Location: Bulle, Switzerland

Activity rate : 100%

Type of contract: Temporary contract

Start date: 05.01.2026

Duration: 6 months (with possible extension)

As a QA Specialist joining UCB QA team, you will review and approve change management and qualification activities within a Biotech environment. You will assess the impact of changes on lab and manufacturing equipment and provide expert guidance on qualification risk strategies. You will also review key documentation for systems such as MES and DCS to ensure full compliance with QA standards. As a subject matter expert, you will help identify critical data assets and support robust QA methodologies.

Your key responsibilities:

Review and approve changes in accordance with UCB processes
Review and approve defined qualification deliverables such as URS, FRA, Testing evidence, defects, Qualification report, etc.
Ensure through risk base approach the right qualification level ensuring compliance with regulation and UCB processes.
Approve through procedures equipment's qualification reports according to current.
Actively participate to quality strategies for projects.
Coordinate relationships with internal/external customers/stakeholders including CMOs in order to provide efficient follow-up of product related deviations, change controls, investigations, incidents, etc.

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