Jobs in Saint-Amable, QC and nearby

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

19,972 listings · 3,035 employers Counted Oct 26, 2026. How we count

About these jobs

Employers hiring include RI-MUHC | Research Institute of the MUHC | #rimuhc (666 listings), Loblaw Companies Limited (590 listings), Desjardins (386 listings).

Common roles: Project manager, Software developer, Sales representative.

1,397 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	30.00	648
CAD / year	80,000.00	637
USD / year	96,750.00	46
USD / hour	60.00	45

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, 36% hybrid, 64% 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-Amable, QC and nearby

Within 25 km

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Added 5 days ago
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Montreal, QC
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Montreal, QC
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Montreal, QC
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Montreal, QC
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Montreal, QC
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Montreal, QC
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Montreal, QC
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Added 5 days ago
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Montreal, QC
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Montreal, QC
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Added 5 days ago
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Montreal, QC
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A
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Added 5 days ago
A
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Montreal, QC
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Added 5 days ago
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Montreal, QC
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Added 5 days ago
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Montreal, QC
- Full-time
Added 5 days ago
CP
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Montreal, QC
- Full-time
Added 5 days ago
Practice Director, Product Experience Management (PXM)
Valtech
Montreal, QC
Added 5 days ago
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Marketing Director
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Montreal, QC
- Full-time

Replimune

Quality Control Analyst I

Montreal, QC, Canada

Full-time

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Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Oct 31, 2026
Posting language: English
Posted: Oct 1, 2026

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

This role will be responsible for performing the routine QC testing following Standard Operating Procedures (SOPs) and established test methods. They will also perform various laboratory based activities such as reagent preparation, tissue culture, equipment maintenance, sample receipt and disposal etc. The role involves getting involved in other tasks such as maintaining sample/reagent/consumable inventory and ordering reagents, updating forms and SOPs and writing as well are reviewing QC documents.

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

Key Responsibilities

The responsibilities of the QC Analyst I include, but are not limited, to the following:

Perform QC testing of various samples according to Standard Operating

Procedures (SOPs).

Maintain various cell lines on regular basis by revival and passaging at set

intervals.

Review testing data and records of other operators and data verification for reports.
Perform QC sample and material receipt and maintain inventory.
Routine equipment maintenance as required.
Write or revise SOPs, protocols, FORMs and update as required.
Participate in QC method transfers, qualification, and stability activities.
Adhere to current Good Manufacturing Practices (cGMP) and Good

Documentation practices (GDP).

General lab tasks such as housekeeping, inventory of supplies, order supplies etc.
Write QC documents and assist with investigations and other documentation as required.
Assist with internal and regulatory agency audits / inspections.

Preferred Educational Requirements

Degree in Chemistry/Biochemistry/ other related science

Skill And Experience Requirements

Competent analytical skills and attention for details.
Understanding of GMP requirements preferred
Computer literacy
Ability to work independently and with others in a team.

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

Perform routine quality control testing and laboratory activities, including cell-line maintenance, sample handling, inventory management, and equipment upkeep. Review testing records, prepare and update QC documentation, support method transfers and stability activities, and assist with investigations and audits.

Requirements

A degree in Chemistry, Biochemistry, or another related science is preferred. Candidates should have analytical skills, attention to detail, computer literacy, and the ability to work independently and collaboratively; familiarity with GMP requirements is preferred.

Skills

Quality Control Testing
Standard Operating Procedures
Cell Culture
Data Review
Data Verification
Sample Receipt
Inventory Management
Equipment Maintenance
SOP Writing and Revision
Method Transfer
Method Qualification
Stability Testing
Good Manufacturing Practices
Good Documentation Practices
Laboratory Housekeeping
Audit Support

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
QC Testing
Standard Operating Procedures
SOPs
Analytical Testing
Cell Culture
Cell-Line Maintenance
Reagent Preparation
Sample Receipt
Inventory Management
Equipment Maintenance
Data Verification
QC Documentation
Method Transfer
Method Qualification
Stability Activities
Good Manufacturing Practices
Good Documentation Practices
Investigations
Internal Audits
Regulatory Inspections
Biotechnology
Oncolytic Immunotherapies
Chemistry
Biochemistry

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