Job Description

As a QC Project Leader at the Visp site, you will act as the central interface between Quality Control, Production, Quality Assurance, MSAT, Engineering, and external customers. You will represent QC as a single point of contact within cross-functional project teams, driving strategic alignment and ensuring efficient, compliant, and cost-effective execution of QC activities in a GMP environment. This role requires a high degree of independence, strong communication skills, and the ability to manage changing priorities while maintaining quality and compliance.



Key Responsibilities



Serve as the QC representative and single point of contact in cross-functional project teams Establish, maintain, and manage customer relationships Prepare, coordinate, and oversee production and QC support for manufacturing campaigns Manage change requests and deviations in accordance with GMP requirements Support and supervise customer audits and regulatory inspections Calculate, monitor, and control QC-related project costs Independently coordinate, prioritize, and schedule QC activities across analytical laboratories Ensure timely, cost-efficient project execution while adapting to changing customer requirements

Required Qualifications & Skills



Master's degree or PhD in natural sciences (biology, biochemistry, pharmaceutical sciences, or related field) Experience in a GMP-regulated environment; experience in Quality Control is a strong advantage Fluent German and English communication skills (written and spoken) Proficient in MS Office; experience with pharmaceutical or laboratory systems (e.g. Documentum, LIMS, Trackwise) is an advantage * Strong organizational skills, analytical thinking, and attention to detail