Octapharma
Group Senior Manager R&D Applications(m/w/x)
Vollzeit
Senior
Keine Angabe
Lachen
OC
Octapharma24 Tage
Group Senior Analyst Quality Applications(m/w/x)
Vollzeit
Senior
Keine Angabe
8853 Lachen
Nejo KI-Zusammenfassung
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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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
Bachelor-Abschluss
Berufserfahrung
5–7 Jahre
Deine 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
Veeva QualityDocsVeeva QMSLIMS
Sprachen
Englisch – verhandlungssicher
Deine Vorteile
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.
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