Computerized System Validation Associate (m/f/d)

• Collaborate with cross-functional teams including IT, Quality Assurance, and Operations to ensure documentation and validation of systems according to internal procedures
• Ensure compliance with internal and external regulatory requirements and guidelines
• Maintain the inventory of software applications
• Conduct periodic reviews and improve existing documentation of systems
• Stay up to date with industry trends, regulatory changes, and best practices in computerized system validation

• Any prior experience in Computerized System Validation within a regulated industry (e.g., pharmaceuticals, biotechnology, medical devices) or basic knowledge of regulatory requirements and guidelines, or certification (FDA 21 CFR Part 11, GxP, etc.) would be beneficial
• MS Office proficiency and good general computer skills
• Good organizational skills, be self-motivated and have a detail-orientated approach
• Good communication skills in written and spoken English. German skills are a plus

• Central Location
• Employee Discounts
• Flexible Hours
• International Environment
• Onboarding
• Workplace Well-Being
• Minimum Salary

StepStone