Stability & Raw Materials QC Expert

Incyte

Yverdon-les-Bains

Vor Ort

CHF 90.000 - 130.000

Vollzeit

vor 44 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Incyte is seeking a QC Specialist Stability and Raw Materials in Yverdon-les-Bains, Switzerland. You will oversee stability studies and RM testing, coordinate analyses, and ensure on-time delivery of results within GMP guidelines.

The role collaborates with QA, Manufacturing, Supply Chain, and external labs; requires strong GMP knowledge, chemical/biotech lab experience, and fluent French with advanced English. Join a fast-paced, quality-driven environment.

Qualifikationen

  • Strong experience in GMP environments in a pharmaceutical/biotech setting.
  • Deep knowledge of analytical testing and pharmacopoeias.
  • Ability to work in a highly regulated and fast-changing environment.

Aufgaben

  • Plan and coordinate RM lab activities for the team of technicians.
  • Coordinate design, initiation, and execution of stability studies per ICH/regulatory requirements.
  • Collaborate with QC analysts and lab supervisors for timely testing completion.
  • Serve as primary contact for stability-related queries across QC/QA/Manufacturing/RA/SC.
  • Support regulatory submissions by providing stability data and summaries.
  • Participate in cross-functional meetings to update timelines and progress.
  • Own deviations, CAPA, and change controls for QC activities.
  • Develop and maintain SOPs, WI, and quality documents related to responsibilities.

Kenntnisse

GMP experience
Analytical testing
Quality systems
Team collaboration
Regulatory compliance
French language
English language

Ausbildung

Bachelor + 5 years / CFC-BTS

Jobbeschreibung

Incyte is seeking a QC Specialist Stability and Raw Materials in Yverdon-les-Bains, Switzerland. You will oversee stability studies and RM testing, coordinate analyses, and ensure on-time delivery of results within GMP guidelines.

The role collaborates with QA, Manufacturing, Supply Chain, and external labs; requires strong GMP knowledge, chemical/biotech lab experience, and fluent French with advanced English. Join a fast-paced, quality-driven environment.

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