Regulatory Affairs Specialist

Il y a 6 mois

Aalst, Belgique Bestinfo Systems LLC Temps plein

**This full-time opportunity is exclusively with this client.**:

- This company is a large multinational medical technology corporation with over 70,000 employees globally. Specializing in medical devices and diagnostic systems, This serves millions of clients worldwide, including healthcare professionals and patients, with innovative solutions in areas such as diagnostics, medical devices, and life sciences.
- **Regulatory Affairs Specialist**:

- **Location: Aalst, Provincie Oost-Vlaanderen, Flanders, Belgium / (HYBRID)**:

- **Base Salary - EUR €10,000 to €70,000**:

- **Industry: Medical Equipment / Devices**:

- **Job Category: Legal - Regulatory / Compliance Law**:

- **Responsibilities**:

- Handling customers’ questions
- Support to customer service for tenders
- Support cross functional teams for products launches
- Review of promotional materials in French and Dutch
- Update of regulatory documents and internal databases
- Monitoring of regulatory changes in Benelux
- Participation to trade associations meeting
- Attend internal meetings with EU Regulatory Affairs team or project teams
- **About you**:

- Master degree in sciences or pharmacy or equivalent
- Previous experience in regulatory affairs of 3 years at least ideally in medical devices or in vitro diagnostics area
- Good communication skills verbal and written in Dutch and English (French is nice to have)
- Ability to handle several projects in parallel and interact with several functions
- Autonomy
- **CANDIDATE DETAILS**:

- Seniority Level - Entry
- Minimum Education - Bachelor's Degree
- Willingness to Travel - Occasionally

HC01

**Salary**: €10.000,00 - €70.000,00 per year

**Benefits**:

- Food allowance
- Hospitalization insurance
- Retirement plan
- Work from home

Schedule:

- Day shift
- Monday to Friday
- Weekend availability

Supplemental pay types:

- Hazard bonus
- Overtime pay

**Education**:

- Master's (required)

**Experience**:

- Regulatory Affairs: 4 years (required)
- medical devices or in vitro diagnostics area: 3 years (required)

Ability to Relocate:

- Aalst: Relocate before starting work (required)

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