Aktuelle Jobs im Zusammenhang mit Emea Regulatory Affairs Trainee - Dülmen - Johnson & Johnson

**Job Function**:
Career Programs
**Job Sub Function**:
Non-LDP Intern/Co-Op
**Job Category**:
Career Program
**All Job Posting Locations**:
Duelmen, Germany

Interne Stellenausschreibung vom 11.06.2025 bis 25.06.2025

We are pleased to offer a 24-month regulatory trainee position to assist the Johnson & Johnson EMEA Regulatory Affairs Organization with a diverse array of regulatory matters and projects. This role presents exceptional opportunities to gain valuable, hands-on in-house regulatory experience within the dynamic, multinational environment of a leading healthcare company.

The EMEA Regulatory Affairs Department is responsible for the registration and maintenance of our Medtech product portfolio across all EMEA countries. In addition to being part of the EMEA Regulatory Affairs Department, you will collaborate closely with the global Johnson & Johnson Regulatory Affairs team, the Supply Chain, marketing and sales teams, as well as our internal legal partners, providing support for Johnson & Johnson Medtech initiatives.

As part of the EMEA Regulatory Affairs team, we are excited to offer the new Regulatory Trainee Program. This program aims to integrate Data science and new technologies while providing insights into the world of regulatory affairs. You will experience a steep learning curve through various challenging activities in a rapidly changing environment allowing you to gain a comprehensive understanding of international regulatory requirements for medical devices on a global scale.
- ** Key Responsibilities**:

- Assist in ensuring compliance with international, European, regulatory requirements for medical devices.
- Independently use technology to provide innovative and creative solutions for reporting metrics and other Regulatory data.
- Respond to inquiries from regulatory authorities, customers and manage correspondence.
- Develop solutions for various challenges of appropriate scope and complexity.
- Create, maintain, and organize regulatory documents.
- Foster positive and cooperative communication with international colleagues at all levels.
- Perform other assigned duties as needed.

**Qualifications**:

- Bachelor’s degree in a scientific discipline such as Medical Engineering, Biology, Life Sciences, Data Science, or a related field; a completed master’s degree is preferred.
- Business acumen and interest in regulatory regulations.
- Knowledge of AI, machine learning, and data analytics is preferred.
- Experience in the medical device or pharmaceutical industry, with international exposure through internships or studies is desirable.
- Familiarity with relevant regulatory standards and regulations: EU MDR, MPDG, DIN EN ISO13485 is a plus.
- Strong analytical skills with a determination to learn and collaborate effectively in a team.
- High degree of flexibility, creativity, and commitment.
- Fluent in German and English, both written and spoken.