Thermo Fisher Scientific is seeking a Quality Specialist II for their Clinical Label Services team in Allschwil, Switzerland. The role focuses on ensuring compliance with GMP requirements through detailed documentation review, process monitoring, and collaboration with cross-functional teams
Job Summary
As a Quality Specialist I, you'll provide essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams.
You'll help maintain GMP compliance, investigate quality events, and drive continuous improvement initiatives while working in a collaborative environment focused on delivering life-changing products to our customers.
Review batch records for completeness, accuracy, and compliance with GMP requirements and manage archiving of quality documentation in accordance with regulatory standards.
Matching Summary
Match Score: 75
Thermo Fisher Scientific is seeking a Quality Specialist II for their Clinical Label Services team in Allschwil, Switzerland. The role focuses on ensuring compliance with GMP requirements through detailed documentation review, process monitoring, and collaboration with cross-functional teams.
Skills & Requirements
Must-have
GMP compliance
documentation review
quality investigations
CAPA and change control
Nice-to-have
continuous improvement initiatives
collaborative environment
life-changing products
Key Requirements
Bachelor's Degree required
Thorough knowledge of EMA and international GMP regulations