Octapharma
Group Senior Manager R&D Applications(m/w/x)
Full-timeOn-siteSenior
Lachen
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OCOctapharma
Group Senior Analyst Quality Applications(m/w/x)
Lachen
Full-timeOn-siteSenior
Nejo AI Summary
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.
Requirements
- 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
Tasks
- 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
Work Experience
- 5 - 7 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Veeva QualityDocs
- Veeva QMS
- LIMS
Benefits
Competitive Pay
- Market-related salary
Family Support
- Family values
Learning & Development
- Skills development
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Octapharma and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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OCOctapharma
Group Senior Analyst Quality Applications(m/w/x)
Lachen
Full-timeOn-siteSenior
Nejo AI Summary
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.
Requirements
- 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
Tasks
- 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
Work Experience
- 5 - 7 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Veeva QualityDocs
- Veeva QMS
- LIMS
Benefits
Competitive Pay
- Market-related salary
Family Support
- Family values
Learning & Development
- Skills development
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Octapharma and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Octapharma
Industry
Pharmaceuticals
Description
Das Unternehmen ist eines der weltweit größten, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt.
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