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Quality Assurance; QA) Specialist

Job in London, Ontario, N0K, Canada
Listing for: Bio Agri Mix, LP
Full Time position
Listed on 2026-10-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Data Analyst, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 55000 - 60000 CAD Yearly CAD 55000.00 60000.00 YEAR
Job Description & How to Apply Below
Position: Quality Assurance (QA) Specialist
Quality Assurance (QA) Specialist – Full-Time, Day Shift

Company Overview
Bio Agri Mix LP has been a leading Canadian manufacturer of  animal feed medicants  and  animal health products  for over 40 years. Located in  Mitchell, Ontario , we are a  Health Canada licensed ,  FDA approved , and  HACCP certified  facility serving the Canadian market.

Position Overview
The  QA Specialist  ensures that all products meet quality standards and comply with  Health Canada ,  FDA , and  HACCP  regulatory requirements while supporting continuous improvement initiatives. The QA Specialist reports to the QA Manager.

Salary Range:  $55,000 – $60,000 per annum. Salary will be commensurate with knowledge and related experience.

Health Benefits:

Eligible after a successful 90 day probation period

Group RSP Plan:  Eligible after a successful 90 day probation period

Holiday Bonus:  $1,000 (pro-rated based on start date and active days worked)

Work Schedule

Day

Shift:  Monday to Thursday | 8:00 AM – 4:30 PM | and Friday 8:00 AM – 4 PM

Work Arrangement
On-site position — reliable daily commuting or relocation  prior to starting  is required.

Please note:

Housing availability in the Mitchell area is limited. Candidates considering relocation are encouraged to plan accordingly.

Key Responsibilities

Review batch records and related documentation to ensure compliance with manufacturing procedures, specifications, and regulatory requirements

Review and approve Quality Control laboratory records, including test results, data sheets, and Certificates of Analysis (CoA). Ensure that test results and analytical data meet established specifications and acceptance criteria. Ensure that investigations into laboratory deviations, non-conformances, or out-of-specification results are conducted in accordance with GMP guidelines and internal SOPs.

Lead and/or participate in investigations of quality incidents, deviations, and non-conformances. Identify root causes of quality issues and implement Corrective and Preventive Actions (CAPAs) to prevent recurrence.

Organize and maintain quality-related documents, records, and files in accordance with company policies and regulatory requirements.

Conduct routine inspections of premises for compliance with Good Manufacturing Practices (GMP) and internal procedures.

Assist in the review and revision of Standard Operating Procedures (SOPs) to ensure accuracy and compliance with regulatory requirements.

Prepare protocols for process validation and cleaning validation studies based on cGMP standards and BAM SOPs.

Assist in preparing reports for manufacturing process and cleaning validations, including statistical analysis of the data.

Assess proposed changes in manufacturing or cleaning processes for their validation and regulatory impact.

Participate in projects that support continuous improvement of the quality system.

Support the QA team in achieving the department’s overall objectives and perform other duties as assigned.

Qualifications

Education:

B.Sc. in Chemistry, Biology, Biological or Pharmaceutical Chemistry, or related field

Experience:

1–2 years in a QA or similar role (pharmaceutical or feed manufacturing preferred)

Certifications:

HACCP certification is an asset

Knowledge of:  GMPs, analytical testing, and statistical analysis tools

Skills

Strong analytical and problem-solving skills

Excellent attention to detail and organizational ability

Clear written and verbal communication

Proficient in Microsoft Office (Word, Excel, PowerPoint) and Adobe software

Dependable, accountable, and team-oriented with a strong attendance record

Please apply only if you:

Applicants must be legally entitled to work in Canada (e.g., Canadian citizen, permanent resident, or valid work permit).

We thank all applicants for their interest; however, only those selected for an interview will be contacted.

Accessibility Statement
Bio Agri Mix LP is an equal opportunity employer. We are committed to an inclusive, accessible workplace. Accommodations are available upon request for candidates during all stages of the recruitment process. Please contact Human Resources to make arrangements.

Recruitment Process
All applications are reviewed by our Human Resources team. We do not rely on automated decision-making tools to screen or select candidates. Hiring decisions are made by qualified personnel based on job-related criteria.
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