33 Quality Control Specialist jobs in Montréal

Job Description

Job Description

Quality Assurance Associate
Are you looking to make your next career move? CellCarta, a Contract Research Organization, is hiring a Quality Assurance Associate to join our dynamic team. As a QA Associate, you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today and take the first step towards an exciting new career with CellCarta!
Summary
Reporting to the Director of Quality Assurance, the Quality Assurance (QA) Associate is responsible for conducting and reporting quality assurance audits and reviews as scheduled. The QA Associate supports the QA department in assessing compliance of clinical and non-clinical studies with applicable regulations, guidelines, study protocols, study plans and company SOPs.
Responsibilities

• Perform audits of company facility and studies for compliance with Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Standard Operating Procedures (SOPs), study protocols, pertinent regulations and guidelines (FDA, Health Canada, EMEA, etc.);
• Perform inspections of Bioanalytical studies, for compliance with the OECD Principles of Good Laboratory Practices, Study Plans and Standard Operating Procedures (SOPs) at the critical phases of the studies;
• Review Workplans, Study plans, CAPAs, Change Controls/Implementations, SOPs;
• Audit pre-study documentation, in-process activities, end-of-study documentation and study reports;
• Conduct various facility audits, including audits of equipment maintenance, training records, computer validation and vendor qualification;
• Keep Management up to date with findings and follow up on corrective actions;
• Assist in the review, writing and distribution of SOPs, as applicable;
• Assist QA management in hosting sponsor and regulatory audits/inspections;
• Assist QA department in the training of personnel on SOPs and GCPs/GLPs.
• Coordinate and interact with other departments to ensure corporate, departmental and study goals are met.

Education

• BSc in life science, or equivalent.

Main Requirements

• 3-5 years QC/QA experience, or related field, preferably including audits of studies in a regulatory environment (GLP preferred);
• Knowledge and understanding of GCP, EMA, OECD, ICH, FDA in relation to Good Laboratory Practice (GLP) and/or GCP/GCLP quality requirements;
• Experience writing and reviewing Standard Operating Procedures (SOPs);
• Clear and concise written and verbal English communication;
• Knowledge in Drug Development, Validation of Analytical Methods, Quality Assurance and Regulatory Compliance;
• Various bioanalysis techniques an asset (e.g. Immunoassays, Quantitation, Mass Spectrometry, etc.);
• High level of attention to detail and accuracy, excellent investigative techniques;
• Strong commitment and self-motivated;
• Excellent organizational skills;
• Proven flexibility to adjust to constantly changing priorities, handle multiple tasks, while maintaining quality;
• Ability to work well in a team environment;
• Ability to identify and/or resolve quality issues, in a proactive, diplomatic, flexible and constructive manner;
• Ability to design and implement quality processes.

Working Conditions

• Onsite/hybrid position in Montreal;
• One year contract, 37.5hrs per week;
• Must accept to perform duties (e.g. inspections) in Bio Safety Level (BSL) 1 and 2 facilities where biological samples may be either naturally or experimentally infected with potentially hazardous viruses such as HIV, HCV, or CMV.

Benefits
We offer a wide range of benefits including:

• Competitive Wages;
• Vacation and Personal Days;
• Dialogue Telemedicine Service and Employee Assistance Program (EAP);
• OPUS & Cie Contribution;
• Parking reimbursement;
• Referral Program.

About CellCarta
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.
Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world! 
Join us as we make an impact on patient therapy!
 

The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact

 

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Job Description

Job Description

Under the supervision of the Quality Manager, the Quality Assurance Technician is responsible for ensuring product compliance with the quality assurance and control procedures established by Cryopak. They will actively participate in the research and development of new products as well as the corrective action process.

