Als neue Jobbenachrichtigung einrichten
Als neue Jobbenachrichtigung einrichten
Geben Sie nachstehend Ihre E-Mail-Adresse ein, um Benachrichtigungen in Ihrem Posteingang zu erhalten, wenn ähnliche Stellenangebote vorliegen.
Indem Sie nachstehend auf „Ja, senden Sie mir Stellenangebote zu“ klicken, stimmen Sie zu, gemäß unserer Datenschutzrichtlinie Stellenangebote auf Basis der von Ihnen gewählten Suchkriterien in Ihrem Posteingang zu erhalten.
Indem Sie nachstehend auf „Ja, senden Sie mir Stellenangebote zu“ klicken, stimmen Sie zu, gemäß unserer Datenschutzrichtlinie Stellenangebote auf Basis der von Ihnen gewählten Suchkriterien in Ihrem Posteingang zu erhalten.
Vielen Dank für Ihre Registrierung zur Jobbenachrichtigung
16392en
- Contract
- English
- Associate
- Research & Development
- Switzerland
- Healthcare & Life Sciences
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: hugo.palejowski@swisslinx.com.
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: hugo.palejowski@swisslinx.com.
I manage this role