Regulatory Affairs Manager

G&L Scientific; Tarragona; Presencial; EUR 50.000 - 75.000; Jornada completa

Descripción de la vacante

Join a leading company in the pharmaceutical sector as a Regulatory Affairs Manager in Tarragona. You will focus on developing regulatory strategies, managing documentation for product registrations, and ensuring compliance with all legal requirements. This role requires over 7 years of experience in regulatory affairs and strong communication skills.

Servicios

Permanent contract

Medical insurance

Pension plan

Flexible remuneration

Formación

• 7+ years in regulatory affairs, at least 3 in a pharmaceutical company.
• Familiar with e-submission portals and multiple therapy areas.
• Fluent in English and Spanish.

Responsabilidades

• Develop and execute a regulatory strategy for product registration.
• Prepare CMC documentation for regulatory submissions.
• Ensure compliance throughout product lifecycle.

Conocimientos

Regulatory Compliance

Project Management

Communication

Analytical Skills

Problem Solving

Educación

Bachelors or Masters degree in health science

Herramientas

MS Office

Descripción del empleo

Are you an experienced Regulatory Affairs professional? Join our team as a Regulatory Affairs Manager and play a vital role within G&L Scientific team. This role focuses on cross-functional activities, managing documentation and ensuring compliance with regulatory and legal requirements.

Responsibilities may include :

• Developing and executing a regulatory strategy to support the registration of products in line with applicable regulatory requirements.
• Preparing, developing and analyzing CMC documentation for Module 3, quality summaries and safety and efficacy documentation.
• Working on safety, efficacy and CMC variations : variation typification and documentation preparation.
• Supporting R&D, manufacturing, quality control and quality assurance departments for potential queries.
• Submitting regulatory documentation to authorities ensuring compliance with the regulatory standards.
• Planning and managing regulatory procedures on behalf of client companies.
• Ensuring ongoing compliance of products throughout their lifecycle by monitoring regulatory changes and assessing potential impacts.
• Managing the authorisation according to national and EU regulations (MRP, DCP and centralized procedures).
• Ensuring all project work aligns with current regulatory guidance and meets internal standards.

Bachelors or masters degree in health science.

Experience :

• 7+ years in regulatory affairs, with at least 3 years of experience in pharmaceutical company.
• Familiarity with European e-submission portals.
• Practical experience working with different National Competent Authorities (NCAs).
• Experience of small and large molecules, ideally across multiple therapy areas / dosage forms.
• Working experience in writing and reviewing module 3, module 4 and module 5.
• Experience in biological products would be a bonus.
• Strong organizational and communication skills with the ability to manage multiple projects.
• Proactive and team-oriented mindset with a commitment to continuous learning.
• Excellent working knowledge of MS Office.
• Fluent written and spoken English and Spanish.
• High degree of attention to detail and troubleshooting skills. Analytical skills and ability to summarize.
• Flexible and adaptable, with innovative problem-solving abilities.
• Expert in interpreting regulatory requirements and determining compliance strategies.

Why working at G&L Scientific?

• Permanent contract.
• Benefits package (medical insurance, disability insurance, pension plan and flexible remuneration).
• Wide variety of projects, new challenges and experiences.