Time for change – time for a new job! You are acompliance specialist and looking fora new professional challenge? Then stop searching! We offer the jobyou are looking for: Our subsidiary Randstad professional solutionsoffers a secure job, fair compensation and exciting new tasks atthe attractive pharmaceutical companyRoche inPenzberg. Apply online now! We welcomeapplications from all suitably qualified persons regardless of anydisabilities.
* Support GxP complianceof all activities in the clinical trial supply management,drug-related distribution and storage
* Responsibility for the project-related GxP documentationand maintenance of lists
* Operational supportand independent performance of operational tasks as process expertin the IMP GxP Compliance Team across diverse clinical trials andR&D Programs (e.g. Batch Record Reviews and TMFFiling)
* Establish and maintain inspectionreadiness for clinical trial supply activities and support inpreparing, accompanying and following up on audits andinspections
* Optimization of processes andworkflows (e.g. support in the creation and review of SOPs andother GxP related documents)
* Completed university degree or a similar education with ascientific focus
* Several years of workexperience in the pharmaceutical or biotech industry
* Knowledge of quality standards (GMP, GCP, GDP) andregulatory requirements in an international environment
* Profound skills in the use of MS Office applications anda quality management system
* Strongcommunications skills, good German language skills and fluency inEnglish
* Option ofpermanent employment with our business partner
* Extensive social benefits, incl. Christmas and holiday bonuses
* Up to 30 days vacation per year