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Added 10 mins ago
NE
Project Manager, Occupational Hygiene
Nichols Environmental + Engineering
AB · Edmonton, AB
- Full-time
Must have ROH or ROHT (Registered Occupational Hygiene Technologist) certification or a CRST (Canadian Registered Safety Technician) certification;
Added 10 mins ago
MT
General Manager
Maxim Truck and Trailer
Brandon, MB
- Full-time
Must hold a valid Driver’s Licence with a clean driving record
Added 10 mins ago
MT
General Manager
Maxim Truck and Trailer
Regina, SK
- Full-time
Must hold a valid Driver’s Licence with a clean driving record
Added 10 mins ago
IW
Vineyard Manager
Iconic Wineries of British Columbia
West Kelowna, BC
- Full-time
The Vineyard Manager is responsible for leading the day-to-day operations of assigned vineyards, ensuring vineyard activities are executed safely, efficiently, and to the highest quality…
Added 10 mins ago
V
ITS Operations & Communications Intern (8-Month Contract)
Vancity
Vancouver, BC
- Full-time
The successful candidate will be expected to attend our office in person approximately 3 days per week
Added 10 mins ago
V
Strategic Insights Analyst
Vancity
Vancouver, BC
- Full-time
This is a Full-time, Permanent role based at our Vancity head office and will report directly to the Manager, Enterprise Intelligence. While this position provides a hybrid work…
Added 10 mins ago
MR
Business Development Manager
Maple Reinders
Remote, Canada
- $120,000 to $160,000 CAD / year
- Full-time
- Remote
Maple Reinders Constructors is seeking an experienced Business Development Manager to join our Buildings team, based in our Burnaby, British Columbia office.
Added 10 mins ago
Vision Rehabilitation Assistant
Vision Loss Rehabilitation Canada
New Westminster, BC
Post-secondary education and/or prior experience in a Rehabilitation Assistant program, Occupational or Physical Therapy Assistant program, Social Work or related field preferred.
Added 10 mins ago
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Vision Loss Rehabilitation Canada
Abbotsford, BC
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Added 10 mins ago
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(CAN) Technician - HVAC/R
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- Full-time
…issues, and coordinating necessary maintenance or repairs under manager and training technician supervision. Uses heavy…
Added 10 mins ago
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(CAN) Technician - HVAC/R
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Lloydminster, AB
- Full-time
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(CAN) Technician - HVAC/R
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Weyburn, SK
- Full-time
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(CAN) Technician - HVAC/R
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(CAN) Technician - HVAC/R
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(CAN) Technician - HVAC/R
Walmart
Thunder Bay, ON
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Sudbury, ON
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Added 10 mins ago
A
QC Reviewer, Flow Cytometry
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Laval, QC
- Full-time
Escalate quality issues or trends to the line manager and participate in their resolution
Added 10 mins ago
IG
Aircraft Deicer
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St. John's, NL · ITC St. John's
- Full-time
Must have ability to lift, push, and pull objects up to 20 pounds regularly; occasionally up to 50 pounds
Added 10 mins ago
VC
Fund Development Officer - Full-time
VON Canada
Halifax, NS
- $27.68 to $29.41 CAD / hour
- Full-time
Must have access to a personal vehicle for work and possess both a current driver’s license and proof of vehicle insurance
Added 10 mins ago
C
Resident Guest Attendant Part time(8:30am-12:30pm) Permanent
Chartwell
Cambridge, ON
- Part-time
Respond to resident and family concerns and report to the Health and Wellness Manager when needed
Added 24 mins ago
IP
Supervisor
Indigo Park Canada
Ottawa, ON
- Full-time
Take certain disciplinary measures with field staff (with involvement by the Area Manager)
Added 24 mins ago
VL
Vision Rehabilitation Assistant
Vision Loss Rehabilitation Canada
New Westminster, BC
- Full-time
Post-secondary education and/or prior experience in a Rehabilitation Assistant program, Occupational or Physical Therapy Assistant program, Social Work or related field preferred
Added 24 mins ago
VL
Vision Rehabilitation Assistant
Vision Loss Rehabilitation Canada
Abbotsford, BC
- Full-time
Post-secondary education and/or prior experience in a Rehabilitation Assistant program, Occupational or Physical Therapy Assistant program, Social Work or related field preferred

