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Apotex

Specialist, Equipment Qualification

Brantford, ON, N3T 6B8, Canada

Pay: $63,482 to $105,804 CAD / year
Experience: Minimum of 5 years experience in the pharmaceutical industry.
Posting language: English
Posted: Jul 16, 2026

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Original job description

About Apotex Inc.

Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.

For more information visit: www.apotex.com.

Job Summary

The Specialist, Equipment Qualification is responsible for planning, authoring, executing (Environmental mapping studies IQOQs and PQs) and maintaining qualification activities for production equipment, facilities, and utilities in accordance with the regulatory guidelines and applicable Apotex Inc. policies and procedures.

Job Responsibilities

Author Installation, Operation, and Performance qualification protocols and reports to ensure that equipment is correctly installed and operates as per the design and user’s specifications and is in compliance with the cGMP requirements.
As required for each equipment/system protocol, document the critical parameters/instruments/attributes, and associated maintenance and calibration requirements and ensure verification in the protocol.
Develop user-friendly tools and guidelines to achieve a consistent approach to Qualification. Support and implement plans to ensure that all Qualification work performed within Apotex Inc. is compliant to current regulatory requirements.
Provide training on qualification topics as required to team members, and potentially to customers and stakeholders outside department or organization.
Review, initiate and recommend changes (as applicable) to SOD’s, and VMP – Validation Master Plan for equipment and facilities qualification within Apotex Inc., specifications, and commissioning documentation.
Coordinate the Equipment and Facility Qualification and Environmental Mapping activities as required.
May provide troubleshooting assistance and suggest remedial and corrective actions in the case of unacceptable validation or qualification results.
Support projects and expansion efforts with respect to qualification of equipment, facilities, and utilities, and attend meetings as required.
Work with Engineering to support authoring, review, or approval of FAT (Factory Acceptance Test) and SAT (Site Acceptance Tests) and participate in execution as required.
Participate in investigations, audits, and improvement initiatives related to equipment, facility, and utilities’ qualification.
Collaborate with Quality, Manufacturing, Engineering, Laboratories, and Information Systems, Safety, Health & Environment, and other departments as required to achieve department objectives and business needs.
Provide qualification technical assistance to outside suppliers and various departments and divisions within Apotex Inc.
Ensure that procedures, work instructions, standard maintenance documents and plant maintenance data describe critical parameters or ranges determined in the qualification or environmental mapping reports are maintained in a qualified status and in an audit ready status.
Assist in implementing and monitoring progress against plans to achieve the company goals and objective within project’s timelines and budget.
Re-qualify controlled spaces, and perform periodic review on the qualification status of designated equipment/facilities at the defined periodic intervals.
Review departmental systems and procedures on a periodic basis for compliance and suggest improvements as required.
Coordinates completion of physical deliverables for the Engineering Change Management Program.
Participate in monthly department meetings as required.
Works in a safe manner collaborating as a team member to achieve all outcomes.
Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
All other relevant duties as assigned.

Job Requirements

Education
- Degree, diploma, or certificate in Engineering, Pharmaceutical Technology, a related science; or equivalent.
Knowledge, Skills and Abilities
- Demonstrated knowledge of qualification concepts and GMP requirement.
- High level of familiarity and proven experience with Excel, Word, Visio, PowerPoint, Access and TrackWise.
- Able to manage multiple priorities in a fast-paced environment.
- Proven organizational, problem solving, customer service, interpersonal and time management skills demonstrated by previous work experience to manage multiple priorities in a fast-paced environment.
- Excellent communication skills.
Experience
- Minimum of 5 years experience in the pharmaceutical industry.

At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed.

We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

The hiring range for this position is $63,482 - $105,804 CAD per year. The final agreed-upon salary may vary based on factors such as job-related knowledge, skills and experience. We are looking for top talent. If your qualifications differ from those listed above, the scope of work and final agreed-upon salary may be adjusted to reflect your individual qualifications. The Apotex Total Rewards package goes beyond base salary. Apotex offers bonus programs based on your position in the organization, you can excel based on our pay-for-performance philosophy. With comprehensive benefits, a pension plan to help you save for retirement and learning and development opportunities, we provide a comprehensive package for your personal and professional development.

Apotex will use artificial intelligence to screen, select and/or assess your application for this job.

This job posting is for a role that is currently available and vacant at Apotex.

Apply About employer

More about this job

Responsibilities

The Specialist is responsible for planning, authoring, and executing qualification protocols for production equipment, facilities, and utilities to ensure cGMP compliance. They also coordinate environmental mapping activities and provide technical support for projects, audits, and investigations.

Requirements

Candidates must hold a degree, diploma, or certificate in Engineering, Pharmaceutical Technology, or a related science. A minimum of 5 years of experience in the pharmaceutical industry and demonstrated knowledge of qualification concepts and GMP requirements are required.

Skills

Equipment qualification
GMP compliance
Protocol authoring
Environmental mapping
Validation master plan
Troubleshooting
Technical writing
Project management
Data analysis
Regulatory compliance
Engineering documentation
Quality assurance
Cross-functional collaboration
Audit readiness
Time management
Communication

Benefits

Bonus programs
Comprehensive benefits
Pension plan
Learning and development opportunities

Visa sponsorship

Not detected in the job text

Keywords

Equipment Qualification
GMP
Pharmaceutical Industry
Validation
IQOQ
PQ
Environmental Mapping
TrackWise
Excel
Word
Visio
PowerPoint
Access
Engineering
Quality Assurance
Compliance
Standard Operating Procedures
Validation Master Plan
Factory Acceptance Test
Site Acceptance Test
Commissioning
Regulatory Guidelines
Technical Documentation
Audit Readiness
Manufacturing
Utilities
Project Management
Risk Assessment
Data Integrity
Process Improvement

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