CSV Manager (m/f/x) | Medical Devices | Munich Area In this exciting CSV role, you will be the main contact person for questions and issues around Computer System Validation and Process Validation. As part of their innovative medical devices team, you will contribute to developing and optimizing systems that enhance the quality and safety of medical products and services.
Ensure compliance and maintain the validated state of all GxP-relevant computerized systems across various departments, in alignment with current regulatory requirements (e.g., Prepare and execute periodic reviews to confirm ongoing system compliance and performance
Collaborate with and advise system owners, end-users, and project leads on Computerized System Validation (CSV) strategies and best practices
Ensure data integrity and regulatory compliance
Oversee (partial) project management tasks, including system administration and coordination across validation initiatives
Studies in Computer Sciences, Business Informatics, Quality Management or a comparable field/qualification
~3+ years of practical experience in Computer System Validation (CSV), ideally in the medical technology industry
~ Experience in the validation and implementation of IT systems and software solutions
~ Fluent German and good English skills, both written and spoken
~ Flat hierarchies with room for your own ideas
Hybrid working environment
Company pension plan
Team events and different sports
Corporate benefits
Our client is a leading German medical technology manufacturer that creates advanced medical devices. Their products are known for their reliability and innovation, and their team of experts includes engineers, scientists, and medical professionals who work together to design and develop new technologies.