OPROMA

DEIN NÄCHSTER SCHRITT

Compliance Specialist (f/m/d)

comp 82377 Penzberg - Deutschland
Compliance-Manager/in Arbeit Vollzeit ab 07.11.2026
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Beschreibung

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

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Bewerben
Ref-Nr.: 14418209
Aktualisiert: 06.11.2026
Quelle: Bundesagentur für Arbeit
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