Job Description

Location:
Mississauga, ON

Date Posted:
8/16/2022

Job Number:
JO-2208-1510



Reports to: Supervisor Quality
Department: Quality

This is a Permanent Full - Time Position

Key Responsibilities:

• Perform accurate analyses on finished products and stability of different dose forms (solid dose, liquids, topicals) in accordance within schedule.
• Perform analyses using HPLC, UPLC, GC, UV, Dissolution, FTIR, and numerous other analytical methodologies and techniques.
• Document all laboratory testing maintaining accurate records through an electronic system (LIMs) or traditional laboratory notebooks.
• Process and integrate chromatographic data using Chromatographic Data System (i.e.Empower).
• Perform all work according to cGMP following regulatory and company standards.
• Assist the Supervisor, Scientists and Senior Chemists in determining the root cause of laboratory deviations providing clear and concise documentation of the event.
• Maintain the highest data integrity following the practices of ALCOA.
• Follow all safety policies and maintain a clean and orderly 5S work area.
• Maintain laboratory systems and participate in projects as required.
• Working closely with others in the group to achieve business objectives.

• University Degree or College Diploma in Chemistry or a related science
• Good theoretical and practical knowledge of instrumental techniques such as HPLC, UPLC, GC, UV-VIS, Dissolution
• Experience with Chromatography Data Acquisition and Laboratory Information Systems.
• Good knowledge of laboratory GMP and demonstrated proficiency in analytical techniques.
• Works well in a fast-paced environment both individually and as part of a team.
• Ability to manage multiple tasks concurrently and effectively
• Excellent oral and written communication skills.
• Demonstrated computer proficiency (Excel and Word)

• Minimum of 2 years Quality Control experience in a pharmaceutical laboratory environment.
• Strong Chromatographic (Empower) and LIMs (LabWare an asset) knowledge.