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Qc Lab Manager Jobs in Whitby, ON (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 ... Coordinate end-to-end materials management including subsampling, external lab shipments, results ...

Aecon Group Inc.

QC Supervisor

Bowmanville, ON

Operate responsibly by managing risk, safety, and environmental considerations across all our ... The QC Supervisor - NI will work with other Aecon sectors and Alliance partners to monitor the ...

Plan Group

QA/QC Manager

Vaughan, ON · On-site

As a QAQC Manager , you will: * Lead and oversee the QA/QC program across assigned projects, ensuring compliance with company standards, drawings, specifications, and contractual requirements * Act ...

ES Fox Limited

QC Receiving Inspector

Bowmanville, ON · On-site

CA$65K - CA$100K/yr

Summary of the Role Reporting to the Project Quality Assurance Manager, the QC Receiving Inspector will be responsible for performing quality control inspections on incoming materials for all ...

TreeHouse Foods

QC Technician-1

Richmond Hill, ON · On-site

Read all plates and fill in the micro record for manager's signature. If any countsfound ... Collect, pack and send samples to outside lab. * Change hot room temperature chart Requirements:

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Qc Lab Manager information

What does a QC Lab Manager do?

A QC (Quality Control) Lab Manager is responsible for overseeing the operations of a laboratory that tests products or materials to ensure they meet required quality standards. They supervise laboratory staff, implement quality control procedures, ensure compliance with regulatory requirements, and analyze test results. The QC Lab Manager also manages lab resources, maintains equipment, and works closely with other departments to resolve quality issues and support product development.

What are some common challenges faced by a QC Lab Manager, and how can they be addressed in a fast-paced laboratory environment?

QC Lab Managers often encounter challenges such as maintaining compliance with strict regulatory standards, managing workflow to ensure timely testing, and leading a diverse team with varying levels of experience. These challenges can be addressed by implementing robust quality management systems, fostering ongoing training programs, and utilizing effective communication tools to coordinate tasks. Additionally, strong organizational skills and the ability to prioritize workload are essential for ensuring accuracy and efficiency in a fast-paced lab setting.

What are the key skills and qualifications needed to thrive as a QC Lab Manager, and why are they important?

To thrive as a QC Lab Manager, you need a strong background in laboratory science, quality control processes, and leadership, typically backed by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (such as GMP or ISO), and relevant certifications like ASQ CQE are highly valued. Excellent problem-solving, communication, and team management skills set exceptional QC Lab Managers apart. These competencies are critical to ensuring accurate results, regulatory compliance, and efficient lab operations.

What is the difference between Qc Lab Manager vs Qc Technician?

AspectQc Lab ManagerQc Technician
CredentialsBachelor's degree in science, quality assurance certifications often preferredAssociate's or bachelor's degree in science or related field
Work EnvironmentSupervises laboratory staff, manages quality processesPerforms testing and data collection in the lab
Employer & Industry UsageUsed across manufacturing, pharmaceuticals, food industriesCommonly employed in similar industries for testing roles

The Qc Lab Manager oversees laboratory operations, staff, and quality systems, while the Qc Technician focuses on executing tests and recording data. Both roles require scientific knowledge, but the manager has additional responsibilities in supervision and process management.

What job categories do people searching Qc Lab Manager jobs in Whitby, ON look for?

The top searched job categories for Qc Lab Manager jobs in Whitby, ON are:

Qc Lab Manager jobs near you
Infographic showing various Qc Lab Manager job openings in Whitby, ON as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution.

QC Analyst

Eli Lilly and Company

Toronto, ON • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 6 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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