Creation, maintenance and further development of requirements and guidelines for validation management, including qualification, process, computer and method validation
Technical review, approval and support of validation activities in development and production
Training employees on validation-related topics
Conducting internal audits and actively supporting inspections and audits as a subject matter expert
Participation in CAPA management, including initiation, implementation and follow-up of corrective and preventive actions
Requirements
Degree in engineering or a natural science
Several years of experience in qualification and validation within a GMP-regulated environment, e.g., pharmaceuticals or medical technology
Very good (C1) German and English skills
Structured working style, strong documentation proficiency and a confident manner
Benefits
Scope for initiative in a stable, growth-oriented environment
Flat hierarchies, short decision-making paths and collegial collaboration
Flexible working hours with a home office option
Attractive compensation, company pension scheme and additional benefits such as Hansefit and bike leasing