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Added 21 mins ago
Job Title Program Resource Worker
Lookout Housing + Health Society
North Vancouver, BC
Internship
The Program Resource Worker (PRW) reports to the Site Manager and works in accordance with the mission and philosophy of Lookout Housing and Health Society, including following Lookout’s…
Added 21 mins ago
Job Title Program Resource Worker
Lookout Housing + Health Society
North Vancouver, BC
Internship
The Program Resource Worker (PRW) reports to the Site Manager and works in accordance with the mission and philosophy of Lookout Housing and Health Society, including following Lookout’s…
Added 21 mins ago
Property and Facilities Manager
Camp Kadesh
Christopher Lake, SK
Full-time
Camp Kadesh is a year-round facility primarily serving the city of Saskatoon and surrounding area. Located northwest of the town of Christopher Lake SK. Summer camp programming under the…
Added 35 mins ago
Temporary Administrative Assistant 6 (up to 12 months)
City of Saint John
Saint John, NB
Temporary
Reporting to the Manager, Customer Service & Operations in Growth and Community Services, the position is responsible for a variety of administrative duties to provide the necessary support…
Added 35 mins ago
Full Time Registered Practical Nurse (RPN) Supervisor
SOAR Community Services
Brantford, ON
Full-time
…activities. The Supervisor works collaboratively with the program’s Manager and fellow Supervisors, as well as with leaders across the Addiction and Mental Health department and community…
Added 35 mins ago
Business Advisor
City of Saint John
Saint John, NB
Full-time
The position serves as backup to the Customer Service Manager and provides leadership to the Customer Experience Specialist.
Added 35 mins ago
Mgr II, Tech Service Sup
Smurfit Westrock
Ajax, ON
Full-time
Job Title: Technical Services Supervisor Manager
Added 51 mins ago
IT Project Manager
TEKsystems
Toronto, ON
Contract
Our client is looking for an experienced IT Project Manager to support the PMO, managing a variety of systems-related projects across the organization. This individual will be responsible…
Added 51 mins ago
Security Guard SOC Operator Floater - Shopping Mall
Allied Universal
Winnipeg, MB
$23 CAD / hour
Full-time
Act as the primary point of contact to coordinate the dispatching of the Contractor’s Personnel and where necessary the Manager’s operations personnel to calls for service as required,…
Added 1 hour ago
(CAN) Cashier
Walmart Canada
Cochrane, AB
Full-time
Ensures safe work practices are followed including proper lifting and keeping a clean work area.
Added 1 hour ago
(CAN) Cashier
Walmart Canada
Cochrane, AB
Full-time
Ensures safe work practices are followed including proper lifting and keeping a clean work area.
Added 1 hour ago
Privacy Analyst
Winnipeg Regional Health Authority
Winnipeg, MB
Added 1 hour ago
Diagnostic Imaging Clerk
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Diagnostic Imaging (DI) Manager of Operations, and while demonstrating a commitment to the Mission, Values and Management Philosophy of St. Boniface…
Added 1 hour ago
Licensed Practical Nurse (LPN) - CD1 Personal Care
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager of Patient Care, the Licensed Practical Nurse (LPN) is responsible for providing professional practical nursing services to designated patients,…
Added 1 hour ago
General Duty Nurse (N2) - Emergency
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager Health Services, the Registered Nurse (RN) is responsible for providing professional registered nursing services for patients, including those…
Added 1 hour ago
General Duty Nurse (N2) - Women's Health Labour & Delivery
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager Health Services, the Registered Nurse (RN) is responsible for providing professional registered nursing services for patients, including those…
Added 1 hour ago
Health Care Aide - Home Care Program - T4 Transcona Access
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager or designate, the Health Care Aide (HCA) assists clients/patients/ residents with activities of daily living, providing direct…
Added 1 hour ago
Nurse 2 - Surgery - Orthopedic
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager, Health Services, the Registered Nurse (RN) is responsible for providing professional registered nursing services for patients, including those…
Added 1 hour ago
Nurse 2 - Surgery - Orthopedic
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager, Health Services, the Registered Nurse (RN) is responsible for providing professional registered nursing services for patients, including those…
Added 1 hour ago
Licensed Practical Nurse (LPN) - Emergency
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager Health Services, the Licensed Practical Nurse (LPN) is responsible for providing professional practical nursing services to designated patients,…
Added 1 hour ago
Licensed Practical Nurse (LPN) - Child Health Float Pool
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager Health Services, the Licensed Practical Nurse (LPN) is responsible for providing professional practical nursing services to designated patients,…
Added 1 hour ago
General Duty Nurse (N2) - Surgery- A3 Thoracic/Vascular/PCU-S
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager, Health Services, the Registered Nurse (RN) is responsible for providing professional registered nursing services for patients, including those…
Added 1 hour ago
General Duty Nurse (N2) - Interventional Radiology - Repost
Winnipeg Regional Health Authority
Winnipeg, MB
Under the direction of the Manager, Health Services (and utilizing the Clinical Resource Nurse as resource for clinical practice issues), the incumbent is responsible for:
Added 1 hour ago
Unit Assistant - ACF Medicine - Repost
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Program Team Manager/Co-Ordinator Pediatric Outpatient Nursing, and while demonstrating a commitment to the Mission, Values and Management Philosophy of…
Added 1 hour ago
General Duty Nurse (N2) - Surgery-A5 Neurosurgery/Spine/Stepdown
Winnipeg Regional Health Authority
Winnipeg, MB
Under the general supervision of the Manager Health Services, the Registered Nurse (RN) is responsible for providing professional registered nursing services for patients, including those…

