Tasks & Responsibilities: • You have end-to-end quality oversight on the qualified state of all assets in your assigned area. • You provide fit for purpose quality support for all the activities related to qualification & CSV, calibration, maintenance & reliability engineering. • You review and approve GMP records that cover technical change management, deviation management & CAPAs, risk assessments and SOPs. • You coordinate and facilitate complex investigations, root cause analyses, technical risk assessments, and continuous improvement projects. • With your operations partner you present topics during health authority inspections and internal audits. Must Haves: • University degree in science or engineering • Min. 3 years demonstrated experience in Quality Assurance at a pharmaceutical manufacturing site • Practical experience in commissioning & qualification projects in highly automated GMP production facilities • Well established confidence in setting precise guidance for QA compliance in technical changes, deviations and CAPAs • Your collaboration with partners is characterized by outstanding communication and team work. • You manage to drive quality awareness with operations partners at all levels by integrating regulatory requirements, analytical problem solving and scientific rationale. • Excellent German and English language skills, both written and spoken. MANPOWER AG – Your Career, Our Focus Become part of our network and take advantage of numerous opportunities ManpowerGroup is the leading global company in staffing solutions. With our three brands – Manpower, Experis, and Talent Solutions – we help companies across various industries with their recruitment needs. For 75 years, we have been active in over 75 countries, and throughout Switzerland, we support our clients in successfully completing their tasks and projects. We are looking for a Quality Assurance Manager (m/f/d) – Basel Metropolitan Area