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Quality Control Analyst Jobs in Ontario (NOW HIRING)

Eli Lilly and Company

QC Analyst

Toronto, ON · On-site

JOB SUMMARY We are looking for a QC Scientist to perform routine and advanced analytical testing, support method verification, and ensure full GMP compliance. The role includes conducting ...

Td

Senior Quality Control Analyst (4743)

Toronto, ON · Hybrid

CA$81K - CA$115K/yr

In addition, the Senior QC Analyst is responsible for RTC approvals, ensuring sound judgment is applied in determining whether to exit or retain the customer. The Senior Analyst will also ensure that ...

Td

Senior Quality Control Analyst (4743)

Ottawa, ON · Hybrid

CA$81K - CA$115K/yr

In addition, the Senior QC Analyst is responsible for RTC approvals, ensuring sound judgment is applied in determining whether to exit or retain the customer. The Senior Analyst will also ensure that ...

BT

Quality Control Specialist

Woodstock, ON · On-site

CA$55K - CA$70K/yr

As a Quality Control Specialist, you will play a crucial role in ensuring that our dairy products ... You will be responsible for conducting thorough inspections, tests, and analyses throughout the ...

L3HHCM20

Quality Control Inspector

Dundas, ON

CA$31 - CA$40/hr

Quality Control inspector Ref# 42264 Waterdown, Ontario Tasks to be Accomplished ... Compile and analyze quality performance data * Develop graphs, charts and quality reports

Amrize

Quality Control Technician

Paris, ON

Execute Job Hazard Analyses for QC Tasks and implement Action Items. * Implement programs and processes to ensure compliance of all products with relevant Codes, Standards, and Specifications.

Amrize

Quality Control Technician

Ayr, ON

Execute Job Hazard Analyses for QC Tasks and implement Action Items. * Implement programs and processes to ensure compliance of all products with relevant Codes, Standards, and Specifications.

Amrize

Quality Control Technician

London, ON · On-site

Execute Job Hazard Analyses for QC Tasks and implement Action Items. * Implement programs and processes to ensure compliance of all products with relevant Codes, Standards, and Specifications.

Amrize

Quality Control Technician

Woodstock, ON · On-site

Execute Job Hazard Analyses for QC Tasks and implement Action Items. * Implement programs and processes to ensure compliance of all products with relevant Codes, Standards, and Specifications.

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All JobsQuality Control Analyst JobsQuality Control Analyst Jobs in Ontario

Quality Control Analyst information

See Ontario salary details

$12

$27

$41

How much do quality control analyst jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for quality control analyst in Ontario is $27.51, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $31.73 per hour, depending on experience, location, and employer.

What is a quality control analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

What are the key skills and qualifications needed to thrive as a quality control analyst?

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by quality control analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

How much does a quality control analyst earn?

The average salary for a quality control analyst typically ranges from $45,000 to $70,000 per year, depending on experience, industry, and location. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. Many roles also include benefits such as health insurance and paid time off.
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For Quality Control Analyst jobs in Ontario, the most frequently searched job titles are:

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Quality Control Analyst jobs near you
Infographic showing various Quality Control Analyst job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $57,225 per year, or $27.5 per hour.

QC Analyst

Eli Lilly and Company

Toronto, ON • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 5 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.


JOB SUMMARY

We are looking for a QC Scientist to perform routine and advanced analytical testing, support method verification, and ensure full GMP compliance. The role includes conducting investigations, maintaining documentation, troubleshooting instruments, collaborating cross-functionally, and contributing to QC KPIs to drive quality and operational excellence.

JOB RESPONSIBILITIES

Analytical Testing & Documentation

  • Perform analytical testing of raw materials, finished products, and stability samples using HPLC, GC, FTIR, and related validated methods.

  • Perform routine inspection of environmental monitoring (EM) samples including viable/non-viable particulate, surface sampling, sterility, and settle plates per cGMP and site SOPs.

  • Support method qualification, product qualification, and verification studies per cGMP and regulatory requirements.

