Για εργοδότες
Regulatory Affairs Specialist
Η θέση δεν δέχεται πλέον αιτήσεις

Requirements

  • 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.

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ΠΕΡΙΛΗΨΗ ΘΕΣΗΣ
Regulatory Affairs Specialist
Άγιοι Ανάργυροι
πριν ένα μήνα
Με κάποια εμπειρία
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