Octapharma
Group Senior Manager R&D Applications(m/w/x)
Vollzeitnur vor OrtSenior
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OCOctapharma
Group Senior Analyst Quality Applications(m/w/x)
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VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Application lifecycle management and validation readiness for GxP-regulated systems at global human protein developer. 5-7 years experience with Veeva QMS, LIMS, or similar quality systems in pharma/life-science required. International team collaboration.
Anforderungen
- Bachelor’s degree in IT, Business Informatics, Life Sciences, or comparable qualification
- 5–7 years of hands-on experience with Quality applications in pharmaceutical or life-science industry
- Strong practical experience with Quality systems such as Veeva QualityDocs, Veeva QMS, LIMS or equivalent
- Solid understanding of GxP requirements, validation principles, and regulated system environments
- Proven experience in requirements management, change coordination, testing, and validation
- Strong analytical and conceptual skills to translate business needs into pragmatic system solutions
- Structured, detail-oriented working style with excellent communication and stakeholder-management skills
- High level of independence, ownership, and initiative with a collaborative and service-oriented mindset
- Fluency in English (spoken and written); additional languages are an asset
Aufgaben
- Act as a subject matter expert for global Quality applications
- Manage the application lifecycle, including configuration and access models
- Ensure documentation and validation readiness in a GxP-regulated environment
- Collect and analyze business requirements from Corporate Quality and local sites
- Translate business requirements into clear solution designs and change requests
- Coordinate system changes and releases, including testing and validation documentation
- Serve as an escalation point for functional support and problem management
- Collaborate with Quality, IT, Validation, and external partners for harmonized processes
- Drive continuous improvement and digitalization through user feedback and best practices
- Build and maintain a global key-user and site administrator network
Berufserfahrung
- 5 - 7 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Veeva QualityDocs
- Veeva QMS
- LIMS
Benefits
Attraktive Vergütung
- Market-related salary
Familienfreundlichkeit
- Family values
Weiterbildungsangebote
- Skills development
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Octapharma erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- Octapharma
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OCOctapharma
Group Senior Analyst Quality Applications(m/w/x)
Lachen
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Application lifecycle management and validation readiness for GxP-regulated systems at global human protein developer. 5-7 years experience with Veeva QMS, LIMS, or similar quality systems in pharma/life-science required. International team collaboration.
Anforderungen
- Bachelor’s degree in IT, Business Informatics, Life Sciences, or comparable qualification
- 5–7 years of hands-on experience with Quality applications in pharmaceutical or life-science industry
- Strong practical experience with Quality systems such as Veeva QualityDocs, Veeva QMS, LIMS or equivalent
- Solid understanding of GxP requirements, validation principles, and regulated system environments
- Proven experience in requirements management, change coordination, testing, and validation
- Strong analytical and conceptual skills to translate business needs into pragmatic system solutions
- Structured, detail-oriented working style with excellent communication and stakeholder-management skills
- High level of independence, ownership, and initiative with a collaborative and service-oriented mindset
- Fluency in English (spoken and written); additional languages are an asset
Aufgaben
- Act as a subject matter expert for global Quality applications
- Manage the application lifecycle, including configuration and access models
- Ensure documentation and validation readiness in a GxP-regulated environment
- Collect and analyze business requirements from Corporate Quality and local sites
- Translate business requirements into clear solution designs and change requests
- Coordinate system changes and releases, including testing and validation documentation
- Serve as an escalation point for functional support and problem management
- Collaborate with Quality, IT, Validation, and external partners for harmonized processes
- Drive continuous improvement and digitalization through user feedback and best practices
- Build and maintain a global key-user and site administrator network
Berufserfahrung
- 5 - 7 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Veeva QualityDocs
- Veeva QMS
- LIMS
Benefits
Attraktive Vergütung
- Market-related salary
Familienfreundlichkeit
- Family values
Weiterbildungsangebote
- Skills development
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Octapharma erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
Octapharma
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist eines der weltweit größten, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt.
Noch nicht perfekt?
- Octapharma
Group Senior Manager R&D Applications(m/w/x)
Vollzeitnur vor OrtSeniorLachen - Octapharma
Group Associate Expert R&D Applications(m/w/x)
Vollzeitnur vor OrtBerufserfahrenLachen - Octapharma
Group Senior Expert HRIS(m/w/x)
Vollzeitnur vor OrtSeniorLachen - Octapharma
Group Associate Engineer MS 365(m/w/x)
Vollzeitnur vor OrtBerufserfahrenLachen - Tecan Trading AG
Senior IT Data Analyst(m/w/x)
Vollzeitnur vor OrtSeniorMännedorf