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.

16,142 listings · 2,700 employers Counted Sep 24, 2026. How we count

About these jobs

Employers hiring include Loblaw Companies Limited (498 listings), Bombardier (391 listings), Walmart Canada (299 listings).

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

777 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 / year	78,000.00	455
CAD / hour	27.97	231
USD / year	90,000.00	45
USD / hour	24.00	33

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, 34% hybrid, 66% 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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Replimune

Scientist I, Analytical Development

Montreal, QC, Canada

Job type: Full-time
Apply by: Oct 21, 2026
Education: Bachelor’s degree
Experience: 4-5+ years industry experience, preferably in a cGMP Quality environment
Posting language: English
Posted: Sep 21, 2026

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Original job description

Overview

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.

At Replimune, We Live By Our Values

United: We Collaborate for a Common Goal.

Audacious: We Are Bold.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.

Join us, as we reshape the future.

Summary Of Job Description

Scientist I, Analytical Development is responsible for performing routine analytical testing to support AD, Process Development (PD), Research and Quality Control (QC) projects. Scientist I also provides support to development, optimization, qualification, and validation of analytical methods and AD characterization projects.

This position is based in our Milton Park location and typically has a 5-day on-site expectation.

Key Responsibilities

Perform in-house in-process and stability testing (PCR, ELISA, chromatography and cell-based analytical tests) to support Process Development, Analytical Development, Research and Quality Control testing.
Provide support by performing analytical method development and product characterisation projects.
Prepare laboratory chemical reagents and biological assay standards and controls for use in routine testing and development projects.
Support the development of robust analytical test methods that are in compliance with regulatory guidelines.
Execute the qualification and validation of analytical test methods and technology transfer in accordance with ICH and other regulatory guidance’s.
Involved in the daily operations of the Analytical Development group and actively participates in method troubleshooting and data analysis.
Oversee and perform internal periodic maintenance, calibration and verification of laboratory equipment.
Perform general laboratory housekeeping tasks, including maintaining stock levels of laboratory consumables.
Operate in accordance with Good Manufacturing Practice (GMP), company procedures and health and safety practices.

Other Responsibilities

Drafts and reviews analytical reports and standard operating procedures (SOPs)
Perform review of assay sheets, lab books and GMP documentation.
Other duties, as assigned.
Training team members in equipment usage and maintenance.

Educational Requirements

Education will be appropriate to specific job requirements. The following educational

Requirements Are a Minimum

Bachelor’s degree in a relevant biological science is required; MSc or PhD preferred.

Experience And Skill Requirement

4-5+ years industry experience, preferably in a cGMP Quality environment
A self-motivated individual, with good time management and able to work in an organised manner.
An ability to work independently and as part of a small team, with effective communication and an ability to work flexibly to meet varying workloads.
Ability to interface effectively with management and other groups or project teams.
Experience in any of cell culture, ELISA, PCR, chromatography.
Good IT skills in core applications e.g. Microsoft Word, Excel, Outlook and experience in statistical analysis

About Replimune

Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.

We are an Equal Opportunity Employer.

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More about this job

Responsibilities

The Scientist I is responsible for performing routine analytical testing including PCR, ELISA, and chromatography to support process and analytical development. They also contribute to method validation, troubleshooting, and the maintenance of laboratory equipment in compliance with GMP standards.

Requirements

Candidates must hold a Bachelor's degree in a biological science, with an MSc or PhD preferred. A minimum of 4-5 years of industry experience, ideally within a cGMP quality environment, is required.

Skills

Analytical testing
PCR
ELISA
Chromatography
Cell-based analytical tests
Method development
Product characterization
GMP
Data analysis
Troubleshooting
Laboratory maintenance
SOP drafting
Statistical analysis
Quality control
Technology transfer

Visa sponsorship

Not detected in the job text

Keywords

Analytical Development
Process Development
Quality Control
PCR
ELISA
Chromatography
Cell culture
GMP
ICH guidelines
Method validation
Technology transfer
SOP
Statistical analysis
Oncolytic immunotherapies
Biotechnology
Laboratory maintenance
Assay development
Regulatory compliance
Biological science
Data analysis

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