20 publicaciones de empleo destacadas de regulatory affairs en madrid, md (¡Están contratando!)

Associate Specialist, Regulatory Affairs HUB SoE
Abacus Medicine Group —Madrid, Madrid provincia
- Trabajo híbrido
- Español
- Doctorado
- Inglés
8d
Manager, Regulatory Affairs HUB SoE
Abacus Medicine Group —Madrid, Madrid provincia
- Trabajo híbrido
- Inglés
- Oficina
- Máster
8d
Life Science - Medical Affairs Consulting Manager
Accenture —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Doctorado
- Inglés
Medical Information Specialist - (Spanish & English Speaking) US hours
EVERSANA —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Microsoft Word
- Español
- Microsoft Excel
Solicitud rápida
Regulatory & Quality Lead – AI IVD Diagnostics
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Bachillerato
Solicitud rápida
Técnico de aseguramiento de la calidad
ZIACOM —Pinto, Madrid provincia
- Jornada completa
- Inglés
- Control de calidad
- Habilidades de comunicación
Medical Science Liaison Dermatology
LEO Pharma A/S —Madrid, Madrid provincia
- Español
- Inglés
- Investigación
14d
Medical Advisor Oncology
OncologyPipeline —Madrid, Madrid provincia
- Media jornada
Director, Medical Affairs (m/f/d)
Abbott Laboratories —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
Associate Director, Medical Affairs
Vertex Pharmaceuticals —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Investigación
- Administración y dirección de empresas
Principal Medical Writer - FSP
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Doctorado
- Investigación
8d
Head of Licensing and Regulatory Authorisations
Tether Operations Limited —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Project management
- Grado
International Policy and Comms Senior Associate (Sustitución)
Pfizer —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
- Grado
2d
Executive Director, Quality & Accreditation- Vice-rectorate for Academic Affairs
IE University —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Senior European Regional Counsel, Regulatory Strategy & Advisory
Morningstar —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Habilidades de análisis
- Servicios financieros
- Liderazgo
Legal Counsel
NBCUniversal —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Máster
18h
Early Asset Medical Manager Breast
AstraZeneca —Madrid, Madrid provincia
- Jornada completa
- Español
- Microsoft Excel
- Investigación
2d
Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)
サイネオス・ヘルス —Madrid, Madrid provincia
- Inglés
Clinical and Marketing Professional Leader
Philips —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Marketing
- Máster
Senior Manager, Medical Devices
Cencora —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Liderazgo

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Associate Specialist, Regulatory Affairs HUB SoE

Abacus Medicine Group
Madrid, Madrid provincia

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Detalles del empleo

Hace 8 días

Cualificaciones

Español
Doctorado
Inglés
Adobe Creative Suite
Máster
Paquetería
Farmacia
Portugués
Cloud
Italiano

Descripción completa del empleo

Do you want to work broadly with Regulatory Affairs in an international pharmaceutical company where you will combine operational regulatory work with process improvements, stakeholder management, and technical ownership?

We are looking for an experienced Regulatory Affairs Specialist to join our South of Europe HUB in Madrid. Here, you will become part of a growing international setup supporting multiple European markets while working closely with colleagues across Regulatory Affairs, QA, Product Development, and Operations.

The opportunity

You will join the Regulatory Affairs South of Europe HUB - a team responsible for handling submissions, approvals, and lifecycle management of parallel import licenses across several European markets.

The team currently consists of two Regulatory Affairs Specialists based in Madrid, working closely together in a highly collaborative and international environment. The role combines operational execution with ownership and continuous improvement, making it ideal for someone who enjoys both detail-oriented regulatory work and driving smarter ways of working.

In this role, you will independently manage complex regulatory tasks across assigned end markets while also contributing to process optimization, training, and operational excellence initiatives.

We would like you to:

Acquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management
Prepare and proofread packaging materials, artwork files, mock-ups, item lists, and regulatory documentation
Communicate with competent authorities and stakeholders across assigned markets
Participate in continuous improvement initiatives and optimization of processes and systems
Support onboarding and training of colleagues within the team
Evaluate regulatory legislation changes and contribute to operational implementation
Participate in projects as an operational SME within Regulatory Affairs
Support maintenance of SOPs, working instructions, and guidelines

What we need you to have:

5+ years of experience within Regulatory Affairs
A Master’s degree or PhD within Pharmacy, Health Sciences, Life Sciences, or similar
Alternatively 8+ years of relevant Regulatory Affairs experience
Strong understanding of EU regulatory requirements and procedures
Professional proficiency in English
Professional proficiency in either Spanish and Portuguese / Italian
Experience working with packaging materials and documentation in a regulated environment
A structured and detail-oriented approach combined with a proactive mindset

It is an advantage if you also have experience working with Adobe Creative Cloud in a technical or regulated environment.

What we offer:

An international workplace with colleagues across Europe
A role with both operational responsibility and influence on improvements and ways of working
A collaborative and supportive team environment
Opportunities for professional and personal development
The possibility to work closely with multiple stakeholders and markets across Europe

Are you interested?

If you want to apply, please use the apply link and attach your resumé.

We look forward to receiving your application!

Moving Healthcare. Moving You.

In Abacus Medicine Group, you’ll experience the power of Moving Healthcare. With our change mindset, we're moving the industry and improving healthcare as we broaden access to medicine.

But it's not just about moving healthcare, it's about Moving You. You’ll be part of a caring community of more than 1,300 people across the World. With us, you will be valued, empowered, and have a direct impact on driving change. Let's access the future of medicine and make a difference together. Your move.

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regulatory affairs empleos en madrid, md

Associate Specialist, Regulatory Affairs HUB SoE

Manager, Regulatory Affairs HUB SoE

Life Science - Medical Affairs Consulting Manager

Medical Information Specialist - (Spanish & English Speaking) US hours

Regulatory & Quality Lead – AI IVD Diagnostics

Técnico de aseguramiento de la calidad

Medical Science Liaison Dermatology

Medical Advisor Oncology

Director, Medical Affairs (m/f/d)

Associate Director, Medical Affairs

Principal Medical Writer - FSP

Head of Licensing and Regulatory Authorisations

International Policy and Comms Senior Associate (Sustitución)

Executive Director, Quality & Accreditation- Vice-rectorate for Academic Affairs

Senior European Regional Counsel, Regulatory Strategy & Advisory

Legal Counsel

Early Asset Medical Manager Breast

Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)

Clinical and Marketing Professional Leader

Senior Manager, Medical Devices

Quiero recibir la alerta de empleo más reciente de regulatory affairs en madrid, md

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Moving Healthcare. Moving You.

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