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Full-time
bachelor degree
Permanent Position, Flexible Schedule, Professional Development Opportunities
Posted 42d ago
Apply by Oct 22
~40 hrs/week
Responsibilities
Responsible for preparing, submitting, and maintaining technical registration dossiers and variations for medicinal products and medical devices. The role involves monitoring submission progress and collaborating with cross-functional teams to ensure regulatory compliance.
Requirements
Requires a Bachelor's Degree in Health Sciences or Engineering and experience in regulatory affairs or technical departments within the pharmaceutical industry. Proficiency in English (C1), Spanish, and MS Office is essential.
Full job description
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, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.
Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Regulatory Affairs Specialist like you.
Mission
The RRAA Specialist will be responsible of the preparation of technical documentation, submission and following up of product registration and/or renewal, variations dossiers, as well as other regulatory documentation.
What your responsibilities will be
Prepare, compile, and maintain registration dossiers and other regulatory documentation for medicinal products and medical devices within the assigned portfolio.
Prepare, review, and submit regulatory documentation for new registrations, renewals, variations, and other regulatory procedures.
Review and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance.
Monitor the progress of regulatory submissions and registration procedures, liaising with regulatory authorities when required.
Maintain up-to-date knowledge of current regulations and regulatory requirements applicable to medicinal products and medical devices, ensuring ongoing compliance.
Coordinate the translation of regulatory documentation, ensuring accuracy, consistency, and compliance with local market requirements.
Collaborate with cross-functional teams and external partners to ensure timely and high-quality regulatory submissions.
Who you are
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).
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. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!
We look forward to receiving your application!
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).
Grifols is a global healthcare company founded in Barcelona in 1909 committed to improving the health and well-being of people all over the world.
A leader in essential plasma-derived medicines and transfusion medicine, we develop, produce and provide innovative healthcare services and solutions in more than 110 countries.
Patient needs and our ever-growing knowledge of many chronic, rare and prevalent diseases, sometimes life-threatening, drive our innovation in plasma-based therapies and other biopharmaceuticals to enhance quality of life.
Grifols is focused on treating conditions across six core therapeutic areas: immunology, neurology, pulmonology, hematology, hepatology and intensive care.
With a workforce of over 25,000 employees in more than 30 countries and regions, we are committed to a sustainable business model that sets the standard for continuous innovation, quality, safety and ethical leadership in the industry. Our work has a positive social and economic impact in the countries where we operate, creating jobs and generating wealth.
People are at the heart of what we do, and we strive to create an inclusive, diverse, fair and equal society. Maintaining and promoting a workforce that reflects this reality leads to enhanced professional relationships and helps us to give our best to patients, donors and customers.
In 2024, Grifols was named one of TIME's 'World's Best Companies' for the second year in a row, reaffirming our commitment to excellence. We were also recognized by Forbes as one of the "Best Employers for Women 2023," reflecting our dedication to fostering an inclusive and supportive workplace for all.
To maintain a positive community and overall respectful communication, please keep our community guidelines in mind.
Offices: Parc Empresarial Can Sant Joan, Av. de la Generalitat, 152-158, Sant Cugat del Vallès, Barcelona 08174, ES · Carrer de Palou, 6, Parets del Valles, Catalonia 08150, ES
PlasmapheresisPlasma derived therapiesDiagnosticsIntravenous therapiesClinical nutritionAutomate drug compounding Drug inventory controland HealthcareHealth CareBiotechnology
How many Manufacturing jobs are open in Sant Cugat del Vallès, Spain right now?
There are currently 33 open manufacturing positions in Sant Cugat del Vallès, Spain listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Sant Cugat del Vallès, Spain?
Companies currently hiring include Grifols, Eurofragance SLU, OCA GLOBAL, Boehringer Ingelheim, HP, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Sant Cugat del Vallès, Spain?
Yes — 17 of the 33 open manufacturing positions offer remote or hybrid work (0 remote, 17 hybrid).
How do I apply for Manufacturing jobs in Sant Cugat del Vallès, Spain?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.