MSAT Process Expert (m/f/d) Freelance/temporary employment for a project Visp Start date: asap Reference number: 858035/1 Responsibilities * Establish and maintain strong customer relationships * Plan, prepare and oversee production campaigns from a QC perspective * Manage GMP-relevant change requests and deviations * Support and host customer audits and regulatory inspections * Calculate, track and report QC cost elements within assigned projects * Coordinate, prioritize and schedule QC activities independently * Ensure close alignment with QA, OPS, MSAT, engineering and other stakeholders * Lead cross-functional QC project activities without direct reports * Drive continuous improvement within QC operations and project workflows * Represent QC in tech transfers and ensure analytical readiness Profile * Master-s or PhD in a natural science discipline (biology, biochemistry, pharmaceuticals or related field) * Solid industry experience * Proven experience in microbial GMP environments * Strong background in biomanufacturing, production operations, MSAT and tech-transfer * Experience in GMP quality control and analytical project coordination is an advantage * Proficient in MS Office; knowledge of Documentum, LIMS, Trackwise or similar software is an advantage * Strong organizational abilities, fast comprehension and high attention to detail * Ability to remain calm, structured and solution-oriented in dynamic or stressful situations * Conversational German and fluent English Benefits * Opportunity to work at a leading biomanufacturing site with cutting-edge technologies * Cross-functional exposure across QC, QA, MSAT, engineering, production and program management * Independent role with high visibility and impact on customer projects * Dynamic, international environment with strong focus on teamwork and scientific excellence