Chemist, QC QS4-(12 months contract)

Job Summary

Summarize the main purpose of the job, and the key outcomes expected. Responsible for generating accurate results while following GMP requirements.  Responsible for analyzing laboratory samples using various chemical and instrumental techniques, in accordance with established compendial and in-house testing methods, while under minimum supervision.

Contract position for 12 months.

Shift- Afternoon Shift- 3:00 pm to 11:00 pm – Monday to Friday (During training shift will be adjusted to day shift- 7:00 am to 3:30 pm).

Job Responsibilities

• Performs analysis of all laboratory samples including raw material, in-process, finished products, purified water, cleaning validation and stability samples using analytical instruments and established analytical procedures and techniques.

• Documents and compiles all observations and data obtained from testing as per established SOPs and good documentation practices.

• Recognizes OOS or out of trend results and under the direction of the Supervisor assists in the completion of lab investigations.  

• Performs calibration of laboratory equipment as required by the department's established calibration program and GMP requirements.

• Works as a member of a team to achieve all outcomes.

• Performs all work in accordance with all established regulatory and compliance and safety requirements.

• Disposes of waste solvents and orders any chemicals or laboratory supplies as required.

• Works in a safe manner collaborating as a team member to achieve all outcomes.
• Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.

• Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. 

• All other relevant duties as assigned.

Job Requirements

• B.Sc. from a recognized educational institution in Chemistry or any related field; or Community College diploma in a related field and a minimum of 1 year of relevant experience in the analysis of pharmaceutical products.

• Knowledge of Excel, Word and other Microsoft Office Programs and/or laboratory software packages is an asset.
• Good theoretical understanding of FT-IR, titration, UV and chromatography (TLC and column).
• Excellent verbal and written English communication skills.

• Knowledge of GMP/GLP.
• Problem solving ability.
• Proven organization and time management skills as demonstrated through previous work and/or educational experience.