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Qa Ra Associate Jobs in Ontario (NOW HIRING)

... Associate is an asset. Work Experience: - Minimum one year relevant work experience in quality assurance experience Apply today! If you feel you would make a great fit for this role please submit an ...

... Associate Quality Assurance Analyst ( Hybrid) Toronto, Ontario, Canada $45.00-$ hours ago Junior Payments Quality Assurance Analyst Co-Op We're unlocking community knowledge in a new way. Experts add ...

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Overview The Quaker Quality Assurance Coordinator is responsible for leading and coordinating the ... our associates to do meaningful work and make a lasting impact in the communities we serve.

Overview The Quaker Quality Assurance Coordinator is responsible for leading and coordinating the ... our associates to do meaningful work and make a lasting impact in the communities we serve.

AML QA Analyst-(Hybrid)

Toronto, ON · Hybrid

CA$50K - CA$56K/yr

As an AML QA Analyst, you will support the accuracy and integrity of Central 1's AML/ATF regulatory ... Filing Support Associates, Analysts, and Investigators. * Validate report content against ...

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Showing results 1-20

Qa Ra Associate information

See Ontario salary details

$23K

$78.5K

$127.5K

How much do qa ra associate jobs pay per year?

As of Sep 10, 2026, the average yearly pay for qa ra associate in Ontario is $78,482.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,000.00 and $104,500.00 per year, depending on experience, location, and employer.

What is a QA RA associate?

QA RA Associates, or Quality Assurance and Regulatory Affairs Associates, are professionals who help ensure that products—especially in industries like pharmaceuticals, medical devices, and biotechnology—meet quality standards and comply with government regulations. They assist in preparing and maintaining documentation, support audits, and help with the submission of regulatory filings. Their work is essential to keeping products safe, effective, and legally approved for market. QA RA Associates typically collaborate with various departments to ensure compliance throughout the product lifecycle.

What are the key skills and qualifications needed to thrive as a QA RA associate?

To thrive as a QA/RA Associate, you need a solid understanding of quality assurance and regulatory affairs principles, typically supported by a degree in life sciences or engineering. Familiarity with regulatory standards like ISO 13485, FDA 21 CFR Part 820, and proficiency in document control systems are essential. Strong attention to detail, analytical thinking, and effective communication skills help ensure compliance and facilitate cross-functional collaboration. These skills are crucial for maintaining regulatory compliance and ensuring product quality in highly regulated industries.

What are some typical challenges faced by a QA RA associate when navigating regulatory submissions?

QA RA Associates often encounter challenges such as staying updated with evolving regulatory requirements, coordinating documentation across departments, and ensuring submission accuracy. Managing tight deadlines while maintaining high-quality standards can be demanding, especially when multiple products or markets are involved. Successful associates proactively communicate with cross-functional teams and utilize strong organizational skills to streamline the submission process.

What cities in Ontario are hiring for Qa Ra Associate jobs?

Cities in Ontario with the most Qa Ra Associate job openings:

Infographic showing various Qa Ra Associate job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $78,482 per year, or $37.7 per hour.

Quality Assurance Associate

Toronto, ON • On-site

CA$52K - CA$60K/yr

Full-time

Medical, Dental

Re-posted yesterday


Job description

Benefits:
  • Gym Access
  • Dental insurance
  • Health insurance

We're Hiring!
The Quality Assurance Associate participates in the completion of milestones associated with specific projects and supports ongoing Annual Product Reviews, Management of Deviations, CAPAs, Change Management, SOP Management, and general quality management systems responsibilities in support of the manufacture, packaging and release of commercial products.
JOB RESPONSIBILITIES

  • Completes APR reports in accordance with the schedule, gathering information available from batch records, investigations, product changes, complaints etc.
  • Collaborate and liaise with business to review and manage Change Control Requests. Ensures GDP and change management procedures are followed.
  • Assists with monitoring all internal QMS compliance through performing internal audits, including production, facilities, validation, and the laboratories.
  • In collaboration with Quality colleagues identifies areas for continuous improvement within the QMS.
  • Acts as Subject Matter Expert (SME) for Investigations & Quality Risk Management. 
  • Reviews deviation and investigation records, includes tracking, follow-up, and reporting/trending. Ensures GDP and deviation procedures are followed.
  • Reviews Corrective and Preventative Actions (CAPA); includes tracking, follow-up, and reporting/trending and evaluating CAPA for effectiveness.
  • Works with all departments to guide the timely completion of Deviations, CAPA, Corrective Work Orders, Change Controls, and Investigations.
  • Helps the Compliance Specialist with the review of batch records for product release.
  • Generates and maintains Quality Assurance and QMS standard operating procedures (SOPs).
  • Oversees controlled document and system changes and performs detailed impact analysis to ensure all necessary GMP and qualification action items have been added to the change controls, as well as executed.
  • Collaborates significantly with cross functional groups, including Quality Assurance, Manufacturing, Process Development, Facilities, and Regulatory Affairs on quality assurance matters. 
  • Cross-train with other QA Associates.
  • Responsible for Logbook issuance, control, and review.
  • Files and maintains controlled documents.
  • Other duties as assigned
JOB REQUIREMENT

  • Minimum 5 years of GMP-related experience in biopharmaceutical or pharmaceutical manufacturing.
  • Bachelor's degree or diploma in Chemistry, Biology, Engineering, or a related field.
  • Strong knowledge of cGMP/GDP requirements, international regulatory compliance, and GMP operations.
  • Proven ability to prioritize tasks and meet internal and external customer needs in a fast-paced environment.
  • Experience supporting Quality projects, including data analysis and evaluation of identifiable factors.
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.