78 Qa Manager jobs in Toronto

About Ya YA Foods:

Ya YA Foods is a dynamic and high-growth manufacturer of liquid food and unique beverages. With over 30 years’ experience, we have evolved into a versatile manufacturer and co-packer of a variety of low acid and high acid beverage and liquid food items. We are a family-owned Canadian business who prides itself in its proven track record of satisfying the needs of global multi-national customers. We are a solution provider for our customers, always striving to exceed expectations on innovation, quality, service, and speed to market. For further information about us, please check our website at yayafoods.com

A career at Ya YA FOODS will offer you the opportunity to…

- Build a career, not just have a job
- Work in a dynamic and high-growth company with very skilled professionals
- Become part of a teamwork focused culture
- Be a part of an organization that supports your future growth path

Report to: Senior Customer Quality Manager

Responsibilities

- Participate and lead all customer meetings related to quality.
- Review customer’s Quality Management System (QMS) and identify any gaps.
- Develop plan to address the gaps internally and with the customer.
- Lead customer quality audits, identify gaps, develop corrective actions and lead the implementation internally.
- Lead line qualification projects for the customer. Liaise with Engineering, Operations, and external resources such as Processing Authorities to ensure production line is qualified based on customer requirement and on-time.
- Ensure supplier and ingredient qualification is performed per customer’s requirement and on-time.
- Ensure quality certifications such as Organic, Halal, Kosher, etc. is obtained per customer requirements.
- Lead record reviews and positive product release for customers.
- Communicate any product quality deviations with customers, work with the internal teams to develop solutions, and prepare deviation reports for the customer.

- Receive, file, and investigate any customer/consumer complaints. Ensure proper investigation is done internally and respond to customer on-time.
- Ensure all product specifications including product formulation are up-to-date and kept securely in company’s document management system.
- Represent the Quality team in any new projects for the customer including launching new or modified products. Ensure all quality aspects of the work is completed according to customer requirements.
- Participate in HACCP program review and update to ensure customer’s requirement are addressed in the HACCP program.
- Lead any other customer initiative and/or corrective action as related to customer quality requirements.
- Compliance with all rules & policies regarding health safety, occupational safety, environmental safety, food safety, legal regulations, company requirements, etc.
- Compliance with the Company's Integrated Management Systems which includes, but is not limited to Production, Quality, Food Safety & GMP.
- Other duties as assigned.

Profile

- Bachelor's Degree in Science (Microbiology, Pharmacy, Chemistry, Food Science), or completion of an Engineering Technology program with a concentration in quality management/food safety systems and/or 5+ years of Quality Assurance experience in a manufacturing setting
- Must have a working knowledge of thermal processing for low acid/high acid beverage manufacturing
- Strong communicator with the ability to interact with customers at all levels of their organization
- Demonstrated accomplishments improving Quality and Operations systems
- Working knowledge of food safety & quality programs such as HACCP and the BRC programs.
- Working knowledge of various government regulations (CFIA, FDA/USDA)
- Demonstrated ability to handle multiple priorities
- Strong attention to details
- Ability to lead projects in a fast paced and growing environment
- Working knowledge of Quality Management System is considered an asset
- NB: Successful candidates will be required to provide photo ID, banking details, a valid SIN number, and (if applicable) a valid work permit

*Why Join Us*

We believe that the key to creating and growing a successful business is by investing in our people—some of whom have been a part of our team for over 30-years. This is at the core of who we are, what we do, and how we grow our business—as a versatile, automated manufacturer and co-packer of a wide-variety of beverages and liquid food items. In our view, a happy team means a better workforce, a better product, and more satisfied customers.

*Furthermore, we encourage different perspectives and celebrate diversity in our workforce. Where every employee* *has the opportunity to* *realize his or her full potential in a working environment that is supportive of everyone. Upon request, we will gladly provide accommodations to any candidate with a disability taking part in the selection process.*

Quality Manager Skills Required: Functional TestingJob Description: Own test strategy and planning for complex epicure leases define quality gates and KPIs. Lead end-to-end testing across dependent systems (policy admin, billing, claims, data ETL, portals).Drive defect prevention early requirement reviews, risk workshops, and story refine-ments. Direct UAT strategy and readiness align business test scenarios to real-world journeys. Oversee regression suites (maintenance, prioritization, automation opportunities).Validate data quality across integrations craft sophisticated SQL for reconciliation. Ensure compliance with priva-cy, security, and accessibility standards (e.g., PIPEDA, WCAG 2.1 AA).Mentor junior intermediate testers uplift test practices and templates. Contribute to release readiness decisions present quali-ty status to leadership.As a Senior Functional Tester, you will be the quality champion for complex initiatives across multi-ple systems and teams. You will drive test strategy, ensure risk-based coverage, mentor testers, and partner with product, architecture, and operations to safeguard customer and regulatory out-comes.Exp Required: 10& above

