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Added 1 min ago
TT
Operations Supervisor
TF Truckload & Logistics
AB · Edmonton, AB
- Full-time
We are growing and looking for an experienced Operations Supervisor to join our team! As the Operations Supervisor, you will oversee daily transportation, yard, and warehouse operations,…
Added 1 min ago
DB
Process Plant Operator, Fixed-Term Contract
De Beers Group
NT · Northwest Territories, Canada
- Contract
…in the Northwest Territories. Reporting to the Process Plant Supervisor, this position is responsible for feeding ore into the process plant from the ore stockpiles. This is a fixed-term…
Added 1 min ago
DB
Heavy Equipment Operator, Multi-Skilled, Mine Operations - Fixed-Term Contract Fly In/Fly Out
De Beers Group
NT · Northwest Territories, Canada
- Contract
…based in the Northwest Territories. Reporting to the Mining Supervisor and working a two (2) week in/ two (2) week out rotation, this position is responsible for operating heavy mobile…
Added 1 min ago
IC
Support Worker - Casual
Island Crisis Care Society
Parksville, BC
- $27.53 to $31.57 CAD / hour
- Part-time
…comes to the client and/or the public. Reports problems to the…
Added 1 min ago
RM
Construction Leader - Borden
REDPATH MINING
Chapleau, ON
- Full-time
Under the supervision of the Shift Supervisor and/or the Underground Superintendent, the primary role of the Construction Leader is to perform construction mining tasks and is able to…
Added 1 min ago
G
Senior HSE Coordinator - Buildings
Graham
Saskatoon, SK
- Full-time
…Saskatoon. The position works closely with the Saskatoon-based supervisor and broader HSE and operations teams, providing construction safety leadership, regulatory guidance, incident…
Added 1 min ago
SC
Sales Solutions Specialist
Sysco Canada Inc.
Toronto, ON · Greater Toronto Area, Canada
- Full-time
Is willing to work safely with minimal environmental impact and understands the importance of reporting all hazards, incidents, and environmental spills immediately to their supervisor.
Added 1 min ago
TO
Operator
Town of Newmarket
Newmarket, ON
- Full-time
Reporting through the Supervisor, Water/Wastewater, and under the direction of the Lead Hand, Water/Wastewater, the Operator – Water/Waste Water is responsible for performing infrastructure…
Added 2 mins ago
Director of Care
Optima Living
Morinville, AB
Added 2 mins ago
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Quality Control Inspector
Leesta
Pointe-Claire, QC
- Full-time
…instructions and perform any other related duties as assigned by their…
Added 2 mins ago
School Age Educator - Ernest Cumberland
YMCA of Simcoe/Muskoka
New Tecumseth, ON
Adhere to work schedule to ensure program stays within ratio and provide adequate notice to supervisor regarding unexpected scheduling changes
Added 2 mins ago
RECE or Equivalent - Split Shift Position
Upper Canada Child Care
Markham, ON
Keeps team and supervisor apprised of compliance issues or problems related to governing regulation and internal policy.
Added 2 mins ago
Maintenance Power Engineers - 3rd Class
Sofina Foods Inc
Wynyard, SK
Reporting to the Maintenance Supervisor, the Power Engineer will operate and maintain Steam Boilers and Ammonia Refrigeration Cooling System at the Wynyard Plant. This position will also be…
Added 2 mins ago
CL
Internal - FT Night Sleep Temporary 9 months - Euphemia (Nov 9 -Nov 18)
Community Living Sarnia-Lambton
Sarnia, ON
- Full-time
Added 2 mins ago
NA
Mental Health Program Specialist (Temporary), Post Secondary Mental Health
Northern Alberta Institute of Technology
St. Catharines, ON · Main Campus
- Full-time
Reporting to the Mental Health Program Supervisor, the Mental Health Program Specialist plays an essential role in the day-to-day coordination and delivery of NAIT’s mental health and…
Added 2 mins ago
CH
Field Service Coordinator Intern - Summer 2027
Clean Harbors
Debert, NS
- Full-time
Assist with proper communication with the foreman/supervisor to ensure that contractual obligations are met to complete requested services.
Added 2 mins ago
TH
Associé(e) aux ventes, Service aux entrepreneurs (temps plein)
The Home Depot
Laval, QC
- Full-time
Strives to meet personal goals (e.g., sales, quotes, credit accounts) set by Supervisor as well as the goals of the team. Creates action plan with Supervisor to develop selling skills.
Added 2 mins ago
TH
Merchandising Execution Team Associate Part Time - 7065 South Common
The Home Depot
Canada
- Part-time
Reports to Merchandising Execution Supervisor (MEAS)
Added 2 mins ago
TH
Head Cashier Part Time - 7255 Cranbrook
The Home Depot
Cranbrook, BC
- Part-time
The Head Cashier plays an important role supporting the Front End Supervisor in motivating front end associates to follow GET behaviours and provide customers a great shopping experience.…
Added 2 mins ago
TH
Lumber Sales Associate: Part time - WHITE ROCK
The Home Depot
Surrey, BC
- Part-time
Added 2 mins ago
TH
Millwork Sales Associate: Part Time - RICHMOND
The Home Depot
Richmond, BC
- Part-time
Added 2 mins ago
TH
Associé(e) ventes aux entrepreneurs (temps partiel)
The Home Depot
Canada
- Part-time
Strives to meet personal goals (e.g., sales, quotes, credit accounts) set by Supervisor as well as the goals of the team. Creates action plan with Supervisor to develop selling skills.
Added 17 mins ago
DT
Merchandising Assistant Manager
Dollar Tree Stores
Edmonton, AB
- Full-time
…perform any other related duties as may be required by their…
Added 17 mins ago
EV
Maintenance, Planner
Elk Valley Resources
Sparwood, BC
- $123,000 to $145,000 CAD / year
Provide backup to the Maintenance Supervisor where required
Added 17 mins ago
UC
Cooks Helper - Full Time & Part Time
Unidine Canada
MB · Dugald, MB
- Full-time
- Part-time
Reports needed maintenance, faulty equipment or accidents to the supervisor immediately.

