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- Employment type
- Full-time
- Experience level
- Lead · 10+ years
- Minimum education
- Bachelor’s degree
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Mid-Senior level
- Application method
- Direct apply is available
Job summary
The QA Manager is responsible for overseeing the quality assurance team, managing daily testing and production data, and ensuring compliance with GMP/cGMP and regulatory standards. They will also lead internal and external audits, mentor staff, and maintain the company's Quality Management Systems.
Job details
Join Our Team at Bio Agri Mix LP – Now Hiring Quality Assurance (QA) Manager Mitchell, Ontario → Perth County is near Stratford (20 minutes), centrally located between London and Kitchener (45 minutes) About Us: Bio Agri Mix LP is a leading Canadian manufacturer of animal feed medicants and animal health care products with over 42 years of success. As a Health Canada licensed, FDA-approved, and HACCP-certified company, we proudly serve the Canadian market with a strong commitment to safety, quality, and innovation. Description: We are seeking a hands-on leader to serve as the QA Manager, with full accountability for the Quality Assurance team for an open position. This role is responsible for managing the day-to-day priorities including review of testing and production data for raw material and finished product release, the oversite of GMP/cGMP compliance, deviations, and investigations. The QA Manager will ensure a safe, efficient, and compliant operating environment aligned with the company objectives. The Quality Assurance Manager reports to the Director of Quality. Compensation & Benefits: Salary Range: $75,000 – $100,000 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 Key Responsibilities: Perform the Finished Product and Raw Material release process, ensuring all necessary documentation, testing, and compliance checks are completed prior to release. Manage and mentor a team of QA professionals, including setting performance goals, providing training, and conducting performance evaluations. Develop, implement, and maintain Quality Management Systems (QMS) in accordance with regulatory requirements such as Health Canada, FDA, and ICH guidelines. Ensure that all documentation is accurate and reflects current practices and regulatory requirements. Analyze and approve product stability data at scheduled intervals to assess product stability and shelf-life predictions. Conduct thorough annual product reviews, ensuring all products meet regulatory requirements and quality standards. This includes collecting and analyzing data related to product performance, including manufacturing processes, quality control results, stability results, and investigations. Assist in executing internal and external audits, including compiling necessary documentation and implementing corrective actions to resolve any deficiencies or gaps identified. Work collaboratively with other departments to address quality concerns and support product development and commercialization. Qualifications: Bachelor’s degree in pharmaceutical sciences, engineering, chemistry, or related field. 10 years of experience within the pharmaceutical industry, with at least 5 years in a managerial role would be an asset. Regulatory Knowledge – In-depth understanding of Canadian and international pharmaceutical regulations and quality standards (e.g., Health Canada, FDA, ICH). Skills Required: Strong knowledge of pharmaceutical quality standards and regulatory requirements. Excellent analytical and problem-solving skills. Proficiency in using quality management systems and statistical analysis tools. Exceptional attention to detail and organizational skills. Effective communication and people skills, with the ability to work collaboratively across departments. Ability to manage multiple tasks and prioritize effectively in a fast-paced environment. Strong leadership and team management skills. Portray a positive attitude that reflects the company’s core values and culture. Why Join Bio Agri Mix LP? Long-standing, reputable company in a growing industry Opportunities to develop a stable, long-term career in pharmaceutical manufacturing Inclusive, accessible workplace that supports employee growth and well-being 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 LinkedIn, BAM website, 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.
What you’ll do
The QA Manager is responsible for overseeing the quality assurance team, managing daily testing and production data, and ensuring compliance with GMP/cGMP and regulatory standards. They will also lead internal and external audits, mentor staff, and maintain the company's Quality Management Systems.
Requirements
Candidates must hold a bachelor's degree in pharmaceutical sciences, engineering, chemistry, or a related field. A minimum of 10 years of experience in the pharmaceutical industry is required, with at least 5 years in a managerial role preferred.
Benefits
- Health benefits
- Group RSP plan
- Holiday bonus
Listed skills
- Quality assurance · Preferred
- Regulatory Compliance · Preferred
- Team Leadership · Preferred
- Data analysis · Preferred
- Problem solving · Preferred
- Communication Skills · Preferred
- Attention to detail · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Quality assurance
- GMP compliance
- cGMP compliance
- Regulatory compliance
- Team leadership
- Data analysis
- Problem-solving
- Quality management systems
- Statistical analysis
- Internal auditing
- External auditing
- Documentation management
- Product stability testing
- Mentoring
- Communication skills
- Attention to detail
Job areas
- Manufacturing
- Management & Leadership
- Science & Research
- Healthcare
- Agriculture
