Close
Application for:

Group Senior Analyst Quality Applications

Group Senior Analyst Quality Applications

Reference: BBBH28380
Date posted: 28/01/2026
Job details
Specialism
Quality Assurance
Expertise
QP
Location
Schwyz, Switzerland
Job type
Permanent
Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

Description

Powering quality systems that keep global operations compliant and connected.

We are seeking a Senior Analyst for Quality Applications to join a high‑performing team within a global life sciences organization. The role is responsible for overseeing and enhancing enterprise-wide quality systems within a regulated GxP environment, ensuring compliance, streamlined processes, and strong user experience.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Act as subject matter expert for global Quality applications (e.g., Veeva QualityDocs, Veeva QMS, LIMS) and related systems.
  • Manage the application lifecycle, including configuration, access models, documentation, validation readiness, and performance monitoring.
  • Collect, analyze, and structure business requirements from Corporate Quality, local sites, and Process Owners, translating them into solution designs and change requests.
  • Coordinate and support system changes and releases, including solution design, testing, validation, documentation, and user acceptance testing.
  • Serve as escalation point for functional support incidents and problem management, ensuring timely resolution with internal IT teams and external vendors.
  • Collaborate closely with Quality, IT Validation, Architecture, and external partners to enable compliant, efficient, and harmonized Quality processes.

Key Skills and Requirements:

  • Bachelor’s degree in IT, Business Informatics, Life Sciences, or a comparable qualification.
  • 5-7 years of hands-on experience working 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

For more information, please contact Jacob Tutt.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

Apply for this role
Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

Related jobs

Discover our latest opportunities in life sciences and apply now.

View all jobs

Get in touch

Have questions or need support? Our team is here to help, contact us to discuss your hiring needs or career goals today.

Contact us