Regulatory Affairs Specialist - Tuttlingen, Deutschland - Clearstone GmbH
Beschreibung
VERTRAGSART- Permanent- BESCHÄFTIGUNGSART- Vollzeit- BRANCHE- Pharma & Health- FÄHIGKEITEN- Alle- BERUFSFELD- Projektmanagement/Führungskräfte, Regulatory Affairs (Life Science)- GEHALTSARTEN- Jährlich- GEHALT- Verhandelbar- JOB-ID- 33137Stellenbeschreibung:
Our client is a world leading Pharmaceutical company, for their Munich office they're currently looking for a:
Regulatory Affairs Specialist - Munich
This role is integral to our Regulatory Affairs department, specifically catering to the European Market.
We seek a meticulous professional to oversee all regulatory affairs and quality assurance endeavors, ensuring adherence to local and international regulatory standards.
Responsibilities:
- Establish and implement a robust quality management system within the European Regulatory Affairs (ERA) domain.
- Identify the necessity for best practices, processes, SOPs, tools, and training sessions, facilitating the development of systemic processes.
- Collaborate with stakeholders and internal teams to ensure regulatory compliance across the product lifecycle.
- Provide comprehensive training and guidance to the team on regulatory and qualityrelated matters.
- Engage in continuous improvement initiatives to bolster compliance and streamline processes.
- Strategically plan ERA projects and systematically track their progress.
- Offer operational support for regulatory submissions and related tasks as required.
Requirements:
- Demonstrated aptitude for learning and adaptation.
- Proficient in project management, with a proven track record of working efficiently under pressure.
- Possess a positive demeanor and foster a collaborative team spirit.
- Excellent interpersonal and communication skills.
- Bachelor's degree or higher, preferably in pharmaceutics.
- Minimum of 7 years of relevant work experience in regulatory affairs or GxP quality assurance.
- Robbert Roos
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