Jobs in Saint-Eustache, QC and nearby

Jobs within 25 km of Saint-Eustache, QC, Canada. Nearby towns and cities are included. Distances are straight-line, not driving distances.

24,903 listings · 3,736 employers Counted Oct 25, 2026. How we count

About these jobs

Employers hiring include Loblaw Companies Limited (770 listings), RI-MUHC | Research Institute of the MUHC | #rimuhc (618 listings), Bombardier (597 listings).

Common roles: Project manager, Retail sales associate, Software developer.

1,846 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / hour	25.19	980
CAD / year	80,000.00	744
USD / hour	55.00	53
USD / year	100,000.00	43

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 0% remote, 33% hybrid, 67% on-site, 0% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Jobs in Saint-Eustache, QC and nearby

Within 25 km

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Added 2 days ago
GD
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A
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Added 2 days ago
M
Localization Services Specialist
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Montreal, QC
- Full-time
Added 2 days ago
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Program Adoption Advisor
Dialogue
Montreal, QC
- $72,400 to $85,975 CAD / year
Added 2 days ago
HP
Software Development Intern, AI-Assisted Development (Winter 2027) / Stagiaire en développement de logiciel, développement assisté par l’IA (Hiver 2027)
Hewlett Packard Enterprise
Montreal, QC
- $17.95 to $31 CAD / hour
- Full-time

Pathogenia Lab

Analytical Data Reviewer-HPLC/GC-Evening Shift

Dorval, QC, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Apr 20, 2027
Posting language: English
Posted: Oct 22, 2026

Original job description

Role Description The Pharmaceutical Laboratory Data Reviewer/Réviseur de données laboratoire pharmaceutique is a full-time, on-site role based at Pathogenia Lab in Dorval, QC. This role is responsible for reviewing, verifying, and approving analytical data generated in the laboratory to ensure accuracy, completeness, and compliance with internal SOPs and regulatory standards.

The person is expected to work in the afternoon shift starting at 2:00 pm.

Responsibilities

Review complete analytical packages: spreadsheets, chromatograms, spectra, laboratory notebooks, raw data, and final reports.
Verify the accuracy of calculations, transcriptions, and units.
Confirm compliance with approved methods, SOPs, specifications, and protocols.
Verify sample traceability and consistency with historical results (trends, OOT/OOS).
Compliance and Data Integrity
Ensure adherence to ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate).
Verify system access, audit trails, and data backups.
Identify anomalies, incidents, deviations, or OOS/OOT results and initiate investigations in accordance with procedures.
Participate in and/or lead Out of specifications Investigations OOS including Client communication
Approve or reject analytical results within the quality system.
Draft or contribute to incident reports, CAPAs, and root cause analyses.
Ensure compliant archiving of analytical records.
Quality Support and Continuous Improvement
Participate in internal audits, external audits, and regulatory inspections.
Contribute to updating SOPs, forms, and work instructions.
Train and mentor analysts on good documentation practices and data integrity.
Participate in periodic reviews of trends and quality indicators.

Qualifications

Strong analytical and data review skills, with the ability to evaluate raw laboratory data, calculations, and reports for accuracy and consistency.
Bachelor of Science degree (or equivalent combination of education and experience such as College with 5-10 years of pharmaceutical QC testing/records review experience) in Chemistry, Biochemistry or related biological science or equivalent in job experience.
Over 2 years of experience working in a pharmaceutical regulated Laboratory environment or Pharmaceutical Company.
Ability to work with electronic systems (eg. LIMS) and other lab equipment to be able to perform audit trail of testing records.
Knowledge of GC, HPLC, UV, IR, ICP-MS/OES and other analytical instrument.
Sound knowledge of Health Canada and FDA regulations.
Quality Assurance /Quality control audit background in pharmaceutical industry is an asset
Extended hours or weekend work may be required from time to time.

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More about this job

Responsibilities

Review, verify, and approve laboratory analytical data packages, calculations, records, and reports for accuracy, traceability, and compliance with approved methods, SOPs, and regulatory standards. Maintain data integrity, investigate anomalies and OOS/OOT results, support audits and quality improvements, and train analysts in documentation practices.

Requirements

Requires a bachelor’s degree in chemistry, biochemistry, or a related biological science, or equivalent education and experience, along with more than two years in a regulated pharmaceutical laboratory or company. Candidates should have strong analytical data review skills, knowledge of laboratory systems and analytical instruments, and familiarity with Health Canada and FDA regulations.

Skills

Analytical Data Review
HPLC
GC
UV Spectroscopy
IR Spectroscopy
ICP-MS/OES
Data Integrity
ALCOA+ Principles
Good Documentation Practices
LIMS
Audit Trail Review
OOS/OOT Investigations
Root Cause Analysis
CAPA
Regulatory Compliance
Quality Auditing

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical Laboratory
Analytical Data Review
HPLC
GC
UV
IR
ICP-MS/OES
LIMS
Chromatograms
Spectra
Raw Data
ALCOA+
Data Integrity
Good Documentation Practices
Audit Trails
SOPs
Regulatory Compliance
Health Canada
FDA Regulations
OOS Investigations
OOT Results
CAPA
Root Cause Analysis
Quality Assurance
Quality Control
Audits
Analytical Methods
Sample Traceability
Trend Analysis
Laboratory Records

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