Quality Management Specialist CSV (m/f/d)

We're on it! Arvato offers you one of the most dynamic working environments you can imagine. We grow, we are innovative, we solve the challenges of our customers all over the world every day. How do we do that? With our global team from 17,000 colleagues: Inside 87 locations in over 17 countries and our special spirit: We're on it! As a strategic growth partner of our customers, we rely on cloud-based e-commerce and IT platforms as well as state-of-the-art automation technology to realize complex global supply chain solutions.

Are you on it? Are you interested in complex systems, think process-oriented and want to actively shape the quality in the healthcare sector? Then become part of our team in Harsewinkel as a specialist quality management CSV (m/w/x) with the focus on computerized system validation. The position must first be fixed for two years.

Are you on it? Are you interested in complex systems, think process-oriented and want to actively shape the quality in the healthcare sector? Then become part of our team in Harsewinkel as a specialist quality management CSV (m/w/x) with the focus on computerized system validation. The position must first be fixed for two years. Turning and fishing point for change control and system validation: You are the central contact person for change control and CSV topics and you are co-ordinatingly independent (re) validation projects of computer-assisted systems. In doing so, you control cooperation with our specialist departments to ensure that regulatory requirements are met at any time Independently editing changes: You first and edit amendments according to internal process specifications. Take the associated information acquisition, test planning, preparation of test matrices and documentation examination completely independently Effective tracking and audit management: You monitor actions in the change process, perform effectiveness controls and securely represent CSV projects in audits or inspections Reporting and documentation of quality-relevant deviations: You report quality-relevant deviations, document them professionally and accompany the corresponding corrective measures

Successfully completed commercial or natural science training, e.g. as an industrial businessman (m/w/x) or pharmaceutical-technical assistant (m/w/x) First experience in quality assurance and computerized system validation (CSV) Contact points with ERP software (e.g. SAP) and very good MS Office knowledge Knowledge of the relevant pharmaceutical and medical regulations and requirements (GxP) High reliability, team skills and very good communication skills in German and English

Open corporate culture: innovative strength and pioneering spirit drives work in our teams and thanks to our “Open Door” Policy we have an open ear for you at any time Growing with us: We live a modern and international corporate culture. You are invited to introduce and unfold - in particular in our innovative and dynamic healthcare environment with a collegial working atmosphere and a lot of design space for your own ideas and your personal development Not only the health of our customers is our heart: therefore, thanks to our health insurance we provide you with additional budget that you can invest in your well-being. Compatibility of job and private: In addition to 30 days of vacation, you can work as it suits you best: in a combination of mobile office and office - for your flexibility in everyday life Extra(s) for you: Our subsidized operating restaurant, Corporate Benefits, own company sickness fund, asset-effective services, etc. .