Weitere Details
LIMS Coordinator m/w/d (DE)
[17498]
LIMS, Labeling
Zu besetzendes Projekt: LIMS Coordinator m/w/d Art der Beschäftigung: Payroll Branche: Biotech Fähigkeiten: LIMS,Labeling Projektstart: 01.06.2026 Projektdauer: 12 months Einsatzort: Basel, Schweiz Key Responsibilities: ·Perform all pull (retrieval, labelling and documentation) activities for stability studies. Login and receive samples in LIMS. Close collaboration with different departments. ·Perform all staging (Packaging, labelling, documentation) activities. Collect and keep updated data in LES (Laboratory Execution System) system. Organize storage of boxes in stability chamber in close collaboration with different departments. ·Support the improvement of the sample management process. ·Ensure safety and health protection by following lab and safety instructions and all cGMP regulations. ·Perform other duties as assigned. Required Qualifications and Skills: ·A degree in e.g. Biotechnology, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or a training on the job as analytical lab technician ·3+ years of experience in the pharmaceutical or chemical industry, preferably in sample management ·Working knowledge in the pharmaceutical industry, preferably in sample management; ·Excellent knowledge of written and spoken English, German is a plus ·Good planning and organisational skills ·Good communication skills ·Good inter-personal skills ·Ability to work independently and in a team environment ·Detail oriented ·Enthusiastic and open-minded ·Willingness to learn and carry out new and complex tasks ·Proactive attitude
- Perform all pull (retrieval, labelling and documentation) activities for stability studies. Login and receive samples in LIMS. Close collaboration with different departments.
- Perform all staging (Packaging, labelling, documentation) activities. Collect and keep updated data in LES (Laboratory Execution System) system. Organize storage of boxes in stability chamber in close collaboration with different departments.
- Support the improvement of the sample management process.
- Ensure safety and health protection by following lab and safety instructions and all cGMP regulations.
- Perform other duties as assigned.
- A degree in e.g. Biotechnology, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or a training on the job as analytical lab technician
- 3+ years of experience in the pharmaceutical or chemical industry, preferably in sample management
- Working knowledge in the pharmaceutical industry, preferably in sample management;
- Excellent knowledge of written and spoken English, German is a plus
- Good planning and organisational skills
- Good communication skills
- Good inter-personal skills
- Ability to work independently and in a team environment
- Detail oriented
- Enthusiastic and open-minded
- Willingness to learn and carry out new and complex tasks
- Proactive attitude
Luca Furler