Randstad Professional
82377 Penzberg - Deutschland
Compliance-Manager/in
Arbeit
Vollzeit
ab 20.01.2026
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.
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
- Performance-based salary package depending on qualifications and
professional experience
- 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
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
- Performance-based salary package depending on qualifications and
professional experience
- 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
Ref-Nr.: 8648503
Aktualisiert:
24.01.2026
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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