Inserat online seit: 19 Juni
Aufgaben der Stelle
For our international and attractive client in Ingelheim , we are currently advertising a position as Project Coordinator Medical Technology / Design Control Processes . Take advantage of this opportunity and submit your application online. We value diversity and are therefore open to all applicants. Randstad is the expert for jobs in your region and throughout Germany. With us, you'll find the right position.
Here's what we offer
With us, you can expect an attractive salary above the standard pay scale, complemented by excellent benefits such as vacation and Christmas bonuses. To ensure your work-life balance isn't compromised, you'll benefit from a discounted Wellhub membership with access to approximately 2,900 sports, leisure, and wellness facilities. We actively support your personal and professional development through a diverse range of e-learning courses, allowing you to continuously expand your skills. And best of all: If you'd like to help us grow our team, we reward every successful employee referral with a €250 bonus.
Your tasks
Documentation & Design Control: You will assume professional responsibility for the creation and maintenance of the English-language project documentation in the design control process and ensure reliable compliance with all official and internal requirements.Project organization & consulting: In close coordination with the Device Team Leader, you will relieve them of organizational work packages and provide technical advice to the team on the application of processes, methods and tools.Process optimization: You actively participate in the "Device Project Management Excellence" initiative and play a key role in shaping the development and implementation of new, future-proof development processes.Interface work in a global environment: You operate in an international, interdisciplinary project environment and ensure the quality and efficiency of the entire product development through close collaboration with various teams. Your profile
Your foundation: You have successfully completed a Master's degree in engineering or natural sciences. Alternatively, you can impress us with a Bachelor's degree and several years of professional experience in the development of medical and combination products or in the design control process.Your expertise: You are a professional in the development of medical and combination products. Especially in the design control process (according to 21 CFR 820.30) as well as in the GMP and change control environment, you are second to none.Your organizational skills: You have solid basic knowledge of project management and ideally have already successfully demonstrated this in technical development projects.Your personality: You are characterized by an independent, structured work style and a high degree of initiative. Since we operate globally, fluent English skills perfectly round out your profile.
