/export applicationspackaging materials reviewregulatory databases managementeCTD submission processes
Soft Skills
communicationtime managementattention to detail
Certifications
BSc in PharmacyBSc in ChemistryBSc in Biology