343686BR
Apr 13, 2022
Switzerland

Job Description

365 days a year, our global manufacturing and supply network works to ensure our patients have the treatments they need to live longer, healthier lives.

A QC Analyst II is responsible for the execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations and the performance of laboratory specific activities such as analyses, maintenance, calibration and qualification of analytical equipment.

Your key responsibilities include, but are not limited to:

• Sample storage and management
• Analytical testing and documentation of API / drug substance / drug product / finished product / complaints / stability / packaging material samples
• Ensure all activities are in compliance with cGxP, incl. data integrity
• Stability testing / sample storage and management
• Analytical documentation of stability samples to cGxP standards
• Ensure compliance with all HSE guidelines
• Detect and report potential accidents, risks and propose solutions
• Responsible for participating in initial training and retraining

The contract will be binding for two years.

Diversity & Inclusion / EEO

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

Minimum Requirements

• Completed apprenticeship as a laboratory assistant or equivalent training
• Basic oral and written communication in English; fluent in German (oral and written)
• Collaborative, result-oriented
• Experience in administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure
• Efficient in Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy
• Understanding of Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling
• Knowledge of TQM and related industry GxP standards and processes

• Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production)


You’ll receive:

We offer you a challenging, international and interdisciplinary work environment. Investment in people is a priority for Novartis. We offer a range of possibilities for personal development and career opportunities within the group to motivated, qualified people. We offer you a competitive salary and benefit package. Novartis also supports a flexible work-life integration (working remotely, flexi-time schedules, ...).

Why consider Novartis?

769 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?

We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.

Imagine what you could do at Novartis!
Novartis Technical Operations
NTO QUALITY
Switzerland
Stein (Säckingen)
Quality
Full Time
Temporary
No
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343686BR

QC Analyst II (temp)

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