Regulatory Affairs Specialist
The chosen candidate, under general supervision responsible for the local coordination and the preparation of documents/packages for regulatory submissions, review and evaluate technical and scientific data and reports required for local submission in support of products.
Main responsabilities:
• Supports regulatory project plan execution
• Maintain awareness of regulatory requirements and ensure continued learning
• Maintain regulatory files in a format consistent with requirements
• Participate as an active team member of project teams as required
• Compile and prepare responses to questions from regulatory authorities according to plan
• Edit and proofread regulatory documentation
• Assist in preparation and review of labeling and other departmental documents
• Compile under supervision regulatory documents for submission
• Track status and progress of regulatory documentation
• Prepare and review AdProm materials for compliance with local regulations
• Understand Regulatory Affairs' position in small project teams
Required skills:
- Bachelor’s degree in a relevant scientific discipline
- Regulatory experience preferably within a healthcare environment
• Knowledge of regulations
• Scientific knowledge
• Administrative and project management skills
• Ability to contribute to multiple projects from a Regulatory Affairs perspective
• Ability to multitask and prioritize
• Interpersonal and communication skills
• Technical system skills (e.g. word processing, spreadsheets, databases, online research)
• Proofreading and editing skills
Contractual and economic offer:
Fixed term contract until december 2024, a subsequent extension will be evaluated.
Salary: CCNL Chimico Farmaceutico Liv. D1
From Monday to Friday / Full Time
Rome (EUR)
Data inizio prevista: 03/06/2024
Categoria Professionale: Scientifico / Farmaceutico
Settore: COMMERCIO ALL'INGROSSO
Città: Roma (Roma)
Conoscenze linguistiche:
- Inglese
Competenze richieste:
- Word Processor - Elaborazione testi - Word
- Fogli di calcolo / elettronici - Excel
- Farmaco-Scientifico - Farmaceutica
Disponibilità oraria:
- Full Time
CCNL: Chimica - Farmaceutica Industria
Livello: D1 Livello D1
I candidati, nel rispetto del D.lgs. 198/2006, D.lgs 215/2003 e D.lgs 216/2003, sono invitati a leggere l'informativa sulla privacy consultabile sotto il form di richiesta dati della pagina di candidatura (Regolamento UE n. 2016/679).
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