Young Innovations

Quality Engineering Specialist

Brantford, ON, Canada

Pay: Compensation Range: $80,000 – 90,000
Posting language: English
Posted: Sep 28, 2026

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Original job description

Job Details: Job Location: Germiphene - Brantford - 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 a Health Canada-licensed manufacturer of dental pharmaceutical, natural health and medical device products, is hiring a Quality Engineering Specialist. Reporting to the Quality Manager, this role is the site owner of all Process Validation, Equipment Control, and Preventive Maintenance Programs, and keeps those programs in a state of continuous compliance with Health Canada GMP, ISO 13485 and regulatory requirements. You will own validation and qualification end to end: risk assessments, determining critical process parameters and acceptance criteria, drafting protocols and statistical sampling plans, directing protocol execution on the floor, interpretation of data, and finalizing reports. You will keep the site's equipment validation, calibration and preventive maintenance program in a state of compliance and are responsible for monitored systems, including the USP Purified Water System. You’ll like this role if: You would rather propose the technical approach and defend it than wait to be handed a method. You like the discipline of validation work: define the parameter, prove the control, and write it up so it holds up three audits from now. You want to own programs rather than work a task queue. You can carry a concurrent portfolio of protocols, qualifications, change controls and CAPAs to agreed dates, coordinating work that depends on Production, Packaging, Maintenance, QC, Microbiology and R&D. You want the impact of your work to be visible. There is no separate validation or metrology group here, so the technical decisions and the programs are yours. 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 are the site owner of validation, calibration and preventive maintenance: you set the technical approach, issue the protocols and reports, and your qualification decisions define how the equipment runs. Who you’ll work with: You will report to the Quality Manager. The position has no direct reports and works daily across Production, Packaging, Maintenance, Quality Control, Microbiology, R&D and Regulatory Affairs at the Brantford site, as well as with Young Innovations corporate Quality counterparts at our sister facilities. What You’ll Do: Validation and qualification Own process validation under the Validation Master Plan: evaluate manufacturing processes to determine critical process parameters, develop protocols and acceptance criteria, apply statistical techniques to set sampling plans, manage execution on the floor, interpret the resulting data, and issue approved reports. Lead risk assessments for process, equipment and cleaning validation, including process FMEA, and drive the resulting action plans. Own equipment qualification for production and laboratory equipment (IQ, OQ, PQ), determine the extent of qualification required based on complexity and intended use, and set the critical operating parameters that follow from it. Assist in the qualification and validation of computerized systems supporting production and laboratory equipment, including data integrity and user access verification, and maintain the qualified status of classified rooms through scheduled airflow and pressure differential verification. Maintain the site's validation status and inventory: periodic review to confirm validations remain current and supported, revalidation decisions driven by change, deviation or trend, and retirement of validations that no longer apply through the document change process. Monitor the ongoing state of control of validated processes, and support product development and production transfer by directing the validation work required to demonstrate a validated state. Calibration, preventive maintenance and equipment control Own the site Calibration and Preventive Maintenance Programs through the calibration management system, including the equipment database, unique identifiers, master records, schedules, frequencies and tolerances. Assess new equipment to determine whether calibration against traceable standards, performance verification against defined acceptance criteria, or preventive maintenance is the appropriate control. Coordinate outside metrology and calibration services and review the resulting certificates and reports before equipment is returned to service. Issue preventive maintenance work orders to Maintenance and system owners ahead of the scheduled date, record completed work, and coordinate HEPA filter certification and replacement for classified rooms, fume hoods and biological safety cabinets. Maintain certified reference standards and metrology equipment, including certificates of conformance and traceability to a recognized national metrology institute. Investigate calibration failures and out-of-tolerance results, assess impact on data and product generated since the previous event, and control equipment status including equipment out of service or removed from service. Monitored systems Monitor the plant temperature and relative humidity systems and the USP Purified Water System: review monitoring data, test results and system parameters at the defined frequency, and respond to alarms and excursions. Perform verification of water system pH, conductivity and total organic carbon instrumentation at the defined