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Excelya

Regulatory Affairs Member

Excelya

. Identify and communicate new Bulgarian legislation, amendments, guidelines and upcoming regulatory developments.

Posted 11/5/2026part-timeRemote • BulgariaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Bulgarian regulatory requirements and EU regulatory submissions, with a strong compliance mindset and the ability to manage tight timelines effectively. Proficient in reviewing and approving promotional materials and product information texts in accordance with local regulations.

Highest-signal resume keywords
Regulatory Affairs ExperienceEU Regulatory SubmissionsBulgarian Regulatory RequirementsLife Sciences DegreeFluency in English and Bulgarian

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Regulatory Submissions ManagementArtwork ReviewTranslation ApprovalCompliance ReviewScientific Expertise
Soft Skills
Detail-OrientedIndependent WorkHigh-Quality Results Delivery
Industry Keywords
Pharmaceutical ProductsMedical DevicesEU Regulatory FrameworkLocal RegulationsRegulatory Consultancies

About the role

Key responsibilities & impact
  • Identify and communicate new Bulgarian legislation, amendments, guidelines and upcoming regulatory developments.
  • Provide expert input on Bulgarian regulatory requirements.
  • Manage EU regulatory submissions (DCP / MRP / National procedures).
  • Review and approve mock-ups (artwork review).
  • Review and approve translations of product information texts.
  • Review and approve promotional materials in compliance with local regulations.
  • Provide scientific expertise required for the successful completion of Excelya’s projects.

Requirements

What you’ll need
  • Degree in Life Sciences.
  • At least 3 years of experience in Regulatory Affairs.
  • Strong familiarity with local Regulatory requirements for pharmaceutical products for human use and medical devices.
  • Experience in EU regulatory submissions (DCP / MRP / National procedures).
  • Good understanding of EU regulatory framework and local regulations in Bulgaria.
  • Detail-oriented with strong compliance mindset.
  • Experience working with pharmaceutical companies or regulatory consultancies.
  • Able to work independently and deliver high-quality results within tight timelines.
  • Fluent in English and Bulgarian language.

Benefits

Comp & perks
  • Best employee experience
  • High-impact projects
  • Space for talents to shine
  • Opportunity to push boundaries and elevate patients’ journeys