ZipRecruiter

Log In

1

Quality Control In Jobs in Pickering, ON (NOW HIRING)

Plan Group

QA/QC Manager

Vaughan, ON · On-site

Minimum 5 years of field experience in QA/QC within electrical, mechanical, or technology construction environments * Post-secondary education in engineering technology, QA/QC, or a related ...

Plan Group

QA/QC Manager

Vaughan, ON · On-site

Minimum 5 years of field experience in QA/QC within electrical, mechanical, or technology construction environments * Post-secondary education in engineering technology, QA/QC, or a related ...

Bird Construction

QA/QC Coordinator

Toronto, ON · On-site

QA/QC Coordinator The QA/QC Coordinator is accountable for supporting the implementation and ... This position will be field based and located in North York, Ontario. What You Will Be Working On

previous pagenext page

Showing results 21-40

All JobsQuality Control In JobsQuality Control In Jobs in Pickering, ON

Quality Control In information

What is the difference between Quality Control In vs Quality Control Inspector?

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

What does a quality control in job do?

A quality control in job involves inspecting products or services to ensure they meet specified standards and quality requirements. It includes tasks such as testing, measuring, and reviewing processes, often using tools like checklists or testing equipment, to identify defects and ensure customer satisfaction.

What cities near Pickering, ON are hiring for Quality Control In jobs?

Cities near Pickering, ON with the most Quality Control In job openings:

Quality Control In jobs near you
Infographic showing various Quality Control In job openings in Pickering, ON as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 88% In-person, and 12% Hybrid job distribution.

QC Lab technician

Toronto, ON • On-site

Apollo Health And Beauty Care
See more jobs at Apollo Health And Beauty Careexternal

CA$45K/yr

Full-time

Medical, Dental

Posted 15 days ago

Job description

Benefits:
  • Gym Access
  • Dental insurance
  • Health insurance

We're Hiring!
We are looking for a QC Lab Technician to join our team on the Afternoon Shift (03:00 PM to 11:00 PM).
Working Schedule: Tuesday to Saturday!

Reporting to the Quality Control Laboratory Team Lead, the QC Lab Technician is responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products. This role ensures all testing is conducted in compliance with approved methods, Standard Operating Procedures (SOPs), and regulatory standards, including current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). The technician plays a key role in maintaining product quality and supporting continuous improvement within the QC laboratory environment.
JOB RESPONSIBILITIES
 
  • Performs physical and chemical testing on raw material, in-process, finished product, stability, and water samples.
  • Responsible for the release of in-process samples and raw material samples upon completion of training and passing the qualification requirements. 
  • Maintains all related records within cGMP & GLP guidelines and provides accurate documentation of tests performed and results obtained.
  • Ensure that all analytical test results are within the acceptable range specified on the Certificate of Analysis (CoA) forms.
  • Ensures samples are submitted to the microbiological laboratory or dispatched to an external laboratory as required, in a timely manner.
  • Performs laboratory equipment calibration in accordance with procedures, records results, and maintains calibration documentation.
  • Investigates and documents out of specification (OOS) results.
  • Files raw materials and external laboratory Certificates of Analysis (CoAs) into their respective binders.
  • Provides experienced input regarding the development and amendment of procedures and practices in the analytical area.
  • Recommend solutions for process improvements in the lab.
  • Follows all Standard Operating Procedures (SOPs), health & safety procedures, and other applicable company policies.
  • Wears, uses, and maintains personal protective equipment (PPE) as required.
  • Uses equipment, materials, and machinery only as authorized.
  • Identifies and reports any hazards, accidents, injuries requiring first aid, health care, lost-time injuries, occupational diseases, spills, or incidents in the workplace.
  • Maintains laboratory equipment.
  • Flexible shifts work as per business needs.
  • Available to work extended hours and/or weekends as required.
  • Performs other duties as assigned.
 
JOB REQUIREMENTS
 
  • Post-secondary degree in a related field.
  • Prior experience working in environments governed by GMP and GLP standards.
  • Familiarity with regulatory requirements from US FDA, Health Canada, and ICH Guidelines.
  • Excellent computer skills, along with strong written and oral communication abilities.
  • High attention to detail and quality in documentation practices.
  • Demonstrated proficiency in General Chemistry and use of analytical instruments, including HPLC, GC, ICP, UV-VIS, FTIR, and Titrations.
  • Strong ability to multi-task and effectively prioritize work.
  • Capable of performing routine and new procedures with minimal supervision.
  • Proven ability to interact across all organizational levels to support goals and influence decisions.
  • Solid understanding of statistics with the ability to analyze and present data in a clear, visual format.

Apollo Health & Beauty Care Ltd. will ensure accommodations are available in consultation with candidates during all stages of the recruitment process. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Duties outlined in this job description may not be all-inclusive, and can be modified at any time if requested by management. Apollo is committed to providing accommodations for people with disabilities in all parts of the hiring process. Apollo will work with applicants to meet accommodation needs that are made known in advance.
We thank all applicants for their interest however only those meeting the minimum qualifications will be interviewed.
Vacancy Status: This posting represents an existing vacancy, and we are actively recruiting to fill this position.