Senior QC Scientist: GMP, Data Integrity & Innovation

Lonza

Oberwallis

Vor Ort

Vertraulich

Vollzeit

vor 36 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Lonza is a global leader in life sciences, and this role sits at the nexus of QC and client-facing CSM activities. You will author, revise and review GMP reference standard qualification protocols and reports for biotechnological reference materials, ensuring timely completion to enable LIMS/LES-related activities.

You will mentor colleagues, drive quality documentation, and lead innovation projects, while collaborating with QC leads, QA Analytics and external clients to uphold data integrity

Qualifikationen

  • Master's degree in Life Sciences (Biology, Chemistry or related field).
  • Proven experience in a cGMP environment; QC or analytical development preferred.
  • Exceptional technical writing skills.
  • Advanced scientific experience in analytical chemistry/biology.
  • Extensive knowledge of QC software (LIMS/LES, DMS, Trackwise, Statistica).
  • Team player with change readiness.
  • English required; German preferred.
  • Excellent project and time management skills.

Aufgaben

  • Act as primary contact between QC customer and CSM for GMP reference standards protocols and reports.
  • Ensure timely qualification protocol/report completion supporting MLP specifications.
  • Provide technical mentoring across the team.
  • Support quality documentation and Trackwise records.
  • Lead innovation projects for cost and efficiency improvements.
  • Contribute SME input during audits and inspections.
  • Ensure compliance with quality, data integrity and safety.
  • Collaborate with QC leads, QA Analytics and external clients.

Ausbildung

Master's degree in Life Sciences

Tools

LIMS/LES
DMS
Trackwise
Statistica

Jobbeschreibung

Lonza is a global leader in life sciences, and this role sits at the nexus of QC and client-facing CSM activities. You will author, revise and review GMP reference standard qualification protocols and reports for biotechnological reference materials, ensuring timely completion to enable LIMS/LES-related activities.

You will mentor colleagues, drive quality documentation, and lead innovation projects, while collaborating with QC leads, QA Analytics and external clients to uphold data integrity

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