* Life Sciences - Quality Management * Wallis * Contracting * Vollzeit * Immediately - 31.07.2026 * Quality Assurance, GMP, Drug Manufacturing Location: Visp Contract duration: 31.07.2026 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 * Act as point of contact for Drug Product QA related questions, topics and complaints from customers related to the manufacturing operations * 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. * Assess, review and approve quality records and release files/dossiers e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions, complaints, APR/PQRs, in line with current local SOPs. 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