Good jobs with fair wages are rare, you say? Well, today is your lucky day! We have a vacant position as compliance specialist at the pharmaceutical company Roche in Penzberg. Applications from individuals with disabilities are warmly welcome.
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 various clinical trials and R&D Programs (eg 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 (eg 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
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Compliance Specialist (f/m/d) in Penzberg Arbeitgeber: GULP Information Services GmbH
Als Compliance Specialist (m/w/d) in unserem Standort Kassel profitieren Sie von einer dynamischen Arbeitsumgebung, die Präzision und Qualität in den Mittelpunkt stellt. Wir bieten Ihnen nicht nur ein attraktives Gehalt und umfassende Sozialleistungen, sondern auch zahlreiche Möglichkeiten zur beruflichen Weiterentwicklung in einem innovativen High-Tech-Umfeld. Unsere offene Unternehmenskultur fördert Teamarbeit und den Austausch von Ideen, sodass Sie als wertvolles Mitglied unseres Teams wachsen können.
Kontaktdaten:
GULP Information Services GmbH Recruiting-Team
