Project and Liaison Manager (m/f/d)

With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry and medical technology, we know the key contact persons who write out demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop professionally and work on their own careers. As a specialized staff consultancy with an international network, we offer you decisive advantages - and this is completely free of charge for you. Register and benefit from interesting and matching positions and projects. About the company

Our client is a growth-oriented company that operates in a technically demanding environment and is characterized by a modern, international working culture. The company pursues a high level of quality, works with various external partners and focuses on future-oriented solutions that make a positive contribution to customers, customers and users in the long term. Employees benefit from short decision-making, open communication culture and the opportunity to take responsibility and actively contribute their own ideas. The company attaches great importance to a structured, reliable way of working, promotes independent work and at the same time offers an environment that supports flexibility and personal development. Interface between departments and external partners Ensuring clear communication and coordination of follow-up tasks Solution of interdisciplinary challenges and promoting cooperation Building and further development of company-wide project management Planning, control and monitoring of projects Management of project meetings and compilation of regular status reports Monitoring schedule, budget, quality and resources Tracking relevant KPIs and identifying and managing project risks Support for EU and US authorisations and compliance with regulatory standards Initiation and implementation of improvement projects

Studies in natural sciences, medical technology, BWL or comparable Found experience in project management in the medical technology industry Good understanding of the product life cycle of medical devices Knowledge of regulatory requirements (ISO 13485, MDR, FDA 21 CFR Part 820) Experience in managing cross-functional projects Certifications such as IPMA, PMI or PRINCE2 desirable High-communication, organized, IT-affin and problem-solving oriented Very good knowledge of German and English Flexibility for international cooperation

Innovative environment in medical technology Work on projects with high impact on patient care Design space and independent work International cooperation and modern work culture Flexible working hours Up to two days of mobile work per week Content information

An attractive remuneration model awaits you. .