frequency. Prepare trending and periodic performance reports for each system, including the annual review and trending of environmental monitoring data, and initiate investigation, deviation or corrective action where trends are adverse or results approach specification limits. Quality system, documentation and audits Act as project manager for change controls and CAPAs you initiate or are assigned, driving each to closure: scope and impact, root cause, corrective and preventive actions, coordination across affected departments, and closure with supporting evidence. Maintain the Validation Master Plan, and author and revise SOPs, forms and work instructions within your areas of responsibility, initiating document change requests and change controls as required. Train and verify the competency of laboratory, production and maintenance personnel performing delegated calibration, monitoring and data collection activities, and confirm training is documented before the work is performed independently. Present the validation, calibration, preventive maintenance and equipment programs in internal, customer and regulatory audits, and own the response to observations arising in those areas. Qualifications: What You’ll Bring: Bachelor’s degree in engineering (mechanical, industrial, manufacturing, chemical or biomedical), chemistry, or related physical science discipline. Minimum five years of experience in quality, validation or metrology within a regulated manufacturing environment, including at least two years with direct responsibility for a validation, calibration or preventive maintenance program. Demonstrated experience independently authoring, executing and closing process, equipment and cleaning validation protocols and reports, including the development of statistical sampling plans. Demonstrated experience administering a computerized calibration and maintenance management system, including equipment records, scheduling, work order generation and calibration history. Working knowledge of Health Canada GMP (Food and Drugs Act, Division 2 and GUI-0001) and ISO 13485, and experience preparing for and participating in regulatory and customer audits. Understanding of metrology principles, including measurement traceability to national standards, calibration tolerance determination, and the distinction between calibration and performance verification. Ability to determine the technical approach to validation, qualification and investigation work independently, presenting a proposed methodology and recommendation for approval rather than requesting direction; analyses technical data, draws defensible conclusions, and reports results clearly in writing. Ability to organize and prioritize a concurrent portfolio of commitments with minimal supervision and deliver to agreed dates. Experience acting as CAPA owner and driving corrective actions to closure, and experience training and delegating technical work to laboratory, production or maintenance personnel, are preferred. Technical Skills Hands-on experience with risk assessment tools, including process FMEA, and risk-based decision-making. Understanding of data integrity principles and regulatory requirements for computerized systems, including audit-trail and user access review. Proficiency with Word and Excel, and with project management tools such as MS Project or Smartsheet. Experience with pharmaceutical purified water systems (RO/EDI), including monitoring, sanitization and USP monograph compliance, is an asset (not required). Travel Requirements Minimal. Occasional travel to supplier sites or sister Young Innovations facilities may be required. Compensation Range: $80,000 – 90,000 The pay range reflects the minimum and maximum target for the position at the time of posting. Within the range, the compensation will be determined based on education/training, skill set, experience, and other organizational needs. 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. 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 Engineering Specialist is responsible for managing process validation, equipment control, and preventive maintenance programs to ensure compliance with Health Canada GMP and ISO 13485 standards. The role involves leading risk assessments, executing validation protocols, and coordinating cross-functional activities across production, maintenance, and quality departments.

Requirements

Candidates must hold a bachelor's degree in engineering or a related physical science and possess at least five years of experience in quality, validation, or metrology within a regulated manufacturing environment. Strong knowledge of GMP, ISO 13485, and experience with computerized calibration management systems are essential.

Skills

Process validation
Equipment qualification
Preventive maintenance
Calibration
GMP compliance
ISO 13485
Risk assessment
Statistical sampling
CAPA management
Change control
Metrology
Data integrity
Regulatory compliance
Technical writing
Project management
Quality assurance

Benefits

Health insurance
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

Not detected in the job text

Keywords

Quality Engineering
Process Validation
Equipment Qualification
IQ/OQ/PQ
GMP
ISO 13485
Health Canada
Metrology
Preventive Maintenance
Calibration
CAPA
Change Control
Risk Assessment
FMEA
Data Integrity
USP Purified Water System
Statistical Sampling
Validation Master Plan
SOP
Regulatory Affairs
Manufacturing
Pharmaceutical
Medical Device
Quality Management
Technical Documentation

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