QC Project Lead m/f/d, Wallis 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
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