Defect Manager Location: Onsite/RemoteExperience: 8+ years in QA or Project DeliveryIndustry - Energy / UtilityRole Overview:The Defect Manager will oversee defect lifecycle management across SAP and non-SAP streams. The role involves coordination between testing, development, and business teams to ensure timely defect resolution and release quality.Key Responsibilities:• Manage end-to-end defect tracking, prioritization, and reporting.• Conduct daily defect triage calls with stakeholders.• Ensure SLA adherence and categorize defects based on severity and impact.• Generate and present defect trend reports and KPIs.• Collaborate with QA and development teams to prevent recurring issues.Required Skills:• Strong experience in defect management using tools like JIRA, HP ALM, or Azure DevOps.• Understanding of SAP testing cycles (SIT, UAT, Regression).• Excellent communication and coordination skills.• Ability to work with cross-functional and multi-location teams.• Analytical and documentation skills to drive defect prevention initiatives.

Job Description
We are seeking a detail-oriented and proactive Quality Control Technician to join our cartridge manufacturing team. This role is critical to ensuring the integrity and performance of our pharmaceutical and biotechnical products. The ideal candidate will have hands-on experience in product testing, visual inspection, and documentation within a cleanroom environment.
Day-to-Day Responsibilities:
- Perform visual inspections of manufactured cartridges using microscopes and other tools.
- Conduct computer-based analysis and maintain accurate documentation using Excel and other digital platforms.
- Follow and enforce Standard Operating Procedures (SOPs) in a cleanroom setting.
- Rotate between different testing stations to evaluate various cartridge models (5-6 types).
- Collaborate with production and quality teams to ensure compliance with internal and regulatory standards.
- Maintain detailed records of test results and report any deviations or anomalies.
- Support afternoon shift operations, which are currently prioritized for staffing.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: and Requirements
Must-Have Requirements
- 1-3 years of experience in a quality control or quality assurance role.
- Background in pharmaceutical or biotechnical industries (preferred over food science).
- Proficiency in microscope-based inspection and computer analysis.
- Familiarity with SOPs, cleanroom protocols, and GMP documentation.
- Strong skills in Excel and digital documentation.
- Ability to work actively across multiple testing stations and adapt to a dynamic environment.
- Excellent attention to detail and organizational skills.