  • Maintain accurate documentation, reports, and laboratory records per GMP standards.

  • Coordinate end-to-end materials management including subsampling, external lab shipments, results review, and specification completion for timely material release.

  • Maintain lab operations: monitor reagent/consumable inventory, initiate purchase orders, log incoming materials, and manage disposal per site and regulatory requirements.

Technical Documentation

  • Prepare method qualification and stability protocols/reports per USP, EP, and ICH guidelines.

  • Author, review, and support SOPs, specifications, test methods, change controls, protocols, and reports.

Change Control

  • Demonstrate thorough understanding of change control as it applies to QC lab activities including methods, instruments, reagents, and procedures.

  • Initiate change control requests with complete technical justification and all required supporting documentation prior to submission.

  • Actively track and follow up on assigned change controls to ensure timely closure within established site timelines.

Deviation, LI & OOS Investigation

  • Understand the OOS investigation process including Phase I (analyst error, instrument, sample prep) and Phase II, ensuring all steps are documented per FDA OOS Guidance and site procedures

  • Perform systematic, objective investigations using root cause analysis tools; document findings clearly per GMP.

  • Develop and implement risk-based CAPAs to prevent recurrence; ensure timely follow-up and verification of effectiveness.

  • Document all OOS and LI steps contemporaneously per ALCOA+ and data integrity principles.

Instrumentation

  • Support calibration, troubleshooting, and routine maintenance of analytical instruments to ensure continuous operational readiness and data integrity.

Microbiological Testing & Environmental Monitoring

  • Perform inspection and reading of environmental monitoring plates, sterility test bottles, and media fill samples per approved SOPs and cGMP requirements, reviewing results for accuracy and compliance prior to disposition.

  • Coordinate shipment of media samples to contract laboratories for Growth Promotion Testing (GPT), ensuring proper chain of custody and timely evaluation of results against acceptance criteria.

  • Support microbiology-related deviation investigations (e.g., unexpected growth, failed GPT) using structured root cause analysis.

EDUCATION & COMPETENCIES

  • BSc in Chemistry or related field from a recognized institution.

  • Minimum of5years of experience in a regulated pharmaceutical or laboratory environment

ADDITIONAL SKILLS

  • Laboratory computer skills (e.g., Empower, Veeva); proficient in MS Teams and Outlook.

  • Excellent written and verbal English communication skills.

  • Detail-oriented with strong problem-solving and organizational skills.

  • In-depth knowledge of GMP, GLP, and data integrity (ALCOA+).

  • Working knowledge of change control, deviation, LI, and OOS investigation processes.

  • Operational and troubleshooting skills for analytical instruments.

  • Proven time management skills as demonstrated through work and educational experience.

  • Knowledge of Radiopharmaceuticals is an asset.

  • Willing to work flexible hours including early mornings, late evenings, or weekends as required.

LILLY CORE EXPECTATIONS (R1-R4)

INCLUDE

Influences & collaborates across peers, teams, and functions.

Listens to learn & understand different views.

Builds relationships across dimensions of difference.

Speaks up with ideas, concerns & to ensure safety of others.

Asks questions & invites others to contribute.

INNOVATE

Anticipates & resolves key technical problems impacting function or project.

Thinks creatively, tries new ideas & applies learnings.

Anticipates, embraces & adapts to change.

Invests in personal development & growth.

Is curious & seeks input from others.

ACCELERATE

Makes decisions based on available information impacting function or project.

Is effective, efficient & decisive.

Is goal &solution-focused.

Is proactive, positive & determined.

Seeks help & support from others when needed.

DELIVER

Impacts own projects, peers, team and/or across teams/business areas.

Performs high quality work.

Demonstrates courage & integrity.

Shares insights & collaborates with others.

Follows through on commitments.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lillydoes not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$69,000 - $101,200

Full-time equivalent employees may also be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a pension plan; vacation benefits; eligibility for healthcare benefits; flexible benefits (if applicable) life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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