What would you do?
Within the Regulatory Affairs Department, the Regulatory Affairs Trainee position is focused on supporting mainly the Regulatory Affairs area in compliance with the quality standards of the products marketed in accordance with current regulations at the national and European level and the guidelines established by the company.
Main Responsibilities:
* Become familiar with EU and ROW regulations and legislation, in relation to medicinal products intended for human use.
* Participate in Regulatory Affairs projects at a global level.
* Participate in the registration of procedures in the different existing databases and maintenance of the physical/electronic file, together with the creation of eCTD sequences.
* Collaborate in the review and completion of SOPs for the area.
* Perform other office tasks as required.
What we offer at Farmaprojects:
* B2B Pharmaceutical company that combines the best of both worlds - agility, flexibility, and a client-centric approach, all while harnessing the strength of Polpharma Group's capabilities.
* 9-12 months development program starting on March-April 2025.
* Monthly remuneration + ticket restaurant + commuting expenses.
* Flexible working hours.
Who are we looking for?
We are looking for candidates with the following qualifications, skills, and education:
Qualifications:
* Excellent level of English (scientific and business terminology).
* Knowledge of Spanish or any other European language.
* University degree in life sciences.
* You are a Bachelor's/Master's/Postgraduate student and have interest and motivation to develop in the pharmaceutical sector.
Skills:
* Solid command of MS Office.
Soft Skills:
* Attention to detail.
* Analytical skills and a proactive attitude.
* Ability to work autonomously and as part of a team, collaborating with people at different levels within the organization, while prioritizing to meet deadlines and maintain high quality results.
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