Compliance Specialist (f/m/d)

• Support GxP compliance of all activities in the clinical trial supply management, drug-related distribution and storage
• Responsibility for the project-related GxP documentation and maintenance of lists
• Operational support and independent performance of operational tasks as process expert in the IMP GxP Compliance Team across diverse clinical trials and R&D Programs (e.g. Batch Record Reviews and TMF Filing)
• Establish and maintain inspection readiness for clinical trial supply activities and support in preparing, accompanying and following up on audits and inspections
• Optimization of processes and workflows (e.g. support in the creation and review of SOPs and other GxP related documents)

• Completed university degree or a similar education with a scientific focus
• Several years of work experience in the pharmaceutical or biotech industry
• Knowledge of quality standards (GMP, GCP, GDP) and regulatory requirements in an international environment
• Profound skills in the use of MS Office applications and a quality management system
• Strong communications skills, good German language skills and fluency in English

Das dürfen Sie erwarten

• Above-average salary
• Extensive social benefits, incl. Christmas and holiday bonuses
• Up to 30 days vacation per year
• Company pension scheme contribution after the end of the probationary period
• A wide range of employee benefits/perks