Die KI-Suchmaschine für Jobs
Group Senior Analyst Quality Applications(m/w/x)
Beschreibung
In this role, you will be the go-to expert for Quality applications, managing their lifecycle and ensuring compliance. Your day-to-day responsibilities will involve collaborating with various teams to enhance processes and drive digital improvements, while also supporting system changes and user training.
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Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
5 - 7 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- •Market-related salary
Familienfreundlichkeit
- •Family values
Weiterbildungsangebote
- •Skills development
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Group Senior Analyst Quality Applications(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will be the go-to expert for Quality applications, managing their lifecycle and ensuring compliance. Your day-to-day responsibilities will involve collaborating with various teams to enhance processes and drive digital improvements, while also supporting system changes and user training.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
5 - 7 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- •Market-related salary
Familienfreundlichkeit
- •Family values
Weiterbildungsangebote
- •Skills development
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.
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