Die KI-Suchmaschine für Jobs
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Beschreibung
As a GCP/GCLP Auditor in the Senior Manager role, you will be at the forefront of ensuring clinical quality by conducting audits, creating essential documentation, and providing training. Your expertise will help maintain inspection readiness and support clinical functions in managing quality deviations.
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Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree in natural sciences or related field
- •5+ years of experience in life sciences companies
- •Experience in general audit execution and investigator site auditing
- •Background in quality management within clinical trial environment
- •Strong knowledge of GCP regulatory requirements
- •Operational clinical trial management experience
- •Comfortable working in a global and matrixed business environment
- •Excellent interdisciplinary and intercultural communication skills in English and preferably German
- •High degree of initiative, analytical reasoning, and strong problem solving skills
- •Structured, reliable, and foresighted task approach
- •Elevated level of individual responsibility, enthusiasm, and strong social skills
Ausbildung
Berufserfahrung
5 Jahre
Aufgaben
- •Conduct internal and external audits
- •Create and review quality-related documents
- •Support implementation of inspection readiness concepts
- •Prepare for and host regulatory inspections
- •Organize and conduct quality-related training
- •Provide quality guidance for protocol and process deviations
- •Assist with change controls and root cause analyses
- •Define CAPA for deviations and inspection observations
- •Support maintenance of the clinical (e)QMS
- •Define and interpret quality metrics and trending reports
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Firmenfahrrad
- •Job bike
Öffi Tickets
- •Job ticket
Gesundheits- & Fitnessangebote
- •Health programs
Kinderbetreuung
- •Childcare benefits
Sonstige Zulagen
- •Relocation allowance
Team Events & Ausflüge
- •Company summer and winter events
- Immatics Biotechnologies GmbHVollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München
- Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
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Qualified Person(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenHerrenberg - Immatics Biotechnologies GmbH
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VollzeitBefristeter Vertragmit HomeofficeBerufserfahrenRastatt, Hechingen
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
As a GCP/GCLP Auditor in the Senior Manager role, you will be at the forefront of ensuring clinical quality by conducting audits, creating essential documentation, and providing training. Your expertise will help maintain inspection readiness and support clinical functions in managing quality deviations.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree in natural sciences or related field
- •5+ years of experience in life sciences companies
- •Experience in general audit execution and investigator site auditing
- •Background in quality management within clinical trial environment
- •Strong knowledge of GCP regulatory requirements
- •Operational clinical trial management experience
- •Comfortable working in a global and matrixed business environment
- •Excellent interdisciplinary and intercultural communication skills in English and preferably German
- •High degree of initiative, analytical reasoning, and strong problem solving skills
- •Structured, reliable, and foresighted task approach
- •Elevated level of individual responsibility, enthusiasm, and strong social skills
Ausbildung
Berufserfahrung
5 Jahre
Aufgaben
- •Conduct internal and external audits
- •Create and review quality-related documents
- •Support implementation of inspection readiness concepts
- •Prepare for and host regulatory inspections
- •Organize and conduct quality-related training
- •Provide quality guidance for protocol and process deviations
- •Assist with change controls and root cause analyses
- •Define CAPA for deviations and inspection observations
- •Support maintenance of the clinical (e)QMS
- •Define and interpret quality metrics and trending reports
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Firmenfahrrad
- •Job bike
Öffi Tickets
- •Job ticket
Gesundheits- & Fitnessangebote
- •Health programs
Kinderbetreuung
- •Childcare benefits
Sonstige Zulagen
- •Relocation allowance
Team Events & Ausflüge
- •Company summer and winter events
Über das Unternehmen
Immatics Biotechnologies GmbH
Branche
Healthcare
Beschreibung
The company combines the discovery of true targets for cancer immunotherapies with the development of T cell receptors to enable robust T cell responses against cancer.
- Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München - Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
Vollzeit/Teilzeitmit HomeofficeManagementTübingen, München - Perrigo Company
Qualified Person(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenHerrenberg - Immatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenTübingen, München - Maquet Cardiopulmonary GmbH
External Audit Specialist - Quality Assurance(m/w/x)
VollzeitBefristeter Vertragmit HomeofficeBerufserfahrenRastatt, Hechingen