Join Us! Pamplona

Asphalion Ltd; Barcelona; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

An established industry player is seeking passionate individuals to join their dynamic team in the Regulatory Affairs sector. This role involves contributing to various scientific projects and ensuring compliance with safety regulations during clinical development and registration processes. You will work collaboratively within an international team, enhancing your skills while tackling diverse challenges. With a focus on employee well-being and a flexible work schedule, this opportunity promises a rewarding career path in a supportive environment. If you are ready to make a difference in the regulatory landscape, this is the perfect role for you.

Servicios

Flexible Schedule

Homeoffice & Hybrid Model

Life / Work Balance

Asphawellbeing Program

Annual Training Plan

Buddy Programme

Formación

• Experience in regulatory affairs or similar role is a plus.
• Strong communication and organisational skills are essential.

Responsabilidades

• Contribute to scientific and regulatory affairs projects.
• Prepare and review documentation for clinical development.

Conocimientos

Communication Skills

Organisational Skills

Collaborative Work

Educación

Background in Life Sciences

Engineering or Related Field

Descripción del empleo

Are you based in Pamplona area and passionate about the Scientific, Regulatory Affairs & Safety sector and looking to join a dynamic and international team?

Asphalion is growing and with our new offices in Pamplona we are looking for different expertise and profiles in the Regulatory Affairs sector to join us!

Our expert team has delivered solutions to over 1,000 Pharmaceutical, Biotechnological and Medical Technology companies from more than 50 countries in over 5,000 projects, covering non-clinical and clinical development, CMC, dossier writing, regulatory procedures, vigilance, eSubmissions and data management, both for medicinal products and medical devices.

Your Role

As a member of our team, you will be involved in various projects, focusing on regulatory related documentation required during clinical development, registration, and safety stages.

Key Responsibilities

• Contribute to a range of scientific and regulatory affairs projects.
• Prepare and review documentation for clinical development and registration processes.
• Ensure compliance with relevant safety regulations and standards.

Qualifications

• Background in life sciences, engineering, or a related field.
• Experience in regulatory affairs or a similar role within the medical device sector is a plus.
• Strong communication and organisational skills.
• Ability to work collaboratively within an international team.

Why working at Asphalion?

• Flexible schedule
• Homeoffice & Hybrid Model
• Life / Work balance
• Asphawellbeing: Asphalion´s programme focused on the physical, psychological and emotional well-being of our employees
• Communication
• Internal activities
• RSC Activities
• Buddy Programme
• Annual training plan and career path
• Wide variety of projects, new challenges and experiences.

Equal Opportunity Employer

Our people and their well-being are our priority