Da Vinci Engineering GmbH
60308 Frankfurt am Main - Deutschland
Ingenieur/in - Elektrotechnik
Arbeit
Teilzeit Vormittag
ab 03.03.2026
Beschreibung
Nothing provides more motivation than success. Da Vinci Engineering is highly committed to ensuring the own employees' success. Become a part of us!
Senior Auditor / R&D Quality Manager (m/f/d)
Stellen-ID: 22169
Standort: Frankfurt am Main
We are searching intelligent and innovative employees. If you are interested in working for a dynamic company with flat hierarchy, we look forward to receiving your application.
Your tasks:
- Plan and conduct clinical project audits, process audits, and su... weiter lesen
Senior Auditor / R&D Quality Manager (m/f/d)
Stellen-ID: 22169
Standort: Frankfurt am Main
We are searching intelligent and innovative employees. If you are interested in working for a dynamic company with flat hierarchy, we look forward to receiving your application.
Your tasks:
- Plan and conduct clinical project audits, process audits, and su... weiter lesen
Nothing provides more motivation than success. Da Vinci Engineering is highly committed to ensuring the own employees' success. Become a part of us!
Senior Auditor / R&D Quality Manager (m/f/d)
Stellen-ID: 22169
Standort: Frankfurt am Main
We are searching intelligent and innovative employees. If you are interested in working for a dynamic company with flat hierarchy, we look forward to receiving your application.
Your tasks:
- Plan and conduct clinical project audits, process audits, and supplier/vendor audits in accordance with GxP and regulatory requirements.
- Develop and maintain risk-based audit plans and study assessment strategies
- Evaluate audit findings, ensure proper documentation, and support CAPA development and follow-up
- Lead and manage quality escalations arising from clinical study activities
- Contribute to the development and maintenance of the Quality Management System, including SOPs, CAPA, deviations, and document control
- Provide quality consultation to Clinical Operations teams on study processes and quality-related topics
- Support qualification and evaluation of clinical service providers such as CROs, laboratories, couriers, and archiving services
- Deliver training on GCP, Good Clinical Laboratory Practice, and other quality-related topics
Your profile:
- University degree in a scientific or technical field such as Life Sciences, Pharmacy, or Medical Technology
- Several years of experience in Quality Management, Clinical Research, or auditing within a GxP/GCP-regulated environment
- Strong knowledge of regulatory requirements for medical devices and pharmaceuticals
- Proven experience in planning, conducting, and following up on internal and external audits
- Solid understanding of CAPA processes, deviation management, and document control systems
- Strong analytical skills and a structured, risk-based approach to quality oversight
- Excellent communication and advisory skills when working with cross-functional teams and external partners
- Very good command of English (written and spoken)
You can expect ...
- Experience in exciting and international projects
- Continuous salary development
- Da Vinci Corporate Benefits
- On-the-job training and language courses
- Appreciation, motivation and commitment
Kontaktdaten für Stellenanzeige
Frau Andrea Cindric
Da Vinci Engineering GmbH
Hauptstätter Straße 149
70178 Stuttgart
+49 711 72240 107
job@davinci.de
Senior Auditor / R&D Quality Manager (m/f/d)
Stellen-ID: 22169
Standort: Frankfurt am Main
We are searching intelligent and innovative employees. If you are interested in working for a dynamic company with flat hierarchy, we look forward to receiving your application.
Your tasks:
- Plan and conduct clinical project audits, process audits, and supplier/vendor audits in accordance with GxP and regulatory requirements.
- Develop and maintain risk-based audit plans and study assessment strategies
- Evaluate audit findings, ensure proper documentation, and support CAPA development and follow-up
- Lead and manage quality escalations arising from clinical study activities
- Contribute to the development and maintenance of the Quality Management System, including SOPs, CAPA, deviations, and document control
- Provide quality consultation to Clinical Operations teams on study processes and quality-related topics
- Support qualification and evaluation of clinical service providers such as CROs, laboratories, couriers, and archiving services
- Deliver training on GCP, Good Clinical Laboratory Practice, and other quality-related topics
Your profile:
- University degree in a scientific or technical field such as Life Sciences, Pharmacy, or Medical Technology
- Several years of experience in Quality Management, Clinical Research, or auditing within a GxP/GCP-regulated environment
- Strong knowledge of regulatory requirements for medical devices and pharmaceuticals
- Proven experience in planning, conducting, and following up on internal and external audits
- Solid understanding of CAPA processes, deviation management, and document control systems
- Strong analytical skills and a structured, risk-based approach to quality oversight
- Excellent communication and advisory skills when working with cross-functional teams and external partners
- Very good command of English (written and spoken)
You can expect ...
- Experience in exciting and international projects
- Continuous salary development
- Da Vinci Corporate Benefits
- On-the-job training and language courses
- Appreciation, motivation and commitment
Kontaktdaten für Stellenanzeige
Frau Andrea Cindric
Da Vinci Engineering GmbH
Hauptstätter Straße 149
70178 Stuttgart
+49 711 72240 107
job@davinci.de
Ref-Nr.: 9685218
Aktualisiert:
03.03.2026
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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