We are looking for 4 Product Care Junior to one of the leading and most innovative dental company in the sector. It is an international company, present worldwide, offering a wide variety of products for dentists and dental technicians.

OBJECTIVE OF THE POST 
Supervision of the Technical Documentation for existing clinical/technical dental medical devices. Monitoring product conformity, in line with current and future global legal and regulatory requirements.

MAIN FUNCTIONS

  • Specialist support for Technical Documentation (MDR).
  • Regular updating of the Technical Documentation as part of post-market surveillance activities (this includes biological evaluation, clinical evaluation, risk management).
  • Creation and supervision of regulatory documents for country-specific registrations.
  • Adaptation of the Technical Documentation in the context of product changes.
  • Regulatory support in creating customer information, including examination and approval.


MAIN REQUIRMENTS

  • University degree in natural sciences or dental technology/dental medicine (biology, chemistry, pharmacy, dentistry…).
  • English for bussines - written and spoken minimun C1 (documentation, writing and communication task with the team in an international environment).


OTHER DESIRABLE REQUIREMENTS

  • Knowledge of regulatory requirements for medical devices (advantageous).
  • Final degree project or master's degree final Project (TFG or TFM) related to the vacancy / good grade due to exhaustive documentation work. 
  • German language skills.
  • ERASMUS experience in an english-speaking country.


PERSONAL SKILLS

  • Ability and enjoyment of document management and Reading tasks.
  • Teamwork.
  • Communication skills.
  • Organization and planning.
  • Positive attitude.
  • Honesty and profesional ethics.
  • Adaptability

¿Conoces a alguien que pudiera interesarle? Cuéntaselo!

Algunos de tus compañeros

Teamtailor

Herramientas de captación de Teamtailor