Regulatory Affairs Manager (m/f/d)

GULP – experts united; Northeim; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

Une entreprise dynamique dans le secteur pharmaceutique recherche un Regulatory Affairs Manager à Northeim. Dans ce rôle, vous serez responsable de la gestion des affaires réglementaires, de la soumission de documents et du mentorat d'une équipe. Vous apporterez votre expertise et collaborerez avec des équipes interfonctionnelles dans un environnement stimulant.

Leistungen

Induction optimale

Avantages mobilité

Accès à une salle de sport gratuite

Produits Apple récents

Qualifikationen

• Formation universitaire avec une spécialisation scientifique.
• Expérience en dispositifs médicaux ou biotechnologie.
• Excellentes compétences en allemand et en anglais.

Aufgaben

• Gérer le département des affaires réglementaires.
• Préparer et soumettre des dossiers aux autorités.
• Former et superviser les employés et consultants.

Kenntnisse

Leadership

Interprétation de règlements

Collaboration internationale

Ausbildung

Formation scientifique

Jobbeschreibung

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Regulatory Affairs Manager (m/f/d), Northeim

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Client:

Location:

Northeim, Germany

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

89910705e680

Job Views:

3

Posted:

21.06.2025

Expiry Date:

05.08.2025

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Job Description:

We are looking for a Regulatory Affairs Manager (m/f/d) in the pharmaceutical industry for a client for direct placement in Northeim.

Here's what our clients offer

• Optimal induction/onboarding
• Mobility benefits
• Free gym & courses as well as numerous health campaigns
• Latest and powerful Apple products with many new collaboration features for daily business
• Managing the Regulatory Affairs department, including the preparation, review, processing and submission of documents to the relevant authorities
• You develop and implement regulatory guidelines
• Reviewing and complying with regulatory procedures and workflows
• Development of optimal strategies
• You will also interface with global regulatory authorities and external consultants
• Training, mentoring and supervising employees, consultants & contractors in the area of regulation as well as developing the team are another part of your responsibilities
• As a Regulatory Affairs Manager (m/f/d), you will continuously support interdisciplinary teams as an advisor on regulatory issues

Your profile

You have successfully completed your studies with a scientific focus

Experience in the field of medical devices or in the biotechnology industry

Proven experience in actively leading a team

Very good knowledge in the interpretation of regulations, guidelines, policy statements

You are experienced in the preparation of marketing authorization applications

Prioritization of work packages, both for yourself and for your team

You enjoy working effectively and cooperatively in cross-functional international teams

Fluent written and spoken German and English and a willingness to travel (max. 10%) round off your profile

You identify with our values of sustainability, openness & joy and are motivated to work in a dynamic company