Regulatory Affairs Technician

JR Spain; Granada; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Regulatory Affairs Technician to support the registration of innovative oncology products. In this role, you'll prepare essential documentation for medical devices, liaise with regulatory bodies, and provide technical assistance to ensure compliance. This position offers a permanent contract with a structured work schedule and opportunities for continuous training and professional development. You'll enjoy a collaborative environment with perks like life insurance and access to an on-site fitness room, making it an attractive opportunity for those passionate about regulatory affairs in the pharmaceutical sector.

Servicios

Permanent Contract

Life Insurance

In-Company Language Courses

Fresh Fruit Weekly

Access to On-Site Fitness Room

Affordable Catering Delivery

Formación

• 1-2 years of experience in a similar role.
• Bachelor's degree in biology, nutrition, chemistry, or related fields.

Responsabilidades

• Prepare technical dossiers for medical device registration.
• Register medical devices with AEMPS and food supplements with health authorities.
• Provide technical support to the QA department.

Conocimientos

Responsibility

Organization

Proactivity

Communication Skills

Team Player

Advanced English (C1)

Fluent Spanish

Microsoft Office Proficiency

Educación

Bachelor's Degree in Sciences

Master's in Regulatory Affairs

Descripción del empleo

Social network you want to login / join with :

Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.

We are currently selecting a Regulatory Affairs Technician fora pharmaceutical company specialized in the development and production of innovative oncology products and high-potency drugs located in Vallès Occidental .

Key Responsibilities :

• Preparation of required technical dossiers and documentation for the registration of medical devices and food supplements.
• Registration of medical devices with the Spanish Agency of Medicines and Medical Devices (AEMPS) and food supplements with the Public Health Department of the Generalitat de Catalunya.
• Requesting Free Sale Certificates for products.
• Continuous communication and assistance to help clients register products in third countries.
• Providing technical support to the QA department, reviewing and approving product labeling according to regulations, and evaluating promotional materials from the marketing department.

Skills :

• Responsible, organized, and proactive.
• Strong communication skills and a team player.
• Advanced level of English (C1).
• Native or fluent in Spanish.
• Proficient in Microsoft Office.

Offered Conditions :

• Permanent contract.
• Monday to Thursday, 8 : 00 AM to 5 : 30 PM, and Fridays from 8 : 00 AM to 2 : 30 PM.
• Continuous training on the job and in-company language courses.
• Life insurance for the employee.
• Affordable catering delivery, fresh fruit every week, and access to an on-site fitness room.

Requirements :

• Bachelor's degree in sciences (biology, nutrition, chemistry, biochemistry, pharmacy, or related fields).
• Preferred : Masters in Regulatory Affairs.
• 1-2 years of experience in a similar role.