Regulatory Affairs Specialist

"Expect to grow", personal y profesionalmente: En Siegfried, ofrecemos desafíos emocionantes y amplias oportunidades para demostrar tu talento. Como socio de confianza y respeto en la industria farmacéutica, mantenemos los más altos estándares en seguridad, calidad y sostenibilidad, mientras fomentamos una cultura que te empodera para prosperar. Únete a una empresa global en rápida expansión, donde diversas perspectivas y experiencias se unen en un entorno colaborativo. Aquí encontrarás un lugar de trabajo que valora tanto el éxito colectivo como tus contribuciones individuales, ofreciendo oportunidades a largo plazo para crecer y generar un impacto.

Your Role:  

At Siegfried we are currently looking for a Regulatory Affairs Specialist to join our Regulatory Affairs team in our site based in Barberà del Vallès.

You will provide support to the company’s business areas and to customers by delivering strategic advice and regulatory expertise for the development and maintenance of products, compiling high-quality documentation and/or registration dossiers. You will support Operations through the communication of manufacturing and/or analytical changes and maintain regulatory compliance.
In addition, you will support licensing, accreditation, and other local activities as required and in coordination with Quality/Compliance, and contribute to the monitoring, evaluation, and implementation of new regulations and guidelines relevant to our business (regulatory intelligence).

Major Accountabilities:

• Lead the preparation, compilation, and maintenance of high-quality regulatory dossiers in compliance with EU, US, and international requirements.

• Provide strategic regulatory guidance to clients and internal teams across product development and lifecycle management.

• Act as the regulatory representative in cross-functional project teams, ensuring alignment with regulatory requirements.

• Manage regulatory lifecycle activities, including variations, change controls, and timely submissions to health authorities.

• Monitor regulatory changes and contribute to regulatory intelligence, ensuring ongoing compliance and proactive strategy adaptation.

Your Profile:

Your Benefits: 

What do we offer?

- Annual Bonus

- Two days of home office per week

- Free parking

- Good public transport available to reach the site

- Subsidized canteen on-site or restaurant ticket: to use when eating out or working from home

- Medical, life, and accident insurance

- Access to "Club Siegfried": an exclusive platform with discounts and offers on over 400 services.
 

If you’re excited by the idea of joining our group, we’d love to hear from you.

Apply today and be part of building something extraordinary!

Fundada en 1873 en Zofingen, Suiza, Siegfried se ha convertido en una red global con 16 centros en tres continentes. Con un equipo de más de 4,200 profesionales altamente capacitados, llevamos las innovaciones de nuestros clientes farmacéuticos a escala industrial y fabricamos medicamentos seguros para pacientes de todo el mundo. Como CDMO totalmente integrada, Siegfried es una de las pocas organizaciones que actualmente puede llevar a cabo el desarrollo y la fabricación de ingredientes farmacéuticos activos (APIs) y formas farmacéuticas terminadas bajo un mismo techo. Esta combinación única de conocimientos y experiencia nos convierte en el socio más confiable de la industria farmacéutica.