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Randstad Professional

Compliance Specialist (f/m/d)

Penzberg, Bayern, Germany

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hirly's read of this role

Seniority
Mid level
Stated salary
€50,000 – €70,000 per year
Country
DE
Work mode
On-site / unstated
First seen by hirly
6 Nov 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

  • 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
Original posting on Randstad Professional's site ↗

Listed on hirly, a job board. hirly is not the employer: Randstad Professional is hiring for this role.

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