14 publicaciones de empleo destacadas de regulatory affairs specialist en sant cugat del vallès barcelona provincia (¡Están contratando!)

Regulatory Affairs Specialist
Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Microsoft Excel
- Inglés
Product Development Specialist
URIACH —Sant Cugat del Vallès, Barcelona provincia
- Doctorado
- Marketing
- Máster
Solicitud rápida
POSITION REGULATORY AFFAIRS SPECIALIST
FARMHISPANIA GROUP —Barcelona, Barcelona provincia
- Inglés
- APIs
Promotional Regulatory Affairs Specialist, Europe
Alcon —Cornellà de Llobregat, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Grado
8d
Senior Staff - Medical & Scientific Affairs Liaison - Acute Care
Beckman Coulter Diagnostics —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Ventas
- Investigación
- Vacaciones pagadas
Product Development Specialist
Uriach Italy —Sant Cugat del Vallès, Barcelona provincia
- Doctorado
- Marketing
- Máster
Solicitud rápida
Regulatory Promotion Specialist - VIE Contract
Sanofi —Barcelona, Barcelona provincia
- Español
- Inglés
- Máster
11d
Sr. Specialist, Regulatory Affairs
Alfasigma Group —Barcelona, Barcelona provincia
- Mantenimiento
- Inglés
- Microsoft Office
- Oportunidades de crecimiento y desarrollo profesional
6d
Product Compliance specialist
Magnera Corporation —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Máster
Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs
Syneos - Clinical and Corporate - Prod —Barcelona, Barcelona provincia
- Jornada completa
8d
Complaints Specialist
Diagnóstic Grifols SA —Parets del Vallès, Barcelona provincia
- Jornada completa
- Teletrabajo
- Inglés
- Habilidades de análisis
- Grado
Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs
サイネオス・ヘルス —Barcelona, Barcelona provincia
8d
Sales Application Specialist Biotechnology
Werfen —Barcelona, Barcelona provincia
- Jornada completa
- Ventas
- Inglés
- Investigación
7d
Clinical Marketing
Werfen —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés

More jobs to discover

Find similar jobs that you might be interested in.

Product Development Specialist
URIACH —Sant Cugat del Vallès, Barcelona provincia
Formulation: Develop the theoretical composition of new products or existing products that require reformulation; supervise and coordinate galenic development…
Solicitud rápida
Product Development Specialist
Uriach Italy —Sant Cugat del Vallès, Barcelona provincia
Formulation: Develop the theoretical composition of new products or existing products that require reformulation; supervise and coordinate galenic development…
Solicitud rápida

Quiero recibir la alerta de empleo más reciente de regulatory affairs specialist en sant cugat del vallès barcelona provincia

Al iniciar sesión en tu cuenta, aceptas las Condiciones del servicio de SimplyHired, nuestra Política sobre cookies y nuestra Política de privacidad.

Explorar empleos en más ubicaciones

regulatory affairs specialist jobs near sant cugat del vallès barcelona provincia

Empleos de Regulatory Affairs Specialist en Barcelona, Barcelona Provincia

Empleos de Application Specialist en Barcelona, Barcelona Provincia

Empleos de Compliance Officer en Barcelona, Barcelona Provincia

Empleos de Public Affairs en Comunidad De Madrid

Empleos de Regulatory Affairs Specialist en Sant Cugat Del Vallès, Barcelona Provincia

Empleos de Application Specialist en Madrid, Madrid Provincia

Empleos de Regulatory Affairs Specialist en San Sebastián De Los Reyes, Madrid Provincia

Empleos de Senior Marketing Manager en Madrid Provincia

Empleos de Contador Publico en Pezuela De Las Torres, Madrid Provincia

Empleos de Contador en Martorell, Barcelona Provincia

Empleos de Hr Specialist en Madrid, Madrid Provincia

Empleos de Content Specialist en Barcelona, Barcelona Provincia

Empleos de Product Specialist en Madrid, Madrid Provincia

Empleos de Fashion Product Manager en Barcelona Provincia

Empleos de Junior Product Owner en Barcelona, Barcelona Provincia

Empleos de Ppa Specialist en Madrid, Madrid Provincia

Empleos de Regulatory Affairs, Medical Device, Iso 13485 en Barcelona, Barcelona Provincia

Empleos de Learning Development Specialist en Málaga, Málaga Provincia

Empleos de Project Engineer en Sant Boi De Llobregat, Barcelona Provincia

Empleos de Learning Development Specialist en Barcelona, Barcelona Provincia

Regulatory Affairs Specialist

Grifols SA -
Sant Cugat del Vallès, Barcelona provincia

Solicitar ahora

Detalles del empleo

Contrato indefinido | Jornada completa

Cualificaciones

Español
Microsoft Excel
Inglés
Microsoft Office
Grado

Descripción completa del empleo

table.MiTabla { max-width: 1020px;!important

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.

Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Regulatory Affairs Specialist like you.

Mission

The RRAA Specialist will be responsible of the preparation of technical documentation, submission and following up of product registration and/or renewal, variations dossiers, as well as other regulatory documentation.

What your responsibilities will be

Prepare, compile, and maintain registration dossiers and other regulatory documentation for medicinal products and medical devices within the assigned portfolio.
Prepare, review, and submit regulatory documentation for new registrations, renewals, variations, and other regulatory procedures.
Review and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance.
Monitor the progress of regulatory submissions and registration procedures, liaising with regulatory authorities when required.
Maintain up-to-date knowledge of current regulations and regulatory requirements applicable to medicinal products and medical devices, ensuring ongoing compliance.
Coordinate the translation of regulatory documentation, ensuring accuracy, consistency, and compliance with local market requirements.
Collaborate with cross-functional teams and external partners to ensure timely and high-quality regulatory submissions.

Who you are

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).

You have a Bachelor's Degree in Health Sciences or engineering.
You have experience in RRAA or technical departments within the pharmaceutical industry.
You have analytical skills, attention to detail, and ability to summarize and evaluate.
You have Advanced level of Spanish and English (C1) and of MS Office (Excel).

What we offer

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!

We look forward to receiving your application!

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Flexibility for U Program: Hybrid Model

Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits package

Contract of Employment: Permanent position.

Location: Sant Cugat del Vallès.

www.grifols.com

#LI-Hybrid

#LI-ER1

Location: SPAIN : España : Sant Cugat del Valles: [[cust_building]]

Learn more about Grifols

Solicitar ahora

Refina tu búsqueda

regulatory affairs specialist empleos en sant cugat del vallès barcelona provincia

Regulatory Affairs Specialist

Product Development Specialist

POSITION REGULATORY AFFAIRS SPECIALIST

Promotional Regulatory Affairs Specialist, Europe

Senior Staff - Medical & Scientific Affairs Liaison - Acute Care

Product Development Specialist

Regulatory Promotion Specialist - VIE Contract

Sr. Specialist, Regulatory Affairs

Product Compliance specialist

Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs

Complaints Specialist

Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs

Sales Application Specialist Biotechnology

Clinical Marketing

More jobs to discover

Quiero recibir la alerta de empleo más reciente de regulatory affairs specialist en sant cugat del vallès barcelona provincia

Explorar empleos en más ubicaciones

Herramientas para candidatos

Herramientas para empresas

Buscar

Mantener la conexión