Manager Validierung managing validation processes in a growing medical technology company in Freiburg, ensuring compliance with regulatory requirements and continuous improvement of methods.
Responsibilities
Developing, maintaining and improving requirements for validation management, including qualification, process, computerized system and method validation
Technical review, approval and oversight 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
Participating in CAPA management, including initiating, implementing and tracking corrective and preventive actions
Requirements
Degree in engineering or natural sciences
Several years of experience in qualification and validation within a GMP-regulated environment, e.g., pharmaceuticals or medical technology
Fluent German and English (C1 level)
Structured working style, high level of documentation accuracy and confident demeanor
Benefits
Opportunity to shape your role in a stable, growth-oriented environment
Flat hierarchies, short decision-making processes and collegial collaboration
Flexible working hours with a home office option
Attractive compensation, company pension scheme and additional benefits such as Hansefit and bicycle leasing
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