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Added 1 hour ago
TC
Shop Technician
Toyota Canada Inc.
Toronto, ON
- Full-time
Initiates and implements appropriate ‘Kaizen’ efforts which results in work efficiencies relating to cost reductions or avoidance, improved time and process efficiencies
Added 3 hours ago
VN
Lab Technician
Verbio North America
Welland, ON
- $24 to $26 USD / hour
- Full-time
The Lab Technician works as part of a team in a continuous process manufacturing environment and reports to the Lab Supervisor. This position provides daily support in monitoring quality…
Added 3 hours ago
TM
Shop Technician
Toyota Motor Corporation
Kamloops, BC · Toyota Canada Inc - Head Office
- Full-time
Initiates and implements appropriate ‘Kaizen’ efforts which results in work efficiencies relating to cost reductions or avoidance, improved time and process efficiencies
Added 4 hours ago
LC
Associate Product Manager, Enterprise Initiatives
Loblaw Companies Limited
Brampton, ON
- Full-time
Associate Product Manager, Enterprise Initiatives - 12mth Contract
Added 7 hours ago
W
Technicien(ne) en amélioration continue de qualité / Quality Continuous Improvement (QCI) Tech - French
Wonderbrands
Longueuil, QC
- Full-time
Added 8 hours ago
P
Planning Supervisor
PHD
Toronto, ON
- Full-time
Identify operational friction and propose practical fixes; implement approved process updates to improve consistency and throughput.
Added 8 hours ago
PG
Supervisor, Digital
Publicis Groupe Holdings B.V
Toronto, ON
- Full-time
Minimum of Associate Degree in Media; Bachelor’s degree a plus/preferred
Added 9 hours ago
PM
Digital Media Supervisor
Publicis Media
Toronto, ON
- Full-time
Minimum of Associate Degree in Media; Bachelor’s degree a plus/preferred
Added 10 hours ago
W
Technicien(ne) en amélioration continue de qualité / Quality Continuous Improvement (QCI) Tech
Wonderbrands
Longueuil, QC
- Other
Added 10 hours ago
AG
Planning Supervisor
Adelphi Group
Toronto, ON
- Full-time
Identify operational friction and propose practical fixes; implement approved process updates to improve consistency and throughput.
Added 1 day ago
SR
QA/QC Associate
STRIVE Recruitment Inc.
Brantford, ON
- Contract
Our client is seeking a QA/QC Associate to join their Quality Assurance team in Brantford, ON. This is a temporary opportunity suited for someone with previous quality assurance, quality…
Added 3 days ago
S
Associate Product Manager Intern (SOTI XSight) (May 2027 - 12 Months)
SOTI
Mississauga, ON
- $55,000 CAD / year
- Full-time
Job Title: Associate Product Manager Intern (SOTI XSight)
Added 3 days ago
S
Associate Product Manager Intern (SOTI Connect) (May 2027 - 12 Months)
SOTI
Mississauga, ON
- $55,000 CAD / year
- Full-time
Added 3 days ago
A
Quality Assurance Specialist
Agropur
Truro, NS
- Full-time
Collaborate with production teams to resolve non-conformities and drive quality improvement initiatives. Verify CAPA effectiveness and process controls are sufficient.
Added 3 days ago
G
Quality Specialist
Ganotec
Toronto, ON
- Full-time
…structural steel erection, heavy mechanical equipment installation, process piping and electrical / instrumentation and…
Added 3 days ago
G
Quality Specialist
Ganotec
Halifax, NS
- Full-time
…structural steel erection, heavy mechanical equipment installation, process piping and electrical / instrumentation and…
Added 4 days ago
RC
Quality Assurance Specialist - Bilingual (EN/FR)
Rethink Canada
Toronto, ON
- Full-time
First round interview with Kyle Hicks, Associate Director of Digital Production
Added 4 days ago
TERM - Specialist I, QA Validation
Emergent Biosolutions
Winnipeg, MB
Deliver CSV education and awareness, to enhance site level awareness of Data Integrity requirements, and associate accountabilities
Added 4 days ago
W
Quality Continuous Improvement Technician (Night Shift)
Wonderbrands
Mississauga, ON
- Other
QCI Techs also champion product quality improvements by actively participating in Quality Huddles as part of the VQS process, ensuring that detailed product information is available for…
Added 4 days ago
PG
Quality Assurance Associate
Pacer Group
Charlottetown, PE
- $30 to $35 CAD / hour
- Full-time
The Quality Assurance Associate will support and execute activities within Quality Operations, Quality Systems, and Compliance. Key responsibilities include document control, change…
Added 4 days ago
Quality Assurance Technician
Give and Go Prepared Foods
Brampton, ON
…successful candidate will focus on quality of the production process, maintenance of standard processes to prevent adulteration or contamination of product, testing of product attributes…
Added 5 days ago
W
(CAN) Team Leader, Quality Assurance (9 month contract) Nights - Sunday to Wednesday - 5pm-3.30am
Walmart
Mississauga, ON
- Full-time
Responsible for interviewing, hiring, training, development, coaching and performance appraisal process for all team members in area of responsibility.
Added 5 days ago
WC
(CAN) Team Leader, Quality Assurance (9 month contract) Nights - Sunday to Wednesday - 5pm-3.30am
Walmart Canada
Mississauga, ON
- Contract
Responsible for interviewing, hiring, training, development, coaching and performance appraisal process for all team members in area of responsibility.
Added 5 days ago
GD
Associate Director, Field Operations
Globalfaces Direct
Toronto, ON · North York, ON
- $85,000 to $115,000 CAD / year
- Full-time
…logistics, territory tracking, and payroll processing - the Associate Director shifts the department focus toward strategic process automation, workflow optimization, and cross-functional…
Added 5 days ago
AE
Quality Assurance Technician
Agrocrop Exports Ltd.
Bolton, ON
- $24 to $27 CAD / hour
- Full-time
Performs inspections of raw materials, materials in process, and finished products.

