Quality Control – evening

  • Anywhere

Groupe PARIMA

The Quality control Analyst carries out chemical and physical activities at the laboratory according to the schedule established by following the specifications, methods, procedures and good Manufacturing Practices (GMP). Responsabilites: Carry out the analyses of finished products, bulks, raw materials and stability according to the methods in forceEnsure the integrity and quality of data at the QC laboratoryTrack interviews or calibrations of all laboratory instrumentsMaintaining equipment records, standards and maintaining reagent, standard and/or consumables inventoryParticipate in investigations, problem solving and the development of R&D methods Compétences et expériences recherchées: Diploma of College Studies (DEC) or a Bachelor of Science (Chemistry, Biochemistry, Pharmaceutical program, or a discipline related)3 to 5 years of experience in quality control in the pharmaceutical industryKnowledge of Canadian Good Manufacturing Practices (GMP) (Health Canada) and American (FDA) Knowledge of laboratory investigation guides (FDA guidance to OOS and OOT investigations, MRHA)Knowledge of Pharmacopoeias (USP, Ph. Eur. and BP) and their applications within a laboratoryKnowledge with the following techniques: HPLC (UPLC) et GC Skills for teamworkAbility to train new employees