Medical Device Regulatory Affairs Assistant

il y a 4 jours

CagnessurMer, France DERMOSCIENCES Temps plein

**_About Dermaceutic_**

Dermaceutic is a dynamic and ambitious laboratory operating in the fast-growing sector of Aesthetic Dermatology, offering a wide range of professional and cosmeceutical products.

Over the last 15 years Dermaceutic has seen significant international growth and is now present in over 70 countries.

At Dermaceutic, we are a young, passionate, and international team working hard in a fast-paced environment. We encourage our employees to learn and grow within their roles, own their projects and be drivers of their own initiatives. Our core business values focus on innovation, efficacy, determination, anticipation, and a search for perfection across our product lines and best-in-class customer brand experience.

**_Mission_**

Within the Regulatory Affairs department, your mission will be to set up and prepare technical files related to medical devices.

**Project list : Constitution of technical files for medical devices**

1) Drafting and implementation of technical files according to the MDR (Medical Device Regulation)
- Write and compile technical files according to MDR 2017/745 medical device regulations.
- Participate in the update of the risk analysis of medical devices.
- Participate in product development and follow-up meetings with other departments (R&D, Sales and Marketing).
- Participate in the drafting of PMS (post market surveillance) reports
- Participate in the regulatory monitoring exercise (guides, technical standards)
- Contribute to the creation of an excel tool for the follow-up of technical documentation and annexes related to medical devices.
- Participate in the implementation or improvement of clinical monitoring of medical devices.

**_Qualifications_**
- Master's degree in regulatory affairs or health products or other degree in health engineering.
- Minimum 1 year experience in regulatory affairs or medical device quality.
- Knowledge of Microsoft Word, Excel, PDF.
- Written English is required. (Files to be written in English)
- Knowledge of Regulation 2017/745 is a plus.
- Juniors accepted.
- You are autonomous, organized and dynamic. You have a good project management, ease in managing documents, follow-up, and are a force of proposal.

**_Other information_**
- Remuneration : To be determined
- Start of contract : ASAP
- Location : Cagnes-sur-Mer
- Type of job : Fixed-term contract (6 months, eventually renewable)

Type d'emploi : Temps plein, CDD
Contract length: 6 months

Salaire : 20 147,40€ à 30 000,00€ par an

Horaires:

- Du Lundi au Vendredi

Rémunération supplémentaire:

- Prime annuelle

Expérience:

- Affaires réglementaires: 1 an (Optionnel)

Langue:

- Anglais (Exigé)

  • Regulatory Manager, EAME Regulatory Affairs

    il y a 1 semaine

    Neuilly-sur-Seine, France International Flavors & Fragrances Temps plein

    Overview Are you passionate about fragrance creation and developing the fragrances of tomorrow? We are seeking a motivated and result-driven talent to join our Scent Regulatory Affairs team. As a Regulatory Manager, you will be responsible for regulatory compliance and conformity to customer requirements for scent products, including fragrances (Fine and...

  • Regulatory Affairs Manager, EAME

    il y a 6 jours

    Neuilly-sur-Seine, Île-de-France IFF Temps plein

    Job SummaryAre you passionate about regulatory affairs, fragrance creation and developing the fragrances of tomorrow?IFF is a global leader in flavors, fragrances, food ingredients and health & biosciences. We deliver sustainable innovations that elevate everyday products.AsRegulatory Affairs Senior Specialist, you will play a key role in ensuring our...

  • Director Cmc Regulatory Affairs

    il y a 4 jours

    Gif-sur-Yvette, France Servier Temps plein

    **Date de parution**:23 oct. 2025- **Ville**:GIF-SUR-YVETTE- **Pays/Région**:FR- **Type de contrat**:CDI- **N° offre**:10219- Director CMC Regulatory Affairs (M/F)- - Nous sommes un groupe pharmaceutique à dimension humaine, international et indépendant, gouverné par une Fondation. Notre modèle, singulier, fait notre fierté mais, surtout, nous permet...

  • Regulatory Affairs Associate Manager

    il y a 2 semaines

    Neuilly-sur-Seine, France International Flavors & Fragrances Temps plein

    Job Summary Who we are Our Pharma Solutions Regulatory Team is growing and we are looking for a dedicated and passionate individual to join our team as a Regulatory Affairs Associate Manager to provide regulatory support including registration for our products used in industrial (non - food, non What we offer Working at an international company with an...

  • Regulatory Affairs Senior Specialist

    il y a 2 semaines

    Neuilly-sur-Seine, France International Flavors & Fragrances Temps plein

    Job SummaryAre you ready to take your skills to the next level and make a real impact? IFF is a global leader in flavors, fragrances, food ingredients and health & biosciences. We deliver sustainable innovations that elevate everyday products. As Regulatory Affairs Senior Specialist, you will have the opportunity to develop a unique skillset by serving as...

  • Director Regulatory Affairs, China, Hong Kong, Japan

    il y a 2 semaines

    Gif-sur-Yvette, Île-de-France Servier France Temps plein

    Date de parution: 29 nov. 2025Ville: GIF-SUR-YVETTEPays/Région: FRType de contrat: CDIN° offre: 9252Director Regulatory Affairs, China, Hong Kong, Japan (H/F)Nous sommes un groupe pharmaceutique à dimension humaine, international et indépendant, gouverné par une Fondation. Notre modèle, singulier, fait notre fierté mais, surtout, nous permet de servir...

  • Cdi - International Regulatory Affairs Manager

    il y a 2 semaines

    Neuilly-sur-Seine, France Sephora Temps plein

    At Sephora we inspire our customers, empower our teams, and help them become the best versions of themselves. We create an environment where people are valued, and differences are celebrated. Every day, our teams across the world bring to life our purpose: to expand the way the world sees beauty by empowering the ExtraOrdinary in each of us. We are united...

  • Regulatory Affairs Specialist Fine Fragrances H/F

    il y a 2 semaines

    Le Bar-sur-Loup, France France 06 - Le Bar sur Loup (siège social) Temps plein

    Le Groupe MANE, un des leaders de l'industrie des arômes et parfums recherche un/une : Regulatory Affairs Specialist Fine Fragrances Les missions principales du poste : -Gestion de certains clients spécifiques (Fine Fragrance) -Avoir des aptitudes au management de personnes -Participation aux réunions clients par Teams et présentiel, chez les clients en...

  • Regulatory Affairs Specialist Fine Fragrances H/F

    il y a 2 semaines

    Le Bar-sur-Loup, France France 06 - Le Bar sur Loup (siège social) Temps plein

    Le Groupe MANE, un des leaders de l'industrie des arômes et parfums recherche un/une : Regulatory Affairs Specialist Fine Fragrances Les missions principales du poste : -Gestion de certains clients spécifiques (Fine Fragrance) -Avoir des aptitudes au management de personnes -Participation aux réunions clients par Teams et présentiel, chez les clients en...

  • Regulatory Affairs Specialist Fine Fragrances

    il y a 6 jours

    Le Bar-sur-Loup, France Mane Temps plein

    Le Groupe MANE, un des leaders de l'industrie des arômes et parfums recherche un/une: Regulatory Affairs Specialist Fine Fragrances Les missions principales du poste: - Gestion de certains clients spécifiques (Fine Fragrance) - Avoir des aptitudes au management de personnes - Participation aux réunions clients par Teams et présentiel, chez les clients...