Job Description:
- 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
Professional experience & skills desired to have:
- 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
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 Timișoara 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