QC Analyst I ( Environmental Monitoring)

Summary

Please note \- this position is being offered as a 2 year temporary contract.

As a QC Analyst I you will be responsible for assigned tasks in the quality control laboratory in accordance with cGxP regulations. You will also be responsible for the performance of laboratory specific activities such as analyses, maintenance, calibration and qualification of analytical equipment.

About the Role

Key tasks:

Operational :

• Sample storage and management


• Analytical testing and documentation of samples

Ensure all activities in compliance with cGxP, incl. data integrity

• HSE :


• Comply with all HSE guidelines


• Detect and report potential accident, risks and propose solutions


• Responsible for participating in initial training and retraining

Relevant Experience

Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique; microbiological analysis.

• Education \& Qualification

Completed apprenticeship as a laboratory assistant or equivalent training

• Languages


• Basic (oral and written) in English; fluent in German

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.

Read our handbook (PDF 30 MB)

Division
Operations
Business Unit
Quality
Location
Switzerland
Site
Stein Aargau
Company / Legal Entity
C046 (FCRS \= CH046\) Novartis Pharma Stein AG
Functional Area
Quality
Job Type
Full time
Employment Type
Befristet (Innendienst) (Befristet)
Shift Work
No

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