Responsibilities:

• Maintain the quality system up to date
• Organize and manage the calibration of measuring instruments (scales and calipers)
• Write and update internal and external specifications for finished products.
• Document identified non-conformities and ensure follow-up
• Train or raise staff awareness on good practices (BPF/GMP, GDP, etc.).
• Actively participate in the problem analysis process (CAPA) related to non-conformities (internal or customer complaints).
• Administer and control the required certifications for raw materials and provide all compliance documentation to our clients (CofC, CofA, others.).
• Manage non-conforming products (identification, quarantine, and communication)
• Review and approve inspection sheets from quality inspectors
• Verify and approve change requests related to the specifications of finished products.
• Support R&D teams during testing or when launching a new product
• Actively participate in the creation of new items
• Participate in internal audits, client audits, and regulatory inspections.
• Contribute to the continuous improvement of processes (5S, CAPA, etc.).
• Maintain close collaboration with the Quality Manager in their involvement with external audits, quality contracts signed with certain clients, and various official regulations (FDA/Health Canada, etc.)
• Train and supervise quality inspectors.
• Any other related tasks

Minimum Education:

DEC or Certificate in Management and Quality Assurance with 2 years of experience in quality.

Experience:

2 to 3 years

Other Required Skills:

Very good knowledge of the Office suite and ERP system.

Fluent in French and advanced level in English.

Knowledge of medical device regulations from Health Canada & FDA (assets)

Knowledge of quality standards (e.g., ISO 9001, BPF/GMP).

Knowledge of quality tools and methods (5 Whys, Ishikawa).

Good analytical and synthesis skills

Exhibits organization with strong time management skills

A good team spirit with a high level of interpersonal relationships

Ability to work with minimal supervision, sense of organization, and autonomy

Knowledge of quality control principles and sampling plans.

Why work for us:

6 sick days

Group insurance premium paid at 70%

RRSP and DPSP employer match to 3%

parking on site

social activities

vacation above the employment standards

Job Description

Job Description

Reporting to the Food Safety Manager, the Quality Assurance Coordinator is responsible for ensuring the certifications, standards, and the ways of working in place at Nature's Touch are maintained and respected at all times. The Quality Assurance Coordinator is a hard-working, detail-oriented individual who's not afraid to roll up her/his sleeves and work closely with all departments in the organization in a highly collaborative atmosphere of continuous improvement.

Localization: Montreal Plant: 5105 rue Fisher, St-Laurent, Qc, H4T 1J8 (Canada).

Duration: Permanent

Shift: Day

Job Responsibilities:

• Provides proper training and coaches the QA technicians' team; regularly visits other shifts, ensures all food safety and quality assurance tasks are completed, replaces the QA Manager when absent, etc.
• Be the HACCP and SQF practitioner.
• Ensures compliance with our factory regulations, certifications in place, documentation, standards, specifications, and GMPs.
• Curious and proactive in detecting potential risks and acts to mitigate the observed risks.
• Ensures effectiveness using thorough investigation, root cause analysis, and CAPA when deviations, non-conformances, or complaints are raised. Completes and documents related documentation and reports. Acts as a problem solver.
• Follows and acts as a reference and a positive mobilizer in ensuring the EMP (Environmental Monitoring Program), GMP (Good Manufacturing Practices), and GDP (Good Documentation Practices) are followed by all employees. Makes tours on the production floor.
• Oversees the day-to-day execution of the quality operations inspections.
• Oversees the day-to-day execution of the raw material and finished goods' hold and release process.
• Works in collaboration and provides technical food safety and quality expertise to colleagues from other departments, such as Maintenance, Production, Warehouse, Corporate, etc.
• Supports internal and external audits.
• Is comfortable communicating with senior management, staff, and corporate.
• Actively contributes to data collection and improvement initiatives to meet target KPIs.
• Participates in the validation and qualification process when new products, equipment, processes, etc.
• Performs other duties as required.

EDUCATION, SKILLS AND EXPERIENCE REQUIRED

• University degree in Food Science and Technology or equivalent (ex: ITA - Institut de Technologie Agroalimentaire).
• Minimum of 5 years of relevant experience in the food manufacturing sector or equivalent.
• Excellent communication skills in English and French (written and spoken to serve our internal and external customers).
• Strong knowledge of Microsoft Office.
• Strong knowledge of HACCP and GFSI. (SQF is an asset.)
• Capable of working in a cold environment for a few hours (with the appropriate clothing provided).
• Required qualities: Excellent ability to work in a team, rigorous, autonomous, organized, and structured, good priority management, sense of urgency, initiative, good analytical skills, and respect for confidentiality.

