Junior Regulatory Affairs Consultant – Hybrid & Intl

Regenold

Almada

Ibrido

EUR 23.000 - 32.000

Tempo pieno

4 giorni fa
Candidati tra i primi

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Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Descrizione del lavoro

Regenold seeks a Junior Regulatory Affairs Consultant to support European regulatory projects and contribute to documentation and strategies. You will work with cross-functional teams across Regenold entities in Germany, the UK, Ireland and Portugal, gradually taking on more responsibility in a dynamic international setting.

The role offers a structured onboarding, mentoring, and increasing responsibility within a multidisciplinary team handling Regulatory Affairs, Quality, Pharmacovigilance,

Competenze

  • University degree in Pharmacy, Pharmaceutical Sciences or life science.
  • Up to 2 years of professional experience in Regulatory Affairs.
  • Basic knowledge of European regulatory procedures and the medicinal product lifecycle.
  • Awareness of EU pharmaceutical legislation.

Mansioni

  • Prepare, compile and review regulatory documentation for submissions in Portugal and across Europe.
  • Collaborate with Quality, Pharmacovigilance, CMC, Medical Devices and Market Access teams.
  • Maintain accurate project records, trackers and regulatory databases, ensuring deadlines are met.
  • Support communications with national authorities, EMA and international clients.

Conoscenze

Regulatory knowledge
Cross-functional collaboration
Project management
English proficiency
Attention to detail
Communication

Formazione

Pharmacy degree

Descrizione del lavoro

Regenold seeks a Junior Regulatory Affairs Consultant to support European regulatory projects and contribute to documentation and strategies. You will work with cross-functional teams across Regenold entities in Germany, the UK, Ireland and Portugal, gradually taking on more responsibility in a dynamic international setting.

The role offers a structured onboarding, mentoring, and increasing responsibility within a multidisciplinary team handling Regulatory Affairs, Quality, Pharmacovigilance,

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