20 publicaciones de empleo destacadas de technical associate en madrid, md (¡Están contratando!)

Associate Specialist, Regulatory Affairs HUB ES
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- Jornada completa
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- Doctorado
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Senior Associate, Capital Markets Accounting Advisory
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- Microsoft Powerpoint
- Español
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Associate, Indirect Tax
Alvarez and Marsal —Madrid, Madrid provincia
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- Español
- Inglés
- Investigación
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Senior Associate, Capital Markets Accounting Advisory
Alvarez and Marsal —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Español
- Microsoft Excel
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Executive Director, Quality & Accreditation- Vice-rectorate for Academic Affairs
IE University —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Associate Director - Cables
AECOM —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Desarrollo de negocios
- Seguro dental
- Vacaciones pagadas
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Accenture —Madrid, Madrid provincia
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- Español
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- Máster
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- Grado
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Lululemon —Madrid, Madrid provincia
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- Disponibilidad fin de semana
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- Vacaciones pagadas
- Flexibilidad horaria
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- Doctorado
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FeverUp —Madrid, Madrid provincia
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- Inglés
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Turner & Townsend —Madrid, Madrid provincia
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The Reuse Company —Madrid, Madrid provincia
- Jornada completa
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2d
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The Reuse Company —Madrid, Madrid provincia
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Mondelēz International —Madrid, Madrid provincia
- Jornada completa
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VML MAP —Madrid, Madrid provincia
- Inglés
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Holtec —Madrid, Madrid provincia
- Máster
- Grado
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Solicitud rápida

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Associate Specialist, Regulatory Affairs HUB ES

Abacus Medicine -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa
Hace 5 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.

Department

Regulatory

Locations

Madrid

Remote status

Hybrid

Employment type

Full-time

Solicitar ahora

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technical associate empleos en madrid, md

Associate Specialist, Regulatory Affairs HUB ES

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Quiero recibir la alerta de empleo más reciente de technical associate en madrid, md

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Moving Healthcare. Moving You.

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