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Apotex

Chemist, QC QS5 (Contract Role)

Toronto, ON, Canada
North York, ON, M9L 1T9, Canada

$48,851 to $81,419 CAD / year

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Job details

Pay: $48,851 to $81,419 CAD / year
Experience: OR Community College diploma in a related field and a minimum of 2 years relevant experience in the analysis of pharmaceutical products.
Posting language: English
Posted: Oct 26, 2026

Original job description

About Apotex Inc.

Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.

For more information visit: www.apotex.com.

Job Summary

Responsible for generating accurate results while following GMP requirements. Responsible for analysing laboratory samples using various chemical and instrumental techniques, in accordance with established compendial and in-house testing methods, while working under minimal supervision. If required, responsible to review documentation for the QC department.

This role is for Afternoon shift - Monday to Friday, 3.00 pm to 11.00 pm

Graduate Chemist Hiring Event – Apotex

Join our Interview Day on November 11 and fast-track your application for Chemist opportunities at Apotex.

To be considered, applications must be submitted by EOD November 5 to allow for résumé review and interview scheduling. Successful applicants will be invited to meet the hiring team and participate in on-site interviews.

Job Responsibilities

Performs analysis of all laboratory samples including raw material, in-process, finished products, purified water, cleaning validation ,stability samples and analysis associated with method transfer or method verification using analytical instruments and established analytical procedures and techniques.
Documents all observations and data obtained from testing as per established SOPs and Good Documentation Practices.
Recognises OOS, OOT or Anomalous results and under the direction of the Supervisor assists in the completion of lab investigations.
Performs general maintenance and daily check of laboratory equipment as required.
Troubleshoots instrumentation and method problems with the supervisor’s assistance.
Disposes of waste solvents and orders any chemicals or laboratory supplies as required.
Performs role of document reviewer as outlined below:
- Reviews and signs off the completed electronic and/or paper data associated with a specific analysis that they have been trained on.
- Ensures accurate results that conform to current specifications, according to Good Manufacturing Practices, in house, compendial and regulatory requirements, and verifies all calculations for mathematical and analytical accuracy.
Demonstrate behaviours that exhibit our organizational Values.
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 a related field and a minimum of 1-year relevant experience in a pharmaceutical lab environment; OR Community College diploma in a related field and a minimum of 2 years relevant experience in the analysis of pharmaceutical products.
Knowledge of Excel, Work and other Microsoft Office Programs and/or laboratory software packages is an asset.
Sound working and theoretical knowledge of automated laboratory instrumentation such as HPLC, AA, UV, Dissolution, IR, UV/VIS spectrophotometry and GC. Detailed oriented with problem solving and instrument troubleshooting ability.
Excellent verbal and written English and communication skills.
Knowledge of GMP/GLP.
Proven organization and time management skills as demonstrated through previous work and/or educational experience.

At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed.

We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

The hiring range for this position is $48,851 - $81,419 CAD per year. The final agreed-upon salary may vary based on factors such as job-related knowledge, skills and experience. We are looking for top talent. If your qualifications differ from those listed above, the scope of work and final agreed-upon salary may be adjusted to reflect your individual qualifications. The Apotex Total Rewards package goes beyond base salary. Apotex offers bonus programs based on your position in the organization, you can excel based on our pay-for-performance philosophy. With comprehensive benefits, a pension plan to help you save for retirement and learning and development opportunities, we provide a comprehensive package for your personal and professional development.

Apotex will use artificial intelligence to screen, select and/or assess your application for this job.

This job posting is for a role that is currently available and vacant at Apotex.

Apply About employer

More about this job

Responsibilities

The chemist is responsible for analyzing laboratory samples using various chemical and instrumental techniques while adhering to GMP requirements. They also document test data, perform equipment maintenance, and review analytical results for accuracy.

Requirements

Candidates must hold a B.Sc. in Chemistry or a related field with at least one year of pharmaceutical lab experience, or a community college diploma with two years of experience. Proficiency in automated laboratory instrumentation and knowledge of GMP/GLP standards are required.

Skills

HPLC
GC
UV/VIS spectrophotometry
Dissolution
IR
AA
GMP
GLP
Laboratory instrumentation
Analytical chemistry
Troubleshooting
Data documentation
Time management
Problem solving
Microsoft Office

Benefits

Bonus programs
Comprehensive benefits
Pension plan
Learning and development opportunities

Visa sponsorship

Not detected in the job text

Keywords

Chemist
QC
Quality Control
Pharmaceutical
GMP
GLP
HPLC
GC
UV/VIS
Dissolution
Analytical chemistry
Laboratory
Raw material testing
Stability samples
Method transfer
SOP
Documentation
Instrumentation
Troubleshooting
Compliance
Biosimilar
Generic pharmaceuticals
Data integrity
Chemical analysis
Quality assurance

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