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Added 2 mins ago
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Staff Product Manager, Professional Experience
ecobee
Toronto, ON
- Full-time
In 2021, ecobee became a subsidiary of Generac Power Systems. Generac introduced the first affordable backup generator and later created the category of automatic home standby generator.…
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…formal people-management activities remain with the accountable…
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Added 32 mins ago
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Senior IT Audit Manager
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Added 32 mins ago
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SENIOR ADVISOR, PROCUREMENT
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Operations Supervisor - Weekend Shift
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Added 32 mins ago
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Staff Product Manager, Professional Experience
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In 2021, ecobee became a subsidiary of Generac Power Systems. Generac introduced the first affordable backup generator and later created the category of automatic home standby generator.…
Added 32 mins ago
Senior Accountant, Foundation Stewardship & Reporting
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Added 32 mins ago
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Added 32 mins ago
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Project Manager - Finance
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Added 32 mins ago
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Meat Assistant Department Manager - Full Time
Longo's
Mississauga, ON
- Full-time
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Added 32 mins ago
EC
AV Specialist
Emily Carr University of Art and Design
Vancouver, BC
- $38.22 to $40.9 CAD / hour
- Temporary
…procedures, and other communications Oversees the University’s AV systems and equipment planning, operations and maintenance, including conference equipment, lecture capture equipment,…

Danaher Corporation

Quality Systems Specialist

Concord, ON, Canada
CAN - Concord - AB Sciex LP, Canada

The annual salary range for this role is $85,167 - $93,000. · Full-time

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Job details

Pay: The annual salary range for this role is $85,167 - $93,000.
Job type: Full-time
Posting language: English
Posted: Oct 27, 2026

Original job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At SCIEX, one of Danaher’s 15+ operating companies, our work saves lives - and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

As part of SCIEX, you will help to influence life changing research and outcomes, while accelerating your potential. For more than 50 years, we have been empowering our customers to solve the most impactful analytical challenges in quantitation and characterization through ground-breaking innovation and outstanding reliability and support. You will be part of a winning team, enabled by DBS, that is passionate about helping life science experts around the world get to answers they can trust.

Learn about the Danaher Business System which makes everything possible.

The Quality Systems Specialist supports the maintenance and continuous improvement of the SCIEX Quality Management System in accordance with ISO 9001, ISO 13485, FDA Quality Management System Regulation, and other applicable requirements. This role supports audits, CAPA, document control, training, eQMS administration, quality metrics, and continuous improvement. The position works cross-functionally to strengthen compliance, process effectiveness, and inspection readiness.

This position reports to the Senior Manager, QMS, and is part of the Quality Assurance & Regulatory Affairs Team located in Concord, Ontario and will be an on-site role.

In this role, you will have the opportunity to:

· Support the maintenance and improvement of QMS processes in accordance with applicable regulatory and internal requirements, including supporting internal and external audit planning, readiness, execution, responses, and action-item closure.

· Administer eQMS activities, including document changes, controlled records, training assignments, reporting, revising QMS procedures, work instructions, forms, and training materials.

· Guide audit NC owners and CAPA owners through investigations, action planning, implementation, documentation, and effectiveness verification.

· Monitor quality metrics, analyze trends, maintain dashboards, identify improvement opportunities and escalate significant compliance risks to QMS leadership.

· Support non-product software validation and cross-functional QMS improvement projects.

The essential requirements of the job include:

· Bachelor’s degree in science, engineering, quality assurance, or a related field, or equivalent education and experience.

· Minimum three years of quality assurance or QMS experience in a regulated development or manufacturing environment such as IVDs, clinical or pharmaceuticals.

· Working knowledge of ISO 9001, ISO 13485, and FDA quality-system requirements.

· Experience supporting QMS audits, CAPA, document control, and quality records.

· Experience with eQMS applications, procedure writing, and quality-data reporting.

It would be a plus if you also possess previous experience in:

· Non-product software validation and AI applications.

· Power BI, and data-analysis or statistical tools.

· Internal auditor or lead auditor training.

SCIEX, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

The annual salary range for this role is $85,167 - $93,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and retirement savings plans for eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

We will ensure that individuals with disabilities are provided reasonable accommodation to access our website, and as applicable participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at 1-202-419-7762 or applyassistance@danaher.com to request accommodation.

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More about this job

Responsibilities

The Quality Systems Specialist supports the maintenance and continuous improvement of the Quality Management System in compliance with ISO and FDA regulations. This role manages audit readiness, CAPA processes, document control, and quality metrics to ensure process effectiveness.

Requirements

Candidates must have a bachelor's degree in science, engineering, or a related field and at least three years of quality assurance experience in a regulated environment. Proficiency in ISO 9001, ISO 13485, and FDA quality-system requirements is essential.

Skills

ISO 9001
ISO 13485
FDA Quality Management System Regulation
CAPA
Document control
eQMS administration
Quality metrics
Internal auditing
Process improvement
Compliance
Non-product software validation
Procedure writing
Data analysis
Quality assurance
Regulatory affairs

Benefits

Health care program
Paid time off
Medical insurance
Dental insurance
Vision insurance
Retirement savings plans
Bonus/incentive pay

Visa sponsorship

Not detected in the job text

Keywords

Quality Management System
ISO 9001
ISO 13485
FDA
CAPA
eQMS
Quality Assurance
Regulatory Affairs
Compliance
Audit
Document Control
Process Improvement
Life Sciences
Biotechnology
Diagnostics
Non-product software validation
Power BI
Data Analysis
Statistical tools
Quality metrics
Danaher Business System
DBS
IVD
Pharmaceuticals
Clinical

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