QA Specialist Validation X3

QA Validation Specialist X3

Currently working with a Global Biotech Client in need of support from 3X QA Validation Specialists for high-level projects in Switzerland. This is an opportunity to work in a new state-of-the-art facility with ground breaking technology for an 8-month contract (extension expected).
 
Interview + offer will take place this week and next, so get in touch ASAP if interested.
 
Responsibilities:

• Support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, GxP contract manufacturing facility.
• In depth awareness of entire process, identifying operational factors which influence the process.
• Provide Quality support.
• Draft and review GMP documents with a technical mindset.

Requirements:

• Previous experience in GMP regulated pharmaceutical industry
• Technical mindset and ability to work efficiently in a fast-paced environment
• English proficiency, German is an asset
• 5 days per week on-site in Valais

Position: QA Validation Specialist
Location: Visp, Switzerland
Start Date: Immediately 

For more information, contact Aliyana Darwesh -

a.darwesh@panda-int.com
+41445514407