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Quality Assurance Specialist

  • Mitchell, ON, Canada

Salary Range: $55,000 - $60,000 per annum. · Full-time

This opening has closed.

The original listing is kept below for reference.

Job details

Pay
Salary Range: $55,000 - $60,000 per annum.
Job type
Full-time
Closing date
Posting language
English
Posted

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Original job description

Archived listing. The details below describe a past opening.

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.

Compensation & Benefits

  • 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.

Why Join Us?

If you are looking for a stable, long-term career with a company that values quality, teamwork, and work-life balance - apply today and become part of the BAM team!

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

Application Instructions

If you are interested in a career with a reliable employer in the animal health industry and meet the requirements, we encourage you to submit your resume for consideration.

Please apply only if you:

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

Apply through the LinkedIn or by Email: hr@bioagrimix.com

or

 Drop-off: 11 Ellens Street, Mitchell, ON

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.

More about this job

Responsibilities

Review manufacturing batch records and laboratory documentation to ensure products meet specifications and regulatory requirements, and maintain quality records and procedures. Investigate quality incidents, implement corrective and preventive actions, support process and cleaning validations, and contribute to continuous improvement of the quality system.

Requirements

A B.Sc. in Chemistry, Biology, Biological or Pharmaceutical Chemistry, or a related field is required, along with 1–2 years of experience in quality assurance or a similar role; pharmaceutical or feed manufacturing experience is preferred. Candidates should know GMP, analytical testing, and statistical analysis, with strong analytical, organizational, communication, and Microsoft Office skills; HACCP certification is an asset.

Skills

  • Quality Assurance
  • Batch Record Review
  • Quality Control Record Review
  • GMP Compliance
  • HACCP
  • Root Cause Analysis
  • Corrective and Preventive Actions
  • Deviation Investigation
  • Document Control
  • Premises Inspection
  • SOP Review
  • Process Validation
  • Cleaning Validation
  • Statistical Analysis
  • Analytical Testing
  • Microsoft Office

Benefits

  • Health Benefits
  • Group RSP Plan
  • Holiday Bonus

Visa sponsorship

Not detected in the job text

Categories

  • Manufacturing
  • Agriculture
  • Science & Research

Keywords

  • Quality Assurance
  • Quality Control
  • Animal Feed Manufacturing
  • Animal Health Products
  • Pharmaceutical Manufacturing
  • Health Canada
  • FDA
  • HACCP
  • GMP
  • cGMP
  • Batch Records
  • Certificates Of Analysis
  • Analytical Testing
  • Laboratory Records
  • Specifications
  • Deviation Investigations
  • Non-Conformances
  • Out-Of-Specification Results
  • Root Cause Analysis
  • Corrective And Preventive Actions
  • Document Control
  • Standard Operating Procedures
  • Process Validation
  • Cleaning Validation
  • Statistical Analysis
  • Continuous Improvement
  • Microsoft Word
  • Microsoft Excel
  • Microsoft PowerPoint
  • Adobe Software

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