Quality Control Technician
Requisition ID: 14209
Location:
Caledon, ON, CA, L0N 1C0
Pay Type: Hourly
**COMPANY OVERVIEW**
Amrize is building North America. From bridges and railways to data centers, schools, offices and homes, our solutions are inside the buildings and infrastructure that connect people and advance how we live. And we invite you to come and build with us.
As the partner of choice for professional builders, we offer advanced branded solutions from foundation to rooftop. Wherever our customers are, whatever their job, we're ready to deliver. Our 19,000 colleagues work across 1,000 sites supported by an unparalleled distribution network. Infrastructure, commercial and residential, new build, repair and refurbishment: We're in every construction market.
Amrize listed on the New York Stock Exchange and the SIX Swiss Exchange on June 23, 2025, following our spinoff as an independent company. Join us and build _your_ ambition.
Learn more at ( Caledon ON
**Job Req ID:** 14209
Join our amazing team and contribute as a:
Quality Control Technician
**ABOUT THE ROLE**
Amrize, Canada's leading supplier of construction materials, has an opportunity for a Quality Control Technician for our Caledon Pit. This role is crucial for ensuring all aggregate products comply with relevant codes, standards, and specifications through the implementation of quality programs, including sampling, testing, reporting, and follow-up. The Quality Control Technician will also contribute to safety initiatives and collaborate with various internal stakeholders to meet customer expectations.
**WHAT YOU'LL ACCOMPLISH**
+ Implement Amrize Safety Policies and comply with Government Legislation.
+ Conduct Safety Inductions for visitors to the Quality Lab or site as required.
+ Execute Job Hazard Analyses for QC Tasks and implement Action Items.
+ Implement programs and processes to ensure compliance of all products with relevant Codes, Standards, and Specifications.
+ Implement Amrize Quality Program, including sampling, testing, reporting, and follow-up for all products.
+ Record, monitor, and communicate Aggregate KPI performance, investigating variances and establishing corrective actions.
+ Participate in or lead the development and implementation of site-specific actions to reduce and/or utilize long products.
+ Provide input to ensure alignment between Sales and Operational staff to ensure product performance meets customer expectations.
+ Demonstrate a commitment to communicating, improving and adhering to health, safety and environmental policies in all work environments and areas. Promote a culture of safety and exhibit these behaviours.
**WHAT WE'RE LOOKING FOR**
+ **Education** : Minimum 2-year College Diploma in Civil Engineering Technology or Environmental Technology, or University Degree in Engineering.
+ **Required Work Experience** : Experience in the construction materials (aggregates, asphalt, and concrete) industry is ideal.
+ **Required Training/Certifications** : Full G-class Drivers License.
+ **Required Technical Skills:** Excellent computer skills.
+ **Travel Requirements:** Zero percent travel.
**Additional Requirements:**
+ Ability to work independently as well as part of a team.
+ Excellent communication skills.
+ Availability for rotating shift work (shifts can extend to 12 hours).
+ Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment ("PPE"), including but not limited to respirators. Employees that are required to wear respirators must be clean shaven where the respirator seal meets the face in order to pass the qualitative and quantitative fit tests.
**WHAT WE OFFER**
+ Flexible Health & Dental benefits coverage for you and your dependents.
+ A generous Pension Plan designed to support you through various stages of your career and life.
+ Access to voluntary programs like RRSP and TFSA for future financial planning.
+ Healthy Living support through an Employee and Family Assistance Program (EFAP), offering confidential assistance for work, health, or life challenges.
+ Easy access to mental health and well-being support.
+ Service recognition awards to celebrate your contributions.
+ Perks & discounts on a variety of products and services.
+ Access to online learning platforms, financial educational assistance, and a culture that fosters career growth and opportunities.
+ Financial support for new parents beyond statutory benefits.
+ An inclusive and welcoming environment where everyone can be themselves.
+ A collaborative work culture in a supportive and team-oriented work environment
+ Company-provided personal protective equipment ensuring your safety and comfort on the job
This posting is for an existing vacancy at Amrize Canada Inc.
**BUILDING INCLUSIVE WORKSPACES**
At Amrize, there is endless opportunity for you to play your part. Whether you're in a technical, managerial, or frontline role, you can shape a career that works for you. We're seeking builders, creative thinkers and innovators. Come put your expertise to work while developing the knowledge and skills to drive your career forward. With us you'll have the chance to build your ambition!
Amrize North America Inc. takes pride in our hiring processes and our commitment that all qualified applicants will receive consideration for employment without regard to age, race, color, ethnicity, religion, creed, national origin, ancestry, gender, gender identity, gender expression, sex, sexual orientation, marital status, pregnancy, parental status, genetic information, citizenship, physical or mental disability, past, current, or prospective service in the uniformed services, or any other characteristic protected by applicable federal, state or local law. Amrize North America Inc, and its respective subsidiaries are Equal Opportunity Employers, deciding all employment on the basis of qualification, merit and business need. Amrize Canada Inc. is committed to the principles of employment equity and encourages the applications from women, visible minorities, and persons with disabilities.
In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request accommodation in order to apply for a position with us, please email . This email address should only be used for accommodations and not general inquiries or resume submittals. In Ontario, our organization/business is committed to fulfilling our requirements under the Accessibility for Ontarians with Disabilities Act. Under the Act, accommodations are available on request for candidates taking part in all aspects of the selection process.
While we sincerely appreciate all applications, only candidates selected for an interview will be contacted.

Job Description

Job Description

JOB DESCRIPTION: QUALITY INSPECTOR

• Read & Interpret drawings, 5 years (Preferred)

• Ensure that existing standard operating procedures, quality programs and welding procedure specifications are being followed by company staff

• Perform weld inspection as per Code

• Supervise welding certification of new hires
• Minimum Level 2 CWB certification

• Review welding specifications and/or requirements for each project and work with team to solve fabrication challenges

• Identify project quality control requirements and ensure they are always met

• Review project drawings and specifications, developing inspection and test plans and implementing them

• Inspect materials and finished goods to ensure they meet Code, customer requirements and/or contract specifications, including but not limited to checking welds, welding consumables, base material, cut & formed parts, layout work and coatings

• Effective verbal and written communication skills, above average level of expertise in business office applications are a must.

• Working knowledge of welding, metal fabrication and machining processes.

