What you’ll do?
Coordinate and manage the registration, notification and lifecycle maintenance of medicinal products, medical devices and cosmetic products.
Prepare, maintain, and translate product technical documentation.
Ensure that submissions and documentation comply with applicable legislation and internal quality standards.
Support vigilance activities related to medicinal products, medical devices and cosmetic products.
Communicate with competent authorities and collaborate with business partners.
Review and coordinate promotional and advertising materials.
Maintain and update regulatory databases and records.
Participate in audits and inspections.
What makes you a great fit?
Degree in Pharmacy, Life Sciences or Medicine.
Understanding of regulatory requirements for medicinal products, medical devices, and/or cosmetic products in Latvia, the Baltic States, and EU.
Previous experience in regulatory affairs and/or pharmacovigilance will be considered an advantage.
High attention to detail, ability to work with large volumes of documentation, and strong time management skills.
Proficiency in Latvian and English languages.
Competency in MS Office applications.
Why join us?
An interesting and meaningful role in an international company.
Monthly salary 1600 EUR gross for a part-time position.
Attractive performance-based bonus system.
Enjoy the flexibility of a hybrid work model.
Health insurance, company mobile phone, covered phone expenses and other company benefits.
Ready to take the next step in your career?
Apply now!
Need more info?
Our Talent and Development Partner Krista Andersone will answer your questions.