Young Innovations

Quality Assurance Supervisor

1379 Colborne St E, Brantford, ON, N3S 0H4, Canada

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Job details

Posting language: English
Posted: Nov 5, 2026

Original job description

Job Details: Job Location: Germiphene - Brantford, ON, Salary Range: Undisclosed, Company Summary: At Young Innovations, we foster a dynamic environment where team members make an impact every day as part of a collaborative, inclusive culture. Together, we serve the dental profession and their patients, united in our mission of achieving a Lifetime of Oral Health™ We embrace diverse perspectives and encourage bold thinking, challenging traditional approaches with a bias for action. Whether you’re looking to expand your skills or grow your career, Young is here to support your goals and continuous learning. At Young, YOU are at the core of what we do. Position Overview: Germiphene Corporation, a Young Innovations company and Health Canada-licensed manufacturer of dental pharmaceutical and natural health products, is hiring a Quality Assurance Supervisor. Reporting to the Quality Manager, this is a hands-on leadership role with accountability for the day-to-day health of the QMS, including investigations, annual product reviews, KPI trending, and SOP authorship across both Drug GMP and ISO 13485 / MDSAP frameworks. The Quality Supervisor leads a team within the Quality Assurance Department and is accountable for the supervision and development of assigned staff to drive timely, defensible closure of deviations, CAPAs, and out-of-specification events. They will be expected to strengthen the QMS through KPI trending, SOP authorship, and continuous improvement work that reduces repeat failures and supports audit readiness. You’ll like this role if: You like structured problem-solving and the satisfaction of getting to a real root cause. You write clearly and plainly, and you can defend what you wrote in front of an auditor. You are comfortable juggling several investigations, CAPAs, and deliverables at once and pushing each forward without losing the thread. You enjoy working with people across Operations, QC, RA, and R&D, and you can mentor junior staff on RCA and quality documentation. You are comfortable leading a small team, and you see developing your direct reports as part of how quality improves. You want to see the impact of your work - in this role, your investigations and trending directly shape how the site improves. Why You’ll Love Working Here: Medium sized company – not too big, not too small – just enough to get things done and see your impact. Did we say benefits? Health, dental, and vision coverage; group RRSP; parental leave; statutory holidays; paid time off; short- and long-term disability insurance; employee assistance program; and more. Real ownership from day one. You will lead investigations end to end, author SOPs that go into production, and see your trending work shape decisions across the site. Who you’ll work with: You will report to the Quality Manager and work closely with QA, QC, Operations, Regulatory Affairs, and R&D colleagues at the Brantford site, as well as Young Innovations corporate Quality counterparts at our sister facilities. What You’ll Do: Investigations and CAPA Lead investigations of deviations, out-of-specification (OOS) results, non-conformances, product complaints, and rework events. Apply structured root cause analysis tools (Fishbone, 5 Whys, FMEA) and author clear, defensible investigation reports. Drive all investigation CAPAs to closure, including verification of effectiveness. Identify systemic issues across investigations and escalate to the Quality Manager as appropriate. Annual Reviews and Summary Reports Lead Annual Product Quality Reviews (APQR) for assigned products, including data compilation, trending, and conclusions on process state of control. Coordinate Annual Summary Reports (ASR) with Regulatory Affairs including literature searches and adverse-event data review. Support pharmacovigilance data collection and prepare Issue-Related Summary Reports (IRSR) at the request of Health Canada or the VP Quality. SOPs, KPIs, Audits, and Continuous Improvement Author, revise, and approve SOPs and forms within delegated authority. Track and report on quality KPIs informed by complaint trends, and deviation/OOS history; identify improvement opportunities and partner with Operations and QC to eliminate recurring failures. Lead internal audit response and act as subject-matter expert during external audits (Health Canada, MDSAP, ISO 13485, customer) under the direction of the Quality Manager. Mentor and provide technical guidance to QA Associates and shop-floor QA staff on investigations, RCA, and documentation. Staff Supervision Supervise assigned quality department direct reports, including day-to-day workload assignment and prioritization. Conduct performance reviews and provide ongoing coaching