You have knowledge in the field of regulatory affairs
Ideally, you have experience with international registrations and approvals in the field of medical devices
You are fluent in English and can write documents confidently in English
German language is a plus
Good communication and problem solving skills
Excel knowledge
Self-responsible, personal motivation, analytical You are responsible for the registration and approval of our medical devices worldwide
You create dossiers and documents for registrations and approvals
You coordinate the timely provision of all necessary documents and information with the departments involved
You organise translations, certifications, apostilles and the mail order of documents
You process enquiries from authorities and partner companies
If required, you will support audits by international authorities
Regulatory review and approval of trade products
Manage regulatory documents in the internal document repository What we offer you:
Competitive salary
Meal tickets
Gift tickets for Christmas, Easter, Children`s Day and Women`s Day
The 13th salary
Annual bonus according to the company performance, bonus for the purchase of glasses, referral bonus
Medical services for you and your family members
Gym and wellness discount package
Transportation from Timisoara and the metropolitan area and Arad
Professional development opportunities and trainings
Bookster (online platform through which employees can borrow books with no charge)
Cafeteria with catering services, free coffee and fruits
Flexible working hours
Vacation days: 23 days/year at employment
We regret to inform you that this job opportunity is no longer available