Responsibilities

Asegúrese de leer detenidamente la información sobre esta posibilidad antes de presentar su candidatura.

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- Acquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management

- Prepare and proofread packaging materials, artwork files, mock-ups, item lists, and regulatory documentation

- Communicate with competent authorities and stakeholders across assigned markets

- Participate in continuous improvement initiatives and optimization of processes and systems

- Support onboarding and training of colleagues within the team

- Evaluate regulatory legislation changes and contribute to operational implementation

- Participate in projects as an operational SME within Regulatory Affairs

- Support maintenance of SOPs, working instructions, and guidelines

Requirements

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- 5+ years of experience within Regulatory Affairs

- A Master’s degree or PhD within Pharmacy, Health Sciences, Life Sciences, or similar

- Alternatively 8+ years of relevant Regulatory Affairs experience

- Strong understanding of EU regulatory requirements and procedures

- Professional proficiency in English

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- Professional proficiency in either Spanish and Portuguese / Italian

- Experience working with packaging materials and documentation in a regulated environment

- A structured and detail-oriented approach combined with a proactive mindset

- Experience working with Adobe Creative Cloud in a technical or regulated environment is an advantage

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📌 Associate Specialist, Regulatory Affairs (Madrid)
🏢 Jobtailor
📍 Madrid