REGULATORY AFFAIRS SPECIALIST
Sant Cugat del Valles, ES
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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.
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.
What your responsibilities will be
- Prepare and manage submissions and follow up of product registrations or any other regulatory activity, ensuring timeliness, accuracy, comprehensiveness, or compliance with regulatory standards.
- Communicate with affiliates, outside companies and Health Authorities.
- Adapt licenses to current regulations.
- Support other Departments, Affiliates and Third Parties in any required regulatory information.
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 Health Sciences or a related field
- Minimum 6 months of related technical and/or regulatory experience in pharmaceutical industry or an equivalent combination of education and experience.
- Ability to work under tight timelines to meet deadlines and business objectives
- Ability to work as part of the regulatory team to meet the objectives
- High degree of attention to detail. Analytical skills and ability to summarize
- Ability to clearly communicate verbally and in writing
- Ability to research regulatory requirements
- Computer skills (such as MS Office, databases, Document Management System)
- Fluent in English and Spanish
What we offer
It’s a brilliant opportunity for someone with the right talents.
Grifols understands you want a challenging and rewarding career in a critical function Regulatory Affairs Specialist help you grow professionally.
Information about Grifols is available at www.grifols.com. If you’re interested in joining our company and you have what it takes, then don’t hesitate to apply.
We look forward to receiving your application.
Grifols is an equal opportunity employer.
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
Benefits package
Contract of Employment: Permanent position
Flexibility for U Program: 2 days remote working
Location: Sant Cugat del Vallès
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Location: SPAIN : España : Sant Cugat del Valles:SC2