• Working knowledge of CWB W47.1, W47.2 and W59 and AWS D1.1 and D1.7standards.
• Experience in development and implementation of QC programs, SOPs, PQRs and WPS.

• Familiarity with requirements of the custom metal fabricating industries.
• Approves incoming materials by confirming specifications, conducting visual and measurement tests, rejecting and returning unacceptable materials
• Perform source inspections, in-process inspections and final inspections
• Communicating required adjustments to shop foreman and returning products for re-work, confirming re-work through proper system (both in ERP and procedurally)
• Documents inspection results by completing reports and logs, summarizing re-work and waste, inputting data into quality database
• Perform all daily inspection and test of the scope and character necessary to achieve the quality required in the drawings and specifications for all works under the contract performed ON or OFF site.
• Taking care of QA/QC documents of the entire project including certificates, calibration, test results, inspection requests, non-compliance reports, materials delivered and other QA/QC documents.
• Perform inspections, reports and archiving documentation and collecting and filing the required Quality Records.
• Carry out inspection and checking for all quality related procedures in all Channel workshops and ensures activity at all shops are as per approved method statement and inspection test plan.
• Evaluates the qualifications of welders and Non Destructive Test-NDT technicians with regard to the activities assigned.
• Perform precision dimensional measurements
• Review production documentation for compliance and adequacy of inspection and as necessary, develop required inspection criteria for the production of quality products
• Analyze compliance with applicable quality elements, relevant standards and processes and initiate any required corrective and preventative actions; verify the response and effectiveness of the implementations
• Ensure products meets or exceeds internal and customer requirements
• Work with production, purchasing and engineering to ensure the quality requirements of production parts are met
• Dealing with the Client for all the Quality matters and coordinates with client’s QA/QC departments for inspection and meeting about quality problems including the closure of Non-Compliance Report.
• Required to participate and oversee all the internal/external audits.
• Accomplish the Quality Control functions/activities of a project or its parts, including Quality Control inspection schedules and the collection of Quality Records.
• Develop and Assesses the implementation of the Quality Plan and Quality Control Plans on shops
• Ensures proper WPS are in place

Job Description

Job Description

Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We're currently searching for a Clinical QC Associate I to join our growing team!

The function of the Clinical QC Associate I is to ensure all prepared study source documents and/or forms of clinical activities are in accordance with the protocols, SOPs and regulations at Pharma Medica Research Inc. (PMRI ). Review study files upon data entry at the screening, check-in, on-study, and post-study procedures. Observe, on a random basis, the clinical procedures during the conduct of studies and make sure that they are performed in accordance with protocols, PMRI SOPs, GCP requirements and regulations. Review study files after study completion and ensure the documentation is in accordance with protocols, PMRI SOPs, GCP requirement and regulations. This position reports to the Manager, Clinical QC and/or designate.

Duties and Responsibilities

1.Prepare study source documents and/or forms in accordance with protocols, PMRI SOPs and regulations.

2.Review and lock the electronic study setting in accordance with protocols.

3.Review study tube arrangement for complicated study procedures based on risk assessment.

4.Review study files upon data entry at the screening, check-in, on-study and post-study procedures.

5.Observe, on a random basis, the clinical procedures during the conduct of studies (i.e. screening procedures, subject entrance, meals, sample bundling, etc.), and make sure that they are performed in accordance with protocols, PMRI SOPs, GCP requirements and regulations.

6.Ensure that study files after study completion are accurate and legible according to protocols, PMRI SOPs, GCP requirements and regulations.

7.Review other study or non-study related documents (e.g. pharmacy and equipment calibration records etc.).

8.Provide reports on the observations/reviewed data to the relevant supervisors/managers and follow up upon resolution.

9.Liaise with other departments to improve the accuracy and quality of data.

10.Perform other assigned duties as required.

Qualifications

• College degree or B.SC. in clinical research, health, or science-related field or equivalent.
• At least 1 year of CRO experience or equivalent is an asset
• Good understanding of Phase I study protocols and conduct.
• Good knowledge of GCP requirements.
• Good communication and interpersonal skills.
• Detail-oriented and good organizational skills.
• Excellent computer skills.
• Ability to work both independently and as a team member.

We Offer

• Competitive compensation plan
• Opportunities for advancement and career progression
• A generous Employee Milestones Awards Program
• Corporate Discounts Program
• Learning Support Programs
• Friendly atmosphere, culture of learning

Please note all applications must be eligible to work within Canada.

PMR I is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.

We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.

If you're looking for an exciting place to work with an incredible team, apply today!