Job Description 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.​​

 

Job Description

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

 

 

Skills Desired

Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Health & Safety Regulations Knowledge, Leadership, Problem Solving Skills, Punctuality, Regulatory Requirements knowledge