About this role
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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. |
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We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
What your responsibilities will be
- Act as an interface with Regulatory Authorities/ Notified Bodies.
- Determines the Regulatory Classification of the products and the applicable standards.
- Create regulatory dossiers and verify compliance with regulatory requirements.
- Coordinates the reviews of labeling in accordance with current regulations.
- Supervises the consistency of the reports that support the registration of products in accordance with current standards (eg Technical Files CE, 510k, BLA, annual reports, etc).
- Draft letters and Technical Technical Documentation that should be submitted to Regulatory Authorities or other Certyfing Bodies
- Determines the Regulatory Impact of changes in Products, Manufacturing Processes and Facilities.
- Is up to date of the standards and regulations applicable to the Diagnostic Business Unit products.
- Draft Technical Documentation related to labeling changes that should be shared with the customers.
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 accommodations may be made to enable individuals with disabilities to perform the essential functions).
- Bachelor’s Degree in Pharmacy, Chemistry, Biology, Biomedical Engineering, or a related Life Sciences/Scientific field.
- Between 2-5 years of experience in technical and regulatory documentation. Prior experience with IVDR and FDA regulations within the Medical Device or IVD industry is highly valued.
- Ability to act as a primary point of contact and lead submissions with international health authorities and Notified Bodies.
- Methodical and detail oriented, with rigorous approach to ensuring regulatory compliance and technical accuracy.
- Ability to work closely with cross-functional teams
- Advanced level of English
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!
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.
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Location: SPAIN : España : Sant Cugat del Valles:[[cust_building]]
Other facts
About GRIFOLS, S.A.
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 a broad range of therapeutic areas: immunology, hepatology and intensive care, pulmonology, hematology, neurology and infectious diseases.
With a workforce of over 23,000 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.
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What you'll do
- The Regulatory Affairs Specialist will act as an interface with Regulatory Authorities and create regulatory dossiers to ensure compliance with applicable standards. They will also supervise the consistency of reports supporting product registration and draft necessary documentation for submission to regulatory bodies.
Ready to join GRIFOLS, S.A.?
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