The Scientist will develop, improve and validate analytical methods within deadlines. He/she will also perform the required analyses for the research and development batches, physical tests, dosages, degradation products (during the process, initial and stability).
Responsibilities:
- Write and run method validation protocols, issue reports
- Maintain accurate experimental records, instrument registers and enter analytical data
- Check the laboratory notebooks
- Actively participate in laboratory investigations
- Follow up on the changes, maintenances, calibrations and qualifications of all laboratory instruments
- Prepare the solutions necessary for the analyses
Skills and experience required:
- Diploma of College Studies (DEC) in Sciences (Chimie, Biochimie), or a discipline related
- Minimum of 1 year experience in development and validation of analytical methods in the pharmaceutical industry
- Knowledge of Canadian Good Manufacturing Practices (GMP) (Health Canada)
- Knowledge of Pharmacopoeias (USP, Ph. Eur. and BP) and their applications within a laboratory
- Knowledge with the following techniques: HPLC (UPLC) et GC
- Communication and problem solving skills