Nov 24, 2022

Job Description

25000+! The total no. of associates in NTO who deliver high quality, affordable medicines on time, every time, safely and efficiently. We strive to become the top manufacturer of innovative and generic medicines in the industry - while keeping our patients at the heart of everything we do.

The QC Analyst II supports all GxP activities in the Quality department and administers Quality Systems / Processes including documentation, metrics and monitoring of actions. This position also supports establishment of Quality operational processes and performs routine GxP Compliance / Operational activities according to Novartis Quality Standards.
As a QC Analyst you will help to optimize and implement analytical methods for new products. In this position you will help to introduce new products for the market and will be responsible to optimize new analytical methods.

Major accountabilities:


• Perform and document lab analysis (standard and more complex technique eg. HPLC, GC, titrations and HPLC-Ms s)
• Ensure all activities in compliance with cGxP, incl. data integrity
• Ensures an adequate level of education, GxP knowledge
• Supports Quality Audits and Health Authority inspection
• Sample storage and management


• Comply with all HSE guidelines
• Detect and report potential accident, risks and propose solutions
• Responsible for participating in initial training and retraining

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

Minimum Requirements

• Professional experience (cca. 3-5 years) in GMP environment and analytics (e.g., Quality Control)
• Good (oral and written) English and German
• Collaboration, as well as being result-oriented
• Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy
• MS Office applications and other standard IT applications supporting Quality activities
• Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; Knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making

*Some restrictions on flexible working options may apply and will be discussed during interview if applicable.

Join our Novartis Network:

If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

Why Novartis?

769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.

We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!

Imagine what you could do here at Novartis!
Novartis Technical Operations
Full Time
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QC Analyst II (80-100%*)

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