Regulatory Affairs Specialist
Η θέση δε δέχεται πλέον αιτήσεις
Άγιοι ΑνάργυροιΤοποθεσία
Άγιοι Ανάργυροιπριν 4 μήνες
Ημ. ανάρτησηςπριν 4 μήνες
Με κάποια εμπειρίαΕπίπεδο εμπειρίας
Με κάποια εμπειρίαΠλήρης απασχόλησηΤύπος απασχόλησης
Πλήρης απασχόλησηΕπιστημονικός ΚλάδοςΚατηγορία θέσης
Επιστημονικός ΚλάδοςRequirements
- Review, compile and keep up to date technical files for medical devices and cosmetic products.
- Monitor European and local regulations and legislation related to medical devices and cosmetics.
- Ensure product compliance with applicable requirements.
- Manage EUDAMED, GREMDIS, and CPNP databases.
- Communicate with relevant authorities and notified bodies.
- Advise other departments on regulatory and compliance matters.
Qualifications
- BSc in Life Sciences (Pharmacy, Chemistry, Biology, relevant field).
- 3+ years of hands-on experience in Regulatory Affairs within the Medical Device and Cosmetics industry
- In depth understanding of medical devices regulations, cosmetics regulations and ISO 13485:2016
- Fluent written and spoken English
- Excellent MS Office skills
- Strong organization skills, multi-tasking and able to meet deadlines
- Excellent communication skills and collaborative mindset
We offer
- Competitive salary.
- Private medical insurance scheme.
- Continuous Education.
- Ability for a successful career in the fast-growing health sub-sector.
All CVs will be treated with strict confidentiality.
ΠΕΡΙΛΗΨΗ ΘΕΣΗΣ
Regulatory Affairs Specialist
Άγιοι Ανάργυροι
πριν 4 μήνες
Με κάποια εμπειρία
Πλήρης απασχόληση