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Added 1 day ago
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Operations Management Associate - Food Manufacturing
Cargill
London, ON
- Full-time
…a result, you will have the possibility of working varying shift hours, 8 to 10-hour shifts, and even 6-day weeks depending on customer demand. As an industry leader, it’s all part of…
Added 1 day ago
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Operations Management Associate - Food Manufacturing
Cargill
High River, AB
- Full-time
…a result, you will have the possibility of working varying shift hours, 8 to 10-hour shifts, and even 6-day weeks depending on customer demand. As an industry leader, it’s all part of…
Added 2 days ago
MC
Stagiaire en affaires médicales / Medical Affairs Intern
Merck Canada
Kirkland, QC
- Internship
Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is…
Added 2 days ago
MC
Stagiaire en affaires médicales / Medical Affairs Intern
Merck Canada
Toronto, ON · Greater Toronto Area, Canada
- Internship
Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is…
Added 2 days ago
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Stagiaire en affaires médicales / Medical Affairs Intern
Merck
Toronto, ON · Kirkland, QC
- Full-time
Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is…
Added 2 days ago
M
Stagiaire en affaires médicales / Medical Affairs Intern
MSD
Toronto, ON · Kirkland, QC
- Full-time
Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is…
Added 2 days ago
Sales Representative - Uniform
Cintas
Edmonton, AB
…energetic Sales Representative to join our growing Outside Sales team. This role provides our customers with solutions to their work apparel needs by offering weekly laundry, delivery,…
Added 2 days ago
CC
Sales Representative - Uniform
Cintas Canada
AB · Edmonton, AB
- Full-time
…energetic Sales Representative to join our growing Outside Sales team. This role provides our customers with solutions to their work apparel needs by offering weekly laundry, delivery,…
Added 3 days ago
CC
Sales Representative - Uniform
Cintas Canada
Cambridge, ON
- Full-time
…energetic Sales Representative to join our growing Outside Sales team. This role provides our customers with solutions to their work apparel needs by offering weekly laundry, delivery,…
Added 3 days ago
Sales Representative - Uniform
Cintas
Cambridge, ON
…energetic Sales Representative to join our growing Outside Sales team. This role provides our customers with solutions to their work apparel needs by offering weekly laundry, delivery,…
Added 3 days ago
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Inside Sales Representative/Shipper Receiver
Air Liquide
London, ON
- Full-time
This position will lead you to build lasting relationships with customers and collaborate on developing business markets. You will have the chance to evolve in an organization where…
Added 3 days ago
CO
Job ID #32083: Arena Clerk (Periodic) - RE-POST
City Of Hamilton
Hamilton, ON
- Temporary
…from the downtown core, and so much more. Join our diverse team of talented and ambitious staff who embody our values of sensational service, courageous change, steadfast integrity,…
Added 4 days ago
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Director, Supply Chain Management (Hybrid)
Merck
Canada
- Full-time
Ability to lead, coach and develop team members.
Added 4 days ago
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Robotic Weld Technician
Martinrea International
Woodbridge, ON
- Full-time
Assure that 1st off/1st Part is inspected and meets Quality Assurance requirements
Added 5 days ago
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Manager, Supply Chain / Gestionnaire, Gestion de la chaîne d’approvisionnement
Merck
Charlottetown, PE
- Full-time
Lead, coach, and develop the Supply Chain team of 9-12 people, establishing clear priorities, accountability, and performance expectations.
Added 5 days ago
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Manager Safety-1st Shift-RVI-Hanceville
Tyson Foods
Hanceville, BC
- Full-time
…throughout the facility. As a key member of the Plant Leadership Team, this position partners with site management to develop, implement, and continuously improve safety programs and…
Added 5 days ago
M&
Robotic Weld Technician
Mitchell & Associates
Vaughan, ON
- Full-time
Assure that 1st off/1st Part is inspected and meets Quality Assurance requirements
Added 5 days ago
JC
Electrical Apprentice 1st
Johnson Controls
Nisku, AB
- Full-time
We offer multiple shift options to fit your lifestyle:
Added 6 days ago
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Sr. IT Manager - IT Application Support
TD
Toronto, ON
- Full-time
This senior support lead position interacts with all users of various vendor and internal developed etrading application like ION , Broadway, Bloomberg including Front Office , Finance &…
Added 11 days ago
MC
Director, Supply Chain Management (Hybrid)
Merck Canada
Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
Ability to lead, coach and develop team members.
Added 11 days ago
CC
Production Supervisor
Cintas Canada
Cambridge, ON
- Full-time
Cintas is seeking a Production Supervisor to lead and direct our Production team. Responsibilities include hiring, training and directing individuals who are performing entry level…
Added 11 days ago
CC
Maintenance Supervisor
Cintas Canada
Toronto, ON · Etobicoke, ON
- Full-time
Cintas is seeking a Maintenance Supervisor to lead all maintenance activities at our Cintas facilities. Responsibilities include improving functionality and reliability of all production…
Added 11 days ago
Production Supervisor
Cintas
Cambridge, ON
Cintas is seeking a Production Supervisor to lead and direct our Production team. Responsibilities include hiring, training and directing individuals who are performing entry level…
Added 11 days ago
Maintenance Supervisor
Cintas
Toronto, ON · Etobicoke, ON
Cintas is seeking a Maintenance Supervisor to lead all maintenance activities at our Cintas facilities. Responsibilities include improving functionality and reliability of all production…
Added 12 days ago
Exterior Cleaner / Groundskeeper – Mall & Parking Lot (Burnaby, BC)
Kandor
Burnaby, BC
This is an exciting opportunity to join the Everclean team and be part of the work that keeps spaces clean, safe, and running smoothly every day.

Pacer Group

Quality Assurance Associate

Charlottetown, PE, Canada

On-site

$30 to $35 CAD / hour · Full-time

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Job details

Pay: $30 to $35 CAD / hour
Job type: Full-time
Workplace: On-site
Apply by: Nov 21, 2026
Posting language: English
Posted: Oct 22, 2026

Original job description

Job Title: Quality Assurance Associate

Location: Charlottetown, PE C1E 0A1, Canada

Duration: 12 Months – Possible Extensions

Schedule: Standard 1st Shift | Monday – Friday

Work Arrangement: On-site

Nature of Job: Contract

Pay Rate: $30.00–$35.00 per hour on W2

Job Type: Contract

Domain: Quality Assurance / Pharmaceutical / Food and Drug Manufacturing

Deadline: 11/06/2026

POSITION OVERVIEW:

The Quality Assurance Associate will support and execute activities within Quality Operations, Quality Systems, and Compliance. Key responsibilities include document control, change control, quality incidents, Corrective and Preventive Actions (CAPA), Good Manufacturing Practice (GMP) data review, batch record review for product release, internal and external audits, and supplier quality management.

The ideal candidate will have experience working in a food or pharmaceutical manufacturing environment, along with direct experience in a Quality Unit. This role ensures that manufacturing operations, quality systems, and compliance activities meet applicable GMP requirements and established Quality Management System (QMS) standards.

SKILLS REQUIRED

Primary Skills

Quality Assurance in food or pharmaceutical manufacturing
Good Manufacturing Practices (GMP)
Quality Management Systems (QMS)
Document Control and Change Control
Quality Incident Management and Investigations
Corrective and Preventive Actions (CAPA)
Batch Record Review and Product Release
Standard Operating Procedures (SOPs)
Internal and External Audits
Supplier Quality Management
GMP Data Review and Compliance

Secondary Skills

Deviation and Laboratory Investigation Management
Out-of-Specification (OOS) Investigation Review
Annual Product Review (APR)
Quality Systems Review (QSR)
Metrics and Scorecard Reporting
Analytical Validation and Process Transfer
Validation and Qualification Documentation
Product Label Management
Facility Inspections and Pest Control
GMP Training and Documentation Archiving
Communication, Critical Thinking, and Problem Solving

