Regulatory Affairs Manager

vor 3 Monaten


Northeim, Deutschland GULP – experts united Vollzeit

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

Full-time employment Personnel development opportunities Attractive fixed salary Comprehensive social package Open corporate culture 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

Your tasks

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