Regulatory Affairs Manager

Grifols; Sant Cugat del Vallès; Híbrido; EUR 45.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid Model

Flexible schedule

Permanent position

Descripción de la vacante

Grifols in Spain is seeking a Regulatory Affairs professional to drive worldwide product registrations, renewals and lifecycle management, coordinating dossiers and responses to Health Authorities.

You will lead a team of Regulatory Affairs Technicians, oversee SOPs, and ensure compliance with evolving regulations while collaborating across functions to support product lifecycle.

Formación

• Bachelor's degree in Health Sciences or engineering required.
• Experience in RRAA or technical departments within the pharmaceutical industry.
• Analytical skills, attention to detail, and ability to summarize and evaluate.
• Advanced level of Spanish and English (C1) and MS Office (Excel).

Responsabilidades

• Assess and define worldwide regulatory strategies for product registrations, renewals, and lifecycle management.
• Review, prepare, and submit regulatory dossiers for new registrations, renewals, variations, and post‑approval changes.
• Prepare, review, and coordinate responses to Health Authority questions within established timelines.
• Manage and coordinate adaptation of product licenses to current regulatory requirements.
• Coordinate and approve packaging materials and labeling documentation for regulatory compliance.
• Organize, coordinate, and supervise Regulatory Affairs Technicians to ensure timely execution.
• Review regulatory impact of changes within the portfolio and oversee required actions.
• Monitor and supervise annual regulatory projects and ensure deliverables on time.
• Represent Regulatory Affairs in communications with affiliates, external partners, and Health Authorities.
• Maintain up‑to‑date knowledge of applicable regulations and provide regulatory guidance.
• Support general activities and strategic initiatives within Regulatory Affairs.
• Coordinate SOPs in Regulatory Affairs and collaborate with cross‑functional teams.

Conocimientos

Analytical skills

Attention to detail

Summarize and evaluate

MS Office

Spanish (C1)

English (C1)

Educación

Bachelor's degree in Health Sciences or engineering

Herramientas

MS Office (Excel)

Descripción del empleo

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

We believe that diversity adds value to our business and to our teams and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.

Mission

Ensuring compliance of the priority plan, as well as coordination of compilation, submission and following up of product registration and/or renewal and/or changes/variations dossiers, and any other regulatory documentation, within the company timelines. Determine and execute actions necessary for licenses and regulatory procedures are in compliance with domestic and international licensing requirements

What Your Responsibilities Will Be

• Assess and define worldwide regulatory strategies for product registrations, renewals, and lifecycle management activities across assigned products and markets.
• Review, prepare, and submit regulatory dossiers for new registrations, renewals, variations, and other post‑approval changes, ensuring compliance with applicable regulations.
• Prepare, review, and coordinate responses to Health Authority questions and requests within established timelines.
• Manage and coordinate the adaptation of product licenses to current regulatory requirements and evolving legislation.
• Coordinate and approve packaging materials and labeling documentation, ensuring regulatory compliance and alignment with local market requirements.
• Organize, coordinate, and supervise the work of Regulatory Affairs Technicians, ensuring the timely and high‑quality execution of assigned activities.
• Review and assess the regulatory impact of product, manufacturing, or process changes within the assigned portfolio and oversee the implementation of required regulatory actions.
• Monitor and supervise the execution of annual regulatory projects and ensure deliverables are achieved according to agreed timelines.
• Represent the Regulatory Affairs function in communications with affiliates, external partners, and Health Authorities, when applicable.
• Maintain up‑to‑date knowledge of applicable regulations and regulatory requirements, providing regulatory guidance for different projects and business initiatives.
• Support general activities and strategic initiatives within the Regulatory Affairs Department.
• Coordinate the preparation, review, implementation, and maintenance of Regulatory Affairs Standard Operating Procedures (SOPs).
• Collaborate with cross‑functional teams to ensure efficient regulatory support throughout the product lifecycle.

Who You Are

• You have a Bachelor's Degree in Health Sciences or engineering.
• You have experience in RRAA or technical departments within the pharmaceutical industry.
• You have analytical skills, attention to detail, and ability to summarize and evaluate.
• You have Advanced level of Spanish and English (C1) and of MS Office (Excel).

What We Offer

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Information about Grifols is available at www.grifols.com.

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Flexibility for U Program:

Hybrid Model

Flexible schedule:

Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits Package

• Contract of Employment: Permanent position.

Location:

Sant Cugat del Vallès.

SPAIN : España : Sant Cugat del Valles:[[cust_building]]

www.grifols.com

Learn more about Grifols