Change Control & Regulatory Specialist
Parets 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 opportunity fostering an inclusive environment where diversity makes us be 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 Change Control & Regulatory Specialist, like you.
Role Mission
Coordinates, supervises, and evaluates the technical management of change controls, assessing their potential impact on products and regulatory licenses. Responsible for preparing, reviewing, and monitoring technical and regulatory documentation.
What your responsibilities will be
- Coordinate and supervise technical aspects of change controls, assessing their impact on products and regulatory approvals.
- Prepare, review, and maintain technical and regulatory documentation related to product changes.
- Provide regulatory guidance and support to internal teams on change implementation and compliance.
- Track the status and effectiveness of change controls to ensure timely execution and regulatory compliance.
- Collaborate with cross-functional teams to ensure all product changes meet company and regulatory standards.
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).
- You have a Bachelor’s degree in Pharmacy, Chemistry, Biotechnology, Life Sciences, or a related field.
- You have an advanced level of English (C1) – indispensable.
- You have at least 2–3 years of experience in regulatory affairs or change control within the pharmaceutical, biotech, or medical device industry.
- You have experience preparing, reviewing, and managing technical and regulatory documentation.
- You have knowledge of regulatory requirements and product licensing processes.
- You have excellent communication and organizational skills to coordinate change controls across teams.
- Experience working with global regulatory authorities and understanding of international regulatory frameworks.
- Familiarity with electronic document management systems (EDMS) and quality systems (e.g., GMP).
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.
Flexible schedule: Monday-Thursday 7:00 -10:00 to 16:00 -19:00h and Friday 8:00-15:00h (with the same flexible start time).
Contract of Employment: Temporary
Flexibility for U Program: 1 day remote working
Location: Parets del Vallès