12 publicaciones de empleo destacadas de regulatory affairs specialist en barcelona, ct (¡Están contratando!)

Regulatory Affairs Specialist
Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
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FARMHISPANIA GROUP —Barcelona, Barcelona provincia
- Inglés
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Alfasigma Group —Barcelona, Barcelona provincia
- Mantenimiento
- Inglés
- Microsoft Office
- Oportunidades de crecimiento y desarrollo profesional
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Axalta Coat. Sys. Spain —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Microsoft Office
- Grado
- Vacaciones pagadas
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1d
Product Stewardship & Regulatory Compliance Specialist (m/f/d) Europe & Asia
Westlake Global Compounds —Santa Perpètua de Mogoda, Barcelona provincia
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- Inglés
Solicitud rápida
Senior Staff - Medical & Scientific Affairs Liaison - Acute Care
Beckman Coulter Diagnostics —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Ventas
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- Vacaciones pagadas
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Fortrea —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
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- Microsoft Excel
1d
Complaints Specialist
Diagnóstic Grifols SA —Parets del Vallès, Barcelona provincia
- Jornada completa
- Inglés
- Habilidades de análisis
- Grado
11d
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Werfen —Barcelona, Barcelona provincia
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iShift Business Enablement – Global Trade services lead
Sanofi —Barcelona, Barcelona provincia
- De 69.200 € a 103.800 € al año
- Inglés
Clinical Marketing
Werfen —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés

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Regulatory Affairs Specialist

Grifols SA -
Sant Cugat del Vallès, Barcelona provincia

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Detalles del empleo

Contrato indefinido | Jornada completa

Cualificaciones

Español
Microsoft Excel
Inglés
Microsoft Office
Grado

Descripción completa del empleo

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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

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regulatory affairs specialist empleos en barcelona, ct

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