Quality Associate QMS (w / m / d), 80%
Duration : ASAP - 31 / 12 / 2026 + possibility of an extension
Location : Solothurn, Switzerland
Workload : 80%, flexible day off during the week
Key Responsibilities
- Support Quality Management System activities at the Solothurn site
- Manage and maintain key QMS processes such as :
o Change Control Management
o CAPA Management
o Deviations
Contribute to site governance initiativesCollaborate with global colleagues (especially US teams) and local stakeholdersDrive continuous improvement initiatives and propose practical solutionsWork independently while engaging proactively with cross-functional teamsKey Requirements
3-5 years of experience in Quality within the pharmaceutical industryStrong background in Quality Management SystemsSolid understanding of GMP regulationsExperience with global quality processes and cross-functional interactionsAbility to work proactively, take initiative, and connect with internal stakeholdersTrackWise experience is a plusFluent in English; German is an advantageEU passport or Swiss CitizenshipSThree_Germany is acting as an Employment Business in relation to this vacancy.