Job Posted by ApplicantPro

Job Description

Job Description

Who we are

Based out of Montreal, Canada, Nature's Touch is one of the largest suppliers of frozen fruit to retailers in North America, Australia, Taiwan, and Japan. We provide a full range of products and support multiple private-label programs in addition to our own brands. We are also one of the largest buyers of fruit globally each year and continue to enjoy strong growth in this emerging category in retail.

The role

Reporting to the QA Manager, the Quality Assurance Technician is responsible for ensuring the production operations are conducted in accordance with food safety rules and are compliant with the quality standards for processes and products.

Responsibilities

• Perform quality testing of food products.
• Sample finish goods when required.
• Record the sampling details.
• Communicate with third party warehouses.
• Raw material approval and allocation.
• Document and record results as instructed.
• Perform GMP inspections in the production room.
• Perform weekly environmental swabs.
• Finish product release.
• Conduct training for new hires.
• Other duties as assigned by operational needs.

Qualifications & Skills:

• One (1) to three (3) years of experience as a Quality Control Technician.
• Prior experience in a food manufacturing environment is an asset.
• Ability to communicate in English or French, written and spoken, to serve internal and external clients.
• Diploma of College Studies (D.E.C.) in Science or another related field is an asset.
• Proficiency with Microsoft Office.
• Ability to lift up to 20 lbs.
• Ability to work in a cold environment.
• Ability to work in a team environment.
• Ability to work in a fast-paced and deadline-oriented environment.

Job Posted by ApplicantPro

Job Description

Job Description

Salary:

Our vision is to create a fully autonomous billing platform. By automating every facet of billing and back-office financial processes, were building a company designed to last 100 yearsanchored in impact and purpose. Pelcro processed over a quarter of a BILLION dollars in cumulative gross merchandise value and our goal is to reach 1 TRILLION .

Check out this video by our CEO:
-ghattas_hiring-fintech-ai-activity-7295493497787240448 -1a4K?utm_source=share &utm_medium=member_ios

Only 19% of global payments occur online, and only 14% of retail sales are digital. This presents vast opportunities, especially with the rise of AI, LLMs, Instant Payments, and crypto. Join us to seize this potential and grow together.

We are seeking individuals who align with Pelcro's vision and valuesstrong communicators with high integrity , who remain disciplined through both good and challenging days. We cultivate a culture of open-mindedness , encourage curiosity , and consistently practice gratitude .

We prioritize investing in our culture, creating countless memories through team activities like field trips, go-karting, skeet shooting, buggies, horse riding, and more. Discover more about our vibrant culture on our careers page.

Responsibilities:

• Own and lead Pelcros QA strategy, processes, and execution across all product releases.
• Manage, mentor, and grow a QA engineers; set a high-performance and accountability culture.
• Define and enforce quality standards, testing practices, and release criteria.
• Design and implement test plans for web applications, APIs, and integrations.
• Lead automated and manual testing efforts to ensure full test coverage and minimal regression.
• Collaborate with engineering and product teams to ensure early testing, CI/CD alignment, and quality gates.
• Investigate and reproduce bugs; analyze root causes and prevent recurring issues.
• Own quality reporting: test coverage, defect rates, regression reports, etc.
• Drive continuous improvements in QA tools, techniques, and practices (e.g., Cypress, Postman, etc.)
• Ensure compliance with security, reliability, and performance standards critical to a SaaS platform.

Qualifications:

• 5+ years of experience in QA, with at least 12 years in a lead or managerial role.
• Proven experience testing SaaS platforms (especially billing, subscriptions, or APIs).
• Strong experience in both manual and automated testing (preferably using tools like Cypress, Selenium, or similar).
• Hands-on experience writing test cases, test scripts, and setting up test environments.
• Strong understanding of software QA methodologies, tools, and processes.
• Comfortable working in Agile/Scrum environments with CI/CD pipelines.
• Excellent problem-solving and communication skills.
• Leadership mindset: ability to mentor, manage, and elevate QA team members.
• Bonus: experience with testing for accessibility, multi-language support, and third-party integrations.

What to Expect:

• A dynamic environment managing various software projects.
• Collaboration with development teams and stakeholders.
• Opportunities to influence project outcomes significantly.
• Regular feedback and growth opportunities.
• Competitive salary and benefits package.

