Senior QC Scientist - GMP Reference Standards

Job-Room; Lalden; Vor Ort; CHF 110.000 - 160.000; Vollzeit

Zusammenfassung

Lonza in Switzerland seeks a senior life sciences professional to author and review GMP reference standard qualification protocols and reports. You will liaise between QC customers and CSM, ensuring timely documentation of LIMS/LES activities, and provide SME input during audits.

You will mentor colleagues, lead cost- and efficiency-focused projects, and maintain data integrity across Trackwise records while collaborating with QA Analytics and external clients.

Qualifikationen

• Master's degree in Life Sciences or related field.
• Proven experience in a cgmp environment, QC or analytical development.
• Exceptional technical writing and ability to document complex data clearly.
• Advanced scientific experience in analytical chemistry/biology.
• Knowledge of QC software such as LIMS/LES, Trackwise, DMS, Statistica.

Aufgaben

• Serve as primary contact between QC customers and CSM for GMP reference standards protocols and reports.
• Ensure timely completion of qualification protocols supporting LIMS/LES activities and test schedules.
• Provide technical mentoring and coaching across teams in a matrix environment.
• Support quality documentation and change management for reference standards (Trackwise records).
• Lead innovation projects and identify cost/efficiency opportunities.
• Provide SME input during audits and inspections.
• Ensure compliance with quality, data integrity and safety requirements.
• Collaborate with QC project leads, QA Analytics and external clients.

Kenntnisse

Exceptional technical writing

Analytical chemistry

Analytical biology

English proficiency

German preferred

Project management

Team player

Change readiness

Ausbildung

Master's degree in Life Sciences

Tools

LIMS/LES

DMS

Trackwise

Statistica

Jobbeschreibung

Lonza in Switzerland seeks a senior life sciences professional to author and review GMP reference standard qualification protocols and reports. You will liaise between QC customers and CSM, ensuring timely documentation of LIMS/LES activities, and provide SME input during audits.

You will mentor colleagues, lead cost- and efficiency-focused projects, and maintain data integrity across Trackwise records while collaborating with QA Analytics and external clients.