Regulatory Affairs Senior Officer

JR Spain; Murcia; A distancia; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking a Regulatory Affairs Senior Officer in Murcia, Spain. The ideal candidate will have over 4 years of experience, strong communication skills, and fluency in English and Spanish. Responsibilities include submitting regulatory documents and managing projects in a diverse, international environment. The role offers a flexible schedule, home office options, and a focus on personal development.

Servicios

Permanent contract

Flexible working schedule

Home office & hybrid model

Training and personal development programs

Employee well-being programs

Formación

• Over 4 years of experience in Regulatory Affairs within Pharma departments.

Responsabilidades

• Submission of MAA, variations, renewals, and procedures worldwide.
• Pricing and Reimbursement.
• Requests to Health Authorities.
• Due Diligence.
• Adapting documentation to the Transparency Policy.
• Providing Strategic Regulatory Advice.
• Reviewing promotional material, packaging, and labeling.
• Leading and managing regulatory projects.

Conocimientos

Fluent in English (C1)

Fluent in Spanish

Proactive communication skills

Detail-oriented

Advanced IT skills (MS Office)

Educación

Academic Degree in Life Sciences

Descripción del empleo

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Regulatory Affairs Senior Officer, Murcia

Client: ASPHALION

Location: Murcia, Spain

Job Category: Other

EU work permit required: Yes

Job Reference:

660463065714864947232460

Job Views:

1

Posted:

23.07.2025

Expiry Date:

06.09.2025

Job Description:

Asphalion is growing and we are looking for a Regulatory Affairs Senior Officer with experience within the pharmaceutical industry. The ideal candidate loves challenges, enjoys working in an international environment, and wants to grow with us.

Main responsibilities include:

• Submission of MAA, variations, renewals, and procedures worldwide, including EU, US, CH, Rest of the World (RoW), etc.
• Pricing and Reimbursement
• Requests to Health Authorities
• Due Diligence
• Adapting documentation to the Transparency Policy 0070
• Providing Strategic Regulatory Advice
• Reviewing promotional material, packaging, and labeling
• Leading and managing regulatory projects to ensure timely and successful execution

Requirements:

• Over 4 years of experience in Regulatory Affairs within Pharma departments
• Fluent in English (C1) and Spanish
• Academic Degree in Life Sciences
• Advanced IT skills (MS Office)
• Proactive, good communication skills, accurate, detail-oriented

Why work at Asphalion?

• Permanent contract
• Flexible working schedule, including Fridays until 15:30
• Home office & hybrid or remote model (located anywhere in Spain)
• Variety of projects, new challenges, and experiences
• Training and personal development programs
• English lessons
• Inclusive, high-performance work environment to develop your skills and grow your career
• Company culture centered on Passion, Flexibility, Commitment, Quality, & Companionship
• Diverse team from over 15 nationalities
• Employee well-being programs and internal activities

Note: The posted date appears to be in the future (23.07.2025), which may be an error.