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 authoritiesYou develop and implement regulatory guidelinesReviewing and complying with regulatory procedures and workflowsDevelopment of optimal strategiesYou will also interface with global regulatory authorities and external consultantsTraining, mentoring and supervising employees, consultants & contractors in the area of regulation as well as developing the team are another part of your responsibilitiesAs a Regulatory Affairs Manager (m / f / d), you will continuously support interdisciplinary teams as an advisor on regulatory issuesYour 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