Senior Bioanalytics QC Specialist — Onsite Basel

C028 (FCRS = CH028) Novartis Pharma AG; Basel; Vor Ort; CHF 85.000 - 159.000; Vollzeit

Benefits dieser Stelle

Hybrid working options

Parental leave (min 14 weeks)

Zusammenfassung

Novartis Pharma AG in Basel, Switzerland seeks a Senior QC Specialist in bioanalytics to support lab activities, review data, and ensure compliance with cGxP and HSE guidelines. This is a fixed-term contract of 18 months.

You will plan sampling, review analytical results for release, stability and projects, and prepare protocols/reports, trend analyses, and KPI documentation. You will lead analytical projects, support method transfers and deviations, and collaborate across functions in a GMP

Qualifikationen

• 3-5 years of relevant experience or a university degree in Pharmacy, Chemistry, or related field.
• Experience in GMP-regulated pharmaceutical environments with analytical testing.
• Ability to review data, contribute to investigations and ensure data integrity.

Aufgaben

• Plan, coordinate and support sampling activities aligned with project needs.
• Review/approve analytical results for release, stability, and projects.
• Prepare/approve protocols, reports, trend analyses and KPIs.
• Lead analytical projects, including method transfers and calibrations.
• Serve as SME for products, audits, and cross-functional governance.
• Manage deviations, CAPAs, investigations, and continuous improvement.
• Ensure compliance with cGxP, data integrity, QA, and HSE requirements.

Kenntnisse

Quality control

GxP compliance

Data integrity

Analytical testing

English communication

Ausbildung

Pharmacy degree

Chemistry degree

Tools

MS Office

Laboratory IT systems

Jobbeschreibung

Novartis Pharma AG in Basel, Switzerland seeks a Senior QC Specialist in bioanalytics to support lab activities, review data, and ensure compliance with cGxP and HSE guidelines. This is a fixed-term contract of 18 months.

You will plan sampling, review analytical results for release, stability and projects, and prepare protocols/reports, trend analyses, and KPI documentation. You will lead analytical projects, support method transfers and deviations, and collaborate across functions in a GMP