Regulatory Affairs Specialist
Want to keep progressing your CMC regulatory affairs experience and be part of a well known Spanish pharmaceutical company located in Barcelona? Are you looking for an hybrid project that gives you the flexibility to work from home occasionally?
This opportunity can be for you!
Main tasks & responsibilities:
- Prepare the documentation to submit to Regulatory Authorities to obtain Marketing Authorization for Medichem products.
- Respond questions and doubts about our registration documentation to customers and Health Authorities.
- Prepare and submit the variations documentation.
- Maintenance of registration files and Marketing Authorizations.
- Identify and interpret relevant regulatory guidelines advise the rest of the company on regulatory matters.
- Possibility to work from home once a week
- Salary: Depending on the experience.
- Flexible schedule
- Social benefits
- Tickets restaurant
Fecha de publicación: 17/06/2022
