Die KI-Suchmaschine für Jobs
BP Regulatory Affairs Manager(m/w/x)
Beschreibung
In this role, you will engage in a variety of tasks, including creating training materials and collaborating with teams and customers. Your focus will be on ensuring compliance with GMP guidelines and supporting quality initiatives across the organization.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Degree in natural science, biotechnology, or comparable
- •Solid quality background with core GxP systems
- •Professional experience in quality or regulatory in pharma manufacturing
- •Professional experience with quality tools in pharmaceutical industry
- •Excellent communication skills in German and English
- •Accurate and detail-oriented mindset
- •Highly skilled in Microsoft Office applications
- •Passionated and motivating attitude
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Author and maintain internal guidance and training documentation
- •Collaborate with global functions, suppliers, and customers to share expertise
- •Review documents for alignment with GMP customer expectations
- •Provide targeted training sessions and participate in global presentations
- •Work closely with the Quality team to align on quality systems
- •Support colleagues in implementing requirements and translating them into solutions
Tools & Technologien
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- •Thirty vacation days per year
- •Company-regulated special leave days
Flexibles Arbeiten
- •Flexible flextime framework
- •Working time account
- •Remote work across Germany
Betriebliche Altersvorsorge
- •Employer-funded retirement plans
Firmenfahrrad
- •Job bike
Öffi Tickets
- •Public transport subsidies
Mitarbeiterrabatte
- •Corporate benefits
Weiterbildungsangebote
- •Freely selectable training sessions
- •Participation in conferences
- •Access to learning platforms
Lockere Unternehmenskultur
- •Diverse and open-minded work environment
- DASGIP Information and Process Technology GmbHVollzeitmit HomeofficeSeniorJülich
- DASGIP Information and Process Technology GmbH
Teamlead Product Support /Manager Technischer Support(m/w/x)
Vollzeitmit HomeofficeManagementJülich - DASGIP Information and Process Technology GmbH
Quality Engineer(m/w/x)
Vollzeitmit HomeofficeJuniorJülich - Stadtwerke Düren GmbH
HR Business Partner(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenDüren - DASGIP Information and Process Technology GmbH
Supplier Quality Engineer(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenJülich
BP Regulatory Affairs Manager(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will engage in a variety of tasks, including creating training materials and collaborating with teams and customers. Your focus will be on ensuring compliance with GMP guidelines and supporting quality initiatives across the organization.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Degree in natural science, biotechnology, or comparable
- •Solid quality background with core GxP systems
- •Professional experience in quality or regulatory in pharma manufacturing
- •Professional experience with quality tools in pharmaceutical industry
- •Excellent communication skills in German and English
- •Accurate and detail-oriented mindset
- •Highly skilled in Microsoft Office applications
- •Passionated and motivating attitude
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Author and maintain internal guidance and training documentation
- •Collaborate with global functions, suppliers, and customers to share expertise
- •Review documents for alignment with GMP customer expectations
- •Provide targeted training sessions and participate in global presentations
- •Work closely with the Quality team to align on quality systems
- •Support colleagues in implementing requirements and translating them into solutions
Tools & Technologien
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- •Thirty vacation days per year
- •Company-regulated special leave days
Flexibles Arbeiten
- •Flexible flextime framework
- •Working time account
- •Remote work across Germany
Betriebliche Altersvorsorge
- •Employer-funded retirement plans
Firmenfahrrad
- •Job bike
Öffi Tickets
- •Public transport subsidies
Mitarbeiterrabatte
- •Corporate benefits
Weiterbildungsangebote
- •Freely selectable training sessions
- •Participation in conferences
- •Access to learning platforms
Lockere Unternehmenskultur
- •Diverse and open-minded work environment
Über das Unternehmen
DASGIP Information and Process Technology GmbH
Branche
Other
Beschreibung
Das Unternehmen bietet Gestaltungsspielraum in der Life-Science Branche und fördert ein wertschätzendes Arbeitsumfeld.
- DASGIP Information and Process Technology GmbH
Head of Global Bioprocess Service(m/w/x)
Vollzeitmit HomeofficeSeniorJülich - DASGIP Information and Process Technology GmbH
Teamlead Product Support /Manager Technischer Support(m/w/x)
Vollzeitmit HomeofficeManagementJülich - DASGIP Information and Process Technology GmbH
Quality Engineer(m/w/x)
Vollzeitmit HomeofficeJuniorJülich - Stadtwerke Düren GmbH
HR Business Partner(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenDüren - DASGIP Information and Process Technology GmbH
Supplier Quality Engineer(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenJülich