50 Maple Leaf Foods jobs in Mississauga

Job Description

Job Description

Intermediate Project Engineer - Food Industry The Danmare Group specializes in providing full-service engineering and design solutions to leading companies in the food and beverage industry. Over the past fourteen years, clients have enlisted our expert team to manage challenging projects from start to finish. We take a collaborative approach that considers all stakeholder requirements to satisfy the unique needs of our clients. Our continued success in our industry has been leveraged by our inclusion in the AGI group of businesses. AGI is a global leader in the planning, engineering and manufacturing of full solutions and systems in the agriculture industry.  AGI partners with customers in six continents to offer unique market solutions. ( This global opportunity provides broader opportunities and experience for our team members. Intermediate Project Engineer The role requires 3 to 5 years of relevant Project Engineering experience to drive and manage multiple projects for a variety of clients in the food, beverage and pet food industries. The ideal candidate should have a thorough knowledge of design engineering principles and project management methodologies, supported with in-depth experienced in the application of project management techniques for clients in the food, beverage or pet food industries. Responsibilities * Support and assist Senior Project Engineers with major project initiatives which includes identifying equipment capabilities, utilities, infrastructure requirements, developing process flow diagrams and layout concepts * Lead and coordinate activities at client sites to ensure proper execution of project designs * Prepare mechanical system designs using AutoCAD, 2D/3D and BIM modelling * Manage contractors, sub-contractors and vendors to ensure compliance to all safety regulations, codes, standards and adherence to client requirements * Monitoring Contractor work for compliance with contract specifications * Generate, review, and take responsibility for contract documents and specifications primarily as they relate to process mechanical requirements * Support site start-up team, troubleshoot and resolve issues by collaborating with vendor equipment technicians during installation and start up * Interact with core disciplines (structural, electrical, controls, process), as well as internal and external clients to coordinate and achieve project objectives in a timely manner * Assist with the development of Engineering Check-out, Equipment Acceptance Testing, start-up and validation documents * Working knowledge of CFIA, USDA and FDA food equipment hygienic design requirements * Understanding GMP requirements, area designations, and clean design requirements Other Essential Requirements * Bachelor of Engineering in any of the following disciplines, Mechanical, Chemical, Industrial, Electrical or Civil * Professional Engineer status or Engineer in Training * Previous experience in food, beverage or pet food industries * Able to work flexible hours, weekends if required * Experience using AutoCAD, Microsoft Project, Excel and Word * Up to 40% travel maybe required to support and service our clients * Valid Ontario driver’s license, Valid passport and ability to obtain TN visa   We provide a competitive compensation including benefits, health spending account, retirement program, fitness allowance, personal and career development and other programs. Check us out at

Job Description

Job Description

About Danmare The Danmare Group specializes in providing full-service engineering and design solutions to leading companies in the food and beverage industry. Over the past fourteen years, clients have enlisted our expert team to manage challenging projects from start to finish. We take a collaborative approach that considers all stakeholder requirements to satisfy the unique needs of our clients Our skilled team of professionals manage the process design, equipment specifications, plant layout, equipment qualifications, construction, and installations, manage vendors so our clients are provided with successful projects, on time and within budget  The Opportunity The role requires a minimum of 10 years of relevant engineering, project management, consulting, or design experiences to drive and manage multiple projects for a variety of clients in the food, beverage, and pet food industries.  The Team Our team is comprised of a diverse and multi-disciplinary discipline, professional engineers, designers, project managers, who have extensive experiences leading, and managing multimillion dollar projects for clients who are leaders in their respective industries Responsibilities and Duties * Lead major project initiatives. Which includes identifying all equipment capabilities, utility & infrastructure requirements and developing layout concepts, etc. * Manage and lead multiple disciplinary teams, providing guidance and mentor team members * Liaise with vendors, contractors to ensure proper installation of all intended project requirements * Lead and support site start-up team, troubleshoot and resolve issues by collaborating with vendor equipment technicians during installation and start up * Oversee the development of Engineering Check-out, Equipment Acceptance Testing, start-up/validation processes * Develop and maintain project plans and coordinate project activities; track critical path milestones * Ensure end-to-end project planning, risk identification, dependency tricking, issues identification /escalation, and change management are being managed appropriately utilizing best practice project management standards * Provide technical guidance and recommendations during project design, implementation, including commissioning, and process qualification * Interact with core disciplines (structural, electrical, controls, process), as well as internal and external clients to coordinate and achieve project objectives in a timely manner * Working knowledge of CFIA, USDA and FDA food equipment clean design requirements * Prepare and issue tender documents to 3rd party vendors/contractors and completing the process with awarding tenders * Interact with core disciplines (structural, electrical, controls, process), as well as internal and external clients to coordinate and achieve project objectives in a timely manner * Recommend, manage, and implement efforts to streamline the organization’s processes and establish best practices. Qualifications * Bachelor of Engineering in any of the following disciplines, Mechanical, Chemical, Industrial, Electrical or Civil * Professional Engineer status * Previous experiences in the food, beverage, pharmaceutical and pet nutrition industries * Working knowledge of FDA and USDA food equipment and clean design standards * Able to work flexible hours, weekends if required * Experience using AutoCAD, Microsoft Project, Excel, Microsoft suite and Visio * Project concept development, design, procurement and installation or equipment experiences * Construction/contractor management, commissioning, and validation experiences * Exceptional interpersonal and communication skills, collaborative, persuasive with strong team building skills, conflict management, influencing, and negotiation skills * Up to 40% travel maybe required to support and service our clients * Valid Ontario driver’s license * Valid passport - US Based projects may require relocation for a period of 9 to 12 months must be able to relocate if required during this period

**Reference No** . R
**Position Title:** Specialist, Quality Assurance
**Department:** Quality DCV & GEM
**Location:** Toronto, ON
**About the Job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Contribute to establishing and maintaining high quality and compliance status of all products handled by Sanofi Canada to meet all Canadian cGMP regulations, as well as corporate requirements.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
**Main Responsibilities:**
+ Coordinates with QA Coordination Call Center to obtain essential information required to document technical complaints
+ Provides support to QA Coordination Call Center to meet needs of the complainant
+ Identifies and confirms inquiries as product technical complaints
+ Evaluates complaints for severity and risk to public safety.
+ Notifies interested departments (eg. Country Quality Head, manufacturing site QA,) upon receipt of critical complaints.
+ Monitors and tracks sample receipt from complaints.
+ Ensures complaints are reviewed and processed within a timely fashion
+ Prioritizes complaints for data entry and processing into the global database
+ Utilizes the customer service database to oversee complaint identification and processing
+ Interacts with both internal and external manufacturing sites regarding technical complaints and their associated investigations
+ Performs QC Checks
+ Understands Health Canada complaint regulations for drug products and medical devices
+ Performs file review and administrative closure for individual complaints
+ Produces trending reports
+ Monitors open complaint activity for each manufacturing site
+ Interacts with Customer Service, Medical Information, Pharmacovigilance and other company departments/associates regarding the identification and evaluation of technical complaints
+ Identifies and reports adverse events within one business day to Pharmacovigilance
+ Provides complaint support to other company departments including Customer Service, Medical Information, Pharmacovigilance, Sales Associates, Regulatory, Commercial Operations, Legal, and Risk Management
+ Participates on ad-hoc teams regarding product-specific complaint issues
+ Supports during regulatory, third party, and internal audits
+ Understands product specific information regarding common product complaints
+ Understands department process flows and complaint databases
+ Coordinates feedback to customers regarding complaint investigations via QA Coordination Call Center
+ Other QA duties, as assigned
**About You**
**Requirements & Qualifications**
+ B.Sc. in Chemistry, Biology or related sciences
+ 5 years of related experience within the pharmaceutical industry.
+ Knowledge of cGMPs and Health Canada regulations regarding drugs, medical devices, combination products, biologics and natural health products
+ Strong understanding of Good Documentation Practices
+ Must be able to understand and utilize complaint database software and reporting tools
+ SAP, MS Office, Adobe Suite
+ Bilingual French strongly preferred
+ Occasional travel: Position is based out of the Toronto office
+ *Persons applying for positions in QA must provide evidence of qualifications, as outlined in current Canadian Good Manufacturing Practices (GMP) Guidelines for review and assessment as a condition of any offers of employment.
**Preferred skills:**
+ Problem Solving mindset who is self-motivated, well organized with attention to detail and strong analytical skills.
+ Customer Service Skills, Project and Time Management Skills
+ Interpersonal skills-must be proactive, personable, flexible, team-oriented
+ Ability to multitask in a stressful environment and to operate in a constantly changing environment
+ Strong Verbal and Written Communication Skills
_*Persons applying for positions in QA must provide evidence of qualifications, as outlined in current Canadian Good Manufacturing Practices (GMP) Guidelines for review and assessment as a condition of any offers of employment._
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs
This position is for a current vacant role that we are actively hiring for.
Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request.
#GD-SG
#LI-GZ
#LI-Onsite
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
_North America Applicants Only_
The salary range for this position is:
$76,200.00 - $10,066.66
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK ( .
La fourchette salariale pour ce poste est la suivante:
76,200.00 - 110,066.66
Toute compensation sera déterminée en fonction de l'expérience démontrée. Les employés peuvent être admissibles à participer aux programmes d'avantages sociau de l'enterprise. Des informations supplémentaires sur les avantages sont disponibles via le lien ( .
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

With Staff Management | SMX, you'll get a weekly paycheck, learn new skills, meet new people, and work with a great management team in a clean and safe environment.
Staff Management | SMX is immediately hiring a Quality Assurance Associate for our food manufacturing Client in Brampton. This is a full time, 2-month contract position.
.
Perks & Benefits: Weekly paychecks.
Shifts: 2nd Shift, 3rd Shift.
Employment Types: Full Time.
Pay Rate: $18.00 - $9.00 / hour
Duties:
+ Conduct routine line checks including temperature, metal detector verification, weights, pouch integrity, and analytical tests (e.g., brix, pH, viscosity, water activity).
+ Monitor Critical Control Points (CCPs) and chart recorders.
+ Record results on controlled documents accurately.
+ Investigate and report on non-conformances to maintain quality standards.
+ Collect various samples for testing.
.
Position Requirements:
+ University degree or college diploma in Science (with Concentration in Chemistry, Biochemistry, or Microbiology) or Food Science.
+ Food industry experience considered a strong asset.
+ Strong ability to work independently, multitask effectively in a fast paced environment.
+ Strong numeracy, written and verbal communication skills.
Requirements: Stand for Shift Duration, Must be at least 18 years old., required education: HS Diploma or GED.
Work Location: Staff Management, Brampton, ON L6S6B7.
Job Types: Food Production, Manufacturing, Production, Warehouse, Quality.
Industry: Manufacturing.
The hourly rate for this position is anticipated between 18.00 - 19.00 per hour. This range is a good-faith estimate, based on the shift you work and other considerations permitted by law. An employee''s pay history will not be a contributing factor where prohibited by local law.
TBI Outsourcing Canada, Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, sexual orientation, age, gender identification, protected veteran status, or any other characteristic protected by law. We consider qualified applicants with arrest and conviction records in accordance with applicable law.
Accommodations are available on request for candidates taking part in the selection process. If you require disability-related accommodation during the recruitment process, please contact your Recruiter or Employee Relations at or . TrueBlue, Inc. and its brands will consult with all applicants who request disability-related accommodation during the recruitment process to ensure that the accommodation provided takes into account the applicant's individual accessibility needs.
SM | SMX is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, sexual orientation, age, gender identification, protected veteran status, or any other characteristic protected by law.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
**A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.**
**That's what makes us Roche.**
At Roche, we thrive to deliver more benefits to our patients as part of our 10-year Pharma vision. We serve our patients through external partnerships because access to quality products is every patient's right. We leverage external partners in order to offer flexibility to our internal capacity at the right cost and quality. We enable our external partners to reliably deliver compliant, quality products to our supply chain customers, so that we can deliver to patients worldwide. We do this through cross-functional collaborations ensuring quality process excellence and continuous improvement.
**The Opportunity:**
+ Provide quality and compliance oversight of external GMP suppliers including CDMOs, CROs/PET centers, CLOs and in-licensing partners to ensure compliance with cGMP and quality agreement requirements.
+ Serve as the Quality Point of Contact for these GMP suppliers and participate as a key member of cross-functional management teams to enable GMP supplier site selection, qualification and implementation, management, and decommissioning
+ Oversee and execute all required quality activities during the lifecycle of a GMP supplier, including but not limited to:
+ Negotiation and maintenance of Quality Agreements and associated documents
+ Monitoring cGMP compliance and reporting quality performance, identifying and mitigating quality risks
+ Supporting Roche audits, ensuring audit responsiveness and CAPA implementation
+ Tech transfers and process validation, and Inspection readiness for commercial CMOs as applicable
***
+ Execute all required activities to support Make Assess and Release commercial and investigational medicinal products, including but not limited to risk assessments, approval of method validation, master batch records and executed records, complex investigations, and changes. Ensure project milestones as well as expectations such as on time closure are met.
+ Serve as Quality Point of Contact to the technical development team, and provide end-to-end quality oversight. Execute the Product Specification File (PSF), intra-company agreements, approve the control system, review CMC sections of Health Authority submissions and related activities.
+ Perform disposition of outsourced investigational medicinal products in SAP, including API and Drug Product of Synthetic Molecules and Biologics
**Who you are:**
+ B.S., M.Sc. or PhD in life sciences or equivalent with at least 8 years Manufacturing and/or Quality experience with Synthetic Molecules including Steriles in the pharmaceutical or related GMP industry. Experience with siRNA (oligos/peptides) and Biologics is a plus.
+ The ideal candidate has GMP QA experience of bulk API and Drug Product clinical supply operations including release.
+ Sound knowledge of cGMP, ISO standards and international regulations for pharmaceuticals. Ability to interpret quality standards as they relate to GMP products.
+ Excellent Quality decision making skills in complex environments
+ Proven ability to influence across cultures and functional reporting lines, and to drive continuous improvement initiatives
+ Ability to operate in a self-managed way of working, with a key focus on collaboration, agility and innovation mindset
+ Ability to work in a purpose driven organization, taking full ownership for assigned roles and tasks, continuously willing to improve individual and team effectiveness

**This position may require up to 10% domestic and/or international travel**
*** Relocation benefits not available for this position***
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**

Job Description
Insight Global is seeking multiple Quality Assurance Testers for a large Canadian banking client. In this role, you will play a key part in supporting the upgrade to a newer version of Certent Disclosure Management (CDM)-a critical platform used for external financial reporting. This initiative requires robust system testing to ensure performance, accuracy, and reliability across multiple users and reporting flows.
Responsibilities:
-Execute manual system testing for the upgraded CDM platform
-Perform stress testing and simulate multi-user scenarios to validate server performance
-Collaborate with internal teams to align testing efforts and ensure coverage
-Validate financial reporting flows including balance sheets, income statements, and cash flow statements
-Support post go-live testing and production verification
-Document test results, defects, and provide feedback to development and business teams
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
-Experience in manual QA testing within enterprise systems
-Familiarity with Certent Disclosure Management (CDM) or similar reporting tools
-Understanding of financial reporting processes and terminology
-Strong communication skills to engage with finance and business teams -Background in accounting or finance
-Experience with TM1 (EPM system) for data pulls
-VBA/macro skills for report validation (not required but beneficial) null
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 employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to 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 oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to

Quality Assurance Analyst
**General Information**
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City
Toronto
State/Province
Ontario
Country
Canada
Department
QUALITY ASSURANCE
Date
Tuesday, August 26, 2025
Working time
Full-time
Ref#

Job Level
Individual Contributor
Job Type
Experienced
Job Field
QUALITY ASSURANCE
Seniority Level
Associate
Currency
CAD - Canada - CA
Annual Base Salary Minimum
41,760
Annual Base Salary Maximum
83,520
The salary range above represents the low and high end in the local currency of Xerox's salary range for this position and is reflected in an annualized amount. Actual salaries will vary based on factors including, but not limited to, geographic location, market competition, and/or the successful applicant's education, experience, knowledge, skills, and abilities. The range listed is just one component of Xerox's total compensation package for employees. Employees are also afforded a comprehensive suite of benefits, that include medical, dental, life insurance, an Employee Assistance Program (EAP), Paid Time Off, holidays, disability, and retirement benefits, please visit Xerox Careers ( . If you are not reviewing this job posting on our Xerox Careers page, we cannot guarantee the validity of this posting. For a list of our current openings, please visit Xerox Job Search ( .
**Description & Requirements**
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**About Xerox Holdings Corporation**
For more than 100 years, Xerox has continually redefined the workplace experience. Harnessing our leadership position in office and production print technology, we've expanded into software and services to sustainably power the hybrid workplace of today and tomorrow. Today, Xerox is continuing its legacy of innovation to deliver client-centric and digitally-driven technology solutions and meet the needs of today's global, distributed workforce. From the office to industrial environments, our differentiated business and technology offerings and financial services are essential workplace technology solutions that drive success for our clients. At Xerox, we make work, work. Learn more about us at .
**OVERVIEW:**
We are seeking a skilled, experienced and detail-oriented Quality Assurance Analyst to join our team at our Scarborough, ON production site. The Quality Assurance Analyst will be responsible for analyzing work processes, creating, managing and executing a Quality Assurance Program that will provide visibility on quality (error rates, systemic issues) that arise from business-as-usual operations. The ideal candidate will possess strong analytical skills, excellent communication abilities, and have a deep understanding of Quality Assurance operations and a general knowledge of IT systems, especially in the insurance or financial services sectors.
**PRIMARY RESPONSIBILITIES** :
+ Create a comprehensive Quality Assurance Program that will measure and report on the error rates of key business processes for a key insurance client in Canada. The goal of the program will be to achieve and exceed contracted Quality targets.
+ Ensure that a statistically based number of daily samples are taken from "in Scope work processes" to calculate error rates, driving both trending as well as possible areas of improvement. Analyze the samples taken for errors, omissions and tabulate the results.
+ Identify opportunities for process improvements and contribute to ongoing optimization efforts.
+ Collaborate with stakeholders on process improvement initiatives (Operations, Technology, Solution Architects and Account Management) to improve the service and seek to create error proof processes over time.
+ Consistently manage expectations and negotiate with stakeholders to determine the most accurate and appropriate definition of quality metrics and priorities.
+ Chair Quality Assurance meetings, informal and formal review meetings and lead Quality Assurance presentations. Develop and document detailed Quality Assurance programs, processes, and methods for client presentation.
+ Lead Quality testing, reporting on results, ensuring quality and adherence to the Quality Assurance requirements. Ensure testing meets or exceeds Quality Assurance requirements.
**QUALIFICATIONS, SKILLSETS & ABILITIES** :
+ Bachelor's degree in Information Technology, Quality Assurance, or related work experience
+ Minimum of 3 years of experience as a Quality Assurance Analyst, preferably in the insurance industry. Experience in the banking industry will also be considered
+ Strong analytical and problem-solving skills
+ Proficiency in data analysis tools and techniques
+ Proficiency with Software Platforms including Microsoft Excel, Microsoft PowerPoint, Microsoft Visio, Microsoft Project, Jira
+ Excellent communication and interpersonal skills
+ Ability to work collaboratively with cross-functional teams
+ Experience with Quality Assurance process workflow and documentation tools
+ Certification in a Quality Assurance role would be an asset
+ Knowledge of Business Analyst and Project Management methodologies and tools
#LI-CB1
Xerox is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, creed, religion, ancestry, national origin, age, gender identity, sex, marital status, sexual orientation, physical or mental disability, use of a guide dog or service animal, military/veteran status, citizenship status, basis of genetic information, or any other group protected by law. Learn more at and explore our commitment to diversity and inclusion: People with disabilities who need a reasonable accommodation to apply or compete for employment with Xerox may request such accommodation(s) by sending an e-mail to Be sure to include your name, the job you are interested in, and the accommodation you are seeking.

Job Description

Job Description

Salary:

About PSD Citywide
PSD Citywide is a leading provider of enterprise asset management, maintenance, financial, GIS, and permitting software solutions, along with advisory services. Offering the only purpose-built, fully unified cloud-based SaaS solution for municipal governments, PSD Citywide supports the management of over $400 billion in municipal assets across North America. With a multidisciplinary advisory team of Asset Management, Finance, Engineering, and Municipal practitioners, combined with an in-house software development group, PSD Citywide delivers comprehensive solutions to ensure best-in-class service for its clients.

The Quality Assurance Analyst works collaboratively within the IT department to execute and validate test cases based upon system requirements. They are responsible for creating an end-to-end test plan; executing the plan and managing all activities in the plan to ensure that all the objectives are met, and the solution works as expected. This Full Time Contract position offers the potential to transition into a Permanent Full Time position. Applicants must reside in Canada to be considered.

What we offer
Competitive Salaries: We recognize and reward your skills and experience with a competitive pay structure.
Remote Work Options: Work from anywhere in Canada that suits you while staying connected with our team.
Social and Charity Events and Initiatives: Join PSD CityKind! A group dedicated to fostering kindness and community engagement across North America.
Career Framework: Clear paths for growth and development, helping you reach your career goals with ongoing learning and mentorship.

Job Duties & Responsibilities

• Ensure technical quality of software through detailed testing and feedback to relevant team members.
• Take a proactive, problem-solving/trouble-shooting approach to identifying and solving software problems; not stopping at identifying the problem, but experiment using available information to try to narrow the possibilities and determine a suggested solution.
• Document, troubleshoot, and isolate issues encountered during testing utilizing internal bug database system and providing accurate and detailed reproduction steps including visuals if possible and/or other required regression information.
• Assist with focus testing sessions and provide summary reports.
• Assist in development and implementation of comprehensive QA test plans and cases.
• Assist in the generation and implementation of procedures for more effective and efficient testing of company products.
• Assist with testing using internal development tools.
• Contribute to a positive work environment by getting involved with all departments of the team, understanding their roles and interacting with the team on a regular basis to help gain a rounded perspective of the project.
• Ensure conformance of all company and departmental standards, policies and procedures.
• Other duties as assigned.
  

Qualifications

• 3-5 years experience in a Software Quality Assurance role.
  
• Post Secondary Degree or Diploma in Computer Science or related technical field or equivalent practical experience.
  
• Working knowledge of Mobile application and Manual and Automation testing.
• ISQTB certification would be considered an asset.
• Extremely familiar with all aspects of software verification including: functionality, performance, and system testing.
• Meticulous attention to detail and strong problem-solving ability, in addition to honesty, strong work ethic.
• Working knowledge of most popular console platforms, Windows operating systems and related hardware.
• Deadline driven individual with strong verbal, technical, and written communication skills, creative and able to collaborate with team members with professionalism and tact.
• Advance skills with MS Word and Excel.
• Professional self-starter with a commitment to constantly upgrade skills through continuous learning.
  

The Candidate Journey

Resume Review: Once you apply, an actual person will review your resume and we are committed to getting back to you with a response.

Phone Interview: PSDs People and Culture team will connect with you to learn about your experience and discuss the role further. Theyll also give you an understanding of what the interview process involves, along with an estimated timeline.

Virtual Interview: Depending on the position, there will be one or two interviews with the Hiring Team that will include questions related to your skills, work experience, values and goals. We provide the opportunity to meet with a wide range of staff members so you can learn more about life at PSD Citywide.

Offer/Feedback: The Hiring Team will debrief and make a decision within a few days of your final interview. If successful, your Recruiter will present you with a verbal offer, followed by a formal offer letter via email. If the timing was not right for this particular opportunity, we will connect with you and provide feedback.

PSD Citywide is committed to ensuring equal access and participation for people with disabilities. We believe in integration, and we are committed to meeting the needs of people with disabilities in a timely manner. We will do so by removing and preventing barriers to accessibility.

We are committed to accommodating people with disabilities. Accommodations are available upon request for candidates taking part in all aspects of the recruitment and selection process. Should you require any accommodation, please indicate this when you apply, and we will work with you to meet your accessibility needs.

remote work

Job Description

Job Description

Belvika Trade & Packaging Ltd. is a leading one-stop contract packaging company, specializing in precision packing of dry foods, chocolate and confectionary products from multiple facilities totaling more than 500,000 ft2. Belvika has grown to be one of the largest co-packers of chocolate, confectionary and snack products in Canada. Belvika uses its extensive experience in managing both manual processes and automated equipment to handle primary and secondary packaging of products for some of the world’s best-known confectionary brands.   Belvika is an equal opportunity employer, offering competitive wages, a bonus plan, benefit plan, ongoing training, and an interesting and challenging work environment. We will provide the tools and training that you require to excel at your role together with access to Senior Management to provide additional support and guidance. We welcome and encourage applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.   Belvika is currently seeking a Quality Assurance Inspector to maintain overall quality standards for all products packed, ensuring that the Company’s and Client’s quality specifications are met at all times. This position will be based at the Export facility located at 450 Export Blvd, Mississauga, and, when needed, must be flexible to work at the Traders facility located at 340 Traders Blvd, Mississauga. The position works on the day shift but must be flexible to work afternoon or night shifts as needed.   Position Summary: * This is a Quality Assurance Inspector position within the Quality Department of a Co-packer in confectionary and snack food products. * Areas include quality element control related to operations, policy and procedure auditing, leads quality improvement projects, and drives defect prevention and detections. * Organizes and reviews all QA aspects of daily production.   The successful candidate will:      * Maintain and ensure consistent execution of current QA programs and internal SOPs and compliance with SQF, CFIA, and client requirements; * Maintain all sensory guidelines for all incoming and outgoing bulk / finished goods; * Oversee the retention samples and storage of product for all customers; * Oversee the proper destruction of any food product and complete any CODs as required; * Prepare all new product start-ups ensuring that all Belvika requirements are met (Belvika and client forms); * Write, review and implement new operating policies and procedures as directed by the QA Manager; * Take the lead on executing various initiatives to improve the quality and safety of our processes; * Assist with Company food safety and quality program updates, maintenance and verifications to ensure the facility is meeting regulatory and compliance requirements for all stakeholders; * Monitor and inspect production lines and quality report forms daily to ensure client quality and food safety standards are being met; * Review shift reports daily to ensure lot traceability and quality checks forms that have been completed are accurate; * Perform Environmental, ATP and allergen tests when needed; * Perform water testing and sampling when required; * Ensure that the allergen program is being followed and make certain quality & food safety standards are being met; * Conduct a variety of monthly internal audits with cross-functional team and identify opportunities for improvement; * Maintain and verify that daily, weekly and monthly cleaning duties have been completed and records are up to date; * Maintain and verify that daily and monthly hold logs have been completed and are up to date; * Take the lead on issuing and following up on any corrective actions, if necessary, based on deviations found or resulting from client complaints; * Ensure that the pest control program is being maintained and liaise with operator to ensure that all Company and regulatory standards are being met; * Drives prevention vs. detection of defects; * Supports client audits, government audits to meet compliance; * Support the ongoing development and improvement of the Quality Management System (QMS). The co-ordination of processes includes managing controlled documents, Quality Records Archiving, employee training of QMS processes and special projects; * Follow all Company health and safety policies and procedures and work in compliance with Occupational Health and Safety Act; * Other tasks as assigned by your supervisor or designate.   Education/Work experience requirements: * Minimum 1-year experience in quality assurance in food processing or food packaging environment; * Knowledge & experience of GMPs, HACCP and & Quality Management systems; * Post-secondary education related to Quality Assurance and/or Food Science is an asset.   Key technical & behavioural competencies: * Self-starter who works well under pressure and has great time management skills; * Proficiency with Microsoft Office such as Word and Excel; * Great interpersonal skills with a proven ability to work well both independently and with multiple departments as required; * Knowledge and basic understanding of allergen and pathogen swabbing techniques; * Knowledge of quality auditing, inspection methods; * Detail oriented; * Strong organizational skills, able to prioritize responsibilities and multi-task; * Excellent reading, writing, and oral communication skills.   We thank all candidates for their interest; however only those most qualified will be contacted.