Senior Scientist QC HPLC (f/m/d)
On-siteVisp, Valais, Switzerland
Job Summary
Conduct investigation and management of deviations as Lead Investigator, performing root cause analysis (RCA) and CAPA implementation for project topics and general lab matters. Execute QC analytical review, extraction and evaluation of data, and preparation of reports and presentations. Manage technical writing, document review, and approval to ensure compliance with regulatory guidelines. Oversee audit readiness in GMP-regulated labs and support optimization of laboratory processes using Lean, 5S, and Six Sigma. Implement, optimize, transfer, and validate analytical methods with a focus on HPLC, CE, and icIEF. Represent the HPLC team in assigned projects and coach junior QC colleagues. Join Lonza's growing international team in Visp to work on interesting projects in the rapidly developing field of Biologics.
Required Qualifications
- Master or PhD in chemistry, biochemistry, biology or related field
- Minimum 5-10 years of proven experience in pharma industry
- Good understanding of GMP
- Proficient in English
Desired Qualifications
- Experience with HPLC, CE or icIEF
- Ideally experience with IT systems like LIMS and CDS
- German
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