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