Regulatory Affairs Trainee

• An opportunity to start your career in Regulatory Affairs in an international pharmaceutical company.
• Training and continuous learning in a highly regulated environment.
• Participation in projects with global impact.
• Working alongside professionals with extensive experience in the regulatory field.
• A dynamic, collaborative environment oriented towards professional development.

At Siegfried El Masnou, we are looking for a Trainee Regulatory Affairs to join our Regulatory Affairs team and develop their professional career in an international and highly specialized environment within the pharmaceutical industry.

If you are passionate about the regulatory field, have an interest in the quality and technical documentation of medicines, and are looking for an opportunity to learn from expert professionals, we want to meet you!

Review quality documentation linked to the Technical Release (Module 3) to ensure its alignment with approved dossiers.

Provide support to our clients as a CDMO in activities related to the product lifecycle, especially in the CMC/Quality (Module 3) field.

Participate in the evaluation and updating of regulatory documentation to ensure compliance with current regulatory requirements.

Perform regulatory assessments of historical dossiers to identify opportunities for updates in accordance with current regulatory guidelines.

Collaborate in the optimization of internal processes, workflows, and the department's document management.

Work transversally with different areas of the company to ensure proper management of regulatory information.

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and broad opportunities to demonstrate your talent. As a trusted and respected partner in the pharmaceutical industry, we maintain the highest standards in safety, quality, and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here you will find a workplace that values both collective success and your individual contributions, offering long-term opportunities to grow and make an impact.

Founded in 1873 in Zofingen, Switzerland, Siegfried has become a global network with 16 centers across three continents. With a team of more than 4,200 highly trained professionals, we bring our pharmaceutical clients' innovations to industrial scale and manufacture safe medicines for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations that can currently carry out the development and manufacture of active pharmaceutical ingredients (APIs) and finished dosage forms under one roof. This unique combination of knowledge and expertise makes us the most trusted partner in the pharmaceutical industry.