GxP QC Analyst II - Quality Systems & Lab Analysis

Novartis AG; Basel; On-site; CHF 90,000 - 110,000; Full time

Job summary

Novartis seeks a QC Analyst to support GxP activities in the quality department. You will manage SOPs, documentation, and records in the QMS, and perform analytical tasks in the pharmaceutical laboratory.

The role may involve shifts and collaboration across functions to ensure data integrity and compliance. Fluency in German and good English are required, along with GMP experience and lab software knowledge (Empower, Chromeleon, TiAmo).

Qualifications

• Experience in quality assurance and analytical skills.
• Proficiency in analytical technologies (e.g., HPLC, GC, titration).
• Knowledge in the use of lab-specific software (e.g., Empower, Chromeleon, TiAmo).
• GMP experience and technological expertise.
• Willingness to work in shifts.
• Fluency in German and good English.

Responsibilities

• Maintain compliance with current Standard Operating Procedures (SOPs), GxP-compliant documentation, and records within the Novartis quality management system.
• Perform and evaluate analytical tasks in a pharmaceutical laboratory, including working in shifts where necessary.
• Ensure the integrity of all quality assurance records and data, as applicable, and foster collaboration between your team and other functions and departments.
• Ensure an appropriate level of education and GxP knowledge.
• Support quality audits and health authority inspections.

Skills

Quality assurance

Analytical skills

GxP knowledge

HPLC

GC

Titration

Empower

Chromeleon

TiAmo

GMP experience

Shift work

German

English

Tools

Empower

Chromeleon

TiAmo

Job description

Novartis seeks a QC Analyst to support GxP activities in the quality department. You will manage SOPs, documentation, and records in the QMS, and perform analytical tasks in the pharmaceutical laboratory.

The role may involve shifts and collaboration across functions to ensure data integrity and compliance. Fluency in German and good English are required, along with GMP experience and lab software knowledge (Empower, Chromeleon, TiAmo).