Compliance Specialist (f/m/d)

• Randstad is one of the world's leading talent companies with the
• ambition to be the world's most equitable and specialized talent
• company. Through our "partner for talent" corporate strategy, we find,
• develop and connect specialized talents with companies - worldwide,
• locally and always at a high speed. We build high-quality, diverse,
• and agile teams, while individuals can enjoy a rewarding career path
• with equitable opportunities.
• Randstad Professional is one of Randstad's four specializations
• and focuses on the placement of specialists and managers in the
• future-oriented sectors of IT, Engineering, Life Science and Office.
• 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: We offer 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