and feedback to support individual development. Identify training needs and coordinate or deliver GMP and role-specific training for direct reports. Escalate performance concerns to the Quality Manager as appropriate. Qualifications: What You’ll Bring: University degree in a science discipline (chemistry, biology, pharmaceutical sciences, microbiology, or related). Minimum five years of progressively responsible quality assurance experience in pharmaceutical or medical device manufacturing. Demonstrated experience leading deviation, OOS, complaint, and CAPA investigations and authoring investigation reports. Working knowledge of Health Canada Drug GMP (GUI-0001) and ISO 13485 / MDSAP requirements; experience supporting external regulatory inspections is preferred. Strong technical and regulatory writing, able to draft defensible SOPs, investigations, and audit responses in clear, plain language. Sound analytical and statistical literacy for KPI trending and stability data interpretation. Sound judgment in assessing risk, scope of impact, and escalation needs; comfortable juggling concurrent priorities under time pressure. Ability to provide constructive technical guidance to junior QA staff. Prior experience managing or supervising quality department staff, including performance management, workload assignment, and development of direct reports. Technical Skills Hands-on experience with structured root cause analysis tools (Fishbone, 5 Whys, FMEA) and risk-based decision-making. Proficiency with electronic QMS systems, including audit-trail reviews. Proficiency with MS Office (Word, Excel, PowerPoint); comfort with data analysis and trending. Experience with HPLC, GC and related analytical method understanding is an asset (not required). Travel Requirements Minimal. Occasional travel to supplier sites or sister Young Innovations facilities may be required. Work Environment Manufacturing/Distribution Environment This position operates in a pharmaceutical manufacturing environment. The role routinely involves working in or around manufacturing and laboratory areas, including machinery, equipment, and moving mechanical parts. The facility may be subject to varying temperatures, noise, and airborne particles such as dust or chemical fumes, depending on the area. PPE and gowning are required when entering production or QC areas. The role may require periods of standing, sitting, or walking throughout the workday. Occasional bending, lifting, or carrying items up to 23 kg may be necessary. Specific vision abilities required by this job include close vision, depth perception and ability to adjust focus. While performing the duties of this Job, the employee is regularly required to sit. Hearing abilities required for this environment include being able to clearly hear and respond to audible alarms, production equipment, forklifts, and other machinery to maintain a safe work environment. Individuals must be able to distinguish and understand verbal communication including instructions, safety warnings, and team discussions, sometimes in an environment with moderate to high background noise. This position is available due to an existing vacancy. In compliance with AODA legislation, if you require accommodation during any part of the recruitment process, please advise Human Resources.

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More about this job

Responsibilities

The Quality Assurance Supervisor leads a team to manage the Quality Management System, including investigations, CAPAs, and SOP development. They are responsible for ensuring regulatory compliance, driving continuous improvement, and mentoring staff within a pharmaceutical manufacturing environment.

Requirements

Candidates must hold a university degree in a science discipline and possess at least five years of quality assurance experience in pharmaceutical or medical device manufacturing. Proficiency in Health Canada Drug GMP, ISO 13485, and structured root cause analysis tools is required.

Skills

Quality Assurance
GMP
ISO 13485
MDSAP
Root Cause Analysis
CAPA
SOP Authorship
KPI Trending
Regulatory Compliance
Staff Supervision
Technical Writing
Risk Assessment
Audit Readiness
Pharmaceutical Manufacturing
Data Analysis
Mentorship

Benefits

Health coverage
Dental coverage
Vision coverage
Group RRSP
Parental leave
Statutory holidays
Paid time off
Short-term disability insurance
Long-term disability insurance
Employee assistance program

Visa sponsorship

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Keywords

Quality Assurance
GMP
ISO 13485
MDSAP
CAPA
SOP
Root Cause Analysis
Fishbone
5 Whys
FMEA
KPI
Health Canada
Pharmaceutical
Medical Device
Regulatory Affairs
Quality Management System
Audit
Pharmacovigilance
APQR
ASR
IRSR
Manufacturing
Laboratory
Compliance
Risk Management
Technical Writing
Data Analysis
Mentoring
Performance Management
Quality Control

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