Emergent Biosolutions

TERM - Specialist I, QA Validation

Winnipeg, MB, R3T 5Y3, Canada

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Job details

Experience: Minimum 5-7 years related industrial experience in the area of validation.
Posting language: English
Posted: Oct 22, 2026

Original job description

Preparedness today, safer tomorrow.

Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.

Job Summary - TERM

This role is responsible for supporting the validation effort and, where required leading projects to ensure that equipment, facilities, utilities, processes and computer systems utilized in the manufacture of product are validated for intended use.

The role will also be responsible for providing leadership and technical guidance aimed at implementing best practices and improving the overall performance of the validation team and quality processes.

Responsibilities

Review, assess and approve (as applicable) CSV related materials for all local and global Computerized System projects
Apply Global GxP requirements as part of a pragmatic validation strategy for computerized systems
Establish and enhance the relationships between IT, validation, and business units, through collaboration, respectful challenge, and ability to strongly support QA decisions
Continually monitor the effectiveness of the DI/CSV program, and recommend optimization opportunities as identified
Participate, as needed, in audits of DI/computerized systems, both internal and external.
Deliver CSV education and awareness, to enhance site level awareness of Data Integrity requirements, and associate accountabilities
QA owner and SME for Data Integrity Assessments/Computer System Risk Assessments, Data Stream Mapping, Remediation Design, Report Creation.
Participate in investigations and corrective actions of data related incidents and report open DI vulnerabilities to site leadership
Responsible for process related activities including the development of validation strategies, the estimation of validation timelines and resource requirements, the generation and approval of the project validation plans, the development of robust and efficient validation test protocols and reports, for new and existing processes.
Working with the cross functional teams in the development and execution of validation activities associated with new equipment, processes or system upgrades.
Participating in project activities including design of systems and equipment to ensure that they comply with applicable regulations & International Standards.
Providing technical input into all phases of the validation lifecycle, i.e. from design through to the commissioning and qualification execution phase and through to validation maintenance.
Review and approval of documents prepared by the validation team, other departments and contractor organizations as required.
Resolving and assisting in the closure of deviations initiated during validation activities or as related to critical process parameters.
Assisting in the implementation of any existing Validation program to ensure continued compliance to the necessary regulations.

The above statements are intended to describe the general nature of work performed by those in this job. It is not an exhaustive list of all duties, and other duties may be assigned.

Education, Experience & Skills

Requirements

BS Engineering/Chemistry/Microbiology or related field.
Minimum 5-7 years related industrial experience in the area of validation.
Expert knowledge of validation principles and concepts.
Demonstrated ability to manage complex validation projects in a fast paced environment is required.

Skills

Possesses Strong knowledge of CSV/GAMP, 21 CFR Part 11, Annex 11, Project Life Cycle and quality systems, cGMP, GDP and FDA/EMEA guidelines and proven ability to apply guidelines to all aspects of validation activities.
Possesses strong knowledge of engineering and related practices, including governmental regulations – ISPE, EU, 21CFR 210, 211, Part 11.
Experience with Aseptic/Sterile Manufacturing and /or Qualification experience within the pharmaceutical or biopharmaceutical industries is preferred.
Experience with systems such as Controlled Temperature units, Critical Utilities, Facilities, and equipment, preferably used in a GMP environment.
Demonstrates success in technical proficiency, creativity, and collaboration with others and independent thought.
Makes decisions exercising judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Ensure alignment and communication of issues and strategies.
Excellent attention to detail, with an ability to work to very tight schedules.
Excellent communication and organizational skills.
Adaptable and flexible.

There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate.

As part of our team, you'll join talented and inspiring colleagues whose sense of purpose complements your own. We offer highly diverse career opportunities, a supportive culture, competitive salaries, flexible work arrangements and an extensive benefits package. Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy.

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More about this job

Responsibilities

This role supports validation efforts for equipment, facilities, and computer systems to ensure compliance with GxP and regulatory standards. The specialist will lead validation projects, conduct data integrity assessments, and collaborate with cross-functional teams to maintain quality processes.

Requirements

Candidates must hold a Bachelor's degree in Engineering, Chemistry, Microbiology, or a related field. A minimum of 5-7 years of industrial experience in validation, specifically with CSV and GxP guidelines, is required.

Skills

Validation
CSV
GAMP
21 CFR Part 11
Data Integrity
cGMP
Quality Assurance
Risk Assessment
Project Management
Technical Writing
Regulatory Compliance
Aseptic Manufacturing
Qualification
Engineering
Investigation
Documentation

Benefits

Competitive salaries
Flexible work arrangements
Extensive benefits package

Visa sponsorship

Not detected in the job text

Keywords

Validation
CSV
GAMP
21 CFR Part 11
Annex 11
Data Integrity
cGMP
GDP
FDA
EMEA
ISPE
EU
21CFR 210
21CFR 211
Aseptic Manufacturing
Sterile Manufacturing
Qualification
Biopharmaceutical
Controlled Temperature Units
Critical Utilities
Quality Systems
Project Life Cycle
Validation Lifecycle
Commissioning
Deviations
Corrective Actions
Data Stream Mapping
Computer System Risk Assessments
Regulatory Compliance
Engineering

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