Regulatory Compliance Jobs in Rheinland-Pfalz
1 - 15 von 26
Suchergebnisse - Regulatory Compliance Jobs in Rheinland-Pfalz
JT International Germany GmbH-Trier
challenging environment. Flexible working concepts, diverse development opportunities and international career paths are part of our everyday life.
To strengthen our team in the area of SRA, we are looking for a
Material Compliance Manager – Regulatory...
stepstone.de -
Michael Page-Trier
Ce poste est basé au LuxembourgLead and shape compliance in a well-established, growing private in strategic decision-making within a professional teamÀ propos de notre clientOur client is a well-established private bank, known for its tailored...
1 ähnliche Jobs: Saarbrücken
JT International Germany GmbH-Trier
Who are we?
JTI is a leading international tobacco company with locations in more than 130 countries and world-famous brands such as Winston, Camel and American Spirit. With our brands Nordic Spirit, Logic and Ploom, we also focus on growth through...
Michael Page-Trier
Ce poste est basé au LuxembourgBuild a career in regulatory complianceAlign group policies with European and local regulationsÀ propos de notre clientOur client is a financial holding company that controls a range of financial institutions...
1 ähnliche Jobs: Saarbrücken
Ryanair Ltd.-Hahn
regulatory and customer requirements.
• Carrying out independent quality audits of the Facilities, Procedures, Vendors and Airworthiness Standards of the organisation in accordance with an audit programme devised by the Compliance Monitoring Manager...
appcast.io -
Michael Page-Trier
Ce poste est basé au LuxembourgJoin a growing multi-cultural compliance Private Bank with solid presence in Luxembourg.À propos de notre clientThis opportunity is with a well-established bank, that has a solid presence in the financial services...
BioNTech SE-Mainz
and continuously improving the global end-to-end Source-to-Pay (S2P) process within BioNTech. The GPO ensures alignment with business objectives, regulatory compliance, and operational excellence while driving standardization, technical innovation, and efficiency...
Eli Lilly and Company-Alzey
the Alzey site. Responsibilities will include but are not limited to: Ensuring regulatory/site/corporate HSE compliance, development of HSE systems/processes/programs, development of the HSE staff, enabling operational excellence, and establishing...
appcast.io -
BioNTech SE-Mainz
the network. The Site Head will also be responsible for ensuring compliance with all regulatory requirements and for maintaining a safe and efficient work environment.
• Lead and manage the Clinical production team, including production, site...
JT International Germany GmbH Karriere-Trier
Who are we?
JTI is a leading international tobacco company with locations in more than 130 countries and world-famous brands such as Winston, Camel and American Spirit. With our brands Nordic Spirit, Logic and Ploom, we also focus on growth through...
BioNTech SE-Mainz
R&D and the future commercial site. The Site Head will also be responsible for ensuring compliance with all regulatory requirements and for maintaining a safe and efficient work environment.
• Lead and manage the Clinical production team, including...
Aktiv Personal-Service GmbH - Mainz-Ingelheim am Rhein
sind Sie für ein vielfältiges und umfangreiches Aufgabengebiet zuständig.
Gesucht wird ab sofort für 6 Monate.
Vergütung: ab 5.000,00€ mtl.
Zur Position:
Tasks:
• Ensure compliance to country regulatory requirements.
• Contribute to the implementation and the maintenance...
jobninja.com -
Boehringer Ingelheim GmbH-Ingelheim am Rhein
focused post-authorisation studies.
• Interpret clinical trial safety data for clinical trial reports and submission documents.
• Review and provide medical-scientific input to regulatory documents (e.g. PSURs, DSURs, RMPs, Clinical Overview Statements...
appcast.io -
Boehringer Ingelheim GmbH-Ingelheim am Rhein
Affairs to develop safety-focused post-authorization studies
• Interpret clinical trial safety data for clinical trial reports and submission documents
• Review and provide medical-scientific input to regulatory documents (e.g. IBs, PSURs, DSURs, RMPs...
appcast.io -
Boehringer Ingelheim GmbH-Ingelheim am Rhein
focused post-authorisation studies.
• Interpret clinical trial safety data for clinical trial reports and submission documents.
• Review and provide medical-scientific input to regulatory documents (e.g. IBs, PSURs, DSURs, RMPs, Clinical Overview...
appcast.io -
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