Position: Quality Control Laboratory Associate Technician
Our client, a pharmaceutical company located in Kirkland, is looking for a Quality Control Laboratory Associate Technician for a permanent position to be filled urgently. Reporting to the laboratory supervisor, the selected candidate will perform chemical and physical analyses in accordance with pharmacopoeia standards (USP/EP) and in compliance with Good Manufacturing Practices (GMP). They will participate in the quality control of raw materials, packaging components, and utility samples while ensuring rigorous documentation.
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The ideal candidate has solid experience in a regulated pharmaceutical laboratory (GMP), strong expertise in documentation, and an excellent understanding of pharmacopoeia requirements. The position demands rigor, proactivity, a strong team spirit, and a keen sense of urgency. Bilingualism is an asset, but unilingual English with functional French (reading and writing) is acceptable.
Shift: Day shift
Location: Montreal
Salary: $65,000 and up, depending on experience
Duration: Permanent
Important: Candidates must be authorized to work in Canada and already reside in the province of Quebec.
Advantages
• Salary starting at $65,000 (adjustable based on experience)
• Full-time permanent position (day shift)
• Stimulating and structured GMP environment
• Professional development opportunities
• Group insurance and paid time off
• Collaborative and dynamic team
Responsibilities
• Perform analytical tests according to USP/EP methods and internal procedures
• Work in a GMP-compliant environment
• Ensure the accuracy and compliance of laboratory results
• Write and review technical documentation (protocols, reports, SOPs)
• Collaborate with quality and production teams to resolve non-conformities
• Actively participate in internal and external audits
• Maintain laboratory equipment and ensure calibration follow-ups
Qualifications
• Degree in Chemistry, Biochemistry, or a related field
• Minimum of 2 years of experience in a pharmaceutical laboratory (GMP environment)
• Excellent knowledge of USP/EP pharmacopoeias
• Strong experience in writing and reviewing technical documentation
• Bilingual (English/French) – French reading and writing essential
• Good knowledge of GMP and regulatory standards
• Strong organizational skills, attention to detail, autonomy, and teamwork skills
Summary
If you are motivated by quality, continuous improvement, and the idea of making a real difference in a growing company, this position is for you! Send me your resume now.
Georges Beauzil
Recruitment Consultant
Quality and Manufacturing Engineering
georges.beauzil@randstad.ca
Let's connect on LinkedIn confidentially:
https://www.linkedin.com/in/georges-beauzil-b89738316/
Randstad Canada is committed to fostering a workforce reflective of all peoples of Canada. As a result, we are committed to developing and implementing strategies to increase the equity, diversity and inclusion within the workplace by examining our internal policies, practices, and systems throughout the entire lifecycle of our workforce, including its recruitment, retention and advancement for all employees. In addition to our deep commitment to respecting human rights, we are dedicated to positive actions to affect change to ensure everyone has full participation in the workforce free from any barriers, systemic or otherwise, especially equity-seeking groups who are usually underrepresented in Canada's workforce, including those who identify as women or non-binary/gender non-conforming; Indigenous or Aboriginal Peoples; persons with disabilities (visible or invisible) and; members of visible minorities, racialized groups and the LGBTQ2+ community.
Randstad Canada is committed to creating and maintaining an inclusive and accessible workplace for all its candidates and employees by supporting their accessibility and accommodation needs throughout the employment lifecycle. We ask that all job applications please identify any accommodation requirements by sending an email to accessibility@randstad.ca to ensure their ability to fully participate in the interview process.
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Position: Quality Control Laboratory Associate Technician
Our client, a pharmaceutical company located in Kirkland, is looking for a Quality Control Laboratory Associate Technician for a permanent position to be filled urgently. Reporting to the laboratory supervisor, the selected candidate will perform chemical and physical analyses in accordance with pharmacopoeia standards (USP/EP) and in compliance with Good Manufacturing Practices (GMP). They will participate in the quality control of raw materials, packaging components, and utility samples while ensuring rigorous documentation.
The ideal candidate has solid experience in a regulated pharmaceutical laboratory (GMP), strong expertise in documentation, and an excellent understanding of pharmacopoeia requirements. The position demands rigor, proactivity, a strong team spirit, and a keen sense of urgency. Bilingualism is an asset, but unilingual English with functional French (reading and writing) is acceptable.
Shift: Day shift
Location: Montreal
Salary: $65,000 and up, depending on experience
Duration: Permanent
Important: Candidates must be authorized to work in Canada and already reside in the province of Quebec.
...
Advantages
• Salary starting at $65,000 (adjustable based on experience)
• Full-time permanent position (day shift)
• Stimulating and structured GMP environment
• Professional development opportunities
• Group insurance and paid time off
• Collaborative and dynamic team
Responsibilities
• Perform analytical tests according to USP/EP methods and internal procedures
• Work in a GMP-compliant environment
• Ensure the accuracy and compliance of laboratory results
• Write and review technical documentation (protocols, reports, SOPs)
• Collaborate with quality and production teams to resolve non-conformities
• Actively participate in internal and external audits
• Maintain laboratory equipment and ensure calibration follow-ups
Qualifications
• Degree in Chemistry, Biochemistry, or a related field
• Minimum of 2 years of experience in a pharmaceutical laboratory (GMP environment)
• Excellent knowledge of USP/EP pharmacopoeias
• Strong experience in writing and reviewing technical documentation
• Bilingual (English/French) – French reading and writing essential
• Good knowledge of GMP and regulatory standards
• Strong organizational skills, attention to detail, autonomy, and teamwork skills
Summary
If you are motivated by quality, continuous improvement, and the idea of making a real difference in a growing company, this position is for you! Send me your resume now.
Georges Beauzil
Recruitment Consultant
Quality and Manufacturing Engineering
georges.beauzil@randstad.ca
Let's connect on LinkedIn confidentially:
https://www.linkedin.com/in/georges-beauzil-b89738316/
Randstad Canada is committed to fostering a workforce reflective of all peoples of Canada. As a result, we are committed to developing and implementing strategies to increase the equity, diversity and inclusion within the workplace by examining our internal policies, practices, and systems throughout the entire lifecycle of our workforce, including its recruitment, retention and advancement for all employees. In addition to our deep commitment to respecting human rights, we are dedicated to positive actions to affect change to ensure everyone has full participation in the workforce free from any barriers, systemic or otherwise, especially equity-seeking groups who are usually underrepresented in Canada's workforce, including those who identify as women or non-binary/gender non-conforming; Indigenous or Aboriginal Peoples; persons with disabilities (visible or invisible) and; members of visible minorities, racialized groups and the LGBTQ2+ community.
Randstad Canada is committed to creating and maintaining an inclusive and accessible workplace for all its candidates and employees by supporting their accessibility and accommodation needs throughout the employment lifecycle. We ask that all job applications please identify any accommodation requirements by sending an email to accessibility@randstad.ca to ensure their ability to fully participate in the interview process.
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