Next Step:

As a next step, we've prepared an assessment to ensure the role is a great fit. Please use one IP address, keep your webcam on, stay in full-screen, and keep your mouse within the test window. Click the link below to start. Good luck!

remote work

Job Responsibilities:

• Maintain QMS: Ensure the QMS is up-to-date and compliant with industry standards, including AS9100, ISO 9001, and NADCAP chemical processing.
• Assist in preparation and following up on internal and external audits.
• Investigate quality issues and perform Root Cause Analysis (RCA) to identify and resolve defects.
• Develop, implement, and monitor corrective and preventive actions (CAPAs) for continuous quality improvement.
• Conduct follow-up audits to assess the effectiveness of corrective actions in anodizing and painting operations.
• Identify process improvement opportunities and enhance quality control in aerospace surface treatments.
• Maintain TNM's specification library, standards and documentation including the procedures up to date.
• Collaborate with cross-functional teams to ensure alignment of quality assurance with production and laboratory processes.

Requirements:

• 2-5 years of experience in the aerospace industry, particularly in chemical processing.
• Knowledge of AS9100, ISO 9001, and NADCAP chemical processing standards.
• Experience in maintaining and improving a Quality Management System (QMS) and conducting root cause analysis.
• Strong communication, analytical, and attention-to-detail skills.
• Ability to stay current with aerospace standards and update the QMS for continued compliance.
• Fluency in English is required. French is an asset.
• Must be eligible to work in Canada.

_When applicable, Bombardier promotes flexible and hybrid work policies._
**Why join us?**
At Bombardier, we design, build and maintain the world's peak-performing aircraft for the world's most discerning people and businesses, governments and militaries. We have been successful in setting the highest standards by putting our people at the heart of it all, and defining excellence, together.
Working at Bombardier means operating at the highest level. Every day, you are part of a team that delivers superior experiences and products, pushing the boundaries of what's possible in our industry and beyond. By prioritizing employee growth and development, we empower everyone to reach their full potential on their own terms, because the best work happens when you are free to be yourself and share your unique expertise.
**Bombardier's Benefits Program**
With our employees' well-being top of mind, we offer a comprehensive and competitive Benefits Program, which includes the following:
+ Insurance plans _(Dental, medical, life insurance, disability, and more)_
+ Competitive base salary
+ Retirement savings plan
+ Employee Assistance Program
+ Tele Health Program
**What are your contributions to the team?**
- Receive, revise and analyze any Quality Investigation Request (QIR) from our costumers and initiate the proper activities with our internal stakeholders.
- Search within Bombardier's documentation (i.e. drawings, processes, etc)
- Inspect aircraft component
- Determine quality issue root cause and corrective action
- Coordinate and manage the containment actions with our stakeholders (Quality, Engineering, Methods, Logistics, etc) involved in the quality escapes
- Lead weekly QIR's reviews
- Present to management new QIR and provide update when required
- Prepare, update and present to leadership the Key Performance Indicators (KPI)
**How to thrive in this role? Skills, knowledge & experience:**
- You hold a college or university degree in a field related to mechanical, aerospace, structure or equivalent.
- You have at least five (5) years of working experience in a regulated field of activity in one (or more) of the following functions: Quality, Engineering, Methods, Production.
- You can work with minimum supervision from home and on-site.
- You are a strong team player, self-motivated, and demonstrate initiative as well as leadership and good interpersonal skills.
- You can work under pressure and manage multiple priorities.
- You possess negotiating skills.
- You are rigorous in monitoring.
- You possess knowledge of aviation regulation.
- You are proficient with the Microsoft Office 365 suite.
- You possess good oral and technical writing skills in English and French. Spanish an asset.
- You possess knowledge of project management and/or problem resolution concepts (an asset).
- You have experience in design, manufacturing, inspection or assembly of aircraft component an asset.
**Now that you can see yourself in this role, apply and join the Bombardier Team!**
Please note: You don't need _all_ the skills, knowledge, and experience listed to apply for this position. We're not looking for the perfect candidate, we're looking for great talent and passionate individuals.
Bombardier is an equal opportunity employer and encourages persons of any race, religion, ethnicity, gender identity, sexual orientation, age, immigration status, disability or other applicable legally protected characteristics to apply.
**Job** Analyst Senior, Quality Assurance
**Primary Location** Administrative Centre (CA)
**Organization** Aerospace Canada
**Shift** Day job
**Employee Status** Regular
**Requisition** 8700 Analyst Senior, Quality Assurance

