Posted 6 days ago
Description
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
- 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
