
Regulatory Affairs Specialist
- Warszawa, mazowieckie
- Stała
- Pełny etat
- Create, submit, and maintain product notifications.
- Review and approve documents to ensure accuracy, completeness, and compliance with regulations.
- Maintain metrics related to product releases, ensuring timely compliance with regulatory requirements.
- Track regulations applicable to medical devices and in vitro diagnostics, monitoring both EU and local requirements.
- Review advertising and promotional materials to ensure compliance with local and corporate requirements.
- Support marketing, sales, and tenders by providing technical support and addressing regulatory questions.
- Input and maintain accurate data, including licenses and registration records, in internal regulatory databases.
- Report product complaints according to corporate and regional requirements.
- Hold a Bachelor's Degree in relevant fields such as Life Sciences, Pharmacy, Biomedical Engineering, or a related discipline.
- Have a minimum of 1-2 years of experience in Regulatory Affairs, preferably within the medical device or in vitro diagnostics industry.
- Possess exceptional verbal and written communication skills for effective interaction with competent authorities, trade associations, and internal teams.
- Demonstrate the ability to work effectively with diverse teams.
- Exhibit strong analytical skills to track, interpret, and apply regulatory changes and their impact on product compliance.
- Show high accuracy and thoroughness in reviewing and approving documents, ensuring compliance with regulations.