Quality Control Analyst

pbLanguage: /b Fluent French + technical English /p pbEligibility: /b Swiss/EU nationality or valid Swiss work permit /p h3Description /h3 pThe Quality Control Analyst will perform routine biochemical QC testing within a cGMP-regulated pharmaceutical laboratory. The role involves hands-on laboratory analysis, documentation, investigations, equipment checks, and support for validation and continuous improvement activities. /p h3Responsibilities /h3 ul liPerform biochemical QC testing according to approved procedures and GMP requirements. /li liPrepare laboratory solutions, reagents, and consumables. /li liComplete logbooks, forms, and documentation in line with GMP, GDP, and ALCOA+. /li liEscalate OOS/invalid results and initiate quality events within required timelines. /li liSupport laboratory investigations and troubleshooting activities. /li liExecute qualification and validation protocols for methods, systems, reagents, and equipment. /li liEnsure equipment calibration and maintenance status is compliant before use. /li liMaintain laboratory organization and 5S standards. /li liCFC Laboratory Technician / Biology qualification or another relevant scientific background. /li liMinimum b3 years of QC laboratory experience in a cGMP environment /b. /li liHands-on experience with biochemical analytical methods. /li liExperience with at least some of the following: bELISA, PCR, HPLC, electrophoresis, Western Blot, enzymatic activity testing /b. /li liStrong GMP and good documentation practice knowledge. /li liFluent French and technical English. /li liSwiss/EU nationality or valid Swiss work authorization. /li /ul h3Preferred Requirements /h3 ul liExperience writing method validation protocols. /li liExperience with laboratory investigations and troubleshooting. /li liBroader experience across multiple biochemical analytical techniques. /li /ul #J-18808-Ljbffr