Do you want to progress professionally and desire a job where you are challenged and supported? With regular working hours, good benefits, and diverse opportunities for further development? Then you've come to the right place: Our subsidiary Randstad professional solutions offers an attractive position as a compliance specialist at the pharmaceutical company Roche in Penzberg. Apply online right away. We value equal opportunities and welcome applications from people with disabilities.
* 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
* Extensive social benefits, incl. Christmas and holiday bonuses
* Up to 30 days vacation per year
* Option of permanent employment with our business partner