Please note this is a one year contract opportunity
Under guidance of Supervisor or senior chemist, responsible for performing all activities in AR&D QC pertaining to full testing of API, in-process, stability samples and finished dosages. Acts as a key member in the project working team.
As per specifications, performs initial testing as well as testing of stability samples, in-process and raw materials.
Under guidance of senior chemist, performs validation of analytical testing procedure for drug substance and drug product.
Conducts other tests required for dosage submissions.
Documents and reports results as per established SOP’s.
Performs additional related duties, as assigned, in accordance with job responsibilities and necessary departmental objectives.
Work as a member of a team to achieve all outcomes.
Demonstrates corporate values in the performance of the work and interactions with others.
Performs all work in accordance with all established regulatory, compliance and safety requirements.
Job Requirements :
Recognized post secondary education in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field.
BSc with 1 year or MSc with 0 year experience in a pharmaceutical lab in an R&D environment.
Knowledge of wet chemistry, analytical bench techniques, Window-based software.
Knowledge of automated data acquisition systems is an asset.
Working knowledge of GC is an asset.
Good written and verbal English communication skills.