Project management support
- Ingelheim Am Rhein
stellenbeschreibung
Job Description The future belongs to those who drive innovation, inspire transformation and fuel collaboration. Our commitment is achieved by working together with our clients in combining the key technologies IT, Engineering and Life Sciences in order to develop innovative solutions for the future. We connect top companies with the sharpest minds in Life Science. All of them united by their burning passion to make use of their talents in order to master the challenges ahead. Are you one of them? If so, you are what we are looking for as a co-worker for a project by one of our customers, a renowned company in the Pharmaceutical Branche located in Ingelheim am Rhein. Commencing immediately, on a temporary basis. What you can do for us * You are responsible as Support Manager for Drug-Delivery Device Development and you support internal and external development teams and project leaders for the device development of biopharmaceutical combination products (CP) * Furthermore you support the planning of CP development projects in cooperation with external suppliers * Utilizing your expertise in project documentation you generate technical and project related documentation and presentations under the guidance of project leaders and subject matter experts for internal and external project teams and decision committees are also part of your position * You run the system-based document management and, if necessary, you author, contribute, review and approve relevant design control, risk management and usability engineering documentation * You contribute with your experience to further improve and strengthen all structures and processes underlying a state-of-the-art CP development, manufacturing and life-cycle management The skills that are needed * PhD or master's degree in pharmacy, engineering or biotechnology * Several years' experience in the medical device industry for biopharmaceutical drug-delivery devices and combination products is required * Additional experience with coordination of activities at third party manufacturers and vendors is preferred (purchasing controls) * Broad expertise around regulatory requirements for parenteral combination products is preferred (mainly 21 CFR parts 4 & 820, ISO 13485, 14971 & IEC 62366 and other guidelines for CP development and required quality system regulations) * Fluent in English with excellent organization and communication skills as well as sound technical writing and documentation Why you are in the right place when working with us We connect the right professionals with the right project, as we do by connecting you with our recruiting projects! Our path together begins with trying to comprehend your ambitions. We shall work together to help you achieve your career objective, by investing in your professional development and mentoring, and by coaching you throughout your career. Modis is a global leader in professional solutions and a dynamic brand with a global focus. We are pursuing ambitious goals in a key market. Our affiliation with Adecco Group opens up a wide array of career choices for you. You can hardly wait to get to know us? Then a simple click will quickly connect you with us. Just click on"APPLY NOW"
to send us your application. Your Contact Frau Svenja Oschwald Modis GmbH Life Science Güterhallenstraße 4 79106 Freiburg Phone +49
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