Language

Aliquotation Operator (50%)

Analytical Laboratory
Pharmaceutical Development
GLP
Laboratory
GMP
Laboratory Automation
Logistics
Inventory
Documentation
SOPS
QM
Description:

This is a temporary contractor opportunity at Novartis 

Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life! 

 Novartis partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit.

 Ready to work with/through Magnit at Novartis? Please read on…

Role Description:
Plans and executes tasks related to the preparation of laboratory aliquots in the areas of stability, release, and reference sample management at site level.

Key Activities (including but not limited to):

  • Execution and coordination of GMP-compliant aliquoting (laboratory bulk materials and analytical samples in the mg/g range)
  • Working in accordance with applicable SOPs, GMP, GLP, QM, HSE, ISRM, and Novartis guidelines
  • Management of inventory (electronic and physical) on behalf of the analytical laboratory in centralized facilities
  • Delivery in accordance with applicable quality standards, ensuring compliance with systems, equipment, and processes
  • Use of complex tools/equipment, laboratory automation tools, and specialized facilities
  • Preparation of raw data documentation for handover to internal and/or external customers
  • Review and/or approval of documents within own area of responsibility in accordance with current processes

Role Requirements:

  • Minimum: Completed vocational training (e.g., pharmaceutical development or logistics in a GMP environment) or equivalent qualification.
  • Fluent in the site-specific language (spoken and written). Basic knowledge of English (spoken and written).
  • At least 3 years of successful professional experience in analytical development
  • Good knowledge of software and computer tools
  • Strong understanding of quality principles (GMP, ALCOA+)
  • High level of organizational skills and ability to work independently

Workload: 50% (20 hours per week)
Role type: Onsite
Required start date: February 2026
Contract: 12 months

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?

EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accommodation: 
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.

QUALIFICATION/ LICENSURE :
  • Work Authorization : N/A
  • Preferred years of experience : 3+ Years
  • Travel Required : No travel required
  • Shift timings: 9 AM to 5 PM
Job Location Basel, Basel-Stadt (On-Site)
Contract Duration 12 month(s)