MAJOR JOB RESPONSIBILITIES

Support quality incident programs, including deviations, laboratory investigations, complaints, and supplier-related incidents. Review incidents, assess severity, approve minor incidents and Phase 1 Out-of-Specification (OOS) investigation outcomes, and participate in major incident investigations.
Participate in internal audits and support external and client audit requirements.
Manage and lead changes to Standard Operating Procedures (SOPs) and review changes initiated by other departments through the change control process.
Support the Annual Product Review (APR) program, metrics and scorecard reporting, and Quality Systems Review (QSR) activities.
Monitor and enforce GMP requirements across all departments during daily operations.
Support supplier quality management and supplier compliance activities.
Inspect and release rooms and conduct facility inspections as part of general quality and compliance activities.
Prepare or assist with reports, protocols, validation documents, and qualification documentation.
Issue, verify, and archive Quality Control (QC) notebooks.
Provide GMP and SOP training to employees across various departments.
Manage product label masters and support product label creation.
Support the CAPA program, including quality improvement and corrective action activities.
Support analytical validation, process transfer, and analytical process lifecycle activities by reviewing and approving analytical validation data, protocols, reports, and work instructions.
Participate in the pest control program, including inspections and investigations.
Perform batch record and data reviews to support the release of critical raw materials, Active Pharmaceutical Ingredients (APIs), and finished products.
Release critical raw materials, APIs, and finished products upon successful completion of the required BioVectra batch release training.
Support the process lifecycle by reviewing and approving the creation and revision of batch records.
Participate in SOP document lifecycle activities, including QA review and approval of SOP changes.

REQUIRED QUALIFICATIONS

Post-secondary education is required.
Three years of work experience with a food or pharmaceutical manufacturing company.
At least one year of direct experience working in a Quality Unit position.
Practical knowledge of GMP requirements and quality assurance processes.
Experience with quality documentation, SOPs, investigations, and compliance activities.
Strong written and verbal communication skills.
Ability to work independently with minimal supervision and collaboratively within a team.
Strong organizational, prioritization, and scheduling skills.
Ability to review documentation accurately and maintain compliance with established quality standards.

Must-Have Requirements:

Experience working with a food or drug manufacturing company.
At least one year of direct experience in a Quality Unit position.

PREFERRED SKILLS

A bachelor's degree in a scientific field is considered an asset.
Experience with CAPA, deviations, OOS investigations, and change control.
Familiarity with batch record review and the release of raw materials, APIs, and finished products.
Experience supporting internal audits, external audits, and supplier quality programs.
Strong critical-thinking and problem-solving abilities.
Effective presentation and interpersonal skills.
Ability to manage multiple priorities and meet deadlines.
Strong attention to detail and commitment to quality and compliance.

BENEFITS

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Retirement Plan
Paid Sick Leave
Other applicable benefits, subject to employer and assignment eligibility.

AI USAGE POLICY

Artificial intelligence tools may be used to assist with administrative tasks and candidate screening. All hiring and selection decisions will be made by human recruiters and authorized hiring personnel.

EEOC COMPLIANCE

We are an equal opportunity employer and consider all qualified applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status, or any other status protected by applicable law. Employment decisions are based on qualifications, skills, experience, and business requirements.

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More about this job

Responsibilities

Support quality operations and compliance by managing quality incidents, CAPAs, document and change control, audits, supplier quality, and GMP training. Review batch records and GMP data, support validation and product lifecycle activities, and release materials and products after required training and review.

Requirements

Requires post-secondary education, at least three years of experience in food or pharmaceutical manufacturing, and at least one year of direct Quality Unit experience. Candidates must have practical GMP and quality assurance knowledge, experience with quality documentation and investigations, and strong communication, organizational, and documentation-review skills.

Skills

Quality Assurance
Good Manufacturing Practices (GMP)
Quality Management Systems (QMS)
Document Control
Change Control
Quality Incident Management
Investigations
Corrective and Preventive Actions (CAPA)
Batch Record Review
Standard Operating Procedures (SOPs)
Internal and External Audits
Supplier Quality Management
GMP Data Review
Out-of-Specification (OOS) Investigations
Analytical Validation
Product Release

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Retirement Plan
Paid Sick Leave

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
Food Manufacturing
Pharmaceutical Manufacturing
Good Manufacturing Practices (GMP)
Quality Management System (QMS)
Quality Operations
Quality Systems
Compliance
Document Control
Change Control
Quality Incidents
Deviations
Laboratory Investigations
Out-of-Specification (OOS) Investigations
Corrective and Preventive Actions (CAPA)
Batch Records
Product Release
Standard Operating Procedures (SOPs)
Internal Audits
External Audits
Supplier Quality Management
Annual Product Review (APR)
Quality Systems Review (QSR)
GMP Training
Analytical Validation
Process Transfer
Validation and Qualification
Active Pharmaceutical Ingredients (APIs)
Product Label Management
Pest Control

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