Global Senior Analyst, Quality Applications (Veeva/LIMS)

Octapharma-Plasma; Lachen; On-site; CHF 90,000 - 130,000; Full time

Job summary

Octapharma is seeking a Group Senior Analyst Quality Applications in Lachen, CH, to serve as a subject matter expert for global Quality applications such as Veeva QualityDocs, Veeva QMS, and LIMS. You will own configuration, validation readiness, and release coordination in a GxP environment.

The ideal candidate has 5–7 years of hands-on Quality apps experience in pharma, strong requirements management skills, and fluency in English.

Qualifications

• Bachelor’s degree in IT, Business Informatics, Life Sciences, or equivalent.
• 5–7 years’ hands‑on experience with Quality applications in the pharmaceutical or life‑sciences industry.
• Strong practical experience with Quality systems such as Veeva QualityDocs, Veeva QMS, LIMS or equivalent regulated platforms.
• 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, with the ability to translate business needs into pragmatic system solutions.
• Structured, detail‑oriented working style with excellent communication and stakeholder management skills.
• High independence, ownership, and initiative, paired with a collaborative mindset.
• Fluency in English (spoken and written); other languages are a plus.

Responsibilities

• Act as subject matter expert for global Quality applications (e.g. Veeva QualityDocs, Veeva QMS, LIMS) ensuring compliance and user‑centric design.
• Manage application lifecycle including configuration, access models, documentation, and validation readiness.
• Translate business requirements into clear solution designs and change requests.
• Coordinate and support system changes and releases including testing and validation documentation.
• Serve as escalation point for support, incidents, and problem management with IT and vendors.
• Collaborate with Quality, IT, Validation, Architecture, and external partners to harmonize processes.
• Drive continuous improvement and digitalization with data‑driven enhancements.
• Build a global network of key users and site administrators, delivering training and roadmaps.

Skills

GxP experience

Veeva QMS/QualityDocs

LIMS

Requirements management

Stakeholder management

English fluency

Education

Bachelor’s degree in IT or Life Sciences

Tools

Veeva QualityDocs

Veeva QMS

LIMS

Job description

Octapharma is seeking a Group Senior Analyst Quality Applications in Lachen, CH, to serve as a subject matter expert for global Quality applications such as Veeva QualityDocs, Veeva QMS, and LIMS. You will own configuration, validation readiness, and release coordination in a GxP environment.

The ideal candidate has 5–7 years of hands-on Quality apps experience in pharma, strong requirements management skills, and fluency in English.