_When applicable, Bombardier promotes flexible and hybrid work policies._
**Why join us?**
At Bombardier, we design, build and maintain the world's peak-performing aircraft for the world's most discerning people and businesses, governments and militaries. We have been successful in setting the highest standards by putting our people at the heart of it all, and defining excellence, together.
Working at Bombardier means operating at the highest level. Every day, you are part of a team that delivers superior experiences and products, pushing the boundaries of what's possible in our industry and beyond. By prioritizing employee growth and development, we empower everyone to reach their full potential on their own terms, because the best work happens when you are free to be yourself and share your unique expertise.
**Bombardier's Benefits Program**
With our employees' well-being top of mind, we offer a comprehensive and competitive Benefits Program, which includes the following:
+ Insurance plans ( _Dental, medical, life insurance, disability, and more_ )
+ Competitive base salary
+ Retirement savings plan
+ Employee Assistance Program
+ Tele Health Program
**What are your contributions to the team?**
Bombardier is currently seeking a Software QA Analyst to join their Digital team. The ideal candidate will have strong technical skills with solid backend experience and excellent communication skills as they will be working closely with Development and Product Management teams to develop and maintain top quality digital applications. This role will require a solid mix of both manual testing with a focus on functional, integration, and regression testing, as well as exposure and understanding of Automation frameworks and scripting.
+ Creating QA test artifacts (Test Strategies, Test Scenarios and Cases, Test Results and Reports) and functional documentation.
+ Active contribution to scrum team ceremonies such as story grooming and refinement sessions, sprint planning & retrospectives, daily scrum meetings.
+ Executing manual and automated test cases at the functional, UI, API, Integration, and Regression levels to ensure requirements have been met.
+ Maintaining up to date Regression suite.
+ Reporting issues in requirements from the onset as well as usability issues once functionality has been released for testing.
+ Communicating test progress, results, and other relevant project information to key stakeholders and management.
+ Troubleshooting issues and clearly reporting them in Jira with an understanding of issue severity based on risk analysis.
+ Recommend process improvements after root cause analysis and report based on findings.
+ Staying up to date on Software QA practices and tools to ensure efficiencies in testing.
**How to thrive in this role?**
+ You have over five (5) years of proven expertise with manual testing experience in such areas as functional, regression, integration, user interface.
+ You have a strong expertise in automated testing frameworks and tools.
+ You have had exposure to non-functional testing such as Performance, Load, Security.
+ You have experience with Accessibility testing.
+ You have experience in writing SQL queries and scripts.
+ You have experience in working within an agile software development team.
+ You have a strong ability to analyze, define, and translate business and functional requirements, use cases, designs, and technical specifications into testing requirements.
+ You have excellent communication skills, both verbal and written, and inter-personal skills.
+ You are a highly developed critical and analytical thinker geared toward first level problem solving.
+ You are well-versed in writing test cases and identifying all test scenarios that provide complete test coverage.
+ You are familiar with tools like Jira, Confluence, Sharepoint, Zephyr, Postman, Playwright.
+ You have the ability to prioritize work with a focus on deadlines and deliverables.
+ You are independently able to solve complex tasks and recognize as well as escalate risks.
+ You are quickly able to demonstrate a high level of productivity, learning, responsibility, and influence, accountable for all quality deliverables in a quest for continuous improvement.
**?Now that you can see yourself in this role, apply and join the Bombardier Team!**
Please note: You don't need _all_ the skills, knowledge, and experience listed to apply for this position. We're not looking for the perfect candidate, we're looking for great talent and passionate individuals.
Bombardier is an equal opportunity employer and encourages persons of any race, religion, ethnicity, gender identity, sexual orientation, age, immigration status, disability or other applicable legally protected characteristics to apply.
**Job** Analyst, Software Quality Assurance
**Primary Location** Administrative Centre (CA)
**Organization** Aerospace Canada
**Shift** Day job
**Employee Status** Regular
**Requisition** 6226 Analyst, Software Quality Assurance