CQV Engineer X3

CQV Engineer X3

Currently working with a Global Biotech Client in need of support from 3X CQV Engineers 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 a 6-month contract (extension expected).
 
Interview + offer will take place this week and next, so get in touch ASAP if interested.
 

• Performing qualification/validation studies, including organization, supervision and documentation of tests and qualifications. 
• Taking care of the development and delivery of the different project phases: planning, implementation, testing and validation up to the final post-processing and handover of the project. 
• Play an active role in troubleshooting during the different project phases. 
• Manage additional administration required on projects (SOP development, user specifications, training strategies, etc.). 

Requirements:

• Previous experience in GMP regulated pharmaceutical industry
• Technical mindset and ability to work efficiently in a fast-paced environment
• English and German proficiency is required 
• 4 days per week on-site in Valais (minimum)

Position: CQV Engineer X3
Location: Visp, Switzerland
Start Date: Immediately 

For more information, contact Aliyana Darwesh -

a.darwesh@panda-int.com
+41445514407