Hays AG

Stellenangebot: Regulatory Affairs Project Manager / Regulatory Affairs Manager (m/f/d)

Mannheim Vollzeit

Jetzt bewerben

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

Leading and supporting regulatory strategies for global product submissions
Ensuring compliance with international regulatory requirements and standards
Collaborating with cross-functional teams, including R&D, Quality and Clinical to drive regulatory initiatives
Providing regulatory guidance to support product development and lifecycle management
Staying abreast of evolving regulatory trends and up- dates, and implementing best practices

Ihr Profil

Bachelor’s Degree in Life Sciences, Regulatory Affairs or a related field / alternatively completed vocational training with comparable experience in the regulatory field
Profound work experience in Regulatory Affairs; preferred in Regulatory, R&D, Quality, and/or Clinical, with some experience in Healthcare regulatory affairs
Profound knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments & software
Organizational and communication skills
Ability to multitask and effectively manage multiple projects simultaneously
Self-motivated and capable of working independently in a self-management environment
Profound English and German skills
Affinity for IT and good MS Office skills