Jobdescription
For our client, we are looking for a QC Analyst(FR) to join their teamin Neuchâtel.
WorkConditions:
* On-site role inNeuchâtel
* 6-month contract via Randstad(17/03/2025 - 16/09/2025)
* Frenchmandatory (English is a plus)
* Variableworking hours, including weekends (1 out of 4 to 6) and on-callperiods
JobResponsibilities
As the entry point forthe Quality Control (QC) laboratories, you will be responsiblefor providing the necessary samples, stability materials, andarticles for analysis. You will ensure the proper handling,documentation, and distribution of samples while maintainingcompliance with Good Manufacturing Practices (GMP) andinternal procedures.
Your main tasks willinclude:
Sample Handling &Logistics
* Control, aliquot, identify,record, distribute, store, or dispose of samples in compliancewith GMP and standard operating procedures(SOPs)
* Ensure proper reception, processing, anddistribution of samples according to establishedguidelines
* Receive and register samples intracking systems (LIMS or similar) within definedtimelines
* Perform sampledestruction and transfers asrequired
Stability & ValidationStudies
* Participate in validationprotocols and stability studies, from sample receptionto analysis, stabilization, anddisposal
* Ensure proper documentation andtraceability of stabilitysamples
Stock & EquipmentManagement
* Manage the stockof consumables and reagents for thelaboratory
* Oversee equipment maintenance,calibration, and temperature alarmmonitoring
* Ensure proper logbookcompletion and review
RegulatoryCompliance & EHS
* Adhereto GMP guidelines and internal qualityprocedures
* Support regulatory audits bymaintaining accuratedocumentation
* Follow EHS (Environment,Health & Safety) regulations and actively report anydeviations
Support for QCTeams
* Assist with non-testingtasks such as preparation of analysis solutions, freezertransfers, and autoclavingactivities
* Collaborate with cross-functionalteams for efficient sampleprocessing
JobRequirements
? Education &Experience
* Previous experiencein sample management, stability studies, or QClogistics within a GMP-regulatedenvironment
* Familiarity with GoodManufacturing Practices (GMP), stability management, and laboratorysample handling
* Experience with LIMS orother sample tracking systems is aplus
? Technical & SoftSkills
* Strong attention todetail and ability to follow SOPsprecisely
* Excellent organizational andmultitasking skills
* Proactive mindsetin ensuring regulatory compliance and safetystandards
* Ability to work bothindependently and in collaboration with QC and regulatoryteams
Thisis a great opportunity to join a dynamic and high-qualityenvironment. If you meet the requirements and are interested, applynow!