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DEIN NÄCHSTER SCHRITT

Compliance Specialist (f/m/d)

comp 82377 Penzberg - Deutschland
Compliance-Manager/in Arbeit Vollzeit ab 16.10.2026
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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,...
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Arbeitgeber: Randstad Professional

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.



Good jobs with fair wages are rare, you say? Well, today is your lucky

day! We have 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
Bewerbungsinfos und Link zur BA ansehen
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Ref-Nr.: 13811995
Aktualisiert: 16.10.2026
Quelle: Bundesagentur für Arbeit
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