Quality Control Analyst – Analytical Chemistry
Introduction
Hello, I’m Anthony Chacon, Recruitment Advisor at FED ManuTech, specializing in engineering, technical and manufacturing positions.
I’m currently recruiting a Quality Control Analyst – Analytical Chemistry for a manufacturing company in the pharmaceutical industry. This is an opportunity to join a structured, highly regulated environment and play an important role in the quality control of raw materials and finished products.
Mission
Your Role :
Perform quality control testing on raw materials and finished products using various analytical techniques.
Operate analytical instrumentation such as HPLC, GC, KF, IR and UV-VIS.
Perform testing in accordance with USP, NF and FCC requirements.
Prepare and document investigations related to out-of-specification (OOS) results under the supervision of the Laboratory Manager.
Review and verify analyses performed by QC analysts.
Accurately document laboratory activities in the appropriate notebooks and systems.
Ensure compliance with GMP/cGMP requirements and internal procedures.
Follow all applicable health and safety requirements.
Support additional laboratory activities and projects as assigned by management.
Working Conditions :
Salary: $58,000 to $65,000 per year
Full-time permanent position.
Fully on-site work environment.
Structured and regulated pharmaceutical manufacturing environment.
Your profile
At least 5 years of relevant experience in analytical chemistry, preferably within the pharmaceutical industry.
DEC or Bachelor’s degree in Science, Chemistry or a related field.
Hands-on experience with analytical instrumentation such as HPLC, GC, IR, UV-VIS or KF.
Previous experience working in a GMP-regulated environment.
Good understanding of FDA and Health Canada regulatory requirements.
Strong analytical skills with the ability to interpret and document laboratory data.
Good computer skills, particularly with Microsoft Office.
Fluency in both French and English.
If you’re looking to bring your analytical chemistry expertise to a quality-focused pharmaceutical environment, I’d be happy to discuss this opportunity with you.
