Compliance Specialist (f/m/d)

GULP – experts united; Penzberg; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading pharmaceutical company is seeking a Compliance Specialist in Penzberg. This role offers the opportunity for professional growth in an environment with strong support and various benefits. You will be responsible for ensuring GxP compliance and managing documentation across clinical trials.

Leistungen

Extensive social benefits, including Christmas and holiday bonuses

Up to 30 days vacation per year

Option of permanent employment

Qualifikationen

• Several years of work experience in pharmaceutical or biotech industry.
• Good German language skills and fluency in English.

Aufgaben

• Support GxP compliance in clinical trial supply management.
• Establish and maintain inspection readiness for clinical trial activities.
• Optimize processes and workflows regarding GxP documentation.

Kenntnisse

Communication

Knowledge of quality standards (GMP, GCP, GDP)

MS Office applications

Quality management systems

Ausbildung

Completed university degree or similar education with a scientific focus

Jobbeschreibung

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Job Opportunity: Compliance Specialist at Roche

If 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.

Here's what we offer

• Extensive social benefits, including Christmas and holiday bonuses
• Up to 30 days vacation per year
• Option of permanent employment with our business partner
• Support GxP compliance of all activities in clinical trial supply management, drug-related distribution, and storage
• Responsibility for project-related GxP documentation and maintenance of lists
• Operational support and independent performance of operational tasks as a 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)

Your profile

• Completed university degree or 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
• Proficient skills in MS Office applications and quality management systems
• Strong communication skills, good German language skills, and fluency in English