Stellenangebot: Regional Regulatory Leader (m/f/d)

Über uns

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Ihre Aufgaben

• Serve as a Regional Regulatory Lead for the assigned product portfolio, Therapeutic area Haematology and countries
• Align all regulatory activities with regional and global strategies, ensuring compliance with local requirements
• Communicate effectively to ensure that dossiers meet regional and local content and format requirements
• Coordinate, compile and track high-quality documentation for submissions, including new license applications and lifecycle activities to enhance connectivity and improve submission and approval timelines.This also involves addressing questions related to regulatory submissions
• Build strong relationships with regional regulatory agencies, utilizing negotiation and influencing skills for positive outcomes
  
• Collaborate with internal functions e.g., Commercial, Manufacturing, Supply Chain, and Medical Affairs to enhance connectivity
  
• Stay informed about international legislation and guidelines for biological products and related initiatives e.g., rare diseases, orphan drugs
  

Ihr Profil

• A degree in Life Sciences, preferably with a post-graduate qualification. Degree e.g. in Drug Regulatory Affairs advantageous
• Experience within the international region, supported by additional pharmaceutical or industry experience
• Profound knowledge of the scientific principles and technical requirements relevant to the development of a pharmaceutical product and understanding of the principles of GMP and GCP
• Proficiency in standard regulatory tools Veeva, DocNet, Trackwise

Wir bieten

• A very renowned company
• A highly motivated team and an open way of communication

Ihr Kontakt

Ansprechpartner
Annalena Käser

Referenznummer
768359/1

Kontakt aufnehmen
E-Mail: annalena.kaeser@hays.ch

Anstellungsart
Freiberuflich für ein Projekt