Evening shift: 1:30PM – 10:00PM – Premium applicable
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 force
- Ensure the integrity and quality of data at the QC laboratory
- Track interviews or calibrations of all laboratory instruments
- Maintaining equipment records, standards and maintaining reagent, standard and/or consumables inventory
- Participate 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 industry
- Knowledge 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 laboratory
- Knowledge with the following techniques: HPLC (UPLC) et GC
- Skills for teamwork
- Ability to train new employees