QC Project Leader
Summary
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
Seniority level
Mid‑Senior level
Employment type
Contract
Job function
Quality Assurance and Science
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