QA Specialist (w/m/d)
Location: Visp, Switzerland
Duration: 02/02/2026 to 31/07/2026
Key responsibilities
* Act as QA representative in Project teams and represent QA in meetings
* Act as QA contact for specific topics and realize the interface for DRs and CRs
* Support and approve risk assessments or regulatory specific risk or gap assessments.
* Review and release product specific documentation such as process descriptions and workflows, recipes, manufacturing protocols, transfer documents, test plans, parameter lists, etc.
* Represent Drug Product QA topics during regulatory inspections.
* Support continuous improvement programs to establish an effective Quality Management System for Visp DPS.
* Represent Quality Assurance in cross-functional teams, establish and maintain interfaces with the Manufacturing teams, QC, Support Functions, Project- and Site Engineering project / technology transfer to effectively execute tasks related to Drug Product processes.
Key requirements
* University degree or equivalent in Chemistry / Biology / Biotechnology or a related field
* Long-term experience working in the GMP environment of the pharmaceutical industry
* Experience working in a QA department Drug Product
* English language skills are required, German language is an advantage
SThree_Germany is acting as an Employment Business in relation to this vacancy.