On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a QC Analyst.
In this role, you will ensure pharmaceutical quality through lab analyses, method validation, and documentation in a GMP environment, collaborating as a reliable and communicative team member.
Contract type - Contract
Start Date - January
Location - Visp
Workload - 100%
Duration - 6 months
Your mission :
- Perform and release in-process controls (HPLC, CE, icIEF, etc.) in compliance with cGMP guidelines
- Support method validation activities
- Maintenance of existing infrastructures
- Carry out routine final analyses and stability samples for time-critical samples
- Test and assess random product samples to ensure minimum pre-defined standards are met.
- Aggregate test data and documents results of testing.
Your background :
- Fluent in English mandatory, German is a plus
- You have completed training and ideally already have experience in analytical work in pharmaceutical industry
- You are a team player, responsible, resilient and communicative
- You have a high level of quality awareness and an efficient way of working
- You have good comprehension skills, are independent and work reliably
- You have a safe handling of potentially hazardous substances
- You are confident in using a PC and standard software
- experienced with HPLC technique
- hands-on lab experience in GMP environment
What's on offer
- A 6 month contract.
- A great opportunity to develop your career at a leading international biotechnology company.
- A competitive salary.
If this sounds like you, don't hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter : [email protected].
1 day ago