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Regulatory Affairs - Europe; Pre-Approval Supervisor

Job in Athena West Colonia, El Paso County, Texas, USA
Listing for: Kariera SA
Full Time position
Listed on 2026-06-24
Job specializations:
  • Healthcare
  • Pharmaceutical
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: Regulatory Affairs - Europe (Pre-Approval) Supervisor
Location: Athena West Colonia

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs - Europe (Pre-Approval) Supervisor to join our team. This position is based in Athens, Kryoneri.

Responsibilities
  • Lead EU pre‑approval regulatory strategy and documentation requirements.
  • Own end‑to‑end dossiers for DCP/MRP/National submissions, ensuring quality and on‑time delivery.
  • Line‑manage/coach Regulatory Affairs Officers & Associates; review and sign off key deliverables.
  • Act as primary liaison with EU Regulatory Authorities; coordinate responses to questions/deficiencies.
  • Drive cross‑functional input for dossier compilation and maintain compliance for the registered portfolio.
  • Understanding of Regulatory strategy and documentation requirements.
  • Act as responsible Regulatory Team member for assigned regulatory projects.
  • Ensure policies and procedures are properly understood, evaluated and carried out. Make sure modifications are investigated if necessary.
  • Liaise with various departments to collect all necessary information and documentation, in accordance with defined guidelines for Pharmaceutical Dossier submission and product registration.
  • Support internal activities of Regulatory department in order to ensure regulatory compliance of registered products.
  • Compile and monitor the progress of scientific responses to deficiencies raised by the Regulatory authorities.
Requirements
  • BSc Degree in Pharmacy, Biology or relevant field.
  • 5+ years of experience in Regulatory within a Pharmaceutical organization ideally in similar position.
  • Fluent in English and good MS Office skills
  • Strong organization skills, multi‑tasking and able to meet deadlines
  • Effective communication and relationship management
  • Knowledge of EU regulatory guidelines
  • Ability to work under pressure, resilience
Benefits

The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.

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