Responsable de Asuntos Regulatorios
Presencial en España·Jornada completa·Añadida hoy
37 ofertas abiertas
Resumen
Detalles del puesto
Jornada completa
Según la oferta.
Requisitos
Trabajar en inglés
Se requiere inglés, según la oferta.
Trabajar presencialmente en Spain
No se menciona ninguna ayuda para la mudanza.
Tener 3+ años de experiencia
Puesto de nivel Mid.
Titulación universitaria
«Degree/studies Required: Bachelor's degree (diplomatura) in Life Sciences, Engineering, or Physical Science.» — según la oferta.
Esta oferta está publicada en inglés.
Resumen en español
Este puesto proporciona soporte regulatorio para productos fabricados y de clientes. Preparará la documentación para registros CE y FDA asegurando el cumplimiento de la legislación. La posición se encuentra en Lliçà d'Amunt, España.
El puesto
This position provides effective regulatory support for company's manufactured products and customer's products. Prepare and submit the documentation according to the corresponding legislation for the different countries. Be responsible for the implementation of new regulatory requirements.
Qué harás
Prepare the required documentation to obtain the CE mark, FDA, or other country registrations for the company's manufactured products or customer's products in accordance with current legislation. Communication and maintenance of products with Spanish authorities.
Support customers with any regulatory aspect.
Follow up and resolve requirements that emerge during registration procedures.
Maintain technical files as necessary to sustain product approval.
Review product materials, labeling, and/or specification sheets for compliance with applicable regulations and customer policies.
Be part of CFT projects as the RA representative.
Support internal and external audits, validations, and product risk analysis.
Follow management indicators/metrics for the proper performance of the department and apply appropriate corrective actions if necessary.
Support the Market Surveillance Department in compiling information for Post-Market Surveillance.
Recommend and manage, if applicable, changes to company procedures/documents (quality system and compliance) to comply with current regulations, guidelines, and/or standards.
Provide support to Customer Service regarding product import/export.
Ensure effective partnering and collaboration with R&D, Quality Operations, Design Quality, and Operations to meet project goals, maintain compliance, and complete defined regulatory submissions.
Ensure all documentation is RA-reviewed before it is shared externally with regulators and/or customers.
Collaborate with other QRA groups, R&D, and Operations to ensure successful Regulatory Inspections.
Job Information
Number
Job function
Job type
Full-time
Location
Lliçà d'Amunt, Cataluña, España
Country
Spain
Internal Networking
To be determined based on department needs, to include interactions such as:
All departments of the company.
Werfen Companies.
Customers.
Regulatory agencies.
Suppliers.
Requisitos
Qué buscan
- Degree/studies
Required: Bachelor's degree (diplomatura) in Life Sciences, Engineering, or Physical Science.
Valuable: Any additional degree higher than required.
- Years of experience
Required: 3 years in a similar position.
- Min knowledge
Software: Fluency in Office Tools (Excel & Word); basic knowledge of SAP is valuable.
Languages: Fluency in Spanish or Catalan; advanced knowledge of English (reading and speaking).
Standards: Knowledge of IVD legislation and the healthcare sector is valuable.
Management of decisions under pressure.
Methodical and well-organized approach.
Teamwork.
Time management skills.
Ability to express information clearly and concisely to staff, ensuring understanding.
Ability to apply a systematic approach with constant control, follow-up, and verification of results.
Analytical thinking and problem-solving.
Ability to collaborate, participate, and coordinate actively with working groups.
Reflects Werfen values in work quality and working relationships.
Sobre Werfen
Werfen es una empresa global de diagnóstico médico con sede en Barcelona, España, especializada en sistemas y reactivos de diagnóstico in vitro para hemostasia, cuidados agudos, transfusiones, autoinmunidad y trasplantes. Con operaciones directas en 30 países y distribución en más de 100 territorios, la compañía generó ventas de casi 2.200 millones de euros en 2024 y emplea a 7.000 personas en todo el mundo. Sus centros tecnológicos se encuentran en Estados Unidos y Europa, y recientemente adquirió Omixon, una empresa con sede en Budapest especializada en secuenciación de nueva generación (NGS), para ampliar su cartera de diagnóstico de trasplantes.
- Sector
- Medical Diagnostics
- Fundación
- 1966
- Plantilla
- 5,000–10,000
- Sede
- Barcelona, Spain
- En España
- Barcelona
- Web
- werfen.com
Datos prácticos
- Con sede en Barcelona, España, que ofrece un estilo de vida mediterráneo y es un importante centro europeo de negocios y tecnología.
- Opera directamente en 30 países, lo que brinda oportunidades de movilidad internacional dentro de la empresa.
- Empresa familiar e innovadora, con un fuerte enfoque en I+D y centros tecnológicos en Estados Unidos y Europa.
- Cuenta con 7.000 empleados, lo que indica una organización grande y consolidada con roles diversos.
- La reciente adquisición de Omixon (Budapest) puede crear nuevas oportunidades en diagnóstico de trasplantes y NGS.
En sus propias palabras
Sobre la empresa y el equipo
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Información adicional
Up to 5% of time.
If you are interested in constantly learning and being challenged on a daily basis, we encourage you to submit your resume or CV.
Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V.
www.werfen.com
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