The position forms part of the QC Laboratory Team. This position reports to the QC Supervisor and forms part of the Quality Control team.
How you’ll spend your dayPrepare glassware, consumables and Mobile Phases / Diluents required to support analysis according to the relevant pharmacopoeia monographs and/or Company standards as per current GMP
Your experience and qualificationsSkills: Good eye for detail - Highly organized - Accurate & methodical in his/her work - Good communication, documentation, & time management skills
Experience: Training will be given
Qualifications: Ordinary level standard of education (preferably knowledgeable in science subjects) - Computer literate - Proficient in Microsoft Office applications
Enjoy a more rewarding choice •Health Insurance •Life Insurance •Performance Bonus •Personal Growth (Internal Training/Training Platform, certified courses, access to Linked In Learning etc.) •Internal Career Opportunities •Free on-site medical services •Company Car Park FacilityMake a difference with Teva Pharmaceuticals Reports ToQuality Control Shift Supv
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