Regulatory Affairs Intern

Vor 6 Tagen


Genf GE, Schweiz Teoxane Vollzeit

**Date**:9 oct. 2024

**Lieu**: Genève, Corporate, 1203

**Entreprise**:teoxanesa

Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global patient care. Using its products, practitioners are able to fill all kinds of wrinkles, from the finest to the deepest, to restore youthful volume to the face, and to treat the neck and décolleté, with natural results. The strength of Teoxane is also its human size and independence. Teoxane has a total freedom of thoughts, action and innovation which makes the company unique.

In the frame of the growth of our business, we are looking for a:
**Regulatory Affairs Intern**

**Main activities**
- Assess Regulatory requirements of MDSAP countries and prepare a compliance plan for the QMS (Quality Management System)
- Asses the UE requirements for EUDAMED and prepare a compliance plan for the QMS
- Support the ROW (Rest of the World) team in the roll-out of the MDR modifications
- Participate in the validation of promotional assets

**Your profile**
- Scientific University, EPF or HES degree
- Strong organizational skills and flexibility
- Enthusiasm and commitment with a good attitude towards teamwork
- Good Scientific writing skills
- Fluency in English and French

TEOXANE promotes equal opportunity and places at the heart of its human resources management policy the fight against all forms of discrimination based on age, gender, origin, disability, or any other personal characteristic.



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