Job description: For our client in the pharmaceutical industry based in Visp, we are looking for a Quality Engineer (m/f) for a 7-month contract, from 03/02/2025 to 01/08/2025 Management of qualification documents: Support, review and approval of documents. Evaluation and approval of change requests: Evaluate changes to ensure they do not affect qualified status and perform quality risk analyses (e.g. GMP FMEA). Dealing with deviations: Investigating and dealing with deviations using deviation reports. Ensuring compliance: Ensuring that QA activities comply with legislation, regulatory requirements and customer expectations. Reporting : Keeping the Group Manager QA Qualification informed of relevant developments and trends. Strategy and training: Support the creation and development of qualification strategies and ongoing training. Audit support: Participate in internal audits, customer audits and regulatory inspections as QA representative. Requirements: Proven experience in biotechnology or pharmaceutical environment Solid experience as QA Qualification Good knowledge on FAT/SAT/IQ/OQ/PQ Excellent communication skills, proactive and able to work in a multidisciplinary teaml. You are fluent in English (spoken and written) - German is an advantage for this position