Senior QC Specialist, Bioanalytics - Basel

Healthcare Businesswomen’s Association; Basel; Vor Ort; CHF 85.000 - 159.000; Vollzeit

Zusammenfassung

Novartis in Basel, Switzerland is seeking a Senior QC Specialist to support bioanalytics and laboratory activities, ensuring GxP compliance and data integrity. This fixed-term 18-month role involves reviewing analytical data, leading projects, and acting as SME for assigned products.

The role requires 3–5 years in pharma/analytical labs, strong QA knowledge, and excellent communication in English. Local language skills are a plus; relocation is not offered.

Qualifikationen

• Experience in Quality Control testing in a GMP-regulated environment.
• Proficiency with sampling procedures and data handling.
• Strong knowledge of GxP standards and data integrity principles.
• Ability to make quality-based decisions and document results clearly.
• Excellent written and spoken English; local language fluency is a plus.

Aufgaben

• Plan, coordinate, and support sampling activities with documentation aligned to project needs.
• Review and approve analytical test results for release, stability, and project activities.
• Prepare and approve analytical protocols, reports, and trend analyses.
• Lead analytical projects including method transfers and new product introductions.
• Serve as SME for assigned products, audits, and external initiatives.
• Manage deviations, CAPA definitions, and continuous improvement actions.
• Support supplier qualification and cross-functional governance meetings.
• Ensure compliance with cGxP, data integrity, and HSE requirements.

Kenntnisse

Quality Control

Sampling

Data integrity

GxP standards

Communication skills

MS Office

Ausbildung

Pharmacy or Chemistry degree

Tools

MS Office

Jobbeschreibung

Novartis in Basel, Switzerland is seeking a Senior QC Specialist to support bioanalytics and laboratory activities, ensuring GxP compliance and data integrity. This fixed-term 18-month role involves reviewing analytical data, leading projects, and acting as SME for assigned products.

The role requires 3–5 years in pharma/analytical labs, strong QA knowledge, and excellent communication in English. Local language skills are a plus; relocation is not offered.