Compliance specialist in Penzberg wanted! Are you interested? With the many benefits at our subsidiary Randstad professional solutions, such as competitive compensation and retirement plans, you certainly can't say "no". If that's the case, apply today for the available position at the pharmaceutical company Roche! Here's another advantage: Applying with us is absolutely straightforward, requiring only your name, email address, and resume. People with disabilities are warmly welcomed at our company.
Das dürfen Sie erwarten
* Extensive social benefits, incl. Christmas and holiday bonuses
* Up to 30 days vacation per year
* Option of permanent employment with our business partner
* Free online courses, e.g. several language courses
Ihre Aufgaben
* 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)
Unsere Anforderungen
* 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