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Zuletzt aktualisiert: vor 14 Stunden
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Senior Auditor Quality Assurance Manager (m / f / x)

Senior Auditor Quality Assurance Manager (m / f / x)

SciProBaden-Württemberg, Germany, Germany
Senior Auditor Quality Assurance Manager (m / f / x) || Hessen || Medical Devices.Lead audits for clinical trials and medical products to ensure compliance with GxP and regulatory standards.Develop and...Mehr anzeigenZuletzt aktualisiert: vor 21 Tagen
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Information Technology Governance Manager

Information Technology Governance Manager

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In this high-impact role, you will take ownership of the.IT, information security, and enterprise risk.IT governance strategy aligns with internal controls, German regulations, and security framewo...Mehr anzeigenZuletzt aktualisiert: vor 13 Tagen
Security Expert (m / w / d)

Security Expert (m / w / d)

HäfeleNagold
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Prüfer ­­ / ­­ Prüfungsgruppenleiter ­­ / ­­ Prüfungsleiter

Prüfer ­­ / ­­ Prüfungsgruppenleiter ­­ / ­­ Prüfungsleiter

vbw Verband baden-württembergischer Wohnungs- und Immobilienunternehmen e.V.Baden-Württemberg, DE
Wir sind der genossenschaftliche Prüfungs- und Interessenverband der rund 300 Wohnungs- und Immobilien­unternehmen in Baden-Württemberg, mit Sitz in Stuttgart. Zur Unterstützung und Erweiterung unse...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Interne : r Auditor : in

Interne : r Auditor : in

JCWStuttgart Region, Germany
Wir suchen im Auftrag einer großen Bank einen Revisor (m / w / d) für das Risikomanagement.Die Stelle bietet die beratende und prüfende Tätigkeit für die Fachbereiche sowie die Überwachung von Maßnahme...Mehr anzeigenZuletzt aktualisiert: vor 2 Tagen
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Supply Chain Quality Engineer - PCA (m / f / d)

Supply Chain Quality Engineer - PCA (m / f / d)

Advantest Europe GmbHHolzgerlingen
Advantest - We enable tomorrowʻs technology.IoT, 5G and Artificial Intelligence.More than half of all the microchips produced worldwide first pass through our hands.As t...Mehr anzeigenZuletzt aktualisiert: vor 14 Stunden
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Senior Auditor Quality Assurance Manager (m / f / x)

Senior Auditor Quality Assurance Manager (m / f / x)

SciProBaden-Württemberg, Germany, Germany
Vor 21 Tagen
Stellenbeschreibung

Senior Auditor Quality Assurance Manager (m / f / x) || Hessen || Medical Devices

Responsibilities :

  • Lead audits for clinical trials and medical products to ensure compliance with GxP and regulatory standards.
  • Develop and implement audit plans based on risk assessments and conduct internal process and vendor audits.
  • Address and escalate serious clinical trial violations, ensuring timely resolution.
  • Contribute to the development and maintenance of the Quality Management System (QMS), focusing on document management, CAPA, deviations, and SOPs.
  • Advise the Clinical Operations team on CAPA management and quality-related issues.
  • Provide independent consultation on GCP-related and quality issues within clinical research.
  • Support the qualification process for clinical development suppliers and lead supplier audits.
  • Train employees on best practices in GCP, GCLP, pharmacovigilance, and clinical trial regulations.
  • Coordinate inspections and audits by regulatory authorities and ensure readiness for external audits.
  • Manage CAPA actions from inspections and support regulatory compliance within R&D

Requirements :

  • Master’s degree in Natural Sciences, Pharmacy, Medicine, or a related field.
  • At least 8 years of experience as a QA Auditor, preferably in clinical research or the medical device industry.
  • Strong knowledge of GxP guidelines, clinical trial processes, and relevant regulatory standards.
  • Experience conducting audits, inspections, and managing compliance.
  • Excellent analytical skills, with the ability to assess complex data and identify risks and trends.
  • Independent, organized, and able to work effectively with cross-functional teams.
  • Strong communication skills and the ability to collaborate internationally.
  • Willingness to travel (approx. 20% of the time).
  • Fluency in English; German is a plus.

    • About the Client :

    This company offers a great working environment with a global perspective and the opportunity to work in an international team. The flexible hybrid model allows you to work 2 days in the office and 3 days remotely. With an average employee tenure of over 8 years, the company provides long-term stability and growth opportunities. In addition to a competitive salary, employees enjoy attractive benefits such as Wellpass, Jobticket, Jobbike, 39 vacation days, a pension plan, and childcare support.

    If you're passionate about driving clinical trials forward in the field of medical devices, with a strong emphasis on cross-functional leadership, efficiency, and quality compliance, we encourage you to apply.

    I´m looking forward to seeing your application!

    Contact details :

    E-Mail : [email protected]

    Tel : 089 26 20 09 25