Randstad Professional
82377 Penzberg - Deutschland
Compliance-Manager/in
Arbeit
Vollzeit
ab 27.02.2026
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 sp... weiter lesen
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 sp... weiter lesen
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
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
Ref-Nr.: 9226334
Aktualisiert:
02.03.2026
Quelle: Bundesagentur für Arbeit
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
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