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Compliance Specialist (f/m/d)

Randstad Professionalpenzberg, Bayern🇩🇪GermanyPosted 4 Mar 2026

Why This Role Stands Out

Advance your career with a hybrid Compliance Specialist role at a leading pharmaceutical company, offering professional growth, a supportive environment, and above-average compensation. You will thrive here if you have a scientific background, experience in the pharmaceutical industry, and a keen eye for quality standards and regulatory requirements. Seize this opportunity to contribute to impactful work and further develop your expertise.

Quick Overview

Seniority
Mid Senior
Employment type
Full Time
Work mode
Hybrid
Location
penzberg, Bayern, Germany
GCPClinical TrialsCompliance

Job Description

Good jobs with fair wages are rare, you say? Well, today is your lucky day! Our subsidiary Randstad professional solutions has a vacant position as compliance specialist  at the pharmaceutical company  Roche  in Penzberg . Tariff-based wages, care by a company medical center, and employee discounts - all advantages that you can count on with Randstad. It's best to apply online right away and secure this job! 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 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
  • Performance-based salary package depending on qualifications and professional experience
  • Up to 30 days vacation per year
  • Extensive social benefits, incl. Christmas and holiday bonuses
  • Definition of career goals
  • Candid corporate culture

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