Thermo Fisher Scientific

Site Quality Head

Mississauga, ON, Canada

Full-time

Apply on thermofisher.wd5.myworkdayjobs.com About employer

Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English
Posted: Nov 13, 2026

Original job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Join our team as Quality Director and make a meaningful impact on health and safety. In this leadership role, you'll guide quality assurance strategy and develop a culture of excellence across our manufacturing sites. Working at the intersection of innovation and compliance, you'll lead quality initiatives that ensure our products meet the highest standards while enabling scientific discoveries. You'll oversee all QA activities, maintain regulatory compliance, and work collaboratively to improve business outcomes. This position offers the opportunity to build and implement quality systems that support our mission of enabling customers to make the world healthier, cleaner, and safer.

Lead and own the quality strategy, regulatory compliance, and Pharmaceutical Quality System execution for an Oral Solid Dose CDMO manufacturing facility. This role ensures consistent delivery of high quality products including tablets, capsules, granules, and soft gel formulations.

The Site Quality Head serves as the independent Quality authority on the Site Leadership Team and holds ultimate responsibility for ensuring that all products manufactured, tested, and released from the site meet global regulatory requirements and Thermo Fisher Scientific quality standards.

REQUIREMENTS:

•Bachelor’s or advanced degree in Life Sciences, Engineering, Pharmaceutical Sciences, or related field.

12 to 15 years of pharmaceutical manufacturing experience including significant leadership roles in quality.

Strong knowledge of OSD manufacturing processes, cGMP requirements, and regulatory expectations.

ASQ Quality Manager Certification preferred
ASQ Lead Auditor Certification preferred
5+ years proven experience as a site quality lead
Demonstrated expertise in FDA CFR 820, ISO 13485/9001, MDR, and risk management (ISO 14971)
Strong experience managing CAPA systems and quality improvement initiatives
Proficiency in quality tools including FMEA, SPC, and risk management methodologies
Experience with problem-solving techniques such as PPI, 8D, DMAIC, and PPS
Experience leading and developing large quality teams (8-10 direct reports, 100+ indirect)
Experience working with external regulatory authorities and managing inspections
Ability to build cross-functional partnerships and collaborate at all organizational levels
Proficiency in strategic planning and execution of quality initiatives
Success in transitioning organizations from quality control to quality assurance
Experience with Lean or Six Sigma improvement systems preferred
Excellent communication and presentation skills
Change management and organizational development capabilities
Ability to travel 25-30% of time
Electromechanical manufacturing experience preferred

Compensation

The estimated annualized pay range for this position in Ontario is $160,000.00–$200,350.00.

Apply on thermofisher.wd5.myworkdayjobs.com About employer

More about this job

Responsibilities

Lead the quality strategy, regulatory compliance, and Pharmaceutical Quality System execution for an Oral Solid Dose CDMO manufacturing facility. Serve as the independent Quality authority on the Site Leadership Team to ensure all products meet global regulatory requirements and company standards.

Requirements

Requires a Bachelor’s or advanced degree in Life Sciences, Engineering, or Pharmaceutical Sciences with 12 to 15 years of pharmaceutical manufacturing experience. Candidates must possess significant leadership experience in quality, strong knowledge of cGMP, and expertise in regulatory standards like FDA CFR 820 and ISO 13485.

Skills

Quality Assurance
Regulatory Compliance
cGMP
Oral Solid Dose Manufacturing
Strategic Planning
Risk Management
CAPA
FMEA
SPC
Problem-solving
Change Management
Leadership
Pharmaceutical Quality System
FDA CFR 820
ISO 13485
ISO 14971

Visa sponsorship

Not detected in the job text

Keywords

Quality Director
Site Quality Head
Pharmaceutical Manufacturing
Oral Solid Dose
CDMO
cGMP
Regulatory Compliance
Quality Assurance
Quality Control
FDA CFR 820
ISO 13485
ISO 9001
ISO 14971
CAPA
FMEA
SPC
PPI
8D
DMAIC
PPS
Lean
Six Sigma
Risk Management
Change Management
Life Sciences
Engineering
Pharmaceutical Sciences
ASQ Quality Manager
ASQ Lead Auditor
